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.
172 related articles for article (PubMed ID: 35768377)
1. [Marsili syndrome manifested by fever: a case report and literature review]. Xiong XM; Wei XY; Wang HY; Wen ZG Zhonghua Jie He He Hu Xi Za Zhi; 2022 Jul; 45(7):686-691. PubMed ID: 35768377 [No Abstract] [Full Text] [Related]
2. 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]
3. A rare case of congenital insensitivity to pain with anhidrosis. Sreenivasan V; Karunakar P; Madhileti S; Govindaswamy Ramamoorthy J; Gulati R Paediatr Int Child Health; 2024 Aug; 44(2):59-62. PubMed ID: 38659257 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. A novel mutation in the SCN9A gene associated with congenital insensitivity to pain, anhidrosis, and mild cognitive impairment. Romagnuolo M; Moltrasio C; Cavalli R; Brena M; Tadini G Pediatr Dermatol; 2024; 41(1):80-83. PubMed ID: 37345838 [TBL] [Abstract][Full Text] [Related]
7. An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis. Bonkowsky JL; Johnson J; Carey JC; Smith AG; Swoboda KJ Pediatrics; 2003 Sep; 112(3 Pt 1):e237-41. PubMed ID: 12949319 [TBL] [Abstract][Full Text] [Related]
8. [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]
9. Identification of novel variations in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis. Li S; Hu HY; Xu JJ; Feng ZK; Sun YQ; Chen X; Yang K; Li YZ; Zhang DL Mol Genet Genomic Med; 2021 Nov; 9(11):e1839. PubMed ID: 34674383 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
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. 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]
15. Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis. Indo Y; Tsuruta M; Hayashida Y; Karim MA; Ohta K; Kawano T; Mitsubuchi H; Tonoki H; Awaya Y; Matsuda I Nat Genet; 1996 Aug; 13(4):485-8. PubMed ID: 8696348 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy. Kurth I; Baumgartner M; Schabhüttl M; Tomni C; Windhager R; Strom TM; Wieland T; Gremel K; Auer-Grumbach M Am J Med Genet B Neuropsychiatr Genet; 2016 Sep; 171(6):875-8. PubMed ID: 27184211 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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] [Next] [New Search]