BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 6312355)

  • 1. Congenital hypomyelination neuropathy in a newborn.
    Hakamada S; Kumagai T; Hara K; Miyazaki S; Miyazaki K; Watanabe K
    Neuropediatrics; 1983 Aug; 14(3):182-3. PubMed ID: 6312355
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Congenital neuropathy caused by hypomyelination].
    Pagès M; Voisin M; Echenne B; Pagés AM; Dumas R; Jean R
    Arch Fr Pediatr; 1983; 40(7):557-60. PubMed ID: 6314923
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital hypomyelination neuropathy with arthrogryposis multiplex congenita.
    Boylan KB; Ferriero DM; Greco CM; Sheldon RA; Dew M
    Ann Neurol; 1992 Mar; 31(3):337-40. PubMed ID: 1637141
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Thin axons relative to myelin spiral length in hereditary motor and sensory neuropathy, type I.
    Nukada H; Dyck PJ; Karnes JL
    Ann Neurol; 1983 Dec; 14(6):648-55. PubMed ID: 6316837
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A case of childhood multiple sclerosis with peripheral neuropathy.
    Tachi N; Ishikawa Y; Tsuzuki A; Minami R; Sasaki K; Shinoda M
    Neuropediatrics; 1985 Nov; 16(4):231-4. PubMed ID: 3001568
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two cases of congenital hypomyelination neuropathy.
    Tachi N; Ishikawa Y; Minami R
    Brain Dev; 1984; 6(6):560-5. PubMed ID: 6099985
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital hypomyelination neuropathy: glial bundles in cranial and spinal nerve roots.
    Towfighi J
    Ann Neurol; 1981 Dec; 10(6):570-3. PubMed ID: 7325606
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pathology of lacquer thinner induced neuropathy.
    Means ED; Prockop LD; Hooper GS
    Ann Clin Lab Sci; 1976; 6(3):240-50. PubMed ID: 182061
    [TBL] [Abstract][Full Text] [Related]  

  • 9. MRI of peripheral nerves and pathology of sural nerves in hereditary motor and sensory neuropathy type III.
    Tachi N; Kozuka N; Ohya K; Chiba S; Naganuma M
    Neuroradiology; 1995 Aug; 37(6):496-9. PubMed ID: 7477868
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A case report of congenital hypomyelination.
    Ono J; Senba E; Okada S; Abe J; Futagi Y; Shimizu H; Sugita T; Hashimoto S; Yabuuchi H
    Eur J Pediatr; 1982 May; 138(3):265-70. PubMed ID: 6288385
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spinal and cranial hypertrophic neuropathy in multiple sclerosis.
    Quan D; Pelak V; Tanabe J; Durairaj V; Kleinschmidt-Demasters BK
    Muscle Nerve; 2005 Jun; 31(6):772-9. PubMed ID: 15793846
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Central hypomyelination associated with congenital hypomyelinating polyneuropathy: report of an autopsied case.
    Johnson MD; Glick AD; Whetsell WO
    Clin Neuropathol; 1989; 8(1):28-34. PubMed ID: 2706841
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nerve and muscle biopsy in a case of hereditary motor and sensory neuropathy type III with basal lamina onion bulbs.
    Bornemann A; Hansen FJ; Schmalbruch H
    Neuropathol Appl Neurobiol; 1996 Feb; 22(1):77-81. PubMed ID: 8866786
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A case of adult cerebral X-linked adrenoleukodystrophy (X-ALD) accompanying typical hypertrophic neuropathy with marked onion-bulb formation].
    Ohori N; Yamashita Y; Ohnishi A
    Rinsho Shinkeigaku; 1999 Nov; 39(11):1144-6. PubMed ID: 10689938
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Widenings of the myelin lamellae in a typical Guillain-Barré syndrome.
    Vallat JM; Leboutet MJ; Jauberteau MO; Tabaraud F; Couratier P; Akani F
    Muscle Nerve; 1994 Apr; 17(4):378-80. PubMed ID: 8170482
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SOX10 mutation with peripheral amyelination and developmental disturbance of axons.
    Parthey K; Kornhuber M; Kunze C; Wand D; Nolte KW; Nikolin S; Weis J; Schröder JM
    Muscle Nerve; 2012 Feb; 45(2):284-90. PubMed ID: 22246888
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1.
    Pitt M; Houlden H; Jacobs J; Mok Q; Harding B; Reilly M; Surtees R
    Brain; 2003 Dec; 126(Pt 12):2682-92. PubMed ID: 14506069
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Arthrogryposis multiplex congenita with posterior column degeneration and peripheral neuropathy: a case report.
    Folkerth RD; Guttentag SH; Kupsky WJ; Kinney HC
    Clin Neuropathol; 1993; 12(1):25-33. PubMed ID: 8382571
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital giant axonal neuropathy.
    Kinney RB; Gottfried MR; Hodson AK; Autilio-Gambetti L; Graham DG
    Arch Pathol Lab Med; 1985 Jul; 109(7):639-41. PubMed ID: 2990373
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Ultrastructural aspects of peripheral nerve lesions in one case of Farber's disease].
    Vital C; Battin J; Rivel J; Hehunstre JP
    Rev Neurol (Paris); 1976 Jun; 132(6):419-23. PubMed ID: 181809
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.