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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 platelets
D 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 acidosis
C 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 vivo
R 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 plasma
G 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 I
C 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 patient
C Dionisi-Vici, C Bachmann, M C Graziani, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 40) with videos related to
Sort By:
Page
of 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 platelets
D 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 acidosis
C 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 vivo
R 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 plasma
G 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 I
C 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 patient
C Dionisi-Vici, C Bachmann, M C Graziani, et al.
Page
of 4