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There are 17406 results for: content related to: Congenital Insensitivity to Pain with Anhidrosis Presenting with Palmoplantar Keratoderma

  1. Novel NTRK1 mutations associated with congenital insensitivity to pain with anhidrosis verified by functional studies

    Journal of the Peripheral Nervous System

    Volume 22, Issue 2, June 2017, Pages: 92–99, Tai-Seung Nam, Wenting Li, Somy Yoon, Gwang Hyeon Eom, Myeong-Kyu Kim, Sung Taek Jung and Seok-Yong Choi

    Version of Record online : 8 JUN 2017, DOI: 10.1111/jns.12205

  2. The Gly571arg mutation, associated with the autonomic and sensory disorder congenital insensitivity to pain with anhidrosis, causes the inactivation of the NTRK1/nerve growth factor receptor

    Journal of Cellular Physiology

    Volume 182, Issue 1, January 2000, Pages: 127–133, Angela Greco, Riccardo Villa, Lisa Fusetti, Rosaria Orlandi and Marco A. Pierotti

    Version of Record online : 18 NOV 1999, DOI: 10.1002/(SICI)1097-4652(200001)182:1<127::AID-JCP14>3.0.CO;2-0

  3. 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

    Human Mutation

    Volume 18, Issue 6, December 2001, Pages: 462–471, Yasuhiro Indo

    Version of Record online : 13 NOV 2001, DOI: 10.1002/humu.1224

  4. Clinical and genetic analysis of Korean patients with congenital insensitivity to pain with anhidrosis

    Muscle & Nerve

    Volume 40, Issue 5, November 2009, Pages: 855–859, Seung-Tae Lee, Jeehun Lee, Munhyang Lee, Jong-Won Kim and Chang-Seok Ki

    Version of Record online : 17 JUL 2009, DOI: 10.1002/mus.21340

  5. You have free access to this content
    Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosis

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 341–350, Y Indo

    Version of Record online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01943.x

  6. Skoura – a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 gene

    Clinical Genetics

    Volume 75, Issue 3, March 2009, Pages: 230–236, C Suriu, M Khayat, M Weiler, N Kfir, C Cohen, A Zinger, C Aslanidis, G Schmitz and TC Falik-Zaccai

    Version of Record online : 31 DEC 2008, DOI: 10.1111/j.1399-0004.2008.01143.x

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    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

    Human Mutation

    Volume 17, Issue 1, 2001, Page: 72, Marek Bodzioch, Katarzyna Lapicka, Charalampos Aslanidis, Marek Kacinski and Gerd Schmitz

    Version of Record online : 22 DEC 2000, DOI: 10.1002/1098-1004(2001)17:1<72::AID-HUMU10>3.0.CO;2-X

  8. 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

    Human Mutation

    Volume 18, Issue 4, October 2001, Pages: 308–318, Yasuhiro Indo, Sek Mardy, Yuichi Miura, Allie Moosa, Essam A.R. Ismail, Ennio Toscano, Generoso Andria, Vito Pavone, Deborah L. Brown, Alice Brooks, Fumio Endo and Ichiro Matsuda

    Version of Record online : 18 SEP 2001, DOI: 10.1002/humu.1192

  9. RET and NTRK1 proto-oncogenes in human diseases

    Journal of Cellular Physiology

    Volume 195, Issue 2, May 2003, Pages: 168–186, Luisella Alberti, Cristiana Carniti, Claudia Miranda, Emanuela Roccato and Marco A. Pierotti

    Version of Record online : 11 MAR 2003, DOI: 10.1002/jcp.10252

  10. Functional characterization of NTRK1 mutations identified in melanoma

    Genes, Chromosomes and Cancer

    Volume 53, Issue 10, October 2014, Pages: 875–880, Claudia Miranda, Mara Mazzoni, Marialuisa Sensi, Marco A. Pierotti and Angela Greco

    Version of Record online : 25 JUN 2014, DOI: 10.1002/gcc.22200

  11. Neurobiology of pain, interoception and emotional response: lessons from nerve growth factor-dependent neurons

    European Journal of Neuroscience

    Volume 39, Issue 3, February 2014, Pages: 375–391, Yasuhiro Indo

    Version of Record online : 4 FEB 2014, DOI: 10.1111/ejn.12448

  12. Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype

    American Journal of Medical Genetics Part A

    Volume 173, Issue 4, April 2017, Pages: 1009–1016, Ruqaiah Altassan, Haya Al Saud, Tariq Ahmad Masoodi, Haya Al Dosssari, Ola Khalifa, Hamad Al-Zaidan, Nadia Sakati, Zuhair Rhabeeni, Zuhair Al-Hassnan, Yousef Binamer, Nadia Alhashemi, William Wade, Zayed Al-Zayed, Moeen Al-Sayed, Mohamed A. Al-Muhaizea, Brian Meyer, Mohammad Al-Owain and Salma M. Wakil

    Version of Record online : 22 MAR 2017, DOI: 10.1002/ajmg.a.38120

  13. Abnormal Pain Conditions in Humans Related to Genetic Mutations

    Pain Genetics: Basic to Translational Science

    Inna Belfer, Luda Diatchenko, Pages: 61–77, 2013

    Published Online : 22 NOV 2013, DOI: 10.1002/9781118398890.ch5

  14. Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 6, September 2016, Pages: 875–878, Ingo Kurth, Manuela Baumgartner, Maria Schabhüttl, Cecilia Tomni, Reinhard Windhager, Tim M. Strom, Thomas Wieland, Kurt Gremel and Michaela Auer-Grumbach

    Version of Record online : 17 MAY 2016, DOI: 10.1002/ajmg.b.32458

  15. Congenital insensitivity to pain with anhidrosis: a case with preserved itch sensation to histamine and partial pain sensation

    British Journal of Dermatology

    Volume 166, Issue 4, April 2012, Pages: 888–891, T. Tanaka, T. Satoh, A. Tanaka and H. Yokozeki

    Version of Record online : 6 FEB 2012, DOI: 10.1111/j.1365-2133.2011.10706.x

  16. Clinical significance of NTRK family gene expression in neuroblastomas

    Pediatric Blood & Cancer

    Volume 59, Issue 2, August 2012, Pages: 226–232, Jennifer E. Light, Hiroshi Koyama, Jane E. Minturn, Ruth Ho, Anisha M. Simpson, Radhika Iyer, Jennifer L. Mangino, Venkatadri Kolla, Wendy B. London and Garrett M. Brodeur

    Version of Record online : 11 OCT 2011, DOI: 10.1002/pbc.23343

  17. Norepinephrine deficiency with normal blood pressure control in congenital insensitivity to pain with anhidrosis

    Annals of Neurology

    Volume 77, Issue 5, May 2015, Pages: 743–752, Lucy Norcliffe-Kaufmann, Stuart D. Katz, Felicia Axelrod and Horacio Kaufmann

    Version of Record online : 13 MAR 2015, DOI: 10.1002/ana.24377

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    NTRK1 re-arrangement in papillary thyroid carcinomas of children after the Chernobyl reactor accident

    International Journal of Cancer

    Volume 80, Issue 6, 15 March 1999, Pages: 842–847, Claudia Beimfohr, Sabine Klugbauer, Evgenij P. Demidchik, Edmund Lengfelder and Hartmut M. Rabes

    Version of Record online : 8 NOV 1999, DOI: 10.1002/(SICI)1097-0215(19990315)80:6<842::AID-IJC7>3.0.CO;2-Z

  19. Hereditary sensory and autonomic neuropathy types IV and V in Japan

    Pediatrics International

    Volume 57, Issue 1, February 2015, Pages: 30–36, Nobuhiko Haga, Masaya Kubota, Zenzo Miwa and on behalf of the Japanese Research Group on Congenital Insensitivity to Pain

    Version of Record online : 25 FEB 2015, DOI: 10.1111/ped.12538

  20. Gene Expression and Localization of NGF and Its Cognate Receptors NTRK1 and NGFR in the Sex Organs of Male Rabbits

    Reproduction in Domestic Animals

    Volume 50, Issue 6, December 2015, Pages: 918–925, M Maranesi, M Zerani, L Leonardi, A Pistilli, J Arruda-Alencar, AM Stabile, M Rende, C Castellini, L Petrucci, F Parillo, A Moura and C Boiti

    Version of Record online : 22 SEP 2015, DOI: 10.1111/rda.12609