Literature DB >> 7745396

Myelin gene dosage and mutation in the hereditary motor and sensory neuropathies: a review.

G Nicholson.   

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Year:  1995        PMID： 7745396      PMCID： PMC1073479          DOI： 10.1136/jnnp.58.5.523

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  35 in total

1.  Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).

Authors:  P F Chance; T D Bird; P O'Connell; H Lipe; J M Lalouel; M Leppert
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

2.  Expression of P0 protein in sural nerve of a patient with hereditary motor and sensory neuropathy type III.

Authors:  N Tachi; K Kasai; S Chiba; M Naganuma; K Uyemura; K Hayasaka
Journal:  J Neurol Sci       Date:  1994-06       Impact factor: 3.181

3.  Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease.

Authors:  D Ellis; S Malcolm
Journal:  Nat Genet       Date:  1994-04       Impact factor: 38.330

4.  A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease.

Authors:  F Barbieri; R Santangelo; C Crisci; M Ragno; A Perretti; L Santoro
Journal:  Clin Neurol Neurosurg       Date:  1990       Impact factor: 1.876

5.  Onion bulb neuropathy in the trembler mouse: a model of hypertrophic interstitial neuropathy (Dejerine-Sottas) in man.

Authors:  M M Ayers; R M Anderson
Journal:  Acta Neuropathol       Date:  1973-06-26       Impact factor: 17.088

6.  DNA duplication associated with Charcot-Marie-Tooth disease type 1A.

Authors:  J R Lupski; R M de Oca-Luna; S Slaugenhaupt; L Pentao; V Guzzetta; B J Trask; O Saucedo-Cardenas; D F Barker; J M Killian; C A Garcia; A Chakravarti; P I Patel
Journal:  Cell       Date:  1991-07-26       Impact factor: 41.582

7.  Penetrance of the hereditary motor and sensory neuropathy Ia mutation: assessment by nerve conduction studies.

Authors:  G A Nicholson
Journal:  Neurology       Date:  1991-04       Impact factor: 9.910

8.  Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17.

Authors:  J M Vance; G A Nicholson; L H Yamaoka; J Stajich; C S Stewart; M C Speer; W Y Hung; A D Roses; D Barker; M A Pericak-Vance
Journal:  Exp Neurol       Date:  1989-05       Impact factor: 5.330

9.  Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B.

Authors:  T Kulkens; P A Bolhuis; R A Wolterman; S Kemp; S te Nijenhuis; L J Valentijn; G W Hensels; F G Jennekens; M de Visser; J E Hoogendijk
Journal:  Nat Genet       Date:  1993-09       Impact factor: 38.330

10.  De-novo mutation in hereditary motor and sensory neuropathy type I.

Authors:  J E Hoogendijk; G W Hensels; A A Gabreëls-Festen; F J Gabreëls; E A Janssen; P de Jonghe; J J Martin; C van Broeckhoven; L J Valentijn; F Baas
Journal:  Lancet       Date:  1992-05-02       Impact factor: 79.321
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  1 in total

1.  Slowing of central conduction in X-linked Charcot-Marie-Tooth neuropathy shown by brain stem auditory evoked responses.

Authors:  G Nicholson; A Corbett
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-07       Impact factor: 10.154
  1 in total

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