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143 results

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Page 1
The Discrepancy between Performance-Based Measures and Questionnaires when Assessing Clinical Outcomes and Quality of Life in Pediatric Patients with Neurological Disorders.
Coutinho V, Câmara-Costa H, Kemlin I, Billette de Villemeur T, Rodriguez D, Dellatolas G. Coutinho V, et al. Among authors: billette de villemeur t. Appl Neuropsychol Child. 2017 Oct-Dec;6(4):255-261. doi: 10.1080/21622965.2016.1146141. Epub 2016 May 16. Appl Neuropsychol Child. 2017. PMID: 27182681
Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene.
Gras D, Jonard L, Roze E, Chantot-Bastaraud S, Koht J, Motte J, Rodriguez D, Louha M, Caubel I, Kemlin I, Lion-François L, Goizet C, Guillot L, Moutard ML, Epaud R, Héron B, Charles P, Tallot M, Camuzat A, Durr A, Polak M, Devos D, Sanlaville D, Vuillaume I, Billette de Villemeur T, Vidailhet M, Doummar D. Gras D, et al. Among authors: billette de villemeur t. J Neurol Neurosurg Psychiatry. 2012 Oct;83(10):956-62. doi: 10.1136/jnnp-2012-302505. Epub 2012 Jul 24. J Neurol Neurosurg Psychiatry. 2012. PMID: 22832740
[Fetal neurology: conditions of diagnostic uncertainty].
Moutard ML, Gélot A, Rodriguez D, Guët A, Mignot C, Ponsot G, Billette de Villemeur T. Moutard ML, et al. Among authors: billette de villemeur t. Arch Pediatr. 2006 Jun;13(6):825-7. doi: 10.1016/j.arcped.2006.03.128. Epub 2006 May 12. Arch Pediatr. 2006. PMID: 16698255 French. No abstract available.
Monoamine neurotransmitters and movement disorders in children and adults.
Doummar D, Moussa F, Nougues MC, Ravelli C, Louha M, Whalen S, Burglen L, Rodriguez D, Billette de Villemeur T. Doummar D, et al. Among authors: billette de villemeur t. Rev Neurol (Paris). 2018 Nov;174(9):581-588. doi: 10.1016/j.neurol.2018.07.002. Epub 2018 Aug 27. Rev Neurol (Paris). 2018. PMID: 30166070 Review.
Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies.
Valence S, Cochet E, Rougeot C, Garel C, Chantot-Bastaraud S, Lainey E, Afenjar A, Barthez MA, Bednarek N, Doummar D, Faivre L, Goizet C, Haye D, Heron B, Kemlin I, Lacombe D, Milh M, Moutard ML, Riant F, Robin S, Roubertie A, Sarda P, Toutain A, Villard L, Ville D, Billette de Villemeur T, Rodriguez D, Burglen L. Valence S, et al. Among authors: billette de villemeur t. Genet Med. 2019 Mar;21(3):553-563. doi: 10.1038/s41436-018-0089-2. Epub 2018 Jul 12. Genet Med. 2019. PMID: 29997391 Free article.
[Creutzfeldt-Jakob disease in 4 children treated with growth hormone].
Billette de Villemeur T, Gourmelen M, Beauvais P, Rodriguez D, Vaudour G, Deslys JP, Dormont D, Richard P, Richardet JM. Billette de Villemeur T, et al. Rev Neurol (Paris). 1992;148(5):328-34. Rev Neurol (Paris). 1992. PMID: 1448646 Review. French.
Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients.
Chérot E, Keren B, Dubourg C, Carré W, Fradin M, Lavillaureix A, Afenjar A, Burglen L, Whalen S, Charles P, Marey I, Heide S, Jacquette A, Heron D, Doummar D, Rodriguez D, Billette de Villemeur T, Moutard ML, Guët A, Xavier J, Périsse D, Cohen D, Demurger F, Quélin C, Depienne C, Odent S, Nava C, David V, Pasquier L, Mignot C. Chérot E, et al. Among authors: billette de villemeur t. Clin Genet. 2018 Mar;93(3):567-576. doi: 10.1111/cge.13102. Epub 2017 Oct 4. Clin Genet. 2018. PMID: 28708303 Free article.
Single-Step Rapid Diagnosis of Dopamine and Serotonin Metabolism Disorders.
Lo A, Guibal P, Doummar D, Rodriguez D, Hautem JY, Couderc R, Billette De Villemeur T, Roze E, Chaminade P, Moussa F. Lo A, et al. Among authors: billette de villemeur t. ACS Omega. 2017 Sep 30;2(9):5962-5972. doi: 10.1021/acsomega.7b01008. Epub 2017 Sep 19. ACS Omega. 2017. PMID: 30023757 Free PMC article.
143 results