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G Parenti

Showing results (211-220 of 226) with videos related to

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Journal of Endocrinological Investigation|February 27, 2003
Microvascular density and vascular endothelial growth factor expression in normal pituitary tissue and pituitary adenomasP Viacava, M Gasperi, G Acerbi, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|March 14, 2014
Liver transplantation in defects of cholesterol biosynthesis: the case of lathosterolosisP L Calvo, A Brunati, M Spada, et al.
Journal of Endocrinological Investigation|September 3, 2010
Evaluation of the anterior pituitary function in the acute phase after spontaneous subarachnoid hemorrhageG Parenti, P C Cecchi, B Ragghianti, et al.
Stroke|March 10, 2001
111In platelet scintigraphy for the noninvasive detection of carotid plaque thrombosisG Manca, G Parenti, R Bellina, et al.
Cell|April 7, 1995
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathyB Franco, G Meroni, G Parenti, et al.
Journal of Endocrinological Investigation|October 7, 2011
A simple ultrasound score for the identification of candidates to fine needle aspiration of thyroid nodulesL Petrone, E Mannucci, M L De Feo, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Respiratory-chain and pyruvate metabolism defects: Italian collaborative survey on 72 patientsU Caruso, A Adami, E Bertini, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentationS Fecarotta, G Parenti, P Vajro, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of delta7-sterol reductase in Italy and report of three novel mutationsD De Brasi, T Esposito, M Rossi, et al.
Human Mutation|August 19, 2006
Mutation profile of the GAA gene in 40 Italian patients with late onset glycogen storage disease type IIA L E Montalvo, B Bembi, M Donnarumma, et al.
Pageof 23

Showing results (211-220 of 226) with videos related to

Sort By:
Pageof 23
Journal of Endocrinological Investigation|February 27, 2003
Microvascular density and vascular endothelial growth factor expression in normal pituitary tissue and pituitary adenomasP Viacava, M Gasperi, G Acerbi, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|March 14, 2014
Liver transplantation in defects of cholesterol biosynthesis: the case of lathosterolosisP L Calvo, A Brunati, M Spada, et al.
Journal of Endocrinological Investigation|September 3, 2010
Evaluation of the anterior pituitary function in the acute phase after spontaneous subarachnoid hemorrhageG Parenti, P C Cecchi, B Ragghianti, et al.
Stroke|March 10, 2001
111In platelet scintigraphy for the noninvasive detection of carotid plaque thrombosisG Manca, G Parenti, R Bellina, et al.
Cell|April 7, 1995
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathyB Franco, G Meroni, G Parenti, et al.
Journal of Endocrinological Investigation|October 7, 2011
A simple ultrasound score for the identification of candidates to fine needle aspiration of thyroid nodulesL Petrone, E Mannucci, M L De Feo, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Respiratory-chain and pyruvate metabolism defects: Italian collaborative survey on 72 patientsU Caruso, A Adami, E Bertini, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentationS Fecarotta, G Parenti, P Vajro, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of delta7-sterol reductase in Italy and report of three novel mutationsD De Brasi, T Esposito, M Rossi, et al.
Human Mutation|August 19, 2006
Mutation profile of the GAA gene in 40 Italian patients with late onset glycogen storage disease type IIA L E Montalvo, B Bembi, M Donnarumma, et al.
Pageof 23