Ryan MM - Search Results

1

The severe epilepsy syndromes of infancy: A population-based study.

Howell KB, Freeman JL, Mackay MT, Fahey MC, Archer J, Berkovic SF, Chan E, Dabscheck G, Eggers S, Hayman M, Holberton J, Hunt RW, Jacobs SE, Kornberg AJ, Leventer RJ, Mandelstam S, McMahon JM, Mefford HC, Panetta J, Riseley J, Rodriguez-Casero V, Ryan MM, Schneider AL, Smith LJ, Stark Z, Wong F, Yiu EM, Scheffer IE, Harvey AS. Howell KB, et al. Among authors: ryan mm. Epilepsia. 2021 Feb;62(2):358-370. doi: 10.1111/epi.16810. Epub 2021 Jan 21. Epilepsia. 2021. PMID: 33475165

2

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

3

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

4

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

5

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

6

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.

7

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

8

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

9

Ascorbic acid for Charcot-Marie-Tooth disease type 1A in children: a randomised, double-blind, placebo-controlled, safety and efficacy trial.

Burns J, Ouvrier RA, Yiu EM, Joseph PD, Kornberg AJ, Fahey MC, Ryan MM. Burns J, et al. Among authors: ryan mm. Lancet Neurol. 2009 Jun;8(6):537-44. doi: 10.1016/S1474-4422(09)70108-5. Epub 2009 May 6. Lancet Neurol. 2009. PMID: 19427269 Clinical Trial.

10

Atypical Silver-Russell phenotype resulting from maternal uniparental disomy of chromosome 7.

Stark Z, Ryan MM, Bruno DL, Burgess T, Savarirayan R. Stark Z, et al. Among authors: ryan mm. Am J Med Genet A. 2010 Sep;152A(9):2342-5. doi: 10.1002/ajmg.a.33590. Am J Med Genet A. 2010. PMID: 20684011

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