Profil

Misson Jean-Paul

Département des sciences cliniques

See author's contact details
Main Referenced Co-authors
Dubru, Jean-Marie  (22)
Leroy, Patricia (18)
Caviness, V. S. (13)
Leroy, P. (11)
Verloes, Alain  (11)
Main Referenced Keywords
Child (6); enfant (6); Humans (5); Female (4); Infant (3);
Main Referenced Disciplines
Pediatrics (130)
Neurology (98)
Anatomy (cytology, histology, embryology...) & physiology (19)
Genetics & genetic processes (6)
Oncology (3)

Publications (total 147)

The most downloaded
7184 downloads
Vaessen, S., DARON, A., DUBRU, J.-M., Ebetiuc, I., Leroy, P., & Misson, J.-P. (2012). Aspects neurologiques associés au Syndrome de Down. Tijdschrift van de Belgische Kinderarts, 14 (2), 40-43. https://hdl.handle.net/2268/129552

The most cited

361 citations (Scopus®)

Misson, J.-P., Edwards, M., Yamamoto, M., & Caviness, V. S. (1988). Identification of radial glial cells within the developing murine central nervous system:studies based upon a new immunohistochemical marker. Developmental Brain Research, 44, 95-108. doi:10.1016/0165-3806(88)90121-6 https://hdl.handle.net/2268/63913

Van Kerkhoven, C., mumba, L., Harvengt, J., & Misson, J.-P. (2024). Severe hypotonia and developmental delay due to an EBF3 pathogenic variant: Clinical implications of a molecular defect and narrative review. Belgian Journal of Paediatrics.
Peer reviewed

DELBOS, M., Allington, N., VAESSEN, S., & Misson, J.-P. (November 2019). L'image du mois. Tibia arque chez le nouveau-ne. Revue Médicale de Liège, 74 (3), 117-119.
Peer reviewed

BARREA, C., VAESSEN, S., BULK, S., HARVENGT, J., & Misson, J.-P. (2018). Phenotype-genotype correlation in children with neurofibromatosis type 1. Neuropediatrics. doi:10.1055/s-0037-1620239
Peer Reviewed verified by ORBi

Alkan, S., Stouffs, K., Jansen, A., Misson, J.-P., Verloes, A., & JACQUINET, A. (16 February 2018). Circumferential skin creases and blepharophimosis are features associated with tubulinopathies : a case report and review of literature [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium.

Geurten, C., de Bilderling, G., Nassogne, M.-C., Misson, J.-P., & Verghote, M. (2018). Pseudotumoral cerebellitis with acute hydrocephalus as a manifestation of EBV infection. Revue Neurologique. doi:10.1016/j.neurol.2017.06.015
Peer Reviewed verified by ORBi

LEROY, P., Meyer, F., Vaessen, S., Doummar, D., & Misson, J.-P. (July 2017). Dystonie de type 12 : un diagnostic rare et difficile. Archives de Pédiatrie, 24 (7), 637-639. doi:10.1016/j.arcped.2017.04.010
Peer Reviewed verified by ORBi

Geurten, C., de Bilderling, G., Nassogne, M.-C., Misson, J.-P., & Verghote, M. (2017). Tableau d’hydrocéphalie aigue sur cérébellite pseudotumorale liée à EBV
 [Poster presentation]. 27ème congrès de la Société Française de Neuropédiatrie, 2017.

Barrea, C., Vigouroux, T., Karam, J., Milet, A., vaessen, S., & MISSON, J.-P. (August 2016). Horner syndrome in children: a clinical condition with serious underlying disease. Neuropediatrics, 47 (4), 268-272. doi:10.1055/s-0036-1584085
Peer Reviewed verified by ORBi

VAESEN, F., Thimmesch, M., BORN, J., & MISSON, J.-P. (2016). Une présentation rare de craniosténose associée à un crâne lacunaire. Revue Médicale de Liège, 71 (3), 120-123.
Peer reviewed

LONGTON, J., DRESSE, M.-F., Florkin, B., FORGET, P., Guidi, O., Hoyoux, M., Piette, C., Cajgfinger, N., Dauphin, G., Renard, M., MISSON, J.-P., & Hoyoux, C. (2016). Purpura thrombocytopénique idiopathique...idiopathique, vraiment? Tijdschrift van de Belgische Kinderarts, 18 (1), 112.
Peer reviewed

Barrea, C., Vigouroux, T., Karam, J., Milet, A., Vaessen, S., & MISSON, J.-P. (2016). Horner syndrome in children: a clinical condition with serious underlying disease [Poster presentation]. 44ème Congrès de la Société Belge de Pédiatrie.

LONGTON, J., DRESSE, M.-F., Hoyoux, M., MISSON, J.-P., & Nicolescu, C. R. (2015). Décrochage de la courbe de périmètre crânien et si l’origine n'était pas neurologique. Tijdschrift van de Belgische Kinderarts, 17 (1), 46.
Peer reviewed

DARON, A., DRESSE, M.-F., Hoyoux, C., Tebache, M., MISSON, J.-P., & DEBRAY, F.-G. (2015). Schizencephaly associated with a severe prothrombotic syndrome caused by antithombin III deficiency. Tijdschrift van de Belgische Kinderarts, 17 (1), 109.
Peer reviewed

kaputu-kalal-malu, C., D'Amour Birindabagabo, J., Walker, T. D., Mafuta-Musalu, E., Ntumba-Tshitenge, O., Preux, P.-M., & MISSON, J.-P. (2014). Evaluation of Adherence to a Convulsion management Protocol for Children in Rwanda. Journal of Tropical Pediatrics, 60 (2), 124-128.
Peer Reviewed verified by ORBi

Malu, C. K. K., Kahamba, D. M., Walker, T. D., Mukampunga, C., Musalu, E. M., Kokolomani, J., Mayamba, R. M. K., Wilmshurst, J. M., DUBRU, J.-M., & Misson, J.-P. (2013). Efficacy of Sublingual Lorazepam Versus Intrarectal Diazepam for Prolonged Convulsions in Sub-Saharan Africa. Journal of Child Neurology. doi:10.1177/0883073813493501
Peer Reviewed verified by ORBi

KAPUTU, K. M. C., MAFUTA, M. E., DUBRU, J.-M., LEROY, P., TOMAT, A.-M., & Misson, J.-P. (April 2013). ÉPIDÉMIOLOGIE ET CARACTÉRISTIQUES DES CONVULSIONS FEBRILES DE L'ENFANT. Revue Médicale de Liège, 68 (4), 180-185.
Peer reviewed

Barrea, C., Vaessen, S., Leroy, P., & Misson, J.-P. (2013). Thromboses veineuses cérébrales chez l'enfant. Belgische Kinderarts, 15 (1), 93.
Peer reviewed

Bequet, E., Remont, L., Verdin, V., Demarche, M., Jamblin, P., Gorur, Y., & MISSON, J.-P. (2013). Occlusion intestinale chez l’enfant : à propos de deux cas particuliers [Poster presentation]. 41ème Congrès de la Société Belge de Pédiatri, Anvers, Belgium.

Barrea, C., Vaessen, S., Leroy, P., & MISSON, J.-P. (2013). Thromboses veineuses cérébrales chez l'enfant [Poster presentation]. 41ème Congrès de la Société Belge de Pédiatrie.

Kaputu Kalala Malu, C., MAFUTA MUSALU, E., OKITUNDU LUWA E-ANDJAFONO, D., LUSAMBA MUTEBA, J., MAPATANO MALA ALI, N., KAYEMBE KALULA, MUKENDI KAVULU MAYAMBA, & Misson, J.-P. (September 2012). PROFILS EVOLUTIFS A COURT TERME DES CONVULSIONS ASSOCIEES A LA FIEVRE CHEZ LE NOURRISSON ET LE JEUNE ENFANT EN MILIEU DE SOINS DE SANTE PRIMAIRES A KINSHASA. African Journal of Neurological Sciences, 31 (1), 23–33.

KAPUTU, K. M. C., Mafuta, E., OKITUNDU, L.-A., LUSAMBA, M., MAPATANO, M., KAYEMBE, K., Misson, J.-P., & MUKENDI, K. (June 2012). Convulsions associées à le fièvre et développement psychomoteur en soins de santé primaires à Kinshasa. Annales Africaine de Médecine, 5 (3), 1106-1111.
Peer reviewed

Vaessen, S., DARON, A., DUBRU, J.-M., Ebetiuc, I., Leroy, P., & Misson, J.-P. (2012). Aspects neurologiques associés au Syndrome de Down. Tijdschrift van de Belgische Kinderarts, 14 (2), 40-43.
Peer reviewed

KAPUTU, K. M. C., Mafuta, M. E., okitundu, L. E.-A. D., Lusamba, M. J., Matapano, M. A. N., Kayembe, K. T., Mukendi, K. M. R., & Misson, J.-P. (2012). Profils evolutifs à court terme des convulsions associées à la Fièvre chez le nourisson et le jeune enfant en milieu de soins de santé primaires à kinshasa. African Journal of Neurological Sciences, 31 (1), 23-33.
Peer reviewed

JACQUINET, A., STEVENS, R., DEMONCEAU, N., LEROY, P., MISSON, J.-P., & DEBRAY, F.-G. (March 2011). Type II GM1 gangliosidosis presenting as isolated psychomotor regression [Poster presentation]. Annual Meeting of The Belgian Society of Pediatrics, Bruxelles, Belgium.

Passoglou, V., Tebache, M., Collignon, L., Weerts, E., Misson, J.-P., & Rausin, L. (2011). Diastematomyelia: pre- and postnatal multimodal diagnostic approach. Journal Belge de Radiologie, 94 (6), 333-5. doi:10.5334/jbr-btr.700
Peer reviewed

Bequet, E., Remont, L., Verdin, V., Demarche, M., Jamblin, P., Gorur, Y., & Misson, J.-P. (2011). An unusual cause of distal occlusion [Paper presentation]. Réunion de la Belgian Association of paediatric surgery, Bruxelles, Belgium.

Jacquinet, A., Gerard, M., Gabbett, M. T., Rausin, L., Misson, J.-P., Menten, B., Mortier, G., Van Maldergem, L., Verloes, A., & Debray, F.-G. (2010). Temple-Baraitser syndrome: a rare and possibly unrecognized condition. American Journal of Medical Genetics. Part A, 152A (9), 2322-6. doi:10.1002/ajmg.a.33574
Peer Reviewed verified by ORBi

Gelaes, S., Lefèbvre, P., Maillart, C., Sadzot, A., Misson, J.-P., & Bourguignon, J.-P. (May 2009). Évaluation préliminaire d'un séminaire pilote mixte "médecine/orthophonie", préalable au développement d'un programme interprofessionnel en sciences de la santé. Pédagogie Médicale, 10 (2), 105.
Peer Reviewed verified by ORBi

HARVENGT, J., poskin, J., etienne, I., Misson, J.-P., & guidi, O. (March 2009). Glucose-galactose transporter DEFICIENCY: a diagnosis based on clinical observations [Poster presentation]. société belge de pédiatrie.

Misson, J.-P., & Evrard, P. (2009). Développement normal et pathologique du neocortex cérébral. In M. Poncelet, S. Majerus, ... M. Van der Linden (Eds.), Traité de neuropsychologie de l'enfant (pp. 29-63). Marseille, France: Solal.

Piette, C., Deprez, M., Born, J., Michotte, A., Munaut, C., Closon, M.-T., Rutten, I., DRESSE, M.-F., Forget, P., Schmitz, V., Misson, J.-P., & Hoyoux, C. (2008). Management of diffuse glioma in children: a retrospective study of 27 cases and review of literature. Acta Neurologica Belgica, 108 (2), 35-43.
Peer Reviewed verified by ORBi

Piette, C., Deprez, M., Born, J., Closon, M.-T., Rutten, I., Micho, A., Misson, J.-P., & Hoyoux, C. (2008). Management of Diffuse Gliomas in Children: a retrospective study of 27 cases and review of the literature [Paper presentation]. Journées Belges de Pédiatrie.

Piette, C., Deprez, M., Munaut, C., Misson, J.-P., & Foidart, J.-M. (2008). Interaxctions MIF-glucocorticoïdes dans la croissance des gliomes [Paper presentation]. EDT Médecine Clinique et Expérimentale.

Carvelli, T., Viellevoye, R., & Misson, J.-P. (Eds.). (2008). Urgences Pédiatriques. Liège, Belgium: ULg - Université de Liège.

Fransolet, A.-C., Born, J. D., Misson, J.-P., Dresse, M.-F., Forget, P., Rausin, L., Otto, B., Weerts, E., Rutten, I., Closon, M.-T., Bolle, S., Lebrethon, M.-C., Mouchamps, M., & Hoyoux, C. (April 2007). Prise en charge du médulloblastome de l'enfant. Revue Médicale de Liège, 62 (4), 200-4.
Peer reviewed

Champagne, C., Hoyoux, M., RIGO, V., Schaaps, J.-P., Rigo, J., & Misson, J.-P. (2007). Dandy-Walker. Tijdschrift van de Belgische Kinderarts, 87.
Peer reviewed

Mohring, M.-P., Dadoumont, C., DARON, A., Leroy, P., & Misson, J.-P. (2007). Intoxication au CO: Mouvements athétosiques. Journal de Pédiatrie belge.
Peer reviewed

Leroy, P., Dubru, J.-M., & Misson, J.-P. (2007). Actualites therapeutiques en neuropediatrie. Revue Médicale de Liège, 62 (5-6, May-Jun), 449-450.
Peer reviewed

Peduzzi, M., Defontaine, E., & Misson, J.-P. (April 2006). Epilepsie chez des enfants infirmes moteurs-cérébraux. Revue Médicale de Liège, 61 (4), 237-239.
Peer reviewed

Salmon, C., Gaillez, S., Pieltain, C., Sacre, F., Misson, J.-P., Rocour-Brumioul, D., Bourguignon, J.-P., & LEBRETHON, M.-C. (2006). Le syndrome de Prader Willi: intérêt d'une prise en charge pluridisciplinaire. Revue Médicale de Liège, 61 (7-8, Jul-Aug), 593-599.
Peer reviewed

Liegeois, S., Lerusse, C., Leroy, P., Remacle, J.-M., Fransolet, A.-C., & Misson, J.-P. (2006). Empyème extradural et ostéite de la voûte crânienne associés à des infections ORL et un déficit immunitaire. Revista de Neurologia.
Peer Reviewed verified by ORBi

de Tourtchaninoff, M., & Misson, J.-P. (2006). Migraine specificities during childhood to adulthood: diagnosis and treatment. Acta Neurologica Belgica.
Peer Reviewed verified by ORBi

Leroy, P., DARON, A., Weerts, E., Born, J.-D., & Misson, J.-P. (2005). Encéphalocéle frontoethimoidale: Encéphalite herpétique comme premier signe d'une méningite récurrente. Revista de Neurologia.
Peer Reviewed verified by ORBi

DARON, A., Leroy, P., & Misson, J.-P. (2005). A propos d'un cas d'hémiparésie aigue chez l'enfant. Percentile, 10, 29.
Peer reviewed

Peduzzi, M., Defontaine, E., Leroy, P., Dubru, J.-M., & Misson, J.-P. (2005). Epilepsy in children with cerebral palsy. European Journal of Paediatric Neurology.
Peer Reviewed verified by ORBi

Verloes, A., Raoul, M., Genevieve, D., Sznajer, Y., Demarche, M., Lombet, J., Rigo, V., Misson, J.-P., Collignon, L., Vanwijck, F., & Vanwijck, R. (October 2004). Bony syngnathia, vertebral segmentation defect, coloboma, microcephaly and mental retardation: confirmation of Dobrow syndrome and review of syndromal syngnathias. Clinical Dysmorphology, 13 (4), 205-211. doi:10.1097/00019605-200410000-00002
Peer Reviewed verified by ORBi

POIRRIER, A.-L., Ngosso-Tetanye, I., Mouchamps, M., & MISSON, J.-P. (2004). Spontaneous arachnoid cyst rupture in a previously asymptomatic child : a case report [Poster presentation]. Annual Scientific Meeting of the Belgian Association for Paediatrics, La Ramée, Belgium.

Lagae, L., Ceulemans, B., & Misson, J.-P. (2004). Febrile convulsions: an update. Acta Neurologica Belgica.
Peer Reviewed verified by ORBi

Misson, J.-P., Dubru, J.-M., & Leroy, P. (2004). Développement normal et anormal du cortex cérébral: un up-date. Percentile, 9 (1), 3-6.
Peer reviewed

Poirrier, A.-L., Ngosso-Tetanye, I., Mouchamps, M., & Misson, J.-P. (2004). Spontaneous arachnoid cyst rupture in a previously asymptomatic child: a case report. European Journal of Paediatric Neurology, 8 (5), 247-251. doi:10.1016/j.ejpn.2004.04.005
Peer Reviewed verified by ORBi

Verloes, A., Massin, M., Fransolet, A.-C., & Misson, J.-P. (2004). Hypertrichosis, fallot tetralogy, growth and developmental delay. Clinical Dysmorphology, 13, 247-250. doi:10.1097/00019605-200410000-00009
Peer Reviewed verified by ORBi

POIRRIER, A.-L., Ngosso-Tetanye, I., Mouchamps, M., & MISSON, J.-P. (2004). Spontaneous arachnoid cyst rupture in a previously asymptomatic child : a case report [Paper presentation]. Spring Meeting of the Belgian Neurological Society, Brussels, Belgium.

POIRRIER, A.-L., & MISSON, J.-P. (2004). Atypical myoclonus, deafness, gait and posture disorders : an unusual syndrome [Poster presentation]. International Symposium on Paediatric Movement Disorders, Barcelona, Spain.

Massin, M., Leroy, P., Misson, J.-P., & Lepage, P. (June 2003). La tachycardie ventriculaire catecholergique du jeune enfant: un diagnostic souvent meconnu. Archives de Pédiatrie, 10 (6), 524-526. doi:10.1016/S0929-693X(03)00150-7
Peer Reviewed verified by ORBi

Verloes, A., Misson, J.-P., Gillet, P., Baumann, C., Spiritus, M., & Deprez, M. (2003). Duane anomaly, congenital myopathy and severe scoliosis in sibs: new AR syndrome? Annales de Génétique, 46 (4), 449-52. doi:10.1016/S0003-3995(03)00018-2
Peer Reviewed verified by ORBi

Lemaire, R., al Azba, S., Brumioul, D., & Misson, J.-P. (March 2001). Comment j'explore certains cas difficiles de meningite tuberculeuse. Revue Médicale de Liège, 56 (3), 181-185.
Peer reviewed

Closset, A., Van der Linden, M., & Misson, J.-P. (1999). Les troubles cognitifs consécutifs à un trauma crânien léger chez l'enfant. Percentile, 4, 61-68.

Misson, J.-P., Dubru, J.-M., Leroy, P., Pirard, S., Takahashi, T., & Caviness, V. S. (1999). Neuronal migration disorders and epilepsies. In A. Nehlig & J. Motte (Eds.), Childhood epilepsies and brain development (pp. 55-70). London, United Kingdom: John Libbey.

Symann, S., Rucquoy, M., Misson, J.-P., Gillain, C., Bonnier, C., & van Rijckevorsel, K. (1999). New hope for CSWS/ESES treatment: Topiramate? European Journal of Paediatric Neurology.
Peer Reviewed verified by ORBi

Deprez, M., D'Hooghe, M., Misson, J.-P., De Leval, L., Ceuterick, C., Reznik, M., & Martin, J. J. (1999). Infantile and juvenile presentations of Alexander's disease: a report of two cases. Acta Neurologica Scandinavica, 99 (3), 158-65. doi:10.1111/j.1600-0404.1999.tb07338.x
Peer Reviewed verified by ORBi

Dubru, J.-M., Leroy, P., & Misson, J.-P. (1998). Electroencéphalographie du prématuré et du nouveau-né à terme. Percentile, 3, 42-44.
Peer reviewed

Senterre, T., Leroy, P., & Misson, J.-P. (1998). Tumeurs cérébrales chez l'enfant : Expérience du département universitaire de pédiatrie de Liège. Percentile, 3 (2), 68-70.

Senterre, T., Leroy, P., & Misson, J.-P. (1998). Tumeurs Cérébrales chez l'Enfant : Expérience du Département Universitaire de Pédiatrie de Liège. Percentile, 3 (1), 26-28.
Peer reviewed

Leroy, P., Dubru, J.-M., & Misson, J.-P. (1998). Traumatismes crâniens et épilepsie. Percentile, 3 (1), 29-32.
Peer reviewed

Chanas-Sacré, G., Leprince, P., Lewin, M., Pirard, S., Thiry, M., Rogister, B., Misson, J.-P., & Moonen, G. (1998). The radial glial cell antigen recognized by the RC2 antibody is an intermediate-filament associated protein [Poster presentation]. European Meeting on Glial Cell Function in Health and Disease, Athens, Greece.

Van Coster, Janssens, S., Misson, J.-P., Verloes, A., & Leroy, J. (1998). Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples. Prenatal Diagnosis, 18, 1041-1044. doi:10.1002/(SICI)1097-0223(1998100)18:10<1041::AID-PD407>3.0.CO;2-J
Peer Reviewed verified by ORBi

Senterre, T., & Misson, J.-P. (19 April 1997). Tumeurs cérébrales chez l'enfant : Expérience du département universitaire de pédiatrie de Liège [Paper presentation]. 20 ans de la Société Belge de Neurologie Pédiatrique, Meise, Belgium.

Verloes, A., Lesenfants, S., Misson, J.-P., Galand, A., & Koulischer, L. (10 February 1997). Microcephaly, muscular build, rhizomelia, and cataracts: Description of a possible recessive syndrome and some comments on the use of electronic databases in syndromology. American Journal of Medical Genetics, 68 (4), 455-60, discussion 461. doi:10.1002/(SICI)1096-8628(19970211)68:4<455::AID-AJMG16>3.0.CO;2-R
Peer Reviewed verified by ORBi

Leprince, P., Chanas-Sacre, G., Lewin, M., Pirard, S., Thiry, M., Misson, J.-P., Rogister, B., & Moonen, G. (1997). Labelling of an intermediate-filament-associated protein in cerebellar radial glial cells with the RC2 antibody [Poster presentation]. Symposium of the DFG study group, Berlin, Germany.

Janssens, S., Van Coster, R., Chang, J., Raes, F., Misson, J.-P., & Verloes, A. (1997). Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples. European Journal of Paediatric Neurology, 1, 105.
Peer Reviewed verified by ORBi

Leroy, P., Dubru, J.-M., & Misson, J.-P. (1997). Epilepsies rebelles de l'enfant: définition et modalités de prise en charge hospitalière. Neurone, 2 (8), 285-288.
Peer reviewed

Misson, J.-P., Leroy, P., & Dubru, J.-M. (1996). Les convulsions fébriles: attitude actuelle. Tempo Médical, 9-13.

Leprince, P., Chanas-Sacre, G., Wattiez, R., Lewin, M., Rogister, B., Mazy-Servais, C., Misson, J.-P., & Moonen, G. (1996). Identification of antigens recognized in the developing mouse brain by the RC2 antibody, a marker of radial glia. International Journal of Developmental Neuroscience, 14 (Sup. 1), 84.
Peer Reviewed verified by ORBi

Dubru, J.-M., Leroy, P., & Misson, J.-P. (1996). Caractéristiques des lésions résultant d'une pathologie périnatale. Acta Paediatrica Belgica, 28 (3), 203-204.
Peer Reviewed verified by ORBi

Misson, J.-P., Dubru, J.-M., & Leroy, P. (1996). Reconnaissance des malformations et pathologies prénatales du système nerveux central. Acta Paediatrica Belgica, 28 (3), 204-215.

Leroy, P., Dubru, J.-M., & Misson, J.-P. (1996). Images liées à la pathologie traumatique du système nerveux central. Acta Paediatrica Belgica, 28 (3), 216.

Misson, J.-P., Leroy, P., Dubru, J.-M., & Carlier, G. (1996). La Biologie clinique en pédiatrie: hypotonie et retard moteur. Acta Paediatrica Belgica, 28 (2), 95.

Leprince, P., Chanas-Sacré, G., Lewin, M., Pirard, S., Thiry, M., Rogister, B., Mazy-Servais, C., COUCKE, P., Misson, J.-P., & Moonen, G. (1996). In vitro expression of RC2-labeled antigens as radial glial cells markers in cultures derived from mouse embryonic brain [Poster presentation]. Second European Meeting on Glial Cell Function in Health and Disease, Arcachon, France.

Misson, J.-P., Dubru, J.-M., Leroy, P., & Carlier, G. (1996). Retard neuromoteur et neuropsychologique: critères de recours à une prise en charge spécialisée. Percentile, . (3), 103-107.
Peer reviewed

Verloes, A., Misson, J.-P., Dubru, J. M., Jamblin, P., & Le Merrer, M. (July 1995). Heterogeneity of sponastrime dysplasia: Delineation of a variant form with severe mental retardation. Clinical Dysmorphology, 4 (3), 208-215.
Peer Reviewed verified by ORBi

Misson, J.-P., Born, J., Collignon, L., Otto, B., HANS, P., Leroy, P., & Brucher, J. M. (1995). Lambdoid synostosis - pachycephaly: diagnosis and treatment. Developmental Medicine and Child Neurology. Supplement, 37 (3), 87.
Peer Reviewed verified by ORBi

Misson, J.-P., Dacier, P., Leroy, P., Otto, B., Rodesch, G., Mouchamps, M., & Born, J. (1995). Méningiome volumineux chez l'enfant: discussion à propos d'un cas chez une fillette de 5 ans. In Société Belge de Neurologie Pédiatrique.
Peer reviewed

Hoyoux, C., Dresse, M.-F., Misson, J.-P., Lenelle, J., & Chantraine, J.-M. (1995). Central neuroblastoma in a 14 year-old girl. In 4th International Symposium on Neuroblastoma Screening.
Peer reviewed

Dacier, P., Leroy, P., Ernould, C., Mouchamps, M., Otto, B., Brucher, J.-M., Burette, V., & Misson, J.-P. (1995). Gliomatose méningée cérébro-spinale diffuse chez un enfant traité par hormone de croissance dans le cadre d'un syndrome de Turner. In Société Belge de Neurologie Pédiatrique.
Peer reviewed

Misson, J.-P., Lombet, J., Rigo, J., Verloes, A., Weerts, E., & Van Coster, R. (1995). Caractéristiques neuroradiologiques du déficit en Pyruvate Carboxylase. In Société Européenne de Neurologie Pédiatrique.
Peer reviewed

Leroy, P., Bakri, A., Dubru, J.-M., Ravet, F., & Misson, J.-P. (1994). Effet préventif du Sabril dans un cas présymtomatique de maladie de Bourneville. In Société Belge de Neurologie Pédiatrique.
Peer reviewed

Verloes, A., Misson, J.-P., Dubru, J.-M., Jamblin, P., & Le Merrer, M. (1994). Sponastrime dysplasia with mental retardation: A distinct entity. In 3ème Dysmorphology Meeting.
Peer reviewed

Van Coster, R., Misson, J.-P., Meire, F., & Obermaier-Kusser, B. (1994). Leber-associateddystonia with putamen necrosis. Annals of Neurology.
Peer Reviewed verified by ORBi

Verloes, A., Journel, H., Elmer, C., Misson, J.-P., Le Merrer, M., Kaplan, J., Van Maldergem, L., Deconinck, H., & Meire, F. (15 April 1993). Heterogeneity versus variability in Neuhauser megalocornea-mental retardation (MMR) syndromes: Report of new cases and delineation of 4 probable types. American Journal of Medical Genetics, 46 (2), 132-137. doi:10.1002/ajmg.1320460206
Peer Reviewed verified by ORBi

Grossman, D., Misson, J.-P., Quacoe, M., Otto, B., Mouchamps, M., & Born, J. (1993). Kyste arachnoïdien suprasellaire post méningitique. Revue Neurologique.
Peer Reviewed verified by ORBi

Misson, J.-P., & Collignon, J. (1993). Schizencephaly of the frontal opercula mimicing sylvian arachnoidal cyst. In 3rd biennal Meeting of European Society of Magnetic Resonance in Pediatric Neurology.
Peer reviewed

Misson, J.-P., Reynaers, A., Ernould, C., & Sadzot, B. (1993). Epilepsie frontale et trouble du comportement: diagnostic, exploration et traitement. In 30ème Congrès de l'Association des Pédiatres de Langue Française.
Peer reviewed

Misson, J.-P., Martin, D., Ries, M., & Lenelle, J. (1993). Hydrocéphalie transitoire, spina bifida occulta, hydromélie: Eléments de discussion en faveur d'une pathogénie tensionnelle dans un cas d'Arnold Chiari Type I. Revue Neurologique, 149, 583.
Peer Reviewed verified by ORBi

Misson, J.-P., Leroy, P., Born, J., Damas, F., & Otto, B. (1993). Transient multiple arterial spasms: stenosis in the corse of a cerebral trauma. In 3rd biennal Meeting of European Society of Magnetic Resonance in Pediatric Neurology.
Peer reviewed

Misson, J.-P., Robbe-Dechamps, M., Pauly, F., & Otto, B. (1993). Postnatal ulegyria due to prolonged postoperative status epilepticus. In 3rd biennal Meeting of European Society of Magnetic Resonance in Pediatric Neurology.
Peer reviewed

Leroy, P., Dubru, J.-M., Pierrard, A., & Misson, J.-P. (1993). Sclérodermie en coup de sabre et hémiatrophie faciale de Perry-Romberg: A propos d'un cas. In 30ème Congrès de l'Association des Pédiatres de Langue Française.
Peer reviewed

Leroy, P., Verloes, A., Born, J., Pierrard, A., Otto, B., & Misson, J.-P. (1993). Syndrome oculo-cérébro-cutané de Delleman. In 30ème Congrès de l'Association des Pédiatres de Langue Française.
Peer reviewed

Jamblin, P., Collignon, J., Flandroy, P., Lenelle, J., Misson, J.-P., & Reznik, M. (1993). Neuroblastome primitif du système nerveux central. Revue Neurologique, 149, 592.
Peer Reviewed verified by ORBi

Gressens, P., Gofflot, F., Van Maele-Fabry, G., Misson, J.-P., Gadisseux, J.-F., Evrard, P., & Picard, J. (March 1992). Early neurogenesis and teratogenesis in whole mouse embryo cultures. Histochemical, immunocytological and ultrastructural study of the premigratory neuronal-glial units in normal mouse embryo and in mouse embryos influenced by cocaine and retinoic acid. Journal of Neuropathology and Experimental Neurology, 51 (2), 206-219. doi:10.1097/00005072-199203000-00010
Peer Reviewed verified by ORBi

Gadisseux, J.-F., Evrard, P., Misson, J.-P., & Caviness, V. S. (1992). Dynamic changes in the density of radial glial fibres of the developing murine cerebral wall: A quantitative immunohistochemical analysis. Journal of Comparative Neurology, 321, 1-9. doi:10.1002/cne.903220210
Peer Reviewed verified by ORBi

Misson, J.-P. (1991). The alignment of migrating neural cells in relation to the murine neopallial radial glial fiber system. Cerebral Cortex, 1, 221-229. doi:10.1093/cercor/1.3.221
Peer Reviewed verified by ORBi

Mascart, F., Pieltain, C., Andoura, B., Philippet, P., Misson, J.-P., & Bourguignon, J.-P. (1991). L'insuffisance surrénale isolée: Une cause inhabituelle d'hypoglycémie du nourrisson. In Journées annuelles de la Société Belge de Pédiatrie.

Misson, J.-P., & Verloes, A. (1991). Familial neuronal heterotopias as cerebral palsy. An inherited disorder of brain histogenesis. In European Society of Human Genetics.
Peer reviewed

Misson, J.-P., Takahashi, T., & Caviness, V. S. (1991). Ontogeny of radial and other astroglial cells in murine cerebral cortex. Glia, 4, 138-148. doi:10.1002/glia.440040205
Peer Reviewed verified by ORBi

Misson, J.-P. (1991). Identification, organization and function of the radial glial cells during mouse neocortex development [Post doctoral thesis, ULiège - Université de Liège]. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/64031

Malfilatre, G., Merken, A., Dubru, J.-M., & Misson, J.-P. (1991). Apport de la résonance magnétique nucléaire dans la mise au point des troubles d'apprentissage scolaires. In Journées annuelles de la Société Belge de Pédiatrie.

Franckart, G., Fakif, K., Trippaerts, M., Foidart-Dessalle, M., & Misson, J.-P. (1990). Paralysie vélo-palatine et oculomotrice d'apparition brutale : une forme particulière de polyradiculonévrite. In Comptes Rendus des Journées Annuelles de la Société Belge de Pédiatrie (pp. 133).

Misson, J.-P., Dubru, J.-M., Gilson, V., & Desprechins, B. (1990). Aspects de pachygyrie dans un cas de troubles d'apprentissage. In Comptes Rendus de la Société Européenne de Neurologie Infantile (pp. 121).

Misson, J.-P., Austin, C., Takahashi, T., Cepko, C., & Caviness, V. S. (1990). Neuronal migration in the murine cerebrum proceeds in parallel to raidial fibers : Analysis based upon double labeling of migrating neurons and radial fibers. In Comptes Rendu des Journées Annuelles de la Société Belge de Pédiatrie (pp. 162).

Crandall, J. E., Butler, D., & Misson, J.-P. (1990). The development of radial glia and radial dendrites during barrel formation in mouse somatosensory cortex. Developmental Brain Research, 55, 87-94. doi:10.1016/0165-3806(90)90108-B
Peer Reviewed verified by ORBi

Takahashi, T., Misson, J.-P., & Caviness, V. S. (1990). Glial process elongation and branching in the developing murine neocortex: A qualitative and quantitative immunohistochemical analysis. Journal of Comparative Neurology, 302, 15-28. doi:10.1002/cne.903020103
Peer Reviewed verified by ORBi

Lyon, G., Arita, F., Le Galloudec, E., Vallée, L., Misson, J.-P., & Ferriere, G. (1990). A disorder of axonal development, necrotizing myopathy, cardiomyopathy and cataracts: A new familial disorder. Annals of Neurology, 27, 193-199. doi:10.1002/ana.410270216
Peer Reviewed verified by ORBi

Misson, J.-P., Takahashi, T., Austin, C., Gadisseux, J.-F., Evrard, P., & Caviness, V. S. (1990). Histogenèse du cortex cérébral et migration neuronale. Acta Paediatrica Belgica, 22, 13-20.
Peer Reviewed verified by ORBi

Mason, C. A., Misson, J.-P., Blazeski, R., & Godement, P. (1990). Retinal axon navigation in the mouse optic chiasm: Middle cues and cell-cell relations. Neuroscience, 1125.
Peer Reviewed verified by ORBi

Caviness, V. S., Misson, J.-P., Takahashi, T., & Gadisseux, J.-F. (1989). Ontogeny of the radial glial fiber system of the developing murine cerebrum. In B. L. Finlay & G. Innocenti (Eds.), The neocortex: Ontogeny and Phylogeny. New York, United States: Plenum.

Misson, J.-P., Austin, C., Takahashi, T., Cepko, C., & Caviness, V. S. (1989). Migrating neurons of the murine cerebrum ascend in parallel to radial fibers: analysis based upon double-labeling of migrating neurons and radial fibers. Neuroscience.
Peer Reviewed verified by ORBi

Crandall, J. E., Butler, D., Caviness, V. S., & Misson, J.-P. (1989). Patterns of the radial dendrites and radial glia in the barrel cortex after whisker removal in neonatal mice. Neuroscience.
Peer Reviewed verified by ORBi

Caviness, V. S., Misson, J.-P., Takahashi, T., & Crandall, J. (1989). Astroglial transformations in the developing murine cerebral wall. Neuroscience.
Peer Reviewed verified by ORBi

Caviness, Misson, J.-P., & Gadisseux, J.-F. (1989). Abnormal neuronal patterns and disorders of neocortical development. In A. M. Galaburda (Ed.), From Reading to neurons (pp. 405-442). Cambridge, MA, United States: MIT Press.

Gadisseux, J.-F., Evrard, P., Misson, J.-P., & Caviness, V. S. (1989). dynamic structure of the radial glial fiber system of the developing murine cerebral wall.an immunocytochemical analysis. Developmental Brain Research, 50, 55-67. doi:10.1016/0165-3806(89)90126-0
Peer Reviewed verified by ORBi

Takahashi, T., Misson, J.-P., & Caviness, V. S. (1989). Developmental evolution in the distribution of radial glial fiber growth cones in the murine cerebral wall. Neuroscience.
Peer Reviewed verified by ORBi

Gadisseux, J.-F., Evrard, P., Misson, J.-P., & Caviness, V. S. (1988). Glial organization in the developing reeler neocortex. Neuroscience, 93.
Peer Reviewed verified by ORBi

Crandall, J.-F., Butler, D., & Misson, J.-P. (1988). Development of the barrel pattern in early postnatal mouse somato sensory cortex as revealed by the distribution of MAP-2 immunoreactive dendrites and RC2-labeled radial glia. Neuroscience, 476.
Peer Reviewed verified by ORBi

Misson, J.-P., Evrard, P., Gadisseux, J.-F., & Caviness, V. S. (1988). Identification of radial glial growth cones. Neuroscience, 748.
Peer Reviewed verified by ORBi

Misson, J.-P., Edwards, M., Yamamoto, M., & Caviness, V. S. (1988). Identification of radial glial cells within the developing murine central nervous system:studies based upon a new immunohistochemical marker. Developmental Brain Research, 44, 95-108. doi:10.1016/0165-3806(88)90121-6
Peer Reviewed verified by ORBi

Misson, J.-P., Yamamoto, M., Edwards, M. A., Scwarting, G., & Caviness, V. S. (1988). Identification of radial glial cells within the developing murine central nervous system using a new immunohistochemical marker. Neuroscience, 1345.
Peer Reviewed verified by ORBi

Misson, J.-P., Edwards, M., Yamamoto, M., & Caviness, V. S. (1988). mitotic cycling of radial glial cells of the fetal murine cerebral wall: a combined autoradiographic and immunohistochemical study. Developmental Brain Research, 38, 183-190. doi:10.1016/0165-3806(88)90043-0
Peer Reviewed verified by ORBi

Gadisseux, J.-F., Evrard, P., Misson, J.-P., & Caviness, V. S. (1987). Fascicular organization of the radial glial fibers in developing murine neocortex: An immunohistochemical study combined with 3H thymidine autoradiography. Neuroscience Research. Supplement, 1117.
Peer Reviewed verified by ORBi

Vamecq, J., Draye, J. P., Van Hoof, F., Misson, J.-P., Evrard, P., Verellen, G., Van Eldere, J., Eyssen, H., Schutgens, R. B. H., Wanders, R. J. A., Roels, F., & Gloldfischer, S. L. (1986). Multiple peroxysomal deficiency syndromes: a comparative and multidisciplinary study in Zellweger and Neonatal Adrenoleukodystrophy patients. American Journal of Pathology, 125, 524-535.
Peer Reviewed verified by ORBi

Misson, J.-P., & Geubelle, F. (1986). Les méningites bactérienne de l'enfant: diagnostic, traitement et pronostic. Revue Médicale de Liège, 41 (19), 713-733.
Peer reviewed

Misson, J.-P., Edwards, M. A., Yamamoto, M., & Caviness, V. S. (1986). Origin of radial glial cells in cerebral mouse cortex: A study using combined immunohistochemical and 3H thymidine labeling. Neuroscience Research. Supplement, 1585.
Peer Reviewed verified by ORBi

Misson, J.-P., Evrard, P., Verellen, G., Van Eldere, J., Eyssen, H., Schutgens, R. B. H., Van Hoof, F., & Vamecq, J. (1985). Multidisciplinary approach in two patients with multiple peroxysomal function deficiency. In Peroxisomes and their metabolites in cellular functions.
Peer reviewed

Massart, B., Misson, J.-P., Henrivaux, P., & Bonnivert, J. (15 May 1985). A propos d'un cas de déficience immunitaire chez un enfant zairois: SIDA ? Revue Médicale de Liège, 40 (10), 433-438.
Peer reviewed

Misson, J.-P., Tshmanga, B., Alexander, M., & Evrard, P. (1985). Encéphalite nécrosante temporale et calcifiante du nourrisson: Une forme de transition. In Progress en neurologie pédiatrique (pp. 87).
Peer reviewed

Misson, J.-P., Evrard, P., Verellen, G., Claus, D., Van Eldere, J., Eyssen, H., Schutgens, R. B. H., Van Hoof, F., & VAMECQ, J. (1985). Aspects cliniques de maladies peroxysiomales. In Comptes Rendus de la Société Belge de Neurologie Infantile.

Misson, J.-P., Baleriaux, D., & Evrard, P. (1985). Intérêt de la résonance magnétique nucléaire dans le diagnostic des tumeurs du tronc cérébral chez l'enfant. In Comptes Rendus de la Société Belge de Neurologie Infantile.

Misson, J.-P., Evrard, P., Verellen, G., Claus, D., Van Eldere, J., Eyssen, H., Schutgens, R. B. H., Van Hoof, F., & Vamecq, J. (1985). Aspects cliniques des maladies peroxisomales [Paper presentation]. Comptes Rendus de la Societé Belge de Neurologie Infantile.

Misson, J.-P., Evrard, P., Verellen, G., Claus, D., Guerit, J.-M., Van Eldere, J., Eyssen, H., Schutgens, R. B. H., Van Hoof, F., & Vamecq, J. (1985). Maladie de Zellweger et adrenoleukodystrophie néonatale: une même maladie ou deux affections distinctes? In Progress en neurologie pédiatrique (pp. 233).
Peer reviewed

Misson, J.-P., Motte, J., Ghislain-Capentier, T., & Lyon, G. (1985). Hématomes cérébraux spontanés et malformations vasculaires cryptique de l'enfant. Comptes rendus de la Société Belge de Neurologie Infantile.

Legrand, B., & Misson, J.-P. (1985). La myosite orbitaire chez l'enfant; Diagnostic et traitement. In Comptes Rendus de la Société Belge de Neurologie Infantile.

Evrard, P., Misson, J.-P., & belpaire, M.-C. (April 1984). Diagnostic antenatal des affections du stystème nerveux central: résultats préliminaires d'une série multicentrique européenne de 350 cas. Journal Français d'Echographie, 2 (4), 123-123.
Peer reviewed

Lyon, G., & Misson, J.-P. (1984). Les vessies neurologiques de l'enfant : rôle du neuropédiatre dans l'approche diagnostique. In Comptes Rendus de la Société Belge d'Urologie.

Misson, J.-P., & Evrard, P. (1984). Neurological aspects of developmental oro-linguo-facial disorders [Paper presentation]. Société Allemande d'Orthodontie, Bruxelles, Belgium.

Misson, J.-P. (01 December 1983). Les convulsions fébriles de l'enfant: leur pronostic et leur traitement. Revue Médicale de Liège, 38 (23), 879-884.
Peer reviewed

CARLIER, G., Misson, J.-P., & Dubru, J.-M. (1983). Epilepsie a paroxysmes rolandiques de l'enfant. In Comptes Rendus de la Société Belge de Neurologie Infantile.

Misson, J.-P., Mossay, C., Francotte, N., & Davin, J.-C. (1983). Insuffisance hépatique et rénale secondaire à une intoxication au trichloréthylène. Acta Paediatrica Belgica.

Mossay, C., Misson, J.-P., Born, J., & HANS, P. (1983). Le syndrome de Reye : Revue de la littérature à propos d'un cas traité par plasmaphérèse et surveillé par monitorage de la pression intracrânienne. Acta Pédiatrica.

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