  | 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 verified by ORBi |
 | 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 |
 | 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 |
 | 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 |
 | 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. |
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. |
 | 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 |
 | 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. |
Carvelli, T., Viellevoye, R., & Misson, J.-P. (Eds.). (2008). Urgences Pédiatriques. Liège, Belgium: ULg - Université de Liège. |
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. |
 | 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 |
 | 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 |
 | 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 |
 | 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 |
 | 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 |
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. |
 | 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 |
 | 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., & 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. |
 | 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 |
 | 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 |
 | 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. |
 | Leroy, P., Dubru, J.-M., & Misson, J.-P. (1998). Traumatismes crâniens et épilepsie. Percentile, 3 (1), 29-32. 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 (1), 26-28. Peer reviewed |
 | 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 |
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. |
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. |
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. |
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 |
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 |
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., 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 |
 | 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 |
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 |
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 |
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 |
 | 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., 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 |
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. (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 |
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. (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 |
 | 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 |
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 |
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 |
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. |
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., 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). 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., 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. |
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. |
Misson, J.-P., Mossay, C., Francotte, N., & Davin, J.-C. (1983). Insuffisance hépatique et rénale secondaire à une intoxication au trichloréthylène. Acta Paediatrica Belgica. |