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Page 1
Duplication 2p16 is associated with perisylvian polymicrogyria.
Amrom D, Poduri A, Goldman JS, Dan B, Deconinck N, Pichon B, Nadaf J, Andermann F, Andermann E, Walsh CA, Dobyns WB. Amrom D, et al. Among authors: dan b. Am J Med Genet A. 2019 Dec;179(12):2343-2356. doi: 10.1002/ajmg.a.61342. Epub 2019 Oct 29. Am J Med Genet A. 2019. PMID: 31660690
Opsoclonus-myoclonus associated with celiac disease.
Deconinck N, Scaillon M, Segers V, Groswasser JJ, Dan B. Deconinck N, et al. Among authors: dan b. Pediatr Neurol. 2006 Apr;34(4):312-4. doi: 10.1016/j.pediatrneurol.2005.08.034. Pediatr Neurol. 2006. PMID: 16638509
Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep.
Coutelier M, Andries S, Ghariani S, Dan B, Duyckaerts C, van Rijckevorsel K, Raftopoulos C, Deconinck N, Sonderegger P, Scaravilli F, Vikkula M, Godfraind C. Coutelier M, et al. Among authors: dan b. Neurology. 2008 Jul 1;71(1):64-6. doi: 10.1212/01.wnl.0000316306.08751.28. Neurology. 2008. PMID: 18591508 No abstract available.
[A new framework for cerebral palsy].
Pelc K, Deconinck N, Monier A, Sékhara T, Bormans J, Dan B. Pelc K, et al. Among authors: dan b. Rev Med Brux. 2006;27 Spec No:Sp33-7. Rev Med Brux. 2006. PMID: 21818891 French.
Somatic mutations in cerebral cortical malformations.
Jamuar SS, Lam AT, Kircher M, D'Gama AM, Wang J, Barry BJ, Zhang X, Hill RS, Partlow JN, Rozzo A, Servattalab S, Mehta BK, Topcu M, Amrom D, Andermann E, Dan B, Parrini E, Guerrini R, Scheffer IE, Berkovic SF, Leventer RJ, Shen Y, Wu BL, Barkovich AJ, Sahin M, Chang BS, Bamshad M, Nickerson DA, Shendure J, Poduri A, Yu TW, Walsh CA. Jamuar SS, et al. Among authors: dan b. N Engl J Med. 2014 Aug 21;371(8):733-43. doi: 10.1056/NEJMoa1314432. N Engl J Med. 2014. PMID: 25140959 Free PMC article.
409 results