These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
181 related articles for article (PubMed ID: 31841741)
1. Congenital insensitivity to pain with anhidrosis syndrome: A series from Jordan. Masri A; Shboul M; Khasawneh A; Jadallah R; ALmustafa A; Escande-Beillard N; Hamamy H; Bakri F; Reversade B Clin Neurol Neurosurg; 2020 Feb; 189():105636. PubMed ID: 31841741 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Identification of a novel mutation of the NTRK1 gene in patients with congenital insensitivity to pain with anhidrosis (CIPA). Wang WB; Cao YJ; Lyu SS; Zuo RT; Zhang ZL; Kang QL Gene; 2018 Dec; 679():253-259. PubMed ID: 30201336 [TBL] [Abstract][Full Text] [Related]
5. Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families. Miura Y; Mardy S; Awaya Y; Nihei K; Endo F; Matsuda I; Indo Y Hum Genet; 2000 Jan; 106(1):116-24. PubMed ID: 10982191 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis. Huehne K; Zweier C; Raab K; Odent S; Bonnaure-Mallet M; Sixou JL; Landrieu P; Goizet C; Sarlangue J; Baumann M; Eggermann T; Rauch A; Ruppert S; Stettner GM; Rautenstrauss B Neuromuscul Disord; 2008 Feb; 18(2):159-66. PubMed ID: 18077166 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. Novel NTRK1 Frameshift Mutation in Congenital Insensitivity to Pain With Anhidrosis. Liu S; Wu N; Liu J; Ming X; Chen J; Pavelec D; Su X; Qiu G; Tian Y; Giampietro P; Wu Z J Child Neurol; 2015 Sep; 30(10):1357-61. PubMed ID: 25316729 [TBL] [Abstract][Full Text] [Related]
15. Congenital insensitivity to pain with anhidrosis presenting with palmoplantar keratoderma. Sayyahfar S; Chavoshzadeh Z; Khaledi M; Madadi F; Yeganeh MH; Sawamura D; Nakano H; Rezaei N Pediatr Dermatol; 2013; 30(6):754-6. PubMed ID: 22957891 [TBL] [Abstract][Full Text] [Related]
16. Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV. Verpoorten N; Claeys KG; Deprez L; Jacobs A; Van Gerwen V; Lagae L; Arts WF; De Meirleir L; Keymolen K; Ceuterick-de Groote C; De Jonghe P; Timmerman V; Nelis E Neuromuscul Disord; 2006 Jan; 16(1):19-25. PubMed ID: 16373086 [TBL] [Abstract][Full Text] [Related]
17. A 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. Sarasola E; Rodríguez JA; Garrote E; Arístegui J; García-Barcina MJ BMC Med Genet; 2011 Jun; 12():86. PubMed ID: 21708027 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Novel NTRK1 mutations in Chinese patients with congenital insensitivity to pain with anhidrosis. Geng X; Liu Y; Ren X; Guan Y; Wang Y; Mao B; Zhao X; Zhang X Mol Pain; 2018; 14():1744806918781140. PubMed ID: 29770739 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]