H P Lipe
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Explore the profile of H P Lipe including associated specialties, affiliations and a list of published articles.
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15
Citations
165
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Recent Articles
1.
Bennett C, Lawson V, Brickell K, Isaacs K, Seltzer W, Lipe H, et al.
Neurology
. 2008 May;
71(1):14-20.
PMID: 18495953
Background: Hereditary motor-sensory neuropathy or the Charcot-Marie-Tooth syndrome is known to represent considerable genetic heterogeneity. Onset is usually in childhood, adolescence, or young adulthood. The objective of this study was...
2.
Chen D, Cimino P, Ranum L, Zoghbi H, Yabe I, Schut L, et al.
Neurology
. 2005 Apr;
64(7):1258-60.
PMID: 15824357
Spinocerebellar ataxia 14 (SCA14) is associated with missense mutations in the protein kinase C gamma gene (PRKCG), rather than a nucleotide repeat expansion. In this large-scale study of PRKCG in...
3.
Street V, Bennett C, Goldy J, Shirk A, Kleopa K, Tempel B, et al.
Neurology
. 2003 Jan;
60(1):22-6.
PMID: 12525712
Background: Charcot-Marie-Tooth (CMT) neuropathy is a heterogeneous group of inherited disorders of the peripheral nervous system. The authors recently mapped an autosomal dominant demyelinating form of CMT type 1 (CMT1C)...
4.
Street V, Meekins G, Lipe H, Seltzer W, Carter G, Kraft G, et al.
Neuromuscul Disord
. 2002 Sep;
12(7-8):643-50.
PMID: 12207932
Charcot-Marie-Tooth Hereditary Neuropathy is a heterogeneous syndrome associated with mutations in several different genes including peripheral myelin protein 22, myelin P0, connexin 32, and early growth response 2. There is...
5.
Bird T, Kraft G, Lipe H, Kenney K, SUMI S
Ann Neurol
. 1997 Apr;
41(4):463-9.
PMID: 9124803
Charcot-Marie-Tooth type 1B is an uncommon form of hereditary motor and sensory neuropathy caused by mutations in the P(0) myelin protein gene on chromosome 1. We report here a 20-year...
6.
Raskind W, Pericak-Vance M, Lennon F, Wolff J, Lipe H, Bird T
Am J Med Genet
. 1997 Feb;
74(1):26-36.
PMID: 9034002
Familial spastic paraparesis (SPG) is a clinically and genetically heterogeneous group of disorders. At least three loci have been implicated in autosomal dominant pure SPG and mutations in either of...
7.
Graf W, Chance P, Lensch M, Eng L, Lipe H, Bird T
Cancer
. 1996 Apr;
77(7):1356-62.
PMID: 8608515
Background: A general predisposition for vincristine-related neuropathy has been observed in persons with a family history of hereditary neuropathies. Methods: In a retrospective case series, we investigated the possible association...
8.
Bird T, Lipe H, Crabtree L
Eur Neurol
. 1994 Jan;
34(3):155-7.
PMID: 8033941
We report 7 men (ages 45-61 years) with impotence associated with the Charcot-Marie-Tooth syndrome (CMT). The range of onset of erectile dysfunction varied from 38 to 55 years of age....
9.
Bird T, Bennett R, Lipe H
N Engl J Med
. 1993 Apr;
328(14):1046.
PMID: 8450869
No abstract available.
10.
Bird T, Boehnke M, Schellenberg G, Deeb S, Lipe H
Arch Neurol
. 1987 Mar;
44(3):273-5.
PMID: 2881531
In five families we have confirmed the close linkage between the genes for myotonic dystrophy and apolipoprotein CII. The total maximum lod (log of the odds) score was 3.32 at...