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Journal Abstract Search

379 related items for PubMed ID: 15467989

  • 1. [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; ; 39(6):525-9. PubMed ID: 15467989
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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 Apr; 75(2):207-11. PubMed ID: 18647521
    [Abstract] [Full Text] [Related]

  • 4. Congenital insensitivity to pain with anhidrosis: morphological and morphometrical studies on the skin and peripheral nerves.
    Itoh Y, Yagishita S, Nakajima S, Nakano T, Kawada H.
    Neuropediatrics; 1986 May; 17(2):103-10. PubMed ID: 2425284
    [Abstract] [Full Text] [Related]

  • 5. Assessment and evaluation of hereditary sensory and autonomic neuropathies with autonomic and neurophysiological examinations.
    Hilz MJ.
    Clin Auton Res; 2002 May; 12 Suppl 1():I33-43. PubMed ID: 12102461
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. [Congenital sensory neuropathy with anhidrosis: type IV. Apropos of 2 new cases].
    Boukthir S, Trabelsi M, Hammami A, Jamel N, Bennaceur B.
    Ann Pediatr (Paris); 1991 Nov; 38(9):611-3. PubMed ID: 1721509
    [Abstract] [Full Text] [Related]

  • 9. [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; 1991 Nov; 41(4):218-22. PubMed ID: 16075400
    [Abstract] [Full Text] [Related]

  • 10. The R3 component of the electrically elicited blink reflex is present in patients with congenital insensitivity to pain.
    Téllez MJ, Axelrod F, Kaufmann H.
    Pain; 2009 Jan; 141(1-2):178-80. PubMed ID: 19084335
    [Abstract] [Full Text] [Related]

  • 11. Inherited autonomic neuropathies.
    Axelrod FB, Hilz MJ.
    Semin Neurol; 2003 Dec; 23(4):381-90. PubMed ID: 15088259
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Proposal for a standardized protocol for the systematic orofacial examination of patients with Hereditary Sensory Radicular Neuropathy.
    Siqueira SR, Okada M, Lino AM, Teixeira MJ, Siqueira JT.
    Int Endod J; 2006 Nov; 39(11):905-15. PubMed ID: 17014530
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. A case of congenital non-progressive sensory neuropathy with tonic pupils.
    Janzer RC, Spycher MA, Boltshauser E, Cserhati M.
    Clin Neuropathol; 1986 Jan; 5(5):209-16. PubMed ID: 3466730
    [Abstract] [Full Text] [Related]

  • 16. 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 Jan; 51(4):206-14. PubMed ID: 15159601
    [Abstract] [Full Text] [Related]

  • 17. Spinal anesthesia in a patient with congenital insensitivity to pain with anhidrosis.
    Oliveira CR, dos Santos FA, Nogueira CS, Mainardes EJ.
    Anesth Analg; 2007 Jun; 104(6):1561-2, table of contents. PubMed ID: 17513658
    [Abstract] [Full Text] [Related]

  • 18. From genes to pain: nerve growth factor and hereditary sensory and autonomic neuropathy type V.
    Capsoni S.
    Eur J Neurosci; 2014 Feb; 39(3):392-400. PubMed ID: 24494679
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. Congenital insensitivity to pain with anhidrosis.
    Rafel E, Alberca R, Bautista J, Navarrete M, Lazo J.
    Muscle Nerve; 1980 Aug; 3(3):216-20. PubMed ID: 6154886
    [Abstract] [Full Text] [Related]

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