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G Andria

Showing results (11-20 of 137) with videos related to

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Clinical Genetics|December 1, 1996
CFC syndrome: report of familial casesM Lecora, G Parenti, G Andria
Clinical Neurology and Neurosurgery|January 1, 1983
Electroencephalographic abnormalities in homocystinuria due to cystathionine synthase deficiencyE Del Giudice, S Striano, G Andria
The Journal of Biological Chemistry|December 25, 1971
The specific binding of three fragments of staphylococcal nucleaseG Andria, H Taniuchi, J L Cone
The New England Journal of Medicine|December 21, 1989
Ultrasonographic detection of arterial disease in treated homocystinuriaP Rubba, F Faccenda, P Strisciuglio, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Protein-bound plasma homocyst(e)ine and identification of heterozygotes for cystathionine-synthase deficiencyR Sartorio, R Carrozzo, L Corbo, et al.
Clinical Genetics|July 1, 1978
Atypical expression of beta-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalitiesG Andria, E Del Giudice, A J Reuser
Bollettino Della Societa Italiana Di Biologia Sperimentale|December 15, 1970
[Comparative submicroscopic findings on the isolated brush border of the rat and human intestine]A Cecio, R V De Masi, G Andria
Bollettino Della Societa Italiana Di Biologia Sperimentale|December 15, 1970
[Study of the isolated membranes of the brush border of the rat intestine]R V De Masi, G Andria, A Cecio
Beitrage Zur Infusionstherapie = Contributions to Infusion Therapy|January 1, 1991
Dietary treatment of liver glycogenosisG Andria, G Parenti, P Strisciuglio, et al.
Acta Paediatrica Scandinavica|May 1, 1971
Arylamidase activities of brush border membrane of rat intestineS Auricchio, M Pierro, G Andria, et al.
Pageof 14

Showing results (11-20 of 137) with videos related to

Sort By:
Pageof 14
Clinical Genetics|December 1, 1996
CFC syndrome: report of familial casesM Lecora, G Parenti, G Andria
Clinical Neurology and Neurosurgery|January 1, 1983
Electroencephalographic abnormalities in homocystinuria due to cystathionine synthase deficiencyE Del Giudice, S Striano, G Andria
The Journal of Biological Chemistry|December 25, 1971
The specific binding of three fragments of staphylococcal nucleaseG Andria, H Taniuchi, J L Cone
The New England Journal of Medicine|December 21, 1989
Ultrasonographic detection of arterial disease in treated homocystinuriaP Rubba, F Faccenda, P Strisciuglio, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Protein-bound plasma homocyst(e)ine and identification of heterozygotes for cystathionine-synthase deficiencyR Sartorio, R Carrozzo, L Corbo, et al.
Clinical Genetics|July 1, 1978
Atypical expression of beta-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalitiesG Andria, E Del Giudice, A J Reuser
Bollettino Della Societa Italiana Di Biologia Sperimentale|December 15, 1970
[Comparative submicroscopic findings on the isolated brush border of the rat and human intestine]A Cecio, R V De Masi, G Andria
Bollettino Della Societa Italiana Di Biologia Sperimentale|December 15, 1970
[Study of the isolated membranes of the brush border of the rat intestine]R V De Masi, G Andria, A Cecio
Beitrage Zur Infusionstherapie = Contributions to Infusion Therapy|January 1, 1991
Dietary treatment of liver glycogenosisG Andria, G Parenti, P Strisciuglio, et al.
Acta Paediatrica Scandinavica|May 1, 1971
Arylamidase activities of brush border membrane of rat intestineS Auricchio, M Pierro, G Andria, et al.
Pageof 14