  | Burglen, L., Van Hoeymissen, E., Qebibo, L., Barth, M., Belnap, N., Boschann, F., Depienne, C., De Clercq, K., Douglas, A. G. L., Fitzgerald, M. P., Foulds, N., Garel, C., Helbig, I., Held, K., Horn, D., Janssen, A., Kaindl, A. M., Narayanan, V., Prager, C., ... Vriens, J. (17 January 2023). Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders. eLife, 12. doi:10.7554/eLife.81032  Peer Reviewed verified by ORBi |
 | Ramaekers, V., & Quadros, E. V. (28 July 2022). Cerebral Folate Deficiency Syndrome: Early Diagnosis, Intervention and Treatment Strategies. Nutrients, 14 (15), 3096. doi:10.3390/nu14153096 Peer Reviewed verified by ORBi |
 | Bobrowski-Khoury, N., Ramaekers, V., Sequeira, J. M., & Quadros, E. V. (24 July 2021). Folate Receptor Alpha Autoantibodies in Autism Spectrum Disorders: Diagnosis, Treatment and Prevention. Journal of Personalized Medicine, 11 (8), 710. doi:10.3390/jpm11080710 Peer Reviewed verified by ORBi |
  | Besnard, T., Sloboda, N., Goldenberg, A., Küry, S., Cogné, B., Breheret, F., Trochu, E., Conrad, S., Vincent, M., Deb, W., Balguerie, X., Barbarot, S., Baujat, G., Ben-Omran, T., Bursztejn, A.-C., Carmignac, V., Datta, A. N., Delignières, A., Faivre, L., ... Isidor, B. (2019). Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome. Genetics in Medicine, 21 (9), 2025-2035. doi:10.1038/s41436-019-0445-x Peer Reviewed verified by ORBi |
 | Moline, S., BARREA, C., RAMAEKERS, V., & SEGHAYE, M.-C. (2018). Neuroborreliosis presenting as Guillain-Barre syndrome: a case report [Poster presentation]. Société Européenne de Neurologie Pédiatrique. |
 | RAMAEKERS, V., SEGERS, K., Sequeira, J. M., Koenig, M., Van Maldergem, L., Bours, V., Kornak, U., & Quadros, E. V. (2018). Genetic assessment and folate receptor autoantibodies in infantile-onset cerebral folate deficiency (CFD) syndrome. Molecular Genetics and Metabolism, 124 (1), 87-93. doi:10.1016/j.ymgme.2018.03.001 Peer Reviewed verified by ORBi |
 | RAMAEKERS, V., SEGERS, K., SEQUEIRA, J., VAN MALDERGEM, L., KOENIG, M., KORNAK, U., & QUADROS, E. (May 2017). Genetic and Folate Receptor Antibody Analysis in the Infantile-onset Cerebral Folate Deficiency Syndrome [Paper presentation]. 11th International Conference on Homocysteine and One-Carbon Metabolism, Aarhus, Denmark. |
 | RAMAEKERS, V., Sequeira, J. M., & Quadros, E. V. (July 2016). The basis for folinic acid treatment in neuro-psychiatric disorders. Biochimie, 126, 79-90. doi:10.1016/j.biochi.2016.04.005 Peer Reviewed verified by ORBi |
 | Boycott, K. M., Beaulieu, C. L., Kernohan, K. D., Gebril, O. H., Mhanni, A., Chudley, A. E., Redl, D., Qin, W., Hampson, S., Kury, S., Tetreault, M., Puffenberger, E. G., Scott, J. N., Bezieau, S., Reis, A., Uebe, S., Schumacher, J., Hegele, R. A., McLeod, D. R., ... Abou Jamra, R. (03 December 2015). Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8. American Journal of Human Genetics, 97 (6), 886-93. doi:10.1016/j.ajhg.2015.11.002 Peer Reviewed verified by ORBi |
 | Kury, S., RAMAEKERS, V., Bezieau, S., & Wolf, B. (2015). Clinical utility gene card for: Biotinidase deficiency-update 2015. European Journal of Human Genetics. doi:10.1038/ejhg.2015.246 Peer Reviewed verified by ORBi |
 | FARHAT, N., DESPRECHINS, B., OTTO, B., RAMAEKERS, V., & SEGHAYE, M.-C. (24 April 2015). Paraspinal arterio-venous fistula in children: two more cases of an exceptional malformation. Clinics and Practice, 5 (2), 707-709. doi:10.4081/cp.2015.707 Peer Reviewed verified by ORBi |
 | Barrea, C., RAMAEKERS, V., & Seghaye, M.-C. (January 2015). Mono- and Biallelic deletion of neurexin - à propos of 3 cases. Tijdschrift van de Belgische Kinderarts, 17 (1), 107. Peer reviewed |
PHILIPPE, P., MAES, N., SCHOLL, J.-M., DELVENNE, V., & RAMAEKERS, V. (08 May 2014). Quelle approche diagnostique et clinique des troubles de la régulation sensorielle chez l’enfant porteur d’autisme (T.S.A. in DSM V) [Paper presentation]. 7° congrès européen de l’AEPEA. Corps à corps. Souffrances du corps et travail psychique chez le bébé, l'enfant, l'adolescent, la famille et les soignants, Bruxelles, Belgium. |
 | BARREA, C., RAMAEKERS, V., OTTO, B., & SEGHAYE, M.-C. (2014). Case report : un cas de glioblastome intra-médullaire chez un enfant de 12 ans. In Belgische Kinderarts 2014;16(1):422. Peer reviewed |
 | BARREA, C., RAMAEKERS, V., OTTO, B., & SEGHAYE, M.-C. (2014). Dissection artérielle cérébrale chez l'enfant. In Tijdschrift van de Belgische Kinderarts. Peer reviewed |
 | RAMAEKERS, V., Thony, B., Sequeira, J. M., Ansseau, M., Philippe, P., BOEMER, F., Bours, V., & Quadros, E. V. (2014). Folinic acid treatment for schizophrenia associated with folate receptor autoantibodies. Molecular Genetics and Metabolism, 113 (4), 307-14. doi:10.1016/j.ymgme.2014.10.002 Peer Reviewed verified by ORBi |
 | Adamsen, D., RAMAEKERS, V., Ho, H. T., BRITSCHGI, C., RÜFENACHT, V., MEILI, D., BOBROWSKI, E., PHILIPPE, P., NAVA, C., VAN MALDERGEM, L., BRUGGMANN, R., WALITZA, S., WANG, J., GRÜNBLATT, E., & THÖNY, B. (2014). Autism spectrum disorder associated with low serotonin in CSF and mutations in the SLC29A4 plasma membrane monoamine transporter (PMAT) gene. Molecular Autism, 5 (43), 1-11. doi:10.1186/2040-2392-5-43 Peer Reviewed verified by ORBi |
PHILIPPE, P., MAES, N., SCHOLL, J.-M., RAMAEKERS, V., & DELVENNE, V. (08 July 2013). Child’s sensory peculiarities in PDD assessment. How? Why? [Poster presentation]. 15th International Congress of ESCAP, Dublin, Ireland. |
PHILIPPE, P., SCHOLL, J.-M., DI DUCA, M., RAMAEKERS, V., & DELVENNE, V. (June 2013). A travers la rencontre avec l’enfant, repérer aussi les particularités sensorielles. Comment ? Pourquoi ? [Paper presentation]. Silence et paroles du corps. Congrès de la ligue des psychomotriciens francophones SNUP - UPBPF, Bruxelles, Belgium. |
 | RAMAEKERS, V., Sequeira, J., & Quadros, E. (March 2013). Clinical recognition and aspects of the cerebral folate deficiency syndromes. Clinical Chemistry and Laboratory Medicine, 51 (3), 497-511. doi:10.1515/cclm-2012-0543 Peer Reviewed verified by ORBi |
 | Sequeira, J., RAMAEKERS, V., & Quadros, E. (01 March 2013). The diagnostic utility of folate receptor autoantibodies in blood. Clinical Chemistry and Laboratory Medicine, 51 (3), 545-54. doi:10.1515/cclm-2012-0577 Peer Reviewed verified by ORBi |
 | RAMAEKERS, V., Quadros, E. V., & Sequeira, J. M. (March 2013). Role of folate receptor autoantibodies in infantile autism [letter to the editor]. Molecular Psychiatry, 18 (3), 270-1. doi:10.1038/mp.2012.22 Peer Reviewed verified by ORBi |
PHILIPPE, P., SCHOLL, J.-M., MAES, N., DI DUCA, M., BOURS, A. F., & RAMAEKERS, V. (21 May 2012). Particularités sensorielles dans les TSA et interventions [Paper presentation]. La prise en charge de l’autisme tout au long de la vie”. Workshop, Bruxelles,, Belgium. |
 | Küry, S., RAMAEKERS, V., Bézieau, S., & Wolf, B. (2012). Clinical utility gene card for: Biotinidase deficiency. European Journal of Human Genetics, 20 (5), 592. doi:10.1038/ejhg.2012.28 Peer Reviewed verified by ORBi |
 | Adamsen, D., Meili, D., Blau, N., Thony, B., & RAMAEKERS, V. (2011). Autism associated with low 5-hydroxyindolacetic acid in CSF and the heterozygous SLC6A4 gene Gly56Ala plus 5-HTTLPR L/L promoter variants. Molecular Genetics and Metabolism, 102 (3), 368-73. doi:10.1016/j.ymgme.2010.11.162 Peer Reviewed verified by ORBi |
 | SEGERS, K., Hanson, J., RAMAEKERS, V., & Bours, V. (02 November 2010). Molecular analysis of the FOLR genes in patients with cerebral folate deficiency [Poster presentation]. 60° American Society of Human Genetics Meeting. |
 | Hasselmann, O., Blau, N., RAMAEKERS, V., Quadros, E. V., Sequeira, J. M., & Weissert, M. (2010). Cerebral folate deficiency and CNS inflammatory markers in Alpers disease. Molecular Genetics and Metabolism, 99 (1), 58-61. doi:10.1016/j.ymgme.2009.08.005 Peer Reviewed verified by ORBi |
 | Opladen, T., Blau, N., & RAMAEKERS, V. (2010). Effect of antiepileptic drugs and reactive oxygen species on folate receptor 1 (FOLR1)-dependent 5-methyltetrahydrofolate transport. Molecular Genetics and Metabolism, 101 (1), 48-54. doi:10.1016/j.ymgme.2010.05.006 Peer Reviewed verified by ORBi |
 | Scholl, U. I., Choi, M., Liu, T., RAMAEKERS, V., Hausler, M. G., Grimmer, J., Tobe, S. W., Farhi, A., Nelson-Williams, C., & Lifton, R. P. (2009). Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10. Proceedings of the National Academy of Sciences of the United States of America, 106 (14), 5842-7. doi:10.1073/pnas.0901749106 Peer Reviewed verified by ORBi |
 | Ramaekers, V., Sequeira, J. M., Blau, N., & Quadros, E. V. (May 2008). A milk-free diet downregulates folate receptor autoimmunity in cerebral folate deficiency syndrome. Developmental Medicine and Child Neurology, 50 (5), 346-352. doi:10.1111/j.1469-8749.2008.02053.x Peer Reviewed verified by ORBi |
 | Garcia-Cazorla, A., Quadros, E. V., Nascimento, A., Garcia-Silva, M. T., Briones, P., Montoya, J., Ormazábal, A., Artuch, R., Sequeira, J. M., Blau, N., Arenas, J., Pineda, M., & RAMAEKERS, V. (15 April 2008). Mitochondrial diseases associated with cerebral folate deficiency. Neurology, 70 (16), 1360-1362. doi:10.1212/01.wnl.0000309223.98616.e4 Peer Reviewed verified by ORBi |
 | Bonkowsky, J. L., RAMAEKERS, V., Quadros, E. V., & Lloyd, M. (2008). Progressive encephalopathy in a child with cerebral folate deficiency syndrome. Journal of Child Neurology, 23 (12), 1460-3. doi:10.1177/0883073808318546 Peer Reviewed verified by ORBi |
 | RAMAEKERS, V., Blau, N., Sequeira, J. M., Nassogne, M.-C., & Quadros, E. V. (December 2007). Folate receptor autoimmunity and cerebral folate deficiency in low-functioning autism with neurological deficits. Neuropediatrics, 38 (6), 276-281. doi:10.1055/s-2008-1065354 Peer Reviewed verified by ORBi |
 | Ramaekers, V., Sequeira, J. M., Artuch, R., Blau, N., Temudo, T., Ormazabal, A., Pineda, M., Aracil, A., Roelens, F., Laccone, F., & Quadros, E. V. (August 2007). Folate receptor autoantibodies and spinal fluid 5-methyltetrahydrofolate deficiency in Rett syndrome. Neuropediatrics, 38 (4), 179-183. doi:10.1055/s-2007-991148 Peer Reviewed verified by ORBi |
 | RAMAEKERS, V., Wels, J., Sequeira, J. M., Quadros, E. V., & Blau, N. (August 2007). Mitochondrial complex I encephalomyopathy and cerebral 5-methyltetrahydrofolate deficiency. Neuropediatrics, 38 (4), 184-187. doi:10.1055/s-2007-991150 Peer Reviewed verified by ORBi |
 | Opladen, T., Ramaekers, V., Heimann, G., & Blau, N. (January 2006). Analysis of 5-methyltetrahydrofolate in serum of healthy children. Molecular Genetics and Metabolism, 87 (1), 61-5. doi:10.1016/j.ymgme.2005.08.011 Peer Reviewed verified by ORBi |
 | Ramaekers, V., Rothenberg, S. P., Sequeira, J. M., Opladen, T., Blau, N., Quadros, E. V., & Selhub, J. (12 May 2005). Autoantibodies to folate receptors in the cerebral folate deficiency syndrome. New England Journal of Medicine, 352 (19), 1985-1991. doi:10.1056/NEJMoa043160 Peer Reviewed verified by ORBi |
 | Moretti, P., Sahoo, T., Hyland, K., Bottiglieri, T., Peters, S., Del Gaudio, D., Roa, B., Curry, S., Zhu, H., Finnell, R. H., Neul, J. L., Ramaekers, V., Blau, N., Bacino, C. A., Miller, G., & Scaglia, F. (22 March 2005). Cerebral folate deficiency with developmental delay, autism, and response to folinic acid. Neurology, 64 (6), 1088-1090. doi:10.1212/01.WNL.0000154641.08211.B7 Peer Reviewed verified by ORBi |
 | Hausler, M., Anhuf, D., Schuler, H., Ramaekers, V., Thron, A., Zerres, K., & Moller-Hartmann, W. (January 2005). White-matter disease in 18q deletion (18q-) syndrome: magnetic resonance spectroscopy indicates demyelination or increased myelin turnover rather than dysmyelination. Neuroradiology, 47 (1), 83-6. doi:10.1007/s00234-004-1309-9 Peer Reviewed verified by ORBi |
 | Ramaekers, V., & Blau, N. (December 2004). Cerebral folate deficiency. Developmental Medicine and Child Neurology, 46 (12), 843-51. doi:10.1017/S0012162204001471 Peer Reviewed verified by ORBi |
 | Korinth, M. C., Ramaekers, V., & Rohde, V. (February 2004). Cervical cord exostosis compressing the axis in a boy with hereditary multiple exostoses: Case illustration. Journal of Neurosurgery, 100 (2 SUPPL.), 223. Peer Reviewed verified by ORBi |
 | Blau, N., Bonafé, L., Krägeloh-Mann, I., Thöny, B., Kierat, L., Häusler, M., & Ramaekers, V. (09 September 2003). Cerebrospinal fluid pterins and folates in Aicardi-Goutières syndrome: A new phenotype. Neurology, 61 (5), 642-647. doi:10.1212/01.WNL.0000082726.08631.E7 Peer Reviewed verified by ORBi |
 | RAMAEKERS, V., Hansen, S., Holm, J., Opladen, T., Senderek, J., Häusler, M., Heimann, G., Fowler, B., Maiwald, R., & Blau, N. (26 August 2003). Reduced folate transport to the CNS in female Rett patients. Neurology, 61 (4), 506-515. doi:10.1212/01.WNL.0000078939.64774.1B Peer Reviewed verified by ORBi |
 | Bergmann, C., Zerres, K., Senderek, J., Rudnik-Schöneborn, S., Eggermann, T., Häusler, M., Mull, M., & RAMAEKERS, V. (July 2003). Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia. Brain: a Journal of Neurology, 126 (7), 1537-1544. doi:10.1093/brain/awg173 Peer Reviewed verified by ORBi |
 | Häusler, M., Schaade, L., Ramaekers, V., Doenges, M., Heimann, G., & Sellhaus, B. (March 2003). Inflammatory pseudotumors of the central nervous system: Report of 3 cases and a literature review. Human Pathology, 34 (3), 253-262. doi:10.1053/hupa.2003.35 Peer Reviewed verified by ORBi |
 | Senderek, J., Bergmann, C., RAMAEKERS, V., Nelis, E., Bernert, G., Makowski, A., Züchner, S., De Jonghe, P., Rudnik-Schöneborn, S., Zerres, K., & Schröder, J. M. (March 2003). Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy. Brain: a Journal of Neurology, 126 (3), 642-649. doi:10.1093/brain/awg068 Peer Reviewed verified by ORBi |
 | Häusler, M., Sellhaus, B., Schweizer, K., Ramaekers, V., Opladen, T., & Kleines, M. (2003). Flow cytometric cerebrospinal fluid analysis in children. Pathology - Research and Practice, 199 (10), 667-675. doi:10.1078/0344-0338-00478 Peer Reviewed verified by ORBi |
 | Ramaekers, V., Häusler, M., Opladen, T., Heimann, G., & Blau, N. (December 2002). Psychomotor retardation, spastic paraplegia, cerebellar ataxia and dyskinesia associated with low 5-methyltetrahydrofolate in cerebrospinal fluid: A novel neurometabolic condition responding to folinic acid substitution. Neuropediatrics, 33 (6), 301-308. doi:10.1055/s-2002-37082 Peer Reviewed verified by ORBi |
 | Häusler, M., Ramaekers, V., Doenges, M., Schweizer, K., Ritter, K., & Schaade, L. (October 2002). Neurological complications of acute and persistent Epstein-Barr virus infection in paediatric patients. Journal of Medical Virology, 68 (2), 253-263. doi:10.1002/jmv.10201 Peer Reviewed verified by ORBi |
 | Hausler, M., Schaade, L., Kemeny, S., Schweizer, K., Schoenmackers, C., & Ramaekers, V. (30 March 2002). Encephalitis related to primary varicella-zoster virus infection in immunocompetent children. Journal of the Neurological Sciences, 195 (2), 111-6. doi:10.1016/S0022-510X(02)00017-5 Peer Reviewed verified by ORBi |
 | Schefels, J., Wenzl, T. G., Merz, U., Ramaekers, V., Holzki, J., Rudnik-Schoeneborn, S., Hermanns, B., & Hörnchen, H. (January 2002). Functional upper airway obstruction in a child with freeman-sheldon syndrome. ORL, 64 (1), 53-56. doi:10.1159/000049271 Peer Reviewed verified by ORBi |
 | Senderek, J., Ramaekers, V., Zerres, K., Rudnik-Schöneborn, S., Schröder, J. M., & Bergmann, C. (15 November 2001). Phenotypic variation of a novel nonsense mutation in the P0 intracellular domain. Journal of the Neurological Sciences, 192 (1-2), 49-51. doi:10.1016/S0022-510X(01)00591-3 Peer Reviewed verified by ORBi |
Hausler, M. G., Jaeken, J., Monch, E., & RAMAEKERS, V. (August 2001). Phenotypic heterogeneity and adverse effects of serine treatment in 3-phosphoglycerate dehydrogenase deficiency: report on two siblings. Neuropediatrics, 32 (4), 191-5. doi:10.1055/s-2001-17373 Peer Reviewed verified by ORBi |
 | RAMAEKERS, V., Senderek, J., Hausler, M., Haring, M., Abeling, N., Zerres, K., Bergmann, C., Heimann, G., & Blau, N. (July 2001). A novel neurodevelopmental syndrome responsive to 5-hydroxytryptophan and carbidopa. Molecular Genetics and Metabolism, 73 (2), 179-87. doi:10.1006/mgme.2001.3187 Peer Reviewed verified by ORBi |
 | Kölker, S., Ramaekers, V., Zschocke, J., & Hoffmann, G. F. (February 2001). Acute encephalopathy despite early therapy in a patient with homozygosity for E365K in the glutaryl-coenzyme A dehydrogenase gene. Journal of Pediatrics, 138 (2), 277-279. doi:10.1067/mpd.2001.110303 Peer Reviewed verified by ORBi |
 | Disselhorst-Klug, C., Bahm, J., RAMAEKERS, V., Trachterna, A., & Rau, G. (October 2000). Non-invasive approach of motor unit recording during muscle contractions in humans. European Journal of Applied Physiology, 83 (2-3), 144-150. doi:10.1007/s004210000272 Peer Reviewed verified by ORBi |
 | Muller, H. D., Mugler, M., RAMAEKERS, V., & Schroder, J. M. (September 2000). Hereditary motor and sensory neuropathy with absence of large myelinated fibers due to absence of large neurons in dorsal root ganglia and anterior horns, clinically associated with deafness, mental retardation, and epilepsy (HMSN-ADM). Journal of the Peripheral Nervous System, 5 (3), 147-57. doi:10.1046/j.1529-8027.2000.00020.x Peer Reviewed verified by ORBi |
Abicht, A., Stucka, R., Karcagi, V., Herczegfalvi, A., Horvath, R., Mortier, W., Schara, U., RAMAEKERS, V., Jost, W., Brunner, J., Janssen, G., Seidel, U., Schlotter, B., Muller-Felber, W., Pongratz, D., Rudel, R., & Lochmuller, H. (22 October 1999). A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin. Neurology, 53 (7), 1564-9. doi:10.1212/wnl.53.7.1564 Peer Reviewed verified by ORBi |
 | Senderek, J., Hermanns, B., Bergmann, C., Boroojerdi, B., Bajbouj, M., Hungs, M., RAMAEKERS, V., Quasthoff, S., Karch, D., & Schroder, J. M. (15 August 1999). X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations(1). Journal of the Neurological Sciences, 167 (2), 90-101. doi:10.1016/S0022-510X(99)00146-X Peer Reviewed verified by ORBi |
 | Kuker, W., & RAMAEKERS, V. (July 1999). Persistent hyperplastic primary vitreous: MRI. Neuroradiology, 41 (7), 520-2. doi:10.1007/s002340050796 Peer Reviewed verified by ORBi |
Hausler, M. G., RAMAEKERS, V., Reul, J., Meilicke, R., & Heimann, G. (August 1998). Early and late onset manifestations of cerebral vasculitis related to varicella zoster. Neuropediatrics, 29 (4), 202-7. doi:10.1055/s-2007-973561 Peer Reviewed verified by ORBi |
 | Senderek, J., Bergmann, C., Quasthoff, S., RAMAEKERS, V., & Schroder, J. M. (May 1998). X-linked dominant Charcot-Marie-Tooth disease: nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln). Acta Neuropathologica, 95 (5), 443-9. doi:10.1007/s004010050823 Peer Reviewed verified by ORBi |
 | Wolf, B., Pomponio, R., Norrgard, K., Lott, I., Baumgartner, E. R., Suormala, T., RAMAEKERS, V., Coskun, T., Tokatli, A., Ozalp, I., & Hymes, J. (1998). Delayed-onset profound biotnidase deficiency. Journal of Pediatrics, 132 (2), 362-365. doi:10.1016/S0022-3476(98)70464-0 Peer Reviewed verified by ORBi |
 | RAMAEKERS, V., Heimann, G., Reul, J., Thron, A., & Jaeken, J. (October 1997). Genetic disorders and cerebellar structural abnormalities in childhood. Brain: a Journal of Neurology, 120 ( Pt 10), 1739-51. doi:10.1093/brain/120.10.1739 Peer Reviewed verified by ORBi |
 | RAMAEKERS, V., Bosman, B., Jansen, G. A., & Wanders, R. J. (September 1997). Increased plasma malondialdehyde associated with cerebellar structural defects. Archives of Disease in Childhood, 77 (3), 231-4. doi:10.1136/adc.77.3.231 Peer Reviewed verified by ORBi |
RAMAEKERS, V., Reul, J., Kusenbach, G., Thron, A., & Heimann, G. (April 1997). Central pontine myelinolysis associated with acquired folate depletion. Neuropediatrics, 28 (2), 126-30. doi:10.1055/s-2007-973686 Peer Reviewed verified by ORBi |
Weis, J., Reul, J., Mayfrank, L., Ramaekers, V., & Thron, A. (1997). Duplication of a vertebral artery associated with epidermoid cyst of the posterior fossa. European Radiology, 7 (3), 412-4. doi:10.1007/s003300050177 |
 | Lissens, W., De Meirleir, L., Seneca, S., Benelli, C., Marsac, C., Poll-The, B. T., Briones, P., Ruitenbeek, W., van Diggelen, O., Chaigne, D., RAMAEKERS, V., & Liebaers, I. (1996). Mutation analysis of the pyruvate dehydrogenase E1 alpha gene in eight patients with a pyruvate dehydrogenase complex deficiency. Human Mutation, 7 (1), 46-51. doi:10.1002/(SICI)1098-1004(1996)7:1<46::AID-HUMU6>3.0.CO;2-N Peer Reviewed verified by ORBi |
 | Suormala, T., RAMAEKERS, V., Schweitzer, S., Fowler, B., Laub, M. C., Schwermer, C., Bachmann, J., & Baumgartner, E. R. (1995). Biotinidase Km-variants: detection and detailed biochemical investigations. Journal of Inherited Metabolic Disease, 18 (6), 689-700. doi:10.1007/BF02436758 Peer Reviewed verified by ORBi |
 | RAMAEKERS, V., Reul, J., Siller, V., & Thron, A. (October 1994). Mesencephalic and third ventricle cysts: diagnosis and management in four cases. Journal of Neurology, Neurosurgery and Psychiatry, 57 (10), 1216-20. doi:10.1136/jnnp.57.10.1216 Peer Reviewed verified by ORBi |
RAMAEKERS, V., Calomme, M., Vanden Berghe, D., & Makropoulos, W. (August 1994). Selenium deficiency triggering intractable seizures. Neuropediatrics, 25 (4), 217-23. doi:10.1055/s-2008-1073025 Peer Reviewed verified by ORBi |
Schroder, J. M., Heide, G., RAMAEKERS, V., & Mortier, W. (October 1993). Subtotal aplasia of myelinated nerve fibers in the sural nerve. Neuropediatrics, 24 (5), 286-91. doi:10.1055/s-2008-1071558 Peer Reviewed verified by ORBi |
RAMAEKERS, V., Casaer, P., & Daniels, H. (October 1993). Cerebral hyperperfusion following episodes of bradycardia in the preterm infant. Early Human Development, 34 (3), 199-208. doi:10.1016/0378-3782(93)90177-V Peer Reviewed verified by ORBi |
Reul, J., RAMAEKERS, V., & Thron, A. (04 June 1993). Suprasellare Raumforderung als Erstmanifestation einer Tuberkulose im Kindesalter. Deutsche Medizinische Wochenschrift, 118 (22), 820-4. doi:10.1055/s-2008-1059394 Peer Reviewed verified by ORBi |
RAMAEKERS, V., Disselhorst-Klug, C., Schneider, J., Silny, J., Forst, J., Forst, R., Kotlarek, F., & Rau, G. (June 1993). Clinical application of a noninvasive multi-electrode array EMG for the recording of single motor unit activity. Neuropediatrics, 24 (3), 134-8. doi:10.1055/s-2008-1071530 Peer Reviewed verified by ORBi |
RAMAEKERS, V., Brab, M., Rau, G., & Heimann, G. (April 1993). Recovery from neurological deficits following biotin treatment in a biotinidase Km variant. Neuropediatrics, 24 (2), 98-102. doi:10.1055/s-2008-1071522 Peer Reviewed verified by ORBi |
 | Hageman, G., RAMAEKERS, V., Hilhorst, B. G., & Rozeboom, A. R. (April 1993). Congenital cervical spinal muscular atrophy: a non-familial, non progressive condition of the upper limbs. Journal of Neurology, Neurosurgery and Psychiatry, 56 (4), 365-8. doi:10.1136/jnnp.56.4.365 Peer Reviewed verified by ORBi |
Otterbach, B., Stoffel, W., & RAMAEKERS, V. (January 1993). A novel mutation in the proteolipid protein gene leading to Pelizaeus-Merzbacher disease. Biological Chemistry Hoppe-Seyler, 374 (1), 75-83. doi:10.1515/bchm3.1993.374.1-6.75 Peer Reviewed verified by ORBi |
 | Jaeken, J., De Cock, P., Stibler, H., Van Geet, C., Kint, J., RAMAEKERS, V., & Carchon, H. (1993). Carbohydrate-deficient glycoprotein syndrome type II. Journal of Inherited Metabolic Disease, 16 (6), 1041. doi:10.1007/BF00711522 Peer Reviewed verified by ORBi |
RAMAEKERS, V., Casaer, P., Daniels, H., & Marchal, G. (October 1992). The influence of blood transfusion on brain blood flow autoregulation among stable preterm infants. Early Human Development, 30 (3), 211-20. doi:10.1016/0378-3782(92)90070-W Peer Reviewed verified by ORBi |
RAMAEKERS, V., Daniels, H., & Casaer, P. (May 1992). Brain oxygen transport related to levels of fetal haemoglobin in stable preterm infants. Journal of Developmental Physiology, 17 (5), 209-13. Peer Reviewed verified by ORBi |
Brab, M., RAMAEKERS, V., Baumgartner, E. R., Heimann, G., & Reim, M. (March 1992). Juvenile Optikoneuropathie durch Km-Variante der Biotinidase. Klinische Monatsblatter für Augenheilkunde, 200 (3), 204-9. doi:10.1055/s-2008-1045738 Peer Reviewed verified by ORBi |
 | RAMAEKERS, V., Suormala, T. M., Brab, M., Duran, R., Heimann, G., & Baumgartner, E. R. (January 1992). A biotinidase Km variant causing late onset bilateral optic neuropathy. Archives of Disease in Childhood, 67 (1), 115-9. doi:10.1136/adc.67.1.115 Peer Reviewed verified by ORBi |
 | RAMAEKERS, V., Stibler, H., Kint, J., & Jaeken, J. (May 1991). A new variant of the carbohydrate deficient glycoproteins syndrome. Journal of Inherited Metabolic Disease, 14 (3), 385-8. doi:10.1007/BF01811710 Peer Reviewed verified by ORBi |
RAMAEKERS, V., Casaer, P., Daniels, H., & Marchal, G. (December 1990). Upper limits of brain blood flow autoregulation in stable infants of various conceptional age. Early Human Development, 24 (3), 249-58. doi:10.1016/0378-3782(90)90032-E Peer Reviewed verified by ORBi |
RAMAEKERS, V., & Casaer, P. (January 1990). Defective regulation of cerebral oxygen transport after severe birth asphyxia. Developmental Medicine and Child Neurology, 32 (1), 56-62. doi:10.1111/j.1469-8749.1990.tb08467.x Peer Reviewed verified by ORBi |
RAMAEKERS, V., Casaer, P., Daniels, H., Smet, M., & Marchal, G. (December 1989). The influence of behavioural states on cerebral blood flow velocity patterns in stable preterm infants. Early Human Development, 20 (3-4), 229-46. doi:10.1016/0378-3782(89)90009-1 Peer Reviewed verified by ORBi |
RAMAEKERS, V., Casaer, P., Marchal, G., Smet, M., & Goossens, W. (June 1988). The effect of blood transfusion on cerebral blood-flow in preterm infants: a Doppler study. Developmental Medicine and Child Neurology, 30 (3), 334-41. doi:10.1111/j.1469-8749.1988.tb14558.x Peer Reviewed verified by ORBi |
Daniels, H., Devlieger, H., Casaer, P., RAMAEKERS, V., van den Broeck, J., & Eggermont, E. (May 1988). Feeding, behavioural state and cardiorespiratory control. Acta Paediatrica Scandinavica, 77 (3), 369-73. doi:10.1111/j.1651-2227.1988.tb10662.x Peer Reviewed verified by ORBi |
RAMAEKERS, V., & Casaer, P. (November 1987). Influence of behavioral states on cerebral blood flow velocity patterns in preterm infants. Journal of Pediatrics, 111 (5), 795. doi:10.1016/S0022-3476(87)80273-1 Peer Reviewed verified by ORBi |
RAMAEKERS, V., Lake, B. D., Harding, B., Boyd, S., Harden, A., Brett, E. M., & Wilson, J. (August 1987). Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight cases. Neuropediatrics, 18 (3), 170-5. doi:10.1055/s-2008-1052474 Peer Reviewed verified by ORBi |