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C Camaschella

Showing results (21-30 of 141) with videos related to

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Recenti Progressi in Medicina|November 1, 1974
[Unusual pathological hemoglobins: Hb unstable, hemoglobins with altered oxygen affinity and Hb M]U Mazza, E Gallo, G Ricco, et al.
Annals of the New York Academy of Sciences|March 27, 1995
Beta-myosin mutations in hypertrophic cardiomyopathiesA Alfarano, L Gastaldi, G G Tos, et al.
American Journal of Hematology|October 1, 1996
Human alpha-thalassemia syndromes: detection of molecular defectsA C Kattamis, C Camaschella, P Sivera, et al.
Haematologica|March 1, 1975
[The aminoacid map from the abnormal peptide in the identification of Hb J Oxford (author's transl)]P G Pich, U Mazza, G Saglio, et al.
Haematologica|September 8, 1999
The influence of hemochromatosis mutations on iron overload of thalassemia majorF Longo, G Zecchina, L Sbaiz, et al.
Blood Cells, Molecules & Diseases|June 22, 2005
Juvenile hemochromatosis due to G320V/Q116X compound heterozygosity of hemojuvelin in an Irish patientF Daraio, E Ryan, F Gleeson, et al.
Lancet (London, England)|February 15, 1986
Fetal diagnosis of beta-thalassaemia by DNA analysis in ItalyC Camaschella, G Saglio, A Serra, et al.
The Journal of Pediatrics|December 25, 2007
Natural history of recessive inheritance of DMT1 mutationsA Iolascon, C Camaschella, D Pospisilova, et al.
Human Genetics|November 1, 1994
A new complex polymorphic repeat close to the HLA-A and HLA-E lociA Totaro, A Grifa, A Roetto, et al.
British Journal of Haematology|May 1, 1990
The homozygous state for the -87 C----G beta + thalassaemiaC Camaschella, A Alfarano, E Gottardi, et al.
Pageof 15

Showing results (21-30 of 141) with videos related to

Sort By:
Pageof 15
Recenti Progressi in Medicina|November 1, 1974
[Unusual pathological hemoglobins: Hb unstable, hemoglobins with altered oxygen affinity and Hb M]U Mazza, E Gallo, G Ricco, et al.
Annals of the New York Academy of Sciences|March 27, 1995
Beta-myosin mutations in hypertrophic cardiomyopathiesA Alfarano, L Gastaldi, G G Tos, et al.
American Journal of Hematology|October 1, 1996
Human alpha-thalassemia syndromes: detection of molecular defectsA C Kattamis, C Camaschella, P Sivera, et al.
Haematologica|March 1, 1975
[The aminoacid map from the abnormal peptide in the identification of Hb J Oxford (author's transl)]P G Pich, U Mazza, G Saglio, et al.
Haematologica|September 8, 1999
The influence of hemochromatosis mutations on iron overload of thalassemia majorF Longo, G Zecchina, L Sbaiz, et al.
Blood Cells, Molecules & Diseases|June 22, 2005
Juvenile hemochromatosis due to G320V/Q116X compound heterozygosity of hemojuvelin in an Irish patientF Daraio, E Ryan, F Gleeson, et al.
Lancet (London, England)|February 15, 1986
Fetal diagnosis of beta-thalassaemia by DNA analysis in ItalyC Camaschella, G Saglio, A Serra, et al.
The Journal of Pediatrics|December 25, 2007
Natural history of recessive inheritance of DMT1 mutationsA Iolascon, C Camaschella, D Pospisilova, et al.
Human Genetics|November 1, 1994
A new complex polymorphic repeat close to the HLA-A and HLA-E lociA Totaro, A Grifa, A Roetto, et al.
British Journal of Haematology|May 1, 1990
The homozygous state for the -87 C----G beta + thalassaemiaC Camaschella, A Alfarano, E Gottardi, et al.
Pageof 15