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C Borrone

Showing results (1-10 of 89) with videos related to

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Rivista Di Patologia Nervosa E Mentale|June 1, 1976
Fucosidosis: a neuropathological studyO Bugiani, C Borrone
Scandinavian Journal of Infectious Diseases|January 1, 1976
Multiple lymphonodular cryptococcosis, cured by 5-fluorocytosineP Tolentino, C Borrone
Helvetica Paediatrica Acta|April 1, 1971
Fucosidosis and mannosidosis, glycoprotein and glycosylceramide storage diseasesP Durand, C Borrone
The Journal of Pediatrics|May 1, 1991
Metabolic defect in arthrogryposis multiplex congenita with renal and hepatic abnormalitiesM DiRocco, C Borrone
Minerva Pediatrica|October 20, 1971
[Active chronic hepatitis in children. Report of 4 cases and research in various childhood chronic liver diseases]A G Marchi, C Borrone
European Journal of Pediatrics|August 1, 1984
The Tay syndrome (congenital ichthyosis with trichothiodystrophy)F Crovato, C Borrone, A Rebora
Pediatric Research|November 1, 1982
Neutral lipid storage with acid lipase deficiency: a new variant of Wolman's disease with features of the Senior syndromeM Philippart, P Durand, C Borrone
Pathologica|January 1, 1979
[Congenital dyserythropoietic anemia, type II (HEMPAS). Description of 2 cases]G Sansone, C Borrone, G Masera
Minerva Medica|July 11, 1975
[Biochemical bases of the hematological aspects of the diseases caused by the accumulation of glycolipids, mucopolysaccharides and oligosaccharides]P Durand, C Borrone, R Gatti
Biochemistry and Experimental Biology|January 1, 1977
Genetical and biochemical studies of two variants of fucosidosisR Gatti, C Borrone, P Durand
Pageof 9

Showing results (1-10 of 89) with videos related to

Sort By:
Pageof 9
Rivista Di Patologia Nervosa E Mentale|June 1, 1976
Fucosidosis: a neuropathological studyO Bugiani, C Borrone
Scandinavian Journal of Infectious Diseases|January 1, 1976
Multiple lymphonodular cryptococcosis, cured by 5-fluorocytosineP Tolentino, C Borrone
Helvetica Paediatrica Acta|April 1, 1971
Fucosidosis and mannosidosis, glycoprotein and glycosylceramide storage diseasesP Durand, C Borrone
The Journal of Pediatrics|May 1, 1991
Metabolic defect in arthrogryposis multiplex congenita with renal and hepatic abnormalitiesM DiRocco, C Borrone
Minerva Pediatrica|October 20, 1971
[Active chronic hepatitis in children. Report of 4 cases and research in various childhood chronic liver diseases]A G Marchi, C Borrone
European Journal of Pediatrics|August 1, 1984
The Tay syndrome (congenital ichthyosis with trichothiodystrophy)F Crovato, C Borrone, A Rebora
Pediatric Research|November 1, 1982
Neutral lipid storage with acid lipase deficiency: a new variant of Wolman's disease with features of the Senior syndromeM Philippart, P Durand, C Borrone
Pathologica|January 1, 1979
[Congenital dyserythropoietic anemia, type II (HEMPAS). Description of 2 cases]G Sansone, C Borrone, G Masera
Minerva Medica|July 11, 1975
[Biochemical bases of the hematological aspects of the diseases caused by the accumulation of glycolipids, mucopolysaccharides and oligosaccharides]P Durand, C Borrone, R Gatti
Biochemistry and Experimental Biology|January 1, 1977
Genetical and biochemical studies of two variants of fucosidosisR Gatti, C Borrone, P Durand
Pageof 9