Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M D Cappellini

Showing results (91-100 of 179) with videos related to

Pageof 18
Sort By:
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittentE Di Pierro, V Besana, V Brancaleoni, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|October 22, 2003
TNFalpha promoter polymorphisms in Italian patients with porphyria cutanea tardaP Dongiovanni, L Valenti, A L Fracanzani, et al.
Haematologica|October 6, 1999
Pulmonary thromboembolism in thalassemia intermedia patientsS Gillis, M D Cappellini, A Goldfarb, et al.
Current Studies in Hematology and Blood Transfusion|January 1, 1991
Characteristics of the membrane receptor for human H-ferritinS Fargion, A L Fracanzani, V Cislaghi, et al.
Annals of Human Genetics|July 1, 1989
Different polymorphic variants of glucose-6-phosphate dehydrogenase (G6PD) in ItalyG Fiorelli, C Manoussakis, M Sampietro, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: FECH. Disease: porphyria, erythropoieticV Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittentValeria Besana, E Di Pierro, V Brancaleoni, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: HMBS. Disease: Porphyria, acute intermittentElena Di Pierro, V Brancaleoni, F Stanzial, et al.
Alcoholism, Clinical and Experimental Research|December 1, 1995
Carbohydrate-deficient transferrin in alcohol and nonalcohol abusers with liver diseaseM Meregalli, V Giacomini, S Lino, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittentElena Di Pierro, V Besana, V Brancaleoni, et al.
Pageof 18

Showing results (91-100 of 179) with videos related to

Sort By:
Pageof 18
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittentE Di Pierro, V Besana, V Brancaleoni, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|October 22, 2003
TNFalpha promoter polymorphisms in Italian patients with porphyria cutanea tardaP Dongiovanni, L Valenti, A L Fracanzani, et al.
Haematologica|October 6, 1999
Pulmonary thromboembolism in thalassemia intermedia patientsS Gillis, M D Cappellini, A Goldfarb, et al.
Current Studies in Hematology and Blood Transfusion|January 1, 1991
Characteristics of the membrane receptor for human H-ferritinS Fargion, A L Fracanzani, V Cislaghi, et al.
Annals of Human Genetics|July 1, 1989
Different polymorphic variants of glucose-6-phosphate dehydrogenase (G6PD) in ItalyG Fiorelli, C Manoussakis, M Sampietro, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: FECH. Disease: porphyria, erythropoieticV Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittentValeria Besana, E Di Pierro, V Brancaleoni, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: HMBS. Disease: Porphyria, acute intermittentElena Di Pierro, V Brancaleoni, F Stanzial, et al.
Alcoholism, Clinical and Experimental Research|December 1, 1995
Carbohydrate-deficient transferrin in alcohol and nonalcohol abusers with liver diseaseM Meregalli, V Giacomini, S Lino, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittentElena Di Pierro, V Besana, V Brancaleoni, et al.
Pageof 18