Literature DB >> 26078659

A case of congenital insensitivity to pain with anhidrosis.

Ahmet Kağan Özkaya1, Ekrem Güler1, Elif Arık1, Ali Rıza Namlı1, Derya Cevizli1, Olcay Güngör1.   

Abstract

Entities:  

Year:  2014        PMID： 26078659      PMCID： PMC4462290          DOI： 10.5152/tpa.2014.1549

Source DB:  PubMed          Journal:  Turk Pediatri Ars


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  6 in total

1.  Congenital insensitivity to pain with anhidrosis.

Authors:  L Sztriha; G G Lestringant; J Hertecant; P M Frossard; I Masouyé
Journal:  Pediatr Neurol       Date:  2001-07       Impact factor: 3.372

2.  Congenital sensory neuropathy with anhidrosis.

Authors:  F Vassella; H M Emrich; R Kraus-Ruppert; F Aufdermaur; O Tönz
Journal:  Arch Dis Child       Date:  1968-02       Impact factor: 3.791

Review 3.  Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): mutations and polymorphisms in TRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor.

Authors:  Y Indo
Journal:  Hum Mutat       Date:  2001-12       Impact factor: 4.878

4.  Muscle involvement in congenital insensitivity to pain with anhidrosis.

Authors:  N Tachi; K Ohya; S Chiba; H Nihira; K Minagawa
Journal:  Pediatr Neurol       Date:  1995-04       Impact factor: 3.372

Review 5.  Variation of muscular structure in congenital insensitivity to pain and anhidrosis.

Authors:  Zamir Shorer; Ruth Shaco-Levy; Vered Pinsk; Leonid Kachko; Jacov Levy
Journal:  Pediatr Neurol       Date:  2013-04       Impact factor: 3.372

6.  Hereditary insensitivity to pain with anhidrosis.

Authors:  M Berkovitch; L Copeliovitch; T Tauber; Z Vaknin; E Lahat
Journal:  Pediatr Neurol       Date:  1998-09       Impact factor: 3.372
  6 in total
  1 in total

Review 1.  Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature.

Authors:  Karim Elhennawy; Seif Reda; Christian Finke; Luitgard Graul-Neumann; Paul-Georg Jost-Brinkmann; Theodosia Bartzela
Journal:  J Med Case Rep       Date:  2017-08-15
  1 in total

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