BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

296 related articles for article (PubMed ID: 11310631)

  • 1. A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V.
    Houlden H; King RH; Hashemi-Nejad A; Wood NW; Mathias CJ; Reilly M; Thomas PK
    Ann Neurol; 2001 Apr; 49(4):521-5. PubMed ID: 11310631
    [TBL] [Abstract][Full Text] [Related]  

  • 2. No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V.
    Toscano E; Simonati A; Indo Y; Andria G
    Ann Neurol; 2002 Aug; 52(2):224-7. PubMed ID: 12210794
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The evaluation of autonomic nervous function in a patient with hereditary sensory and autonomic neuropathy type IV with novel mutations of the TRKA gene.
    Ohto T; Iwasaki N; Fujiwara J; Ohkoshi N; Kimura S; Kawade K; Tanaka R; Matsui A
    Neuropediatrics; 2004 Oct; 35(5):274-8. PubMed ID: 15534759
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Congenital insensitivity to pain with anhidrosis in Taiwan: a morphometric and genetic study.
    Guo YC; Liao KK; Soong BW; Tsai CP; Niu DM; Lee HY; Lin KP
    Eur Neurol; 2004; 51(4):206-14. PubMed ID: 15159601
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two novel mutant alleles of the gene encoding neurotrophic tyrosine kinase receptor type 1 (NTRK1) in a patient with congenital insensitivity to pain with anhidrosis: a splice junction mutation in intron 5 and cluster of four mutations in exon 15.
    Bodzioch M; Lapicka K; Aslanidis C; Kacinski M; Schmitz G
    Hum Mutat; 2001; 17(1):72. PubMed ID: 11139246
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two brothers with a variant of hereditary sensory neuropathy.
    Pavone L; Huttenlocher P; Siciliano L; Micali G; Rizzo R; Anastasi M; Maimone D; Woolmann R
    Neuropediatrics; 1992 Apr; 23(2):92-5. PubMed ID: 1376446
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy.
    Polo A; Aldegheri R; Bongiovanni LG; Cavallaro T; Rizzuto N
    Neuropediatrics; 2000 Jun; 31(3):148-50. PubMed ID: 10963103
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Hereditary sensory and autonomic neuropathies. The neurophysiological and pathological aspects of two cases with congenital insensitivity to pain].
    Esteban-García A; Salinero-Paniagua E; Traba A; Prieto-Montalvo J; Polo-Arrondo AP; Godes-Medrano B; Fernández-Lorente J
    Rev Neurol; 2004 Sep 16-30; 39(6):525-9. PubMed ID: 15467989
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial insensitivity to pain (HSAN V) and a mutation in the NGFB gene. A neurophysiological and pathological study.
    Minde J; Toolanen G; Andersson T; Nennesmo I; Remahl IN; Svensson O; Solders G
    Muscle Nerve; 2004 Dec; 30(6):752-60. PubMed ID: 15468048
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Skoura - a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 gene.
    Suriu C; Khayat M; Weiler M; Kfir N; Cohen C; Zinger A; Aslanidis C; Schmitz G; Falik-Zaccai TC
    Clin Genet; 2009 Mar; 75(3):230-6. PubMed ID: 19250380
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A case of hereditary sensory autonomic neuropathy type II with late onset].
    Shimoya K; Ishimoto S; Ohnishi A; Yamamoto T
    Rinsho Shinkeigaku; 1999 May; 39(5):551-4. PubMed ID: 10424148
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital insensitivity to pain (hereditary sensory and autonomic neuropathy type V): a rare case report.
    Singla S; Marwah N; Dutta S
    J Dent Child (Chic); 2008; 75(2):207-11. PubMed ID: 18647521
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.
    Tüysüz B; Bayrakli F; DiLuna ML; Bilguvar K; Bayri Y; Yalcinkaya C; Bursali A; Ozdamar E; Korkmaz B; Mason CE; Ozturk AK; Lifton RP; State MW; Gunel M
    Neurogenetics; 2008 May; 9(2):119-25. PubMed ID: 18322713
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation.
    Rotthier A; Baets J; De Vriendt E; Jacobs A; Auer-Grumbach M; Lévy N; Bonello-Palot N; Kilic SS; Weis J; Nascimento A; Swinkels M; Kruyt MC; Jordanova A; De Jonghe P; Timmerman V
    Brain; 2009 Oct; 132(Pt 10):2699-711. PubMed ID: 19651702
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.