Neurolipidose juvénile atypique Étude ultrastructurale d'une biopsie cérébrale
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J. Hassoun | J. Pellissier | M. Toga | D. Gambarelli | J. Roger | K. Suzuki
[1] J. Opitz,et al. Juvenile GM1 gangliosidosis: Clinical, pathological, chemical and enzymatic studies , 1972, Clinical genetics.
[2] J. O'brien,et al. Juvenile GM2 gangliosidosis. Biochemical and ultrastructural studies on a new variant of Tay-Sachs disease. , 1971, Archives of neurology.
[3] O. Bugiani,et al. Juvenile G M2 -gangliosidosis: a morphological and chemical study of a cerebral biopsy. , 1971, Acta neurologica Belgica.
[4] I. Rapin,et al. Juvenile GM2‐gangliosidosis , 1970, Neurology.
[5] Elfenbein Ib,et al. Juvenile dystonic lipidosis. , 1969 .
[6] J. Martín,et al. Niemann-Pick disease. Morphologic and biochemical studies in the visceral form with late central nervous system involvement (Crocker's group C). , 1969, Archives of neurology.
[7] S. Aronson,et al. Some ultrastructural and histochemical aspects of lipidoses. , 1968, Pathologia Europaea.
[8] M. Adachi,et al. Fine structure of central nervous system in early infantile Gaucher's disease. , 1967, Archives of pathology.
[9] A. Tingey,et al. The juvenile form of Niemann-Pick disease. , 1967, Archives of disease in childhood.
[10] S. Luse. THE FINE STRUCTURE OF THE BRAIN AND OTHER ORGANS IN NIEMANN–PICK DISEASE* , 1967 .
[11] B. Banker,et al. The Cerebral Pathology of Infantile Gaucher's Disease1 , 1962 .
[12] A. Crocker. THE CEREBRAL DEFECT IN TAY‐SACHS DISEASE AND NIEMANN‐PICK DISEASE * , 1961, Journal of neurochemistry.
[13] S. Korey,et al. Membranous Cytoplasmic Granules in Infantile Amaurotic Idiocy , 1960, Nature.
[14] J. Cumings,et al. A CASE OF JUVENILE GAUCHER'S DISEASE WITH INTRANEURONAL LIPID STORAGE , 1960, Journal of neurology, neurosurgery, and psychiatry.