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154 related items for PubMed ID: 1637141

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Hypomyelination neuropathy in a female newborn presenting as arthrogryposis multiplex congenita.
    Seitz RJ, Wechsler W, Mosny DS, Lenard HG.
    Neuropediatrics; 1986 Aug; 17(3):132-6. PubMed ID: 3762869
    [Abstract] [Full Text] [Related]

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

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

  • 5. 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
    [Abstract] [Full Text] [Related]

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

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

  • 8. [Schwann cell pathology and axonal reduction in a case of congenital neuropathy with hypomyelinization].
    Landrieu P, Selva J, Cau D, Barre M, Metral S, Leonard C.
    Arch Fr Pediatr; 1985 Dec; 42(7):497-502. PubMed ID: 4083969
    [Abstract] [Full Text] [Related]

  • 9. Myelin and axon pathology in a long-term study of PMP22-overexpressing mice.
    Verhamme C, King RH, ten Asbroek AL, Muddle JR, Nourallah M, Wolterman R, Baas F, van Schaik IN.
    J Neuropathol Exp Neurol; 2011 May; 70(5):386-98. PubMed ID: 21487305
    [Abstract] [Full Text] [Related]

  • 10. Congenital hypomyelination polyneuropathy. Pathological findings compared with polyneuropathies starting later in life.
    Guzzetta F, Ferrière G, Lyon G.
    Brain; 1982 Jun; 105(Pt 2):395-416. PubMed ID: 7082995
    [Abstract] [Full Text] [Related]

  • 11. Dysmyelinating sensory-motor neuropathy in merosin-deficient congenital muscular dystrophy.
    Di Muzio A, De Angelis MV, Di Fulvio P, Ratti A, Pizzuti A, Stuppia L, Gambi D, Uncini A.
    Muscle Nerve; 2003 Apr; 27(4):500-6. PubMed ID: 12661054
    [Abstract] [Full Text] [Related]

  • 12. P2, P1, and P0 myelin protein expression in developing rat sixth nerve: a quantitative immunocytochemical study.
    Hahn AF, Whitaker JN, Kachar B, Webster HD.
    J Comp Neurol; 1987 Jun 22; 260(4):501-12. PubMed ID: 2440915
    [Abstract] [Full Text] [Related]

  • 13. Congenital absence of peripheral myelin: abnormal Schwann cell development causes lethal arthrogryposis multiplex congenita.
    Charnas L, Trapp B, Griffin J.
    Neurology; 1988 Jun 22; 38(6):966-74. PubMed ID: 2835709
    [Abstract] [Full Text] [Related]

  • 14. Central hypomyelination associated with congenital hypomyelinating polyneuropathy: report of an autopsied case.
    Johnson MD, Glick AD, Whetsell WO.
    Clin Neuropathol; 1989 Jun 22; 8(1):28-34. PubMed ID: 2706841
    [Abstract] [Full Text] [Related]

  • 15. Mitochondrial schwannopathy and peripheral myelinopathy in a rabbit model of dideoxycytidine neurotoxicity.
    Anderson TD, Davidovich A, Feldman D, Sprinkle TJ, Arezzo J, Brosnan C, Calderon RO, Fossom LH, DeVries JT, DeVries GH.
    Lab Invest; 1994 May 22; 70(5):724-39. PubMed ID: 7515130
    [Abstract] [Full Text] [Related]

  • 16. Multiply myelinated axons in the optic nerve of mice deficient for the myelin-associated glycoprotein.
    Bartsch U, Montag D, Bartsch S, Schachner M.
    Glia; 1995 Jun 22; 14(2):115-22. PubMed ID: 7558238
    [Abstract] [Full Text] [Related]

  • 17. Progressive white matter pathology in the spinal cord of transgenic mice expressing mutant (P301L) human tau.
    Lin WL, Zehr C, Lewis J, Hutton M, Yen SH, Dickson DW.
    J Neurocytol; 2005 Dec 22; 34(6):397-410. PubMed ID: 16902761
    [Abstract] [Full Text] [Related]

  • 18. Dysmaturation neuromyopathy: correlation with minimal neuropathy in sural nerve biopsies.
    Verity MA, Gao YH.
    J Child Neurol; 1988 Oct 22; 3(4):276-91. PubMed ID: 3198895
    [Abstract] [Full Text] [Related]

  • 19. Muscle and intramuscular nerve pathology in congenital hypomyelination neuropathy.
    Nara T, Akashi M, Nonaka I, Nakanishi Y, Hamano S, Ochiai Y, Tsuzura S.
    J Neurol Sci; 1995 Apr 22; 129(2):170-4. PubMed ID: 7608732
    [Abstract] [Full Text] [Related]

  • 20. A case of congenital hypomyelination neuropathy. Clinical, morphological, and chemical studies.
    Kennedy WR, Sung JH, Berry JF.
    Arch Neurol; 1977 Jun 22; 34(6):337-45. PubMed ID: 871259
    [Abstract] [Full Text] [Related]

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