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 *

249 related articles for article (PubMed ID: 8777805)

  • 1. [Progressive cerebellar ataxia and distal amyotrophy of Charcot-Marie-Tooth type with hyperglutamataemia:two sibling cases].
    Tanji H; Takeda A; Tateyama M; Mochizuki H; Itoyama Y
    Rinsho Shinkeigaku; 1995 Jul; 35(7):793-7. PubMed ID: 8777805
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [A case of hereditary motor and sensory neuropathy type I with optic atrophy, neural deafness and pyramidal tract signs].
    Saito T; Nishioka M; Ogino M; Endo K; Kowa H
    Rinsho Shinkeigaku; 1993 May; 33(5):519-24. PubMed ID: 8365058
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Two siblings of distal hereditary motor neuropathy with choroideremia].
    Kawata A; Hayashi H; Yoshida H; Kanda T; Tanabe H
    Rinsho Shinkeigaku; 1990 Sep; 30(9):1010-2. PubMed ID: 2265499
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A case of peroneal muscular atrophy with cerebellar ataxia, pyramidal signs and loss of deep sensations].
    Shinoda H; Kitaguchi T; Kobayashi T; Goto I; Kuroiwa Y
    Rinsho Shinkeigaku; 1987 Mar; 27(3):356-9. PubMed ID: 3608327
    [No Abstract]   [Full Text] [Related]  

  • 5. [A family with progressive neural muscular atrophy--with special reference to relation with allied diseases (author's transl)].
    Hayashi Y; Tomita M; Shimizu K; Takamiya M; Watanabe H
    Rinsho Shinkeigaku; 1978 Oct; 18(10):593-600. PubMed ID: 709963
    [No Abstract]   [Full Text] [Related]  

  • 6. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy.
    McLeod JG; Low PA; Morgan JA
    Proc Aust Assoc Neurol; 1975; 12():23-5. PubMed ID: 1215391
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Identification of a new genetic entity in the form of an autosomal dominant axonal Charcot-Marie-Tooth disease associated with periodic paralyses and pyramidal syndrome].
    Chokri B; Salem M; Faycel H
    Tunis Med; 2005 Sep; 83(9):547-55. PubMed ID: 16383201
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [A patient of Charcot-Marie-tooth disease with rigid spine and respiratory failure].
    Takamure M; Nakamuro T; Sugie K; Suzumura A; Takayanagi T
    Rinsho Shinkeigaku; 2000 May; 40(5):433-8. PubMed ID: 11002724
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Carbamazepine-sensitive neuromyotonia and Charcot-Marie-Tooth disease of the neuronal type].
    Serratrice G; Pouget J; Pellissier JF; Cros D
    Rev Neurol (Paris); 1989; 145(12):867-8. PubMed ID: 2694289
    [TBL] [Abstract][Full Text] [Related]  

  • 10. NEFL N98S mutation: another cause of dominant intermediate Charcot-Marie-Tooth disease with heterogeneous early-onset phenotype.
    Berciano J; Peeters K; García A; López-Alburquerque T; Gallardo E; Hernández-Fabián A; Pelayo-Negro AL; De Vriendt E; Infante J; Jordanova A
    J Neurol; 2016 Feb; 263(2):361-369. PubMed ID: 26645395
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene.
    Sevilla T; Cuesta A; Chumillas MJ; Mayordomo F; Pedrola L; Palau F; Vílchez JJ
    Brain; 2003 Sep; 126(Pt 9):2023-33. PubMed ID: 12821518
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [A case with posterior column ataxia associated with cerebellar ataxia and sensory neuropathy].
    Kikuchi Y; Ogawa M; Shigetoh H; Kawai M; Satoyoshi E
    Rinsho Shinkeigaku; 1999 Sep; 39(9):944-7. PubMed ID: 10614159
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Charcot-Marie-Tooth disease associated with a pyramidal syndrome: clinical, electrophysiological, and neuropathological study of neuro-muscular biopsies in 14 cases].
    Thiam A; Sene FD; Ndao AK; Ndiaye M; Ndiaye IP
    Dakar Med; 2002; 47(2):182-7. PubMed ID: 15776672
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Charcot-Marie-tooth disease.
    Casasnovas C; Cano LM; Albertí A; Céspedes M; Rigo G
    Foot Ankle Spec; 2008 Dec; 1(6):350-4. PubMed ID: 19825739
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Familial idiopathic vitamin E deficiency associated with cerebellar atrophy].
    Aoki K; Washimi Y; Fujimori N; Maruyama K; Yanagisawa N
    Rinsho Shinkeigaku; 1990 Sep; 30(9):966-71. PubMed ID: 2265507
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
    Bouhouche A; Birouk N; Azzedine H; Benomar A; Durosier G; Ente D; Muriel MP; Ruberg M; Slassi I; Yahyaoui M; Dubourg O; Ouazzani R; LeGuern E
    Brain; 2007 Apr; 130(Pt 4):1062-75. PubMed ID: 17347251
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [An autopsy case of neuronal type Charcot-Marie-Tooth disease (HMSN type II) with nerve deafness and psychiatric symptoms].
    Yoshimura I; Yoshimura N; Hanazono T; Usutani S; Muramoto Y; Fukushima Y
    No To Shinkei; 1992 Jun; 44(6):571-8. PubMed ID: 1389565
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A case of hereditary motor and sensory neuropathy with vocal cords palsy and diaphragmatic weakness].
    Fukuda H; Kitani M; Imaoka K
    Rinsho Shinkeigaku; 1993 Feb; 33(2):175-81. PubMed ID: 8319389
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Nosology of Von Graefe-Lindenov syndrome. Study of mental disorders in this genetic neurosensory disease].
    Nehlil J
    Ann Med Psychol (Paris); 1981 Mar; 139(3):352-6. PubMed ID: 7325492
    [No Abstract]   [Full Text] [Related]  

  • 20. Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene.
    Birouk N; Azzedine H; Dubourg O; Muriel MP; Benomar A; Hamadouche T; Maisonobe T; Ouazzani R; Brice A; Yahyaoui M; Chkili T; Le Guern E
    Arch Neurol; 2003 Apr; 60(4):598-604. PubMed ID: 12707075
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.