Literature DB >> 4123669

Congenital sensory neuropathy.

T J Murray.   

Abstract

Entities:  

Mesh:

Year:  1973        PMID: 4123669     DOI: 10.1093/brain/96.2.387

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


× No keyword cloud information.
  17 in total

1.  Novel mutation in the HSN2 gene in a Korean patient with hereditary sensory and autonomic neuropathy type 2.

Authors:  Hyun-Jung Cho; Byoung Joon Kim; Yeon-Lim Suh; Jae-Young An; Chang-Seok Ki
Journal:  J Hum Genet       Date:  2006-09-01       Impact factor: 3.172

2.  Thomas John (Jock) Murray, OC, MD, FRCP(C), MACP, LLD(HON), DSc(Hon), FRCP(Lon): a conversation with the editor. Interview by William Clifford Roberts.

Authors:  Thomas John Murray
Journal:  Proc (Bayl Univ Med Cent)       Date:  2003-10

Review 3.  Autonomic involvement in inherited neuropathies.

Authors:  P K Thomas
Journal:  Clin Auton Res       Date:  1992-02       Impact factor: 4.435

4.  Soradic ulcerative mutilating acropathy with imbalance of free amino acids in the cerebrospinal fluid.

Authors:  F Monaco; A Riccio; A Covacich; L Durelli; M T Giordana; L Palmucci
Journal:  J Neurol Neurosurg Psychiatry       Date:  1975-08       Impact factor: 10.154

5.  A new variety of hereditary sensory neuropathy.

Authors:  G C Robinson; J E Jan; J R Miller
Journal:  Hum Genet       Date:  1977-02-11       Impact factor: 4.132

6.  Congenital insensitivity to pain: a 20 year follow up.

Authors:  A J Larner; J Moss; M L Rossi; M Anderson
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-08       Impact factor: 10.154

7.  Congenital indifference to pain.

Authors:  N Biswal; V M Sundaram; B Mathai; S Balasubramanian
Journal:  Indian J Pediatr       Date:  1998 Sep-Oct       Impact factor: 1.967

8.  Editorial: Insensitivity to pain.

Authors: 
Journal:  Br Med J       Date:  1973-10-27

9.  A new neurological rat mutant "mutilated foot".

Authors:  J M Jacobs; F Scaravilli; L W Duchen; J Mertin
Journal:  J Anat       Date:  1981-06       Impact factor: 2.610

10.  Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II.

Authors:  Masoud Shekarabi; Nathalie Girard; Jean-Baptiste Rivière; Patrick Dion; Martin Houle; André Toulouse; Ronald G Lafrenière; Freya Vercauteren; Pascale Hince; Janet Laganiere; Daniel Rochefort; Laurence Faivre; Mark Samuels; Guy A Rouleau
Journal:  J Clin Invest       Date:  2008-07       Impact factor: 14.808

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.