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A novel syndrome of episodic muscle weakness maps to xp22.3.
Ryan MM, Taylor P, Donald JA, Ouvrier RA, Morgan G, Danta G, Buckley MF, North KN. Ryan MM, et al. Am J Hum Genet. 1999 Oct;65(4):1104-13. doi: 10.1086/302588. Am J Hum Genet. 1999. PMID: 10486330 Free PMC article.
Influenza A encephalitis with movement disorder.
Ryan MM, Procopis PG, Ouvrier RA. Ryan MM, et al. Pediatr Neurol. 1999 Sep;21(3):669-73. doi: 10.1016/s0887-8994(99)00062-4. Pediatr Neurol. 1999. PMID: 10513697
Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin gene.
Ilkovski B, Cooper ST, Nowak K, Ryan MM, Yang N, Schnell C, Durling HJ, Roddick LG, Wilkinson I, Kornberg AJ, Collins KJ, Wallace G, Gunning P, Hardeman EC, Laing NG, North KN. Ilkovski B, et al. Among authors: ryan mm. Am J Hum Genet. 2001 Jun;68(6):1333-43. doi: 10.1086/320605. Epub 2001 Apr 27. Am J Hum Genet. 2001. PMID: 11333380 Free PMC article.
Hereditary peripheral neuropathies of childhood.
Ryan MM, Ouvrier R. Ryan MM, et al. Curr Opin Neurol. 2005 Apr;18(2):105-10. doi: 10.1097/01.wco.0000162849.37273.af. Curr Opin Neurol. 2005. PMID: 15791138 Review.
Outcome of noninvasive ventilation in children with neuromuscular disease.
Young HK, Lowe A, Fitzgerald DA, Seton C, Waters KA, Kenny E, Hynan LS, Iannaccone ST, North KN, Ryan MM. Young HK, et al. Among authors: ryan mm. Neurology. 2007 Jan 16;68(3):198-201. doi: 10.1212/01.wnl.0000251299.54608.13. Neurology. 2007. PMID: 17224573 Clinical Trial.
293 results