Molecular subunits and transamidase activity of factor XIII during disseminated intravascular coagulation in acute leukaemia.
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Acute Disease↗
Biomedical subjects
R Battista
Publications and source records attributed to R Battista.
[Further experiences with iron-chelating therapy (desferrioxamine and ascorbic acid) in siderochromatosis and Cooley's disease].
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Adolescent↗
Relationship between Hb and HbA2 concentrations in beta-thalassemia trait and effect of iron deficiency anaemia.
The relationship of HbA2 to total Hb has been measured in 204 cases of Beta-Thalassaemia (beta-th-t) where the total Hb varied from 3.6 to 16 g/100 ml. The variation of total Hb in the study population was due, as far as could be defined, only to beta-th-t and a superimposed iron deficiency anaemia (IDA). Superimposed IDA decreases HbA2 proportionately more than it does total Hb (P less than 0.001). A not previously described relationship between HbA2 and total Hb was demonstrated and probably conformed to a second degree parabola.
Anemia, Hypochromic↗
Red blood cell survival and hyperbilirubinaemia in the Gilbert's syndrome.
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Adolescent↗
Fibrinogen survival with 75-seleniomethionine in acute myeloblastic leukemia during polychemotherapy.
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Adult↗
[Treatment of 17 cases of non-lymphoblastic acute leukemia with a combination of daunorubicin, cytosine and arabinoside].
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Adolescent↗
[Type II congenital dyserythropoietic anemia (HEMPAS) with high familial incidence].
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Adolescent↗
[The question of thrombocytopathy in Von Willebrand's disease].
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Adenosine Diphosphate↗
[Bromsulphalein clearance and hyperbilirubinemia in Gilbert's syndrome].
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Biliary Tract↗
[Question of thrombocytopathy in von Willebrand's disease].
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Adenosine Diphosphate↗
Congenital dyserythropoietic anemia, type II (Hempas). First five reported cases in Italy.
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Acids↗
Relationship between ristocetin-induced platelet aggregation and factor VIII (activity and antigen) in v. Willebrand's disease.
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Antigens↗
Von Willebrand's disease in Italy. A study of 13 families from a small area in the province of Vicenza.
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Adenosine Diphosphate↗
Platelet functions in von Willebrand's disease.
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Humans↗
Spontaneous platelet aggregation in myeloproliferative disorders. A preliminary study.
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Blood Cell Count↗
[Siderinuria caused by deferoxamine. II. The siderinuric increment obtained by association with ascorbic acid].
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Adolescent↗
[Significance of some humoral and cytological indices in active stages of Hodgkin's disease].
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Alpha-Globulins↗
[Semiautomatic study of platelet aggregation].
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Adenosine Diphosphate↗