An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis.
about
Oral and craniofacial manifestations and two novel missense mutations of the NTRK1 gene identified in the patient with congenital insensitivity to pain with anhidrosisA short in-frame deletion in NTRK1 tyrosine kinase domain caused by a novel splice site mutation in a patient with congenital insensitivity to pain with anhidrosis.Mechanisms of disease in hereditary sensory and autonomic neuropathies.Congenital insensitivity to pain with anhydrosis in a Malaysian family: a genetic analysis.Congenital Insensitivity to Pain and Anhydrosis: Diagnostic and Therapeutic Dilemmas revisited.Update Review and Clinical Presentation in Congenital Insensitivity to Pain and Anhidrosis.Molecular genetics of hereditary sensory neuropathies.NGF-TrkA Signaling by Sensory Nerves Coordinates the Vascularization and Ossification of Developing Endochondral Bone.Thermosensory and mechanosensory perception in human genetic disease.Mutations in TrkA Causing Congenital Insensitivity to Pain with Anhidrosis (CIPA) Induce Misfolding, Aggregation, and Mutation-dependent Neurodegeneration by Dysfunction of the Autophagic Flux.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.Congenital Insensitivity to Pain and Anhydrosis (CIPA) Syndrome; A Report of 4 Cases.Congenital insensitivity to pain and anhidrosis: a case report from South India.A Case Report of Congenital Insensitivity to Pain and Anhidrosis (CIPA).Cardiac arrest after anesthetic management in a patient with hereditary sensory autonomic neuropathy type IV.Expression of Nerve Growth Factor (NGF), TrkA, and p75(NTR) in Developing Human Fetal TeethNerve growth factor signalling in pathology and regeneration of human teeth.NGF-TrkA signaling in sensory nerves is required for skeletal adaptation to mechanical loads in mice.Phenotypic heterogeneity of intellectual disability in patients with congenital insensitivity to pain with anhidrosis: A case report and literature review.Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.Genetic studies of human neuropathic pain conditions: a review.
P2860
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P2860
An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis.
description
2003 nî lūn-bûn
@nan
2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
An infant with primary tooth l ...... ivity to pain with anhidrosis.
@ast
An infant with primary tooth l ...... ivity to pain with anhidrosis.
@en
An infant with primary tooth l ...... ivity to pain with anhidrosis.
@nl
type
label
An infant with primary tooth l ...... ivity to pain with anhidrosis.
@ast
An infant with primary tooth l ...... ivity to pain with anhidrosis.
@en
An infant with primary tooth l ...... ivity to pain with anhidrosis.
@nl
prefLabel
An infant with primary tooth l ...... ivity to pain with anhidrosis.
@ast
An infant with primary tooth l ...... ivity to pain with anhidrosis.
@en
An infant with primary tooth l ...... ivity to pain with anhidrosis.
@nl
P2093
P356
P1433
P1476
An infant with primary tooth l ...... ivity to pain with anhidrosis.
@en
P2093
A Gordon Smith
John C Carey
Joshua L Bonkowsky
Justine Johnson
Kathryn J Swoboda
P304
P356
10.1542/PEDS.112.3.E237
P407
P433
P577
2003-09-01T00:00:00Z