Search research articles
Contact Us
Filters
Showing results (61-70 of 94) with videos related to
Page
of 10
Sort By:
American Journal of Obstetrics and Gynecology
|
October 18, 2000
Low-dose folic acid supplementation reduces plasma levels of the cardiovascular risk factor homocysteine in postmenopausal women
V De Leo, A La Marca, G Morgante, et al.
Polish Journal of Veterinary Sciences
|
September 28, 2019
Antioxidant supplementation to medium for in vitro embryo production in Felis catus
N Cocchia, S Tafuri, C Del Prete, et al.
American Journal of Hypertension
|
March 1, 1990
The beneficial effect of atrial natriuretic peptide on cyclosporine nephrotoxicity
G Capasso, C Rosati, F Ciani, et al.
Human Mutation
|
March 29, 2000
Lymphocyte mRNA analysis of the ornithine transcarbamylase gene in Italian OTCD male patients and manifesting carriers: identification of novel mutations
M Giorgi, A Morrone, M A Donati, et al.
Journal of Inherited Metabolic Disease
|
September 14, 2002
Two new mutations in children affected by partial biotinidase deficiency ascertained by newborn screening
S Funghini, M A Donati, E Pasquini, et al.
Polish Journal of Veterinary Sciences
|
November 24, 2018
Reactive oxygen metabolites in alpha-herpesvirus-seropositive Mediterranean buffaloes (Bubalus bubalis): a preliminary study
S Tafuri, A Marullo, F Ciani, et al.
Nephron
|
November 30, 2000
Inhibition of neutral endopeptidase potentiates the effects of atrial natriuretic peptide on acute cyclosporin-induced nephrotoxicity
G Capasso, R Unwin, F Ciani, et al.
Amino Acids
|
February 22, 2008
Possible antioxidant role of SPA therapy with chlorine-sulphur-bicarbonate mineral water
M Costantino, G Giuberti, M Caraglia, et al.
The Journal of Pediatrics
|
November 5, 1997
Neonatal onset of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with favorable outcome
E Zammarchi, F Ciani, E Pasquini, et al.
Molecular Genetics and Metabolism
|
November 1, 2002
Two novel genetic lesions and a common BH4-responsive mutation of the PAH gene in Italian patients with hyperphenylalaninemia
T Bardelli, M A Donati, S Gasperini, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 94) with videos related to
Sort By:
Page
of 10
American Journal of Obstetrics and Gynecology
|
October 18, 2000
Low-dose folic acid supplementation reduces plasma levels of the cardiovascular risk factor homocysteine in postmenopausal women
V De Leo, A La Marca, G Morgante, et al.
Polish Journal of Veterinary Sciences
|
September 28, 2019
Antioxidant supplementation to medium for in vitro embryo production in Felis catus
N Cocchia, S Tafuri, C Del Prete, et al.
American Journal of Hypertension
|
March 1, 1990
The beneficial effect of atrial natriuretic peptide on cyclosporine nephrotoxicity
G Capasso, C Rosati, F Ciani, et al.
Human Mutation
|
March 29, 2000
Lymphocyte mRNA analysis of the ornithine transcarbamylase gene in Italian OTCD male patients and manifesting carriers: identification of novel mutations
M Giorgi, A Morrone, M A Donati, et al.
Journal of Inherited Metabolic Disease
|
September 14, 2002
Two new mutations in children affected by partial biotinidase deficiency ascertained by newborn screening
S Funghini, M A Donati, E Pasquini, et al.
Polish Journal of Veterinary Sciences
|
November 24, 2018
Reactive oxygen metabolites in alpha-herpesvirus-seropositive Mediterranean buffaloes (Bubalus bubalis): a preliminary study
S Tafuri, A Marullo, F Ciani, et al.
Nephron
|
November 30, 2000
Inhibition of neutral endopeptidase potentiates the effects of atrial natriuretic peptide on acute cyclosporin-induced nephrotoxicity
G Capasso, R Unwin, F Ciani, et al.
Amino Acids
|
February 22, 2008
Possible antioxidant role of SPA therapy with chlorine-sulphur-bicarbonate mineral water
M Costantino, G Giuberti, M Caraglia, et al.
The Journal of Pediatrics
|
November 5, 1997
Neonatal onset of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with favorable outcome
E Zammarchi, F Ciani, E Pasquini, et al.
Molecular Genetics and Metabolism
|
November 1, 2002
Two novel genetic lesions and a common BH4-responsive mutation of the PAH gene in Italian patients with hyperphenylalaninemia
T Bardelli, M A Donati, S Gasperini, et al.
Page
of 10