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G Sabetta

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Haematologica|January 1, 1971
[Congenital deficiency of factor VII associated with abnormal electrophoretic mobility of prothrombin--preliminary note]G Ballati, D Del Principe, G Sabetta
Thrombosis Et Diathesis Haemorrhagica|May 15, 1974
Letter: NBT test in newborn plateletsD Del Principe, L Balducci, G Sabetta
Minerva Pediatrica|March 31, 1975
[Serum levels of the 3d and 4th complement factors in children with cytomegalic virus disease with predominantly hepatic involvement]G Ballati, M A Castello, G Sabetta, et al.
The Journal of Pediatrics|April 1, 1988
Carnitine in lactic acidosisC Dionisi Vici, E Bertini, A Bartuli, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Methylmalonic acidaemia due to mutase apoenzyme defect: responsive to vitamin B12 in intact fibroblasts but not in vivoR Baumgartner, O Giardini, A Cantani, et al.
Minerva Pediatrica|April 7, 1975
[Electroencephalographic findings in children with acute lymphatic leukemia during treatment with vincristine]P Iannetti, G Multari, G Sabetta, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1981
[Celiac disease: correlation of different diagnostic methods (author's transl)]M Castro, G Sabetta, V Lucidi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 12, 1973
Phosphatidylserine metabolism in normal and hemophylic human plasmaG Giovannozzi-Sermanni, D Del Principe, D Tricoli, et al.
Acta Paediatrica Scandinavica|October 1, 1990
Early introduction of uncooked cornstarch for the treatment of glycogen storage disease type IC Dionisi Vici, A Bartuli, M R Mazziotta, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Laryngeal stridor as a leading symptom in a biotinidase-deficient patientC Dionisi-Vici, C Bachmann, M C Graziani, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Haematologica|January 1, 1971
[Congenital deficiency of factor VII associated with abnormal electrophoretic mobility of prothrombin--preliminary note]G Ballati, D Del Principe, G Sabetta
Thrombosis Et Diathesis Haemorrhagica|May 15, 1974
Letter: NBT test in newborn plateletsD Del Principe, L Balducci, G Sabetta
Minerva Pediatrica|March 31, 1975
[Serum levels of the 3d and 4th complement factors in children with cytomegalic virus disease with predominantly hepatic involvement]G Ballati, M A Castello, G Sabetta, et al.
The Journal of Pediatrics|April 1, 1988
Carnitine in lactic acidosisC Dionisi Vici, E Bertini, A Bartuli, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Methylmalonic acidaemia due to mutase apoenzyme defect: responsive to vitamin B12 in intact fibroblasts but not in vivoR Baumgartner, O Giardini, A Cantani, et al.
Minerva Pediatrica|April 7, 1975
[Electroencephalographic findings in children with acute lymphatic leukemia during treatment with vincristine]P Iannetti, G Multari, G Sabetta, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1981
[Celiac disease: correlation of different diagnostic methods (author's transl)]M Castro, G Sabetta, V Lucidi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 12, 1973
Phosphatidylserine metabolism in normal and hemophylic human plasmaG Giovannozzi-Sermanni, D Del Principe, D Tricoli, et al.
Acta Paediatrica Scandinavica|October 1, 1990
Early introduction of uncooked cornstarch for the treatment of glycogen storage disease type IC Dionisi Vici, A Bartuli, M R Mazziotta, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Laryngeal stridor as a leading symptom in a biotinidase-deficient patientC Dionisi-Vici, C Bachmann, M C Graziani, et al.
Pageof 4