Chance PF - Search Results

1

Autosomal dominant transmission of Dejerine-Sottas disease (HMSN III).

Lynch DR, Hara H, Yum SW, Chance PF, Scherer SS, Bird SJ, Fischbeck KH. Lynch DR, et al. Among authors: chance pf. Neurology. 1997 Aug;49(2):601-3. doi: 10.1212/wnl.49.2.601. Neurology. 1997. PMID: 9270606

2

Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies.

Chance PF, Fischbeck KH. Chance PF, et al. Hum Mol Genet. 1994;3 Spec No:1503-7. doi: 10.1093/hmg/3.suppl_1.1503. Hum Mol Genet. 1994. PMID: 7849745 Review.

3

Connexin mutations in X-linked Charcot-Marie-Tooth disease.

Bergoffen J, Scherer SS, Wang S, Scott MO, Bone LJ, Paul DL, Chen K, Lensch MW, Chance PF, Fischbeck KH. Bergoffen J, et al. Among authors: chance pf. Science. 1993 Dec 24;262(5142):2039-42. doi: 10.1126/science.8266101. Science. 1993. PMID: 8266101

4

Linkage localization of X-linked Charcot-Marie-Tooth disease.

Bergoffen J, Trofatter J, Pericak-Vance MA, Haines JL, Chance PF, Fischbeck KH. Bergoffen J, et al. Among authors: chance pf. Am J Hum Genet. 1993 Feb;52(2):312-8. Am J Hum Genet. 1993. PMID: 8430694 Free PMC article.

5

A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4) localizes to a 500-kb interval on chromosome 9q34.

Blair IP, Bennett CL, Abel A, Rabin BA, Griffin JW, Fischbeck KH, Cornblath DR, Chance PF. Blair IP, et al. Among authors: chance pf. Neurogenetics. 2000 Sep;3(1):1-6. doi: 10.1007/pl00022976. Neurogenetics. 2000. PMID: 11085590

6

Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C.

Street VA, Bennett CL, Goldy JD, Shirk AJ, Kleopa KA, Tempel BL, Lipe HP, Scherer SS, Bird TD, Chance PF. Street VA, et al. Among authors: chance pf. Neurology. 2003 Jan 14;60(1):22-6. doi: 10.1212/wnl.60.1.22. Neurology. 2003. PMID: 12525712

7

Autosomal dominant juvenile amyotrophic lateral sclerosis.

Rabin BA, Griffin JW, Crain BJ, Scavina M, Chance PF, Cornblath DR. Rabin BA, et al. Among authors: chance pf. Brain. 1999 Aug;122 ( Pt 8):1539-50. doi: 10.1093/brain/122.8.1539. Brain. 1999. PMID: 10430837

8

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disorders.

Chance PF, Lensch MW, Lipe H, Brown RH Sr, Brown RH Jr, Bird TD. Chance PF, et al. Neurology. 1994 Dec;44(12):2253-7. doi: 10.1212/wnl.44.12.2253. Neurology. 1994. PMID: 7991108

9

Myelin genes: getting the dosage right.

Scherer SS, Chance PF. Scherer SS, et al. Among authors: chance pf. Nat Genet. 1995 Nov;11(3):226-8. doi: 10.1038/ng1195-226. Nat Genet. 1995. PMID: 7581438 No abstract available.

10

Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy.

Jeannet PY, Watts GD, Bird TD, Chance PF. Jeannet PY, et al. Among authors: chance pf. Neurology. 2001 Dec 11;57(11):1963-8. doi: 10.1212/wnl.57.11.1963. Neurology. 2001. PMID: 11739810

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