Literature DB >> 9620018

Congenital insensitivity to pain with anhidrosis: lack of eccrine sweat gland innervation confirmed.

E A Ismail1, N Al-Shammari, J T Anim, A Moosa.   

Abstract

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Mesh：

Year:  1998        PMID： 9620018     DOI： 10.1177/088307389801300511

Source DB:  PubMed          Journal:  J Child Neurol        ISSN： 0883-0738            Impact factor:   1.987


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  4 in total

1.  Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor.

Authors:  S Mardy; Y Miura; F Endo; I Matsuda; L Sztriha; P Frossard; A Moosa; E A Ismail; A Macaya; G Andria; E Toscano; W Gibson; G E Graham; Y Indo
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

2.  Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.

Authors:  Beyhan Tüysüz; Fatih Bayrakli; Michael L DiLuna; Kaya Bilguvar; Yasar Bayri; Cengiz Yalcinkaya; Aysegul Bursali; Elif Ozdamar; Baris Korkmaz; Christopher E Mason; Ali K Ozturk; Richard P Lifton; Matthew W State; Murat Gunel
Journal:  Neurogenetics       Date:  2008-03-06       Impact factor: 2.660

Review 3.  Hereditary sensory and autonomic neuropathies: types II, III, and IV.

Authors:  Felicia B Axelrod; Gabrielle Gold-von Simson
Journal:  Orphanet J Rare Dis       Date:  2007-10-03       Impact factor: 4.123

4.  A Comprehensive Functional Analysis of NTRK1 Missense Mutations Causing Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV).

Authors:  Samiha S Shaikh; Ya-Chun Chen; Sally-Anne Halsall; Michael S Nahorski; Kiyoyuki Omoto; Gareth T Young; Anne Phelan; Christopher Geoffrey Woods
Journal:  Hum Mutat       Date:  2016-11-26       Impact factor: 4.878
  4 in total

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