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Journal Abstract Search

100 related items for PubMed ID: 576735

  • 1. 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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  • 2. Congenital Pelizaeus-Merzbacher disease (Seitelberger type), malformation and cystic degeneration of the central nervous system.
    Vuia O.
    Neuropadiatrie; 1978 May; 9(2):172-84. PubMed ID: 581221
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  • 5. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.
    Pascual-Castroviejo I, Gutierrez M, Morales C, Gonzalez-Mediero I, Martínez-Bermejo A, Pascual-Pascual SI.
    Neuropediatrics; 1994 Aug; 25(4):183-90. PubMed ID: 7824090
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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. Cerebellar loss and brain-stem atrophy associated with neonatal alloimmune thrombocytopenia in a discordant twin.
    Mohila CA, Kubicka ZJ, Ornvold KT, Harris BT.
    Pediatr Dev Pathol; 2010 Mar 31; 13(1):55-62. PubMed ID: 19589002
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  • 9. [Spongy encephalopathy of the van Bogaert-Bertrand type. Intrafamilial association with other degenerative diseases].
    Vuia O, Gutermuth M.
    J Genet Hum; 1973 Dec 31; 21(4):287-96. PubMed ID: 4366365
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  • 11. Electron microscopic and enzyme histochemical studies of the cerebellum in spongy degeneration (van Bogaert and Bertrans type).
    Adachi M, Torii J, Schneck L, Volk BW.
    Acta Neuropathol; 1972 Dec 31; 20(1):22-31. PubMed ID: 4112017
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  • 15. A mild variant of pontocerebellar hypoplasia type 1 in a 12-year-old Indian boy.
    Kalpana D, Parvathy L, Ahamed SM, Iype M, Kunju MP.
    Pediatr Neurol; 2009 Apr 31; 40(4):302-5. PubMed ID: 19302945
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  • 16. [Familial olivo-ponto-cerebellar atrophy with myoclonus. Limits of cerebellar myoclonic dyssynergia (Ramsay-Hunt syndrome)].
    Bonduelle M, Escourolle R, Bouygues P, Lormeau G, Gray F.
    Rev Neurol (Paris); 1976 Feb 31; 132(2):113-24. PubMed ID: 973068
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  • 17. [The cerebral peduncle lesion in multiple system atrophy].
    Yasui K, Hashizume Y, Yoshida M, Sobue G.
    Rinsho Shinkeigaku; 1999 Nov 31; 39(11):1125-31. PubMed ID: 10689934
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  • 18. [Progressive myoclonic epilepsy: anatomo - clinical study of a sporadic case with a marked cerebellar symptomatology (author's transl)].
    Nardelli E, Buonanno F, Onnis L, Rizzuto N.
    Riv Patol Nerv Ment; 1975 Nov 31; 96(4):221-32. PubMed ID: 1232666
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  • 19. Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology.
    Aronica E, van Kempen AA, van der Heide M, Poll-The BT, van Slooten HJ, Troost D, Rozemuller-Kwakkel JM.
    Acta Neuropathol; 2005 Apr 31; 109(4):433-42. PubMed ID: 15714316
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  • 20. 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
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