Literature DB >> 7218272

Genetic aspects of hereditary motor and sensory neuropathy (types I and II).

A E Harding, P K Thomas.   

Abstract

Entities:  

Mesh：

Year:  1980        PMID： 7218272      PMCID： PMC1048594          DOI： 10.1136/jmg.17.5.329

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


× No keyword cloud information.
  19 in total

1.  Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.

Authors:  P S Harper; P R Dyken
Journal:  Lancet       Date:  1972-07-08       Impact factor: 79.321

2.  Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.

Authors:  P J Dyck; E H Lambert
Journal:  Arch Neurol       Date:  1968-06

3.  Onion bulbs in a nerve biopsy specimen from an original case of Roussy-Lévy disease.

Authors:  J Lapresle; P Salisachs; L Kremlin-Bicêtre
Journal:  Arch Neurol       Date:  1973-11

4.  Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneity.

Authors:  P K Thomas; D B Calne
Journal:  J Neurol Neurosurg Psychiatry       Date:  1974-01       Impact factor: 10.154

5.  Wide spectrum of motor conduction velocity in Charcot-Marie-Tooth disease. An anatomico-physiological interpretation.

Authors:  P Salisachs
Journal:  J Neurol Sci       Date:  1974-09       Impact factor: 3.181

6.  Nerve conduction studies in Charcot-Marie-Tooth disease.

Authors:  P M Humberstone
Journal:  Acta Neurol Scand       Date:  1972       Impact factor: 3.209

7.  A recessively inherited mixed polyneuropathy of early onset.

Authors:  M Mahloudji
Journal:  J Med Genet       Date:  1969-12       Impact factor: 6.318

8.  A distal form of chronic spinal muscular atrophy.

Authors:  J C Meadows; C D Marsden
Journal:  Neurology       Date:  1969-01       Impact factor: 9.910

9.  Distal muscular dystrophy in an English family.

Authors:  D Sumner; M D Crawfurd; D G Harriman
Journal:  Brain       Date:  1971       Impact factor: 13.501

10.  Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations.

Authors:  P J Dyck; E H Lambert
Journal:  Arch Neurol       Date:  1968-06
View more
  47 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.  Estimation of the inbreeding coefficient through use of genomic data.

Authors:  Anne-Louise Leutenegger; Bernard Prum; Emmanuelle Génin; Christophe Verny; Arnaud Lemainque; Françoise Clerget-Darpoux; Elizabeth A Thompson
Journal:  Am J Hum Genet       Date:  2003-07-29       Impact factor: 11.025

3.  Therapeutic strategies for the inherited neuropathies.

Authors:  Michael E Shy
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

4.  Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene region.

Authors:  R V Lebo; P F Chance; P J Dyck; M T Redila-Flores; E D Lynch; M S Golbus; T D Bird; M C King; L A Anderson; J Hall
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

5.  Charcot-Marie-Tooth disease subtypes and genetic testing strategies.

Authors:  Anita S D Saporta; Stephanie L Sottile; Lindsey J Miller; Shawna M E Feely; Carly E Siskind; Michael E Shy
Journal:  Ann Neurol       Date:  2011-01       Impact factor: 10.422

Review 6.  Hereditary motor and sensory neuropathies.

Authors:  J M Vance
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

7.  Degeneration of anterior horn cell in neuronal type of Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type II): a Golgi study.

Authors:  S Ono; K Hara; H Sasaki; I Sugano; K Nagao
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

8.  Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathy.

Authors:  P R Fain; D F Barker; P F Chance
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

9.  MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs.

Authors:  Obaid M Albulym; Marina L Kennerson; Matthew B Harms; Alexander P Drew; Anna H Siddell; Michaela Auer-Grumbach; Alan Pestronk; Anne Connolly; Robert H Baloh; Stephan Zuchner; Stephen W Reddel; Garth A Nicholson
Journal:  Ann Neurol       Date:  2016-01-13       Impact factor: 10.422

10.  Homozygous hypertrophic hereditary motor and sensory neuropathies.

Authors:  A Sghirlanzoni; D Pareyson; R Marazzi; G Cavaletti; E Bellone; P Mandich; M R Balestrini; D Riva
Journal:  Ital J Neurol Sci       Date:  1994-02
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.