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M D Cappellini

Showing results (171-180 of 179) with videos related to

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Hepatology (Baltimore, Md.)|January 13, 1998
High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tardaM Sampietro, A Piperno, L Lupica, et al.
The Journal of Biological Chemistry|August 15, 1998
cDNA cloning and functional characterization of the mouse Ca2+-gated K+ channel, mIK1. Roles in regulatory volume decrease and erythroid differentiationD H Vandorpe, B E Shmukler, L Jiang, et al.
Calcified Tissue International|October 29, 2014
Spine bone texture assessed by trabecular bone score (TBS) to evaluate bone health in thalassemia majorM Baldini, F M Ulivieri, S Forti, et al.
Blood|October 27, 1998
A multicenter prospective study on the risk of acquiring liver disease in anti-hepatitis C virus negative patients affected from homozygous beta-thalassemiaD Prati, A Zanella, E Farma, et al.
European Journal of Internal Medicine|April 14, 2018
Clinical outcomes of Clostridium difficile infection according to strain type. A prospective study in medical wardsS Serafino, D Consonni, M Migone De Amicis, et al.
Blood|August 1, 1980
Hemoglobin synthesis in individual bursts from normal adult blood: all bursts and subcolonies synthesize G gamma-and A gamma-globin chainsC Peschle, G Migliaccio, A Covelli, et al.
Annals of the New York Academy of Sciences|December 13, 2005
Survival and complications in thalassemiaC Borgna-Pignatti, M D Cappellini, P De Stefano, et al.
Journal of Inherited Metabolic Disease|May 30, 2008
Management of non-neuronopathic Gaucher disease with special reference to pregnancy, splenectomy, bisphosphonate therapy, use of biomarkers and bone disease monitoringT M Cox, J M F G Aerts, N Belmatoug, et al.
Molecular Genetics and Metabolism Reports|July 14, 2017
Home infusion program with enzyme replacement therapy for Fabry disease: The experience of a large Italian collaborative groupD Concolino, L Amico, M D Cappellini, et al.
Pageof 18

Showing results (171-180 of 179) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 179 results.
Hepatology (Baltimore, Md.)|January 13, 1998
High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tardaM Sampietro, A Piperno, L Lupica, et al.
The Journal of Biological Chemistry|August 15, 1998
cDNA cloning and functional characterization of the mouse Ca2+-gated K+ channel, mIK1. Roles in regulatory volume decrease and erythroid differentiationD H Vandorpe, B E Shmukler, L Jiang, et al.
Calcified Tissue International|October 29, 2014
Spine bone texture assessed by trabecular bone score (TBS) to evaluate bone health in thalassemia majorM Baldini, F M Ulivieri, S Forti, et al.
Blood|October 27, 1998
A multicenter prospective study on the risk of acquiring liver disease in anti-hepatitis C virus negative patients affected from homozygous beta-thalassemiaD Prati, A Zanella, E Farma, et al.
European Journal of Internal Medicine|April 14, 2018
Clinical outcomes of Clostridium difficile infection according to strain type. A prospective study in medical wardsS Serafino, D Consonni, M Migone De Amicis, et al.
Blood|August 1, 1980
Hemoglobin synthesis in individual bursts from normal adult blood: all bursts and subcolonies synthesize G gamma-and A gamma-globin chainsC Peschle, G Migliaccio, A Covelli, et al.
Annals of the New York Academy of Sciences|December 13, 2005
Survival and complications in thalassemiaC Borgna-Pignatti, M D Cappellini, P De Stefano, et al.
Journal of Inherited Metabolic Disease|May 30, 2008
Management of non-neuronopathic Gaucher disease with special reference to pregnancy, splenectomy, bisphosphonate therapy, use of biomarkers and bone disease monitoringT M Cox, J M F G Aerts, N Belmatoug, et al.
Molecular Genetics and Metabolism Reports|July 14, 2017
Home infusion program with enzyme replacement therapy for Fabry disease: The experience of a large Italian collaborative groupD Concolino, L Amico, M D Cappellini, et al.
Pageof 18