Ryan MM - Search Results

1

Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome.

Woodcock IR, Menezes MP, Coleman L, Yaplito-Lee J, Peters H, White SM, Stapleton R, Phelan DG, Chong B, Lunke S, Stark Z, Pitt J, Ryan MM, Robertson C, Yiu EM. Woodcock IR, et al. Among authors: ryan mm. Semin Pediatr Neurol. 2018 Jul;26:2-9. doi: 10.1016/j.spen.2017.03.001. Epub 2017 Apr 5. Semin Pediatr Neurol. 2018. PMID: 29961509

2

Anterior horn cell disease and olivopontocerebellar hypoplasia.

Ryan MM, Cooke-Yarborough CM, Procopis PG, Ouvrier RA. Ryan MM, et al. Pediatr Neurol. 2000 Aug;23(2):180-4. doi: 10.1016/s0887-8994(00)00166-1. Pediatr Neurol. 2000. PMID: 11020648

3

The pharyngeal-cervical-brachial form of Guillain-Barré syndrome in childhood.

Mogale KD, Antony JH, Ryan MM. Mogale KD, et al. Among authors: ryan mm. Pediatr Neurol. 2005 Oct;33(4):285-8. doi: 10.1016/j.pediatrneurol.2005.04.012. Pediatr Neurol. 2005. PMID: 16194730

4

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

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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