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Journal Abstract Search

167 related items for PubMed ID: 1857496

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

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. [Hereditary motor and sensory neuropathy].
    Guo YP.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1992 Oct; 25(5):261-3, 315. PubMed ID: 1291244
    [Abstract] [Full Text] [Related]

  • 4. Sensory nerve pathology in multifocal motor neuropathy.
    Corse AM, Chaudhry V, Crawford TO, Cornblath DR, Kuncl RW, Griffin JW.
    Ann Neurol; 1996 Mar; 39(3):319-25. PubMed ID: 8602750
    [Abstract] [Full Text] [Related]

  • 5. Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0.
    Simonati A, Fabrizi GM, Taioli F, Polo A, Cerini R, Rizzuto N.
    J Neurol; 2002 Sep; 249(9):1298-302. PubMed ID: 12242557
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entity.
    Sabatelli M, Mignogna T, Lippi G, Servidei S, Zollino M, Padua L, Lo Monaco M, De Armas L, Mereu ML, Tonali P.
    Am J Med Genet; 1998 Jan 23; 75(3):309-13. PubMed ID: 9475604
    [Abstract] [Full Text] [Related]

  • 8. [Giant axonal neuropathy. Presentation of 2 familial cases].
    Maraví Petri E, García-Bragado F, Martín Ruiz E, Guarch R, Ruiz de Azúa Y, Yoldi ME.
    Neurologia; 1989 Jan 23; 4(1):24-30. PubMed ID: 2698683
    [Abstract] [Full Text] [Related]

  • 9. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan 23; 46(1):1-18. PubMed ID: 16541790
    [Abstract] [Full Text] [Related]

  • 10. [A family of hereditary motor and sensory neuropathy with spastic paraplegia (HMSN type V)].
    Murayama T, Nagamatsu M, Sugimura K, Matsuoka Y, Takahashi A.
    Rinsho Shinkeigaku; 1989 Oct 23; 29(10):1272-7. PubMed ID: 2691166
    [Abstract] [Full Text] [Related]

  • 11. Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding.
    Ohnishi A, Murai Y, Ikeda M, Fujita T, Furuya H, Kuroiwa Y.
    Muscle Nerve; 1989 Jul 23; 12(7):568-75. PubMed ID: 2779605
    [Abstract] [Full Text] [Related]

  • 12. 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 Jul 23; 197(3):193-8. PubMed ID: 11314784
    [Abstract] [Full Text] [Related]

  • 13. The giant axonal neuropathy--clinical and hisotological aspects, differential diagnosis and a new case.
    Nafe R, Trollmann R, Schlote W.
    Clin Neuropathol; 2001 Jul 23; 20(5):200-11. PubMed ID: 11594505
    [Abstract] [Full Text] [Related]

  • 14. [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 Jul 23; 42(7):497-502. PubMed ID: 4083969
    [Abstract] [Full Text] [Related]

  • 15. 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 23; 22(1):77-81. PubMed ID: 8866786
    [Abstract] [Full Text] [Related]

  • 16. Motor-sensory neuropathy without minifascicles in a patient with 46XY gonadal dysgenesis.
    Malandrini A, Gambelli S, Muglia M, Berti G, Gaudiano C, Patitucci A, Sugie K, Umehara F, Quattrone A, Dotti MT, Federico A.
    Brain Dev; 2008 Apr 23; 30(4):291-4. PubMed ID: 17768021
    [Abstract] [Full Text] [Related]

  • 17. Hereditary demyelinating motor and sensory neuropathy.
    Gabreëls-Festen A, Gabreëls F.
    Brain Pathol; 1993 Apr 23; 3(2):135-46. PubMed ID: 8293175
    [Abstract] [Full Text] [Related]

  • 18. Chronic peripheral neuropathy in childhood: an overview.
    Ouvrier RA, McLeod JG.
    Aust Paediatr J; 1988 Apr 23; 24 Suppl 1():80-2. PubMed ID: 2849398
    [Abstract] [Full Text] [Related]

  • 19. [Hereditary neuropathy with liability to pressure palsies (tomaculous neuropathy). Clinical, electrophysical and molecular study of two affected families].
    Eirís-Punal J, Vidal-Lijó M, Barros-Angueira F, Lopez-Fernández MJ, Pintos-Martínez E, Beiras-Iglesias A, Castro-Gago M.
    Rev Neurol; 1988 Apr 23; 31(6):506-10. PubMed ID: 11055050
    [Abstract] [Full Text] [Related]

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