C Camaschella|P Gasparini - JoVE Visualize

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Blood|November 26, 1999

Defective recovery and severe renal damage after acute hemolysis in hemopexin-deficient miceE Tolosano, E Hirsch, E Patrucco, et al.

Blood|February 15, 1990

A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancerC Camaschella, A Serra, E Gottardi, et al.

Haematologica|January 1, 1990

Molecular diagnosis of A gamma hereditary persistence of fetal hemoglobin using polymerase chain reaction and oligonucleotide analysisE Gottardi, A Alfarano, A Serra, et al.

Haematologica|May 1, 1992

Molecular characterization and functional studies on Hb Kempsey, beta 99 (G-1) Asp----Asn, a high-oxygen affinity variantG Ricco, F Scaroina, M C Amprimo, et al.

Minerva Medica|December 18, 1998

[Diagnosis of hereditary hemochromatosis with molecular analysis of DNA in patients with anti-HCV positive liver cirrhosis. Clinical case]A M Carella, G Bianco, M Carella, et al.

Molecular and Cellular Probes|February 1, 1992

Restriction site generating-polymerase chain reaction (RG-PCR) for the probeless detection of hidden genetic variation: application to the study of some common cystic fibrosis mutationsP Gasparini, A Bonizzato, M Dognini, et al.

Clinical Dysmorphology|May 13, 1999

Confirmation of Kapur-Toriello syndrome in an Italian patientL Zelante, M A Candela, A Savoia, et al.

Cardiologia (Rome, Italy)|December 1, 1995

[Hypertrophic obstructive cardiomyopathy in a patient with Turner syndrome]M R Conte, G Bonfiglio, F Orzan, et al.

Blood|June 1, 1990

Prenatal diagnosis of fetal hemoglobin Lepore-Boston disease on maternal peripheral bloodC Camaschella, A Alfarano, E Gottardi, et al.

Blood|February 1, 1978

Interaction between Hb Hasharon and alpha-thalassemia: an approach to the problem of the number of human alpha lociP Pich, G Saglio, C Camaschella, et al.

Pageof 25

Showing results (61-70 of 250) with videos related to

Sort By:

Pageof 25

Blood|November 26, 1999

Defective recovery and severe renal damage after acute hemolysis in hemopexin-deficient miceE Tolosano, E Hirsch, E Patrucco, et al.

Blood|February 15, 1990

A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancerC Camaschella, A Serra, E Gottardi, et al.

Haematologica|January 1, 1990

Molecular diagnosis of A gamma hereditary persistence of fetal hemoglobin using polymerase chain reaction and oligonucleotide analysisE Gottardi, A Alfarano, A Serra, et al.

Haematologica|May 1, 1992

Molecular characterization and functional studies on Hb Kempsey, beta 99 (G-1) Asp----Asn, a high-oxygen affinity variantG Ricco, F Scaroina, M C Amprimo, et al.

Minerva Medica|December 18, 1998

[Diagnosis of hereditary hemochromatosis with molecular analysis of DNA in patients with anti-HCV positive liver cirrhosis. Clinical case]A M Carella, G Bianco, M Carella, et al.

Molecular and Cellular Probes|February 1, 1992

Restriction site generating-polymerase chain reaction (RG-PCR) for the probeless detection of hidden genetic variation: application to the study of some common cystic fibrosis mutationsP Gasparini, A Bonizzato, M Dognini, et al.

Clinical Dysmorphology|May 13, 1999

Confirmation of Kapur-Toriello syndrome in an Italian patientL Zelante, M A Candela, A Savoia, et al.

Cardiologia (Rome, Italy)|December 1, 1995

[Hypertrophic obstructive cardiomyopathy in a patient with Turner syndrome]M R Conte, G Bonfiglio, F Orzan, et al.

Blood|June 1, 1990

Prenatal diagnosis of fetal hemoglobin Lepore-Boston disease on maternal peripheral bloodC Camaschella, A Alfarano, E Gottardi, et al.

Blood|February 1, 1978

Interaction between Hb Hasharon and alpha-thalassemia: an approach to the problem of the number of human alpha lociP Pich, G Saglio, C Camaschella, et al.

Pageof 25