Fenichel GM - Search Results

1

Nonsense and missense mutations of the muscle chloride channel gene in patients with myotonia congenita.

George AL Jr, Sloan-Brown K, Fenichel GM, Mitchell GA, Spiegel R, Pascuzzi RM. George AL Jr, et al. Among authors: fenichel gm. Hum Mol Genet. 1994 Nov;3(11):2071-2. Hum Mol Genet. 1994. PMID: 7874130 No abstract available.

2

Three new mutations in patients with myophosphorylase deficiency (McArdle disease).

Tsujino S, Shanske S, Nonaka I, Eto Y, Mendell JR, Fenichel GM, DiMauro S. Tsujino S, et al. Among authors: fenichel gm. Am J Hum Genet. 1994 Jan;54(1):44-52. Am J Hum Genet. 1994. PMID: 8279469 Free PMC article.

3

Sneddon and antiphospholipid antibody syndromes causing bilateral thalamic infarction.

Charles PD, Fenichel GM. Charles PD, et al. Among authors: fenichel gm. Pediatr Neurol. 1994 May;10(3):262-3. doi: 10.1016/0887-8994(94)90037-x. Pediatr Neurol. 1994. PMID: 8060434

4

Dystonia and unique muscle features. A 23-year follow-up and correction of diagnosis in two brothers.

Charles PD, Davis TL, Robertson D, Fenichel GM. Charles PD, et al. Among authors: fenichel gm. Arch Neurol. 1995 Aug;52(8):825-6. doi: 10.1001/archneur.1995.00540320109018. Arch Neurol. 1995. PMID: 7639635

5

Neurological examination of the newborn.

Fenichel GM. Fenichel GM. Brain Dev. 1993 Nov-Dec;15(6):403-10. doi: 10.1016/0387-7604(93)90079-n. Brain Dev. 1993. PMID: 8147498 Review.

6

Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia.

Hedera P, Fenichel GM, Blair M, Haines JL. Hedera P, et al. Among authors: fenichel gm. Arch Neurol. 2004 Oct;61(10):1600-3. doi: 10.1001/archneur.61.10.1600. Arch Neurol. 2004. PMID: 15477516

7

Chronic post-traumatic headache often a myth?

Warner JS, Fenichel GM. Warner JS, et al. Among authors: fenichel gm. Neurology. 1996 Apr;46(4):915-6. doi: 10.1212/wnl.46.4.915. Neurology. 1996. PMID: 8780063 No abstract available.

8

Genetic forms of myasthenia gravis.

Misulis KE, Fenichel GM. Misulis KE, et al. Among authors: fenichel gm. Pediatr Neurol. 1989 Jul-Aug;5(4):205-10. doi: 10.1016/0887-8994(89)90076-3. Pediatr Neurol. 1989. PMID: 2679583 Review.

9

A beneficial effect of oxandrolone in the treatment of Duchenne muscular dystrophy: a pilot study.

Fenichel G, Pestronk A, Florence J, Robison V, Hemelt V. Fenichel G, et al. Neurology. 1997 May;48(5):1225-6. doi: 10.1212/wnl.48.5.1225. Neurology. 1997. PMID: 9153447

10

Long-term benefit from prednisone therapy in Duchenne muscular dystrophy.

Fenichel GM, Florence JM, Pestronk A, Mendell JR, Moxley RT 3rd, Griggs RC, Brooke MH, Miller JP, Robison J, King W, et al. Fenichel GM, et al. Neurology. 1991 Dec;41(12):1874-7. doi: 10.1212/wnl.41.12.1874. Neurology. 1991. PMID: 1745340 Clinical Trial.

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