Ryan MM - Search Results

1

King-denborough syndrome caused by a novel mutation in the ryanodine receptor gene.

D'Arcy CE, Bjorksten A, Yiu EM, Bankier A, Gillies R, McLean CA, Shield LK, Ryan MM. D'Arcy CE, et al. Among authors: ryan mm. Neurology. 2008 Sep 2;71(10):776-7. doi: 10.1212/01.wnl.0000324929.33780.2f. Neurology. 2008. PMID: 18765655 No abstract available.

2

Nemaline myopathy: a clinical study of 143 cases.

Ryan MM, Schnell C, Strickland CD, Shield LK, Morgan G, Iannaccone ST, Laing NG, Beggs AH, North KN. Ryan MM, et al. Ann Neurol. 2001 Sep;50(3):312-20. doi: 10.1002/ana.1080. Ann Neurol. 2001. PMID: 11558787 Review.

3

Clinical course correlates poorly with muscle pathology in nemaline myopathy.

Ryan MM, Ilkovski B, Strickland CD, Schnell C, Sanoudou D, Midgett C, Houston R, Muirhead D, Dennett X, Shield LK, De Girolami U, Iannaccone ST, Laing NG, North KN, Beggs AH. Ryan MM, et al. Neurology. 2003 Feb 25;60(4):665-73. doi: 10.1212/01.wnl.0000046585.81304.bc. Neurology. 2003. PMID: 12601110

4

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.

5

Concomitant transverse myelitis and acute motor axonal neuropathy in an adolescent.

Howell KB, Wanigasinghe J, Leventer RJ, Ryan MM. Howell KB, et al. Among authors: ryan mm. Pediatr Neurol. 2007 Nov;37(5):378-81. doi: 10.1016/j.pediatrneurol.2007.05.020. Pediatr Neurol. 2007. PMID: 17950429

6

Dietary L-tyrosine supplementation in nemaline myopathy.

Ryan MM, Sy C, Rudge S, Ellaway C, Ketteridge D, Roddick LG, Iannaccone ST, Kornberg AJ, North KN. Ryan MM, et al. J Child Neurol. 2008 Jun;23(6):609-13. doi: 10.1177/0883073807309794. Epub 2007 Dec 13. J Child Neurol. 2008. PMID: 18079309

7

Central nervous system signs in X-linked Charcot-Marie-Tooth disease after hyperventilation.

Srinivasan J, Leventer RJ, Kornberg AJ, Dahl HH, Ryan MM. Srinivasan J, et al. Among authors: ryan mm. Pediatr Neurol. 2008 Apr;38(4):293-5. doi: 10.1016/j.pediatrneurol.2007.12.003. Pediatr Neurol. 2008. PMID: 18358413

8

Adolescent spinal muscular atrophy with calf hypertrophy and a deletion in the SMN gene.

Yiu EM, Ravat S, Ryan MM, Shield LK, Smith LJ, Kornberg AJ. Yiu EM, et al. Among authors: ryan mm. Muscle Nerve. 2008 Jul;38(1):930-2. doi: 10.1002/mus.21013. Muscle Nerve. 2008. PMID: 18508340

9

Neurophysiologic abnormalities in children with Charcot-Marie-Tooth disease type 1A.

Yiu EM, Burns J, Ryan MM, Ouvrier RA. Yiu EM, et al. Among authors: ryan mm. J Peripher Nerv Syst. 2008 Sep;13(3):236-41. doi: 10.1111/j.1529-8027.2008.00182.x. J Peripher Nerv Syst. 2008. PMID: 18844790

10

Acute transverse myelitis and acute disseminated encephalomyelitis in childhood: spectrum or separate entities?

Yiu EM, Kornberg AJ, Ryan MM, Coleman LT, Mackay MT. Yiu EM, et al. Among authors: ryan mm. J Child Neurol. 2009 Mar;24(3):287-96. doi: 10.1177/0883073808323522. J Child Neurol. 2009. PMID: 19258287

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