Role of folate receptor autoantibodies in infantile autism von Ramaekers, V T, Quadros, E V, Sequeira, J M

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Folate Receptor Autoimmunity and Cerebral Folate Deficiency in Low-Functioning Autism with Neurological Deficits von Ramaekers, V. T., Blau, N., Sequeira, J. M., Nassogne, M.-C., Quadros, E. V.

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Genetic assessment and folate receptor autoantibodies in infantile-onset cerebral folate deficiency (CFD) syndrome von Ramaekers, V.Th, Segers, K., Sequeira, J.M., Koenig, M., Van Maldergem, L., Bours, V., Kornak, U., Quadros, E.V.

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Psychomotor Retardation, Spastic Paraplegia, Cerebellar Ataxia and Dyskinesia Associated with Low 5-Methyltetrahydrofolate in Cerebrospinal Fluid: A Novel Neurometabolic Condition... von Ramaekers, V. T., Häusler, M., Opladen, T., Heimann, G., Blau, N.

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Genetic disorders and cerebellar structural abnormalities in childhood von RAMAEKERS, V. T, HEIMANN, G, REUL, J, THRON, A, JAEKEN, J

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Cerebral folate deficiency with developmental delay, autism, and response to folinic acid von MORETTI, P, SAHOO, T, NEUL, J. L, RAMAEKERS, V. T, BLAU, N, BACINO, C. A, MILLER, G, SCAGLIA, F, HYLAND, K, BOTTIGLIERI, T, PETERS, S, DEL GAUDIO, D, ROA, B, CURRY, S, ZHU, H, FINNELL, R. H

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Mitochondrial Complex I Encephalomyopathy and Cerebral 5-Methyltetrahydrofolate Deficiency von Ramaekers, V. T., Weis, J., Sequeira, J. M., Quadros, E. V., Blau, N.

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Cerebrospinal fluid pterins and folates in Aicardi-Goutières syndrome: A new phenotype von BLAU, N, BONAFE, L, KRÄGELOH-MANN, I, THÖNY, B, KIERAT, L, HÄUSLER, M, RAMAEKERS, V

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Oligophrenin 1 (OPHN1) gene mutation causes syndromic X‐linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia von Bergmann, Carsten, Zerres, Klaus, Senderek, Jan, Rudnik‐Schöneborn, Sabine, Eggermann, Thomas, Häusler, Martin, Mull, Michael, Ramaekers, Vincent T.

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3.072 AUTISM SPECTRUM DISORDER ASSOCIATED WITH LOW BRAIN SEROTONIN AND MUTATIONS IN THE SEROTONIN TRANSPORTER SLC29A 4 AND IN SEROTONIN RELATED GENES von Adamsen, D, Ramaekers, V, Bruggmann, R, Ho, H, Wang, J, Thöny, B

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Selenium Deficiency Triggering Intractable Seizures von Ramaekers, V. Th, Calomme, M., Vanden Berghe, D., Makropoulos, W.

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A common mutation (∈1267delG) in congenital myasthenic patients of Gypsy ethnic origin von ABICHT, A, STUCKA, R, JANSSEN, G, SEIDEL, U, SCHLOTTER, B, MÜLLER-FELBER, W, PONGRATZ, D, RÜDEL, R, LOCHMÜLLER, H, KARCAGI, V, HERCZEGFALVI, A, HORVATH, R, MORTIER, W, SCHARA, U, RAMAEKERS, V, JOST, W, BRUNNER, J

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Neurological complications of acute and persistent Epstein-Barr virus infection in paediatric patients von Häusler, Martin, Ramaekers, Vincent Thomas, Doenges, Martin, Schweizer, Klaus, Ritter, Klaus, Schaade, Lars

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Early and Late Onset Manifestations of Cerebral Vasculitis Related to Varicella Zoster von Häusler, M. G., Ramaekers, V. Th, Reul, J., Meilicke, R., Heimann, G.

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Encephalitis related to primary varicella-zoster virus infection in immunocompetent children von Häusler, M, Schaade, L, Kemény, S, Schweizer, K, Schoenmackers, C, Ramaekers, V.Th

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X-linked dominant Charcot-Marie-Tooth disease : nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln) von SENDEREK, J, BERGMANN, C, QUASTHOFF, S, RAMAEKERS, V. T, SCHRÖDER, J. M

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Non-invasive approach of motor unit recording during muscle contractions in humans von Disselhorst-Klug, C, Bahm, J, Ramaekers, V, Trachterna, A, Rau, G

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Increased plasma malondialdehyde associated with cerebellar structural defects von Ramaekers, V Th, Bosman, B, Jansen, G A, Wanders, R J A

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Delayed-onset profound biotinidase deficiency von Wolf, Barry, Pomponio, Robert J., Norrgard, Karen J., Lott, Ira T., Baumgartner, E.Regula, Suormala, Terttu, Ramaekers, Vincent Th, Coskun, Turgay, Tokatli, Aysegul, Ozalp, Imran, Hymes, Jeanne

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Cerebral folate deficiency von Ramaekers, Vincent Th, Blau, Nenad

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