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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 16551448)

  • 41. [Hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Molecular-genetic aspects].
    Hertz MJ; Jensen AD; Brandt CA; Bisgård C
    Ugeskr Laeger; 1995 Jun; 157(25):3613-8. PubMed ID: 7652980
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Electrodiagnostic evidence of phrenic nerve demyelination in Charcot-Marie-Tooth disease 1A.
    Sagliocco L; Orlandi G; Calabrese R; Pellegrinetti A; Baglini O; Castelli F; Baldinotti F; Sartucci F
    Am J Phys Med Rehabil; 2003 Oct; 82(10):754-9. PubMed ID: 14508405
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred.
    Butinar D; Zidar J; Leonardis L; Popovic M; Kalaydjieva L; Angelicheva D; Sininger Y; Keats B; Starr A
    Ann Neurol; 1999 Jul; 46(1):36-44. PubMed ID: 10401778
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Clinical practice of hereditary motor neuropathy (HMN) and hereditary sensory and autonomic neuropathy (HSAN)].
    Takashima H
    Rinsho Shinkeigaku; 2014; 54(12):957-9. PubMed ID: 25672680
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Autosomal recessive form of hereditary motor and sensory neuropathy type I.
    Gabreëls-Festen AA; Gabreëls FJ; Jennekens FG; Joosten EM; Janssen-van Kempen TW
    Neurology; 1992 Sep; 42(9):1755-61. PubMed ID: 1513466
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Hereditary motor and sensory neuropathy caused by a novel mutation in LITAF.
    Gerding WM; Koetting J; Epplen JT; Neusch C
    Neuromuscul Disord; 2009 Oct; 19(10):701-3. PubMed ID: 19541485
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Clinical and electrophysiological studies of a family with probable X-linked dominant Charcot-Marie-Tooth neuropathy and ptosis.
    Wu T; Wang HL; Chu CC; Yu JM; Chen JY; Huang CC
    Chang Gung Med J; 2004 Jul; 27(7):489-500. PubMed ID: 15508871
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Charcot-Marie-Tooth disease in northern Finland.
    Rantala H; Tolonen U; Myllylä V
    Ann Clin Res; 1986; 18(3):154-9. PubMed ID: 3740791
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I).
    Bird TD; Ott J; Giblett ER; Chance PF; Sumi SM; Kraft GH
    Ann Neurol; 1983 Dec; 14(6):679-84. PubMed ID: 6651251
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Rehabilitation medicine approach to Charcot-Marie-Tooth disease.
    Njegovan ME; Leonard EI; Joseph FB
    Clin Podiatr Med Surg; 1997 Jan; 14(1):99-116. PubMed ID: 9030448
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Variability of presentation in hereditary neuropathy with liability to pressure palsy results in underrecognition.
    Kumar N; Cole J; Parry GJ
    Ann N Y Acad Sci; 1999 Sep; 883():344-50. PubMed ID: 10586259
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood: a longitudinal clinical and electrophysiologic study.
    García A; Combarros O; Calleja J; Berciano J
    Neurology; 1998 Apr; 50(4):1061-7. PubMed ID: 9566395
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Electrophysiological findings in hereditary motor and sensory neuropathy type I and II--a conduction velocity study.
    Emeryk-Szajewska B; Badurska B; Kostera-Pruszczyk A
    Electromyogr Clin Neurophysiol; 1998 Mar; 38(2):95-101. PubMed ID: 9553747
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Ballerina steps, symptom disclosing hypertrophic Charcot-Marie disease with dominant transmission. Value of electrophysiological studies].
    Bady B; Chauplannaz G; Brunon AM
    Rev Neurol (Paris); 1982; 138(11):827-38. PubMed ID: 7167695
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease.
    Barbieri F; Santangelo R; Crisci C; Ragno M; Perretti A; Santoro L
    Clin Neurol Neurosurg; 1990; 92(3):289-94. PubMed ID: 2171842
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Neuropathy progression in Charcot-Marie-Tooth disease type 1A.
    Shy ME; Chen L; Swan ER; Taube R; Krajewski KM; Herrmann D; Lewis RA; McDermott MP
    Neurology; 2008 Jan; 70(5):378-83. PubMed ID: 18227419
    [TBL] [Abstract][Full Text] [Related]  

  • 57. F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II.
    Scaioli V; Pareyson D; Avanzini G; Sghirlanzoni A
    J Neurol Neurosurg Psychiatry; 1992 Nov; 55(11):1027-31. PubMed ID: 1469398
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Somatosensory and brainstem auditory evoked potentials in neurodegenerative system disorders.
    Rossini PM; Cracco JB
    Eur Neurol; 1987; 26(3):176-88. PubMed ID: 3569372
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Screening for hereditary neuromuscular disorders with molecular genetic methods in the Roma population of Hungary].
    Herczegfalvi A; Pikó H; Karcagi V
    Ideggyogy Sz; 2008 Nov; 61(11-12):426-30. PubMed ID: 19070320
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Electromyographic tendon reflex recording: An accurate and comfortable method for diagnosis of charcot-marie-tooth disease type 1a.
    García A; Pelayo-Negro AL; Álvarez-Paradelo S; Antolín FM; Berciano J
    Muscle Nerve; 2015 Jul; 52(1):39-44. PubMed ID: 25363904
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.