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Human Genetics
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January 1, 1982
Alpha-1-antitrypsin (alpha 1AT) phenotypes and PiM subtypes in Italy. Evidence of considerable geographic variability
G Massi, R Cotumaccio, P Auconi
Minerva Medica
|
September 22, 1982
[Congenital alpha 1-antitrypsin deficiency as an aggravating factor in alveolar injury from cigarette smoke]
G Massi, R Cotumaccio, P Auconi
The New England Journal of Medicine
|
October 27, 1983
Molecular heterogeneity of inherited antithrombin III deficiency
G Leone, V M Valori, R Cotumaccio
Digestion
|
January 1, 1982
Congenital deficiency of alpha-1-antitrypsin and acute viral hepatitis in infancy. No evidence of association
G Massi, R Cotumaccio, G Anzidei, et al.
Haematologica
|
November 1, 1983
Antithrombin III Roma: a familial quantitative-qualitative AT-III deficiency identifiable by crossed immunoelectrofocusing and by crossed immunoelectrophoresis
G Leone, R Cotumaccio, V De Stefano, et al.
Haemostasis
|
January 1, 1983
Human antithrombin III heterogeneity: a study by isoelectrofocusing and crossed immunoelectrofocusing
G Leone, V M Valori, R Cotumaccio, et al.
Helvetica Paediatrica Acta
|
May 1, 1982
PiM subtypes in bronchiolitis
G Massi, P Auconi, R Cotumaccio, et al.
Scandinavian Journal of Haematology
|
November 1, 1984
Different forms of AT-III congenital defect: a study by crossed immunoelectrofocusing
G Leone, R Cotumaccio, V De Stefano, et al.
The Journal of Pediatrics
|
December 1, 1981
Evidence for the maternal origin of alpha1-antitrypsin in amniotic fluid
G Massi, R Cotumaccio, G Orsini, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Human Genetics
|
January 1, 1982
Alpha-1-antitrypsin (alpha 1AT) phenotypes and PiM subtypes in Italy. Evidence of considerable geographic variability
G Massi, R Cotumaccio, P Auconi
Minerva Medica
|
September 22, 1982
[Congenital alpha 1-antitrypsin deficiency as an aggravating factor in alveolar injury from cigarette smoke]
G Massi, R Cotumaccio, P Auconi
The New England Journal of Medicine
|
October 27, 1983
Molecular heterogeneity of inherited antithrombin III deficiency
G Leone, V M Valori, R Cotumaccio
Digestion
|
January 1, 1982
Congenital deficiency of alpha-1-antitrypsin and acute viral hepatitis in infancy. No evidence of association
G Massi, R Cotumaccio, G Anzidei, et al.
Haematologica
|
November 1, 1983
Antithrombin III Roma: a familial quantitative-qualitative AT-III deficiency identifiable by crossed immunoelectrofocusing and by crossed immunoelectrophoresis
G Leone, R Cotumaccio, V De Stefano, et al.
Haemostasis
|
January 1, 1983
Human antithrombin III heterogeneity: a study by isoelectrofocusing and crossed immunoelectrofocusing
G Leone, V M Valori, R Cotumaccio, et al.
Helvetica Paediatrica Acta
|
May 1, 1982
PiM subtypes in bronchiolitis
G Massi, P Auconi, R Cotumaccio, et al.
Scandinavian Journal of Haematology
|
November 1, 1984
Different forms of AT-III congenital defect: a study by crossed immunoelectrofocusing
G Leone, R Cotumaccio, V De Stefano, et al.
The Journal of Pediatrics
|
December 1, 1981
Evidence for the maternal origin of alpha1-antitrypsin in amniotic fluid
G Massi, R Cotumaccio, G Orsini, et al.
Page
of 1