Neumeyer AM - Search Results

1

Pilot study of myoblast transfer in the treatment of Becker muscular dystrophy.

Neumeyer AM, Cros D, McKenna-Yasek D, Zawadzka A, Hoffman EP, Pegoraro E, Hunter RG, Munsat TL, Brown RH Jr. Neumeyer AM, et al. Neurology. 1998 Aug;51(2):589-92. doi: 10.1212/wnl.51.2.589. Neurology. 1998. PMID: 9710042 Clinical Trial.

2

Arterial delivery of myoblasts to skeletal muscle.

Neumeyer AM, DiGregorio DM, Brown RH Jr. Neumeyer AM, et al. Neurology. 1992 Dec;42(12):2258-62. doi: 10.1212/wnl.42.12.2258. Neurology. 1992. PMID: 1461375

3

Identification of two mutations and a polymorphism in the chloride channel CLCN-1 in patients with Becker's generalized myotonia.

Esteban J, Neumeyer AM, McKenna-Yasek D, Brown RH. Esteban J, et al. Among authors: neumeyer am. Neurogenetics. 1998 Mar;1(3):185-8. doi: 10.1007/s100480050027. Neurogenetics. 1998. PMID: 10737121

4

Large genomic deletions: a novel cause of Ullrich congenital muscular dystrophy.

Foley AR, Hu Y, Zou Y, Yang M, Medne L, Leach M, Conlin LK, Spinner N, Shaikh TH, Falk M, Neumeyer AM, Bliss L, Tseng BS, Winder TL, Bönnemann CG. Foley AR, et al. Among authors: neumeyer am. Ann Neurol. 2011 Jan;69(1):206-11. doi: 10.1002/ana.22283. Ann Neurol. 2011. PMID: 21280092 Free PMC article.

5

Understanding relationships between autism, intelligence, and epilepsy: a cross-disorder approach.

van Eeghen AM, Pulsifer MB, Merker VL, Neumeyer AM, van Eeghen EE, Thibert RL, Cole AJ, Leigh FA, Plotkin SR, Thiele EA. van Eeghen AM, et al. Among authors: neumeyer am. Dev Med Child Neurol. 2013 Feb;55(2):146-153. doi: 10.1111/dmcn.12044. Epub 2012 Dec 4. Dev Med Child Neurol. 2013. PMID: 23205844 Free PMC article.

6

A novel fast-channel myasthenia caused by mutation in β subunit of AChR reveals subunit-specific contribution of the intracellular M1-M2 linker to channel gating.

Shen XM, Di L, Shen S, Zhao Y, Neumeyer AM, Selcen D, Sine SM, Engel AG. Shen XM, et al. Among authors: neumeyer am. Exp Neurol. 2020 Sep;331:113375. doi: 10.1016/j.expneurol.2020.113375. Epub 2020 Jun 3. Exp Neurol. 2020. PMID: 32504635 Free PMC article.

7

A Pilot Study of Autism-Specific Care Plans During Hospital Admission.

Broder-Fingert S, Shui A, Ferrone C, Iannuzzi D, Cheng ER, Giauque A, Connors S, McDougle CJ, Donelan K, Neumeyer A, Kuhlthau K. Broder-Fingert S, et al. Pediatrics. 2016 Feb;137 Suppl 2:S196-204. doi: 10.1542/peds.2015-2851R. Pediatrics. 2016. PMID: 26908475

8

Clinical and laboratory features distinguishing juvenile polymyositis and muscular dystrophy.

Mamyrova G, Katz JD, Jones RV, Targoff IN, Lachenbruch PA, Jones OY, Miller FW, Rider LG; Childhood Myositis Heterogeneity Collaborative Study Group. Mamyrova G, et al. Arthritis Care Res (Hoboken). 2013 Dec;65(12):1969-75. doi: 10.1002/acr.22088. Arthritis Care Res (Hoboken). 2013. PMID: 23925923 Free PMC article.

9

Hyperpyrexia in an adolescent on desipramine treatment.

Squires LA, Neumeyer AM, Bloomberg J, Krishnamoorthy KS. Squires LA, et al. Among authors: neumeyer am. Clin Pediatr (Phila). 1992 Oct;31(10):635-6. doi: 10.1177/000992289203101012. Clin Pediatr (Phila). 1992. PMID: 1395373 No abstract available.

10

Bone density in peripubertal boys with autism spectrum disorders.

Neumeyer AM, Gates A, Ferrone C, Lee H, Misra M. Neumeyer AM, et al. J Autism Dev Disord. 2013 Jul;43(7):1623-9. doi: 10.1007/s10803-012-1709-3. J Autism Dev Disord. 2013. PMID: 23124396 Free PMC article.

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