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Journal Abstract Search

83 related items for PubMed ID: 568685

  • 1. [Spongious cerebral dystrophy at an infant age (Canavan-Bogaert-Bertrand types) in three siblings of a non-Jewish family in upper Franconia (author's transl)].
    Schmidt H, Rott HD, Neuhäuser G, Neumann W.
    Klin Padiatr; 1978 Nov; 190(6):580-5. PubMed ID: 568685
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  • 2. Spongy degeneration of the central nervous system (van Bogaert and Bertrand type; Canavan's disease). A review.
    Adachi M, Schneck L, Cara J, Volk BW.
    Hum Pathol; 1973 Sep; 4(3):331-47. PubMed ID: 4593851
    [No Abstract] [Full Text] [Related]

  • 3. [Indicative constellation of symptoms in Canavan-van Bogaert-Bertrand disease].
    Kotlarek F, Schütz E, Zeumer H.
    Rofo; 1982 Nov; 137(5):608-10. PubMed ID: 6217138
    [No Abstract] [Full Text] [Related]

  • 4. [van Bogaert-Bertrand spongy cerebral dystrophy].
    Strompen W, Diekmann L.
    Klin Padiatr; 1984 Nov; 196(2):111-4. PubMed ID: 6737947
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  • 5. Congenital spongy degeneration of the brain (van Bogaert - Bertrand) associated with micrencephaly and ponto - cerebellar atrophy (contributions to the pathology of glial dystrophy of intrauterin origin).
    Vuia O.
    Neuropadiatrie; 1977 Feb; 8(1):73-87. PubMed ID: 576735
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  • 6. Spongy degeneration of the central nervous system (van Bogaert-Bertrand type?) in a newborn infant. A light and electron microscopic study.
    Towfighi J, Friedman Z, Maisels MJ.
    Acta Neuropathol; 1977 Mar 31; 37(3):267-70. PubMed ID: 855648
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  • 8. [Acute spongiform leucoencephalopathy with selective intramyelinic involvement of U fibers associated with an ovarian carcinoma. Syndrome of disconnection of U fibers (author's transl)].
    Buge A, Escourolle R, Rancurel G, Gray F, Tempier P, Denvil D.
    Rev Neurol (Paris); 1980 Mar 31; 136(11):741-51. PubMed ID: 7209238
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  • 10. Spongy degeneration of the central nervous system (Van Bogaert-Bertrand disease): report of a case in a Saudi family.
    Mahdi AH, Elidirssy AT, Wright EA.
    J Child Neurol; 1986 Jan 31; 1(1):61-3. PubMed ID: 3598110
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  • 11. [Spongious glioneuronal dystrophy with diffuse fatty degeneration of the liver].
    Werner M, Künnert B, Lehmann J.
    Zentralbl Pathol; 1991 Jan 31; 137(4):380-4. PubMed ID: 1768691
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  • 12. [Amaurotic familial idiocy within the scope of GM2-gangliosidosis. Apropos of a case of Sandhoff's disease studied on the clinical, neuropathological, enzymatic, and genetic levels].
    Mounoud RL.
    J Genet Hum; 1974 Jun 31; 22(2):139-83. PubMed ID: 4609324
    [No Abstract] [Full Text] [Related]

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  • 14. Familial spongy degeneration of the central nervous system (Van Bogaert-Bertrand disease). An ultrastructural study.
    Gambetti P, Mellman WJ, Gonatas NK.
    Acta Neuropathol; 1969 Jan 31; 12(2):103-15. PubMed ID: 5789730
    [No Abstract] [Full Text] [Related]

  • 15. [A contribution concerning the infantile neuro-axonal dystrophy. Comparison to Hallervorden-Spatz disease regarding histopathologic findings and clinical symptoms].
    Richter E.
    Z Neurol; 1972 Jan 31; 201(2):160-95. PubMed ID: 4112646
    [No Abstract] [Full Text] [Related]

  • 16. Biochemistry and molecular biology of Canavan disease.
    Matalon R, Michals-Matalon K.
    Neurochem Res; 1999 Apr 31; 24(4):507-13. PubMed ID: 10227683
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  • 19. [Congenital familial spongy idiocy (van Bogaert-Bertrand syndrome) in a non-Jewish family (study of a 2d Italian family)].
    Morcaldi L, Salvati G, Giordano GG, Guazzi GC.
    Acta Genet Med Gemellol (Roma); 1969 Apr 31; 18(2):142-57. PubMed ID: 5369099
    [No Abstract] [Full Text] [Related]

  • 20. [Spondylocostal dysostosis. An easily recognizable syndrome with a difficult genetic counselling (author's transl)].
    Calabro A, Mastroiacovo P.
    Pediatr Med Chir; 1981 Apr 31; 3(6):559-62. PubMed ID: 7343955
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