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Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease.
Rice GI, Kitabayashi N, Barth M, Briggs TA, Burton ACE, Carpanelli ML, Cerisola AM, Colson C, Dale RC, Danti FR, Darin N, De Azua B, De Giorgis V, De Goede CGL, Desguerre I, De Laet C, Eslahi A, Fahey MC, Fallon P, Fay A, Fazzi E, Gorman MP, Gowrinathan NR, Hully M, Kurian MA, Leboucq N, Lin JS, Lines MA, Mar SS, Maroofian R, Martí-Sanchez L, McCullagh G, Mojarrad M, Narayanan V, Orcesi S, Ortigoza-Escobar JD, Pérez-Dueñas B, Petit F, Ramsey KM, Rasmussen M, Rivier F, Rodríguez-Pombo P, Roubertie A, Stödberg TI, Toosi MB, Toutain A, Uettwiller F, Ulrick N, Vanderver A, Waldman A, Livingston JH, Crow YJ. Rice GI, et al. Among authors: roubertie a. Neuropediatrics. 2017 Jun;48(3):166-184. doi: 10.1055/s-0037-1601449. Epub 2017 Apr 10. Neuropediatrics. 2017. PMID: 28561207 Free PMC article.
[Benign familial infantile convulsions].
Echenne B, Rivier F, Humbertclaude V, Roubertie A, Cheminal R, Malafosse A. Echenne B, et al. Among authors: roubertie a. Arch Pediatr. 1999 Jan;6(1):54-8. doi: 10.1016/S0929-693X(99)80075-X. Arch Pediatr. 1999. PMID: 9974098 French.
McArdle's disease in childhood: report of a new case.
Roubertie A, Patte K, Rivier F, Pages AM, Maire I, Echenne B. Roubertie A, et al. Eur J Paediatr Neurol. 1998;2(5):269-73. doi: 10.1016/s1090-3798(98)80041-x. Eur J Paediatr Neurol. 1998. PMID: 10726830
[The varied etiologies of childhood-onset dystonia].
Roubertie A, Rivier F, Humbertclaude V, Tuffery S, Cavalier L, Cheminal R, Coubes P, Echenne B. Roubertie A, et al. Rev Neurol (Paris). 2002 Apr;158(4):413-24. Rev Neurol (Paris). 2002. PMID: 11984483 Review. French.
181 results