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 *

168 related articles for article (PubMed ID: 8293175)

  • 1. Hereditary demyelinating motor and sensory neuropathy.
    Gabreëls-Festen A; Gabreëls F
    Brain Pathol; 1993 Apr; 3(2):135-46. PubMed ID: 8293175
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Molecular genetics of inherited neuropathies].
    Takashima H
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three cases.
    Schenone A; Abbruzzese M; Uccelli A; Mandich P; James R; Bellone E; Giunchedi M; Rolando S; Capello E; Mandich R [corrected to Mandich P]
    J Neurol Sci; 1994 Mar; 122(1):20-7. PubMed ID: 8195799
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The status of HMSN type III.
    Gabreëls-Festen AA; Gabreëls FJ; Jennekens FG; Janssen-van Kempen TW
    Neuromuscul Disord; 1994 Jan; 4(1):63-9. PubMed ID: 8173353
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteria.
    Gabreëls-Festen AA; Gabreëls FJ; Hoogendijk JE; Bolhuis PA; Jongen PJ; Vingerhoets HM
    Acta Neuropathol; 1993; 86(6):630-5. PubMed ID: 8310819
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Demyelinating hereditary neuropathies in children: a morphometric and ultrastructural study.
    Guzzetta F; Rodríguez J; Deodato M; Guzzetta A; Ferrière G
    Histol Histopathol; 1995 Jan; 10(1):91-104. PubMed ID: 7756749
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Occurrence of active demyelinating lesions in children with hereditary motor and sensory neuropathy (HMSN) type I.
    Vital A; Vital C; Julien J; Fontan D
    Acta Neuropathol; 1992; 84(4):433-6. PubMed ID: 1441924
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inherited peripheral neuropathy.
    Keller MP; Chance PF
    Semin Neurol; 1999; 19(4):353-62. PubMed ID: 10716658
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Homozygous hypertrophic hereditary motor and sensory neuropathies.
    Sghirlanzoni A; Pareyson D; Marazzi R; Cavaletti G; Bellone E; Mandich P; Balestrini MR; Riva D
    Ital J Neurol Sci; 1994 Feb; 15(1):5-14. PubMed ID: 8206746
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Infantile hereditary neuropathy with hypomyelination: report of two siblings with different expressivity.
    Balestrini MR; Cavaletti G; D'Angelo A; Tredici G
    Neuropediatrics; 1991 May; 22(2):65-70. PubMed ID: 1857496
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary motor and sensory neuropathy: HMSN type II (neuronal type) and X-linked HMSN.
    Hahn AF
    Brain Pathol; 1993 Apr; 3(2):147-55. PubMed ID: 8293176
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The phenotypic manifestations of chromosome 17p11.2 duplication.
    Thomas PK; Marques W; Davis MB; Sweeney MG; King RH; Bradley JL; Muddle JR; Tyson J; Malcolm S; Harding AE
    Brain; 1997 Mar; 120 ( Pt 3)():465-78. PubMed ID: 9126058
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication.
    Uncini A; Di Guglielmo G; Di Muzio A; Gambi D; Sabatelli M; Mignogna T; Tonali P; Marzella R; Finelli P; Archidiacono N
    Muscle Nerve; 1995 Jun; 18(6):628-35. PubMed ID: 7753126
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths.
    Gabreëls-Festen AA; Joosten EM; Gabreëls FJ; Stegeman DF; Vos AJ; Busch HF
    Brain; 1990 Dec; 113 ( Pt 6)():1629-43. PubMed ID: 2276038
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Four novel cases of periaxin-related neuropathy and review of the literature.
    Marchesi C; Milani M; Morbin M; Cesani M; Lauria G; Scaioli V; Piccolo G; Fabrizi GM; Cavallaro T; Taroni F; Pareyson D
    Neurology; 2010 Nov; 75(20):1830-8. PubMed ID: 21079185
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and pathological features of an autosomal recessive neuropathy.
    Bouldin TW; Riley E; Hall CD; Swift M
    J Neurol Sci; 1980 Jun; 46(3):315-23. PubMed ID: 6247456
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation].
    Ohnishi A; Yoshimura T; Takazawa A; Hashimoto T; Yamamoto T; Fukushima Y
    Rinsho Shinkeigaku; 1995 Aug; 35(8):843-9. PubMed ID: 8665724
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Infantile demyelinating neuropathy associated with a de novo point mutation on Ser72 in PMP22 and basal lamina onion bulbs in skin biopsy.
    Ceuterick-de Groote C; De Jonghe P; Timmerman V; Van Goethem G; Löfgren A; Ceulemans B; Van Broeckhoven C; Martin JJ
    Pathol Res Pract; 2001; 197(3):193-8. PubMed ID: 11314784
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.