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British Journal of Haematology
|
July 27, 2001
TFR2 Y250X mutation in Italy
M De Gobbi, M R Barilaro, G Garozzo, et al.
British Journal of Haematology
|
April 12, 2000
A new mutation (G51C) in the iron-responsive element (IRE) of L-ferritin associated with hyperferritinaemia-cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteins
C Camaschella, G Zecchina, G Lockitch, et al.
Human Genetics
|
April 1, 1996
Allelic association of microsatellites of 6p in Italian hemochromatosis patients
C Camaschella, A Roetto, P Gasparini, et al.
Cancer
|
October 15, 1983
Increased proportion of suppressor/cytotoxic (OKT8+) cells in patients with Hodgkin's disease in long-lasting remission
F Lauria, R Foa, M Gobbi, et al.
Blood
|
August 1, 1987
The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobases
C Camaschella, A Serra, G Saglio, et al.
Blood
|
November 26, 1999
Defective recovery and severe renal damage after acute hemolysis in hemopexin-deficient mice
E 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 enhancer
C Camaschella, A Serra, E Gottardi, et al.
Haematologica
|
May 1, 1983
Thrombotic thrombocytopenic purpura successfully treated by plasma exchange: a report of two cases
A Sardi, A Novarino, F Peyretti, et al.
Haematologica
|
January 1, 1990
Molecular diagnosis of A gamma hereditary persistence of fetal hemoglobin using polymerase chain reaction and oligonucleotide analysis
E Gottardi, A Alfarano, A Serra, et al.
Molecular and Cellular Probes
|
October 1, 1993
Construction of a genetic map telomeric to HLA-A by microsatellite analysis
C Camaschella, A Roetto, G De Sandre, et al.
Page
of 15
Search research articles
Search
Showing results (51-60 of 141) with videos related to
Sort By:
Page
of 15
British Journal of Haematology
|
July 27, 2001
TFR2 Y250X mutation in Italy
M De Gobbi, M R Barilaro, G Garozzo, et al.
British Journal of Haematology
|
April 12, 2000
A new mutation (G51C) in the iron-responsive element (IRE) of L-ferritin associated with hyperferritinaemia-cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteins
C Camaschella, G Zecchina, G Lockitch, et al.
Human Genetics
|
April 1, 1996
Allelic association of microsatellites of 6p in Italian hemochromatosis patients
C Camaschella, A Roetto, P Gasparini, et al.
Cancer
|
October 15, 1983
Increased proportion of suppressor/cytotoxic (OKT8+) cells in patients with Hodgkin's disease in long-lasting remission
F Lauria, R Foa, M Gobbi, et al.
Blood
|
August 1, 1987
The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobases
C Camaschella, A Serra, G Saglio, et al.
Blood
|
November 26, 1999
Defective recovery and severe renal damage after acute hemolysis in hemopexin-deficient mice
E 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 enhancer
C Camaschella, A Serra, E Gottardi, et al.
Haematologica
|
May 1, 1983
Thrombotic thrombocytopenic purpura successfully treated by plasma exchange: a report of two cases
A Sardi, A Novarino, F Peyretti, et al.
Haematologica
|
January 1, 1990
Molecular diagnosis of A gamma hereditary persistence of fetal hemoglobin using polymerase chain reaction and oligonucleotide analysis
E Gottardi, A Alfarano, A Serra, et al.
Molecular and Cellular Probes
|
October 1, 1993
Construction of a genetic map telomeric to HLA-A by microsatellite analysis
C Camaschella, A Roetto, G De Sandre, et al.
Page
of 15