270 related articles for article (PubMed ID: 31395116)
1. Congenital Insensitivity to Pain with Anhidrosis: A Case with Self-Inflicted Oral Ulcerations.
Soussou R; Cheung WS; Campbell KM
J Dent Child (Chic); 2019 May; 86(2):109-112. PubMed ID: 31395116
[TBL] [Abstract][Full Text] [Related]
2. A 5-Year-Old Palestinian Bedouin Girl with Repeated Self-Induced Injuries to the Digits, a Diagnosis of Congenital Insensitivity to Pain, and Anhidrosis.
Hanatleh OM; Kofahi NK; Aburahma SK; Bintareef EM; Al-Bashtawy M; Alkhawaldeh A; Ibnian AM
Am J Case Rep; 2021 Nov; 22():e933486. PubMed ID: 34732685
[TBL] [Abstract][Full Text] [Related]
3. Genetics of congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV. Clinical, biological and molecular aspects of mutations in TRKA(NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor.
Indo Y
Clin Auton Res; 2002 May; 12 Suppl 1():I20-32. PubMed ID: 12102460
[TBL] [Abstract][Full Text] [Related]
4. Congenital Loss of Permanent Teeth in a Patient With Congenital Insensitivity to Pain With Anhidrosis due to 2 Novel Mutations in the NTRK1 Gene.
Xue XM; Liu YQ; Pang P; Sun CF
J Oral Maxillofac Surg; 2018 Dec; 76(12):2582.e1-2582.e9. PubMed ID: 30075136
[TBL] [Abstract][Full Text] [Related]
5. Clinical and genetic characteristics of three patients with congenital insensitivity to pain with anhidrosis: Case reports and a review of the literature.
Cho JH; Hwang S; Kwak YH; Yum MS; Seo GH; Koh JY; Ju YS; Yoon JH; Kang M; Do HS; Kim S; Kim GH; Bae H; Lee BH
Mol Genet Genomic Med; 2024 Apr; 12(4):e2430. PubMed ID: 38581121
[TBL] [Abstract][Full Text] [Related]
6. [Congenital insensitivity to pain with anhidrosis associated with congenital myasthenic syndrome].
Raspall-Chaure M; Del Toro-Riera M; Gratacós M; Cuenca-León E; Ferrer I; Indo Y; Roig-Quilis M; Macaya-Ruiz A
Rev Neurol; 2005 Aug 16-31; 41(4):218-22. PubMed ID: 16075400
[TBL] [Abstract][Full Text] [Related]
7. Oral manifestations of hereditary sensory and autonomic neuropathy type IV. Congenital insensitivity to pain with anhidrosis.
Amano A; Akiyama S; Ikeda M; Morisaki I
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 1998 Oct; 86(4):425-31. PubMed ID: 9798226
[TBL] [Abstract][Full Text] [Related]
8. Clinical and genetic analysis of Korean patients with congenital insensitivity to pain with anhidrosis.
Lee ST; Lee J; Lee M; Kim JW; Ki CS
Muscle Nerve; 2009 Nov; 40(5):855-9. PubMed ID: 19618435
[TBL] [Abstract][Full Text] [Related]
9. Novel nonsense and frameshift NTRK1 gene mutations in Chinese patients with congenital insensitivity to pain with anhidrosis.
Li M; Liang JY; Sun ZH; Zhang H; Yao ZR
Genet Mol Res; 2012 Aug; 11(3):2156-62. PubMed ID: 22653642
[TBL] [Abstract][Full Text] [Related]
10. NTRK1 gene-related congenital insensitivity to pain with anhidrosis: a nationwide multicenter retrospective study.
Echaniz-Laguna A; Altuzarra C; Verloes A; De La Banda MGG; Quijano-Roy S; Tudorache RA; Jaxybayeva A; Myrzaliyeva B; Tazir M; Vallat JM; Francou B; Urtizberea JA
Neurogenetics; 2021 Oct; 22(4):333-341. PubMed ID: 34405299
[TBL] [Abstract][Full Text] [Related]
11. Identification of a novel nonsense mutation of the neurotrophic tyrosine kinase receptor type 1 gene in two siblings with congenital insensitivity to pain with anhidrosis.
Wang T; Li H; Xiang J; Wei B; Zhang Q; Zhu Q; Liu M; Sun M; Li H
J Int Med Res; 2017 Apr; 45(2):549-555. PubMed ID: 28345382
[TBL] [Abstract][Full Text] [Related]
12. Novel NTRK1 mutations associated with congenital insensitivity to pain with anhidrosis verified by functional studies.
Nam TS; Li W; Yoon S; Eom GH; Kim MK; Jung ST; Choi SY
J Peripher Nerv Syst; 2017 Jun; 22(2):92-99. PubMed ID: 28177573
[TBL] [Abstract][Full Text] [Related]
13. 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.
Indo Y
Hum Mutat; 2001 Dec; 18(6):462-71. PubMed ID: 11748840
[TBL] [Abstract][Full Text] [Related]
14. Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency.
Indo Y; Mardy S; Miura Y; Moosa A; Ismail EA; Toscano E; Andria G; Pavone V; Brown DL; Brooks A; Endo F; Matsuda I
Hum Mutat; 2001 Oct; 18(4):308-18. PubMed ID: 11668614
[TBL] [Abstract][Full Text] [Related]
15. Molecular genetic analysis in 21 Chinese families with congenital insensitivity to pain with or without anhidrosis.
Zhao F; Mao B; Geng X; Ren X; Wang Y; Guan Y; Li S; Li L; Zhang S; You Y; Cao Y; Yang T; Zhao X
Eur J Neurol; 2020 Aug; 27(8):1697-1705. PubMed ID: 32219930
[TBL] [Abstract][Full Text] [Related]
16. Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.
Altassan R; Saud HA; Masoodi TA; Dosssari HA; Khalifa O; Al-Zaidan H; Sakati N; Rhabeeni Z; Al-Hassnan Z; Binamer Y; Alhashemi N; Wade W; Al-Zayed Z; Al-Sayed M; Al-Muhaizea MA; Meyer B; Al-Owain M; Wakil SM
Am J Med Genet A; 2017 Apr; 173(4):1009-1016. PubMed ID: 28328124
[TBL] [Abstract][Full Text] [Related]
17. Congenital insensitivity to pain with anhidrosis: A report of two siblings with a novel mutation in (TrkA) NTRK1 gene in a Saudi family.
Algahtani H; Naseer MI; Al-Qahtani M; Abdulrahman SA; Boker F; Shirah B
J Neurol Sci; 2016 Nov; 370():35-38. PubMed ID: 27772781
[TBL] [Abstract][Full Text] [Related]
18. Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type IV).
Rosemberg S; Marie SK; Kliemann S
Pediatr Neurol; 1994 Jul; 11(1):50-6. PubMed ID: 7527213
[TBL] [Abstract][Full Text] [Related]
19. Identification of founder and novel mutations that cause congenital insensitivity to pain (CIP) in palestinian patients.
Khaled B; Alzahayqa M; Jaffal A; Sallam H; Thawabta R; Mansour M; Alian A; Salah Z
BMC Med Genomics; 2023 May; 16(1):120. PubMed ID: 37248554
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
