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Alcohol Dehydrogenase: An Autoantibody Target in Patients with Alcoholic Liver Disease.
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- International Journal of Immunopathology & Pharmacology, 2005, v. 18, n. 1, p. 173, doi. 10.1177/039463200501800118
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- Article
Coagulation and Splenectomy: An Overview.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 317, doi. 10.1196/annals.1345.039
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- Article
PLASMA DEHYDROEPIANDROSTERONE SULPHATE IN HYPOTHYROID PREMENOPAUSAL WOMEN.
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- Clinical Endocrinology, 1980, v. 13, n. 1, p. 111, doi. 10.1111/j.1365-2265.1980.tb01031.x
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- Article
SEMINAL PLASMA LEVELS OF TESTOSTERONE AND 5α-DIHYDROTESTOSTERONE IN AZOOSPERMIC PATIENTS.
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- Clinical Endocrinology, 1979, v. 11, n. 1, p. 11, doi. 10.1111/j.1365-2265.1979.tb03042.x
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- Article
A RAPID RADIOIMMUNOASSAY FOR DETERMINATION OF DEHYDROEPIANDROSTERONE SULPHATE IN HUMAN PLASMA.
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- Clinical Endocrinology, 1975, v. 4, n. 5, p. 505, doi. 10.1111/j.1365-2265.1975.tb01561.x
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- Article
RADIOIMMUNOASSAY OF PLASMA TESTOSTERONE.
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- Clinical Endocrinology, 1974, v. 3, n. 1, p. 5, doi. 10.1111/j.1365-2265.1974.tb03291.x
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- Article
Analysis of T Helper and Suppressor Lymphocyte Subsets in Relation to the Clinical Stage of Solid Neoplasms.
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- Oncology, 1990, v. 47, n. 5, p. 381, doi. 10.1159/000226852
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- Article
Lactate Dehydrogenase and Aspartate Aminotransferase Isoenzymes in Normal and Hypertrophic Human Heart.
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- Cardiology, 1970, v. 55, n. 1, p. 28, doi. 10.1159/000169262
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- Article
Protection from concanavalin A (Con A)-induced T cell-dependent hepatic lesions and modulation of cytokine release in mice by sodium fusidate.
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- Clinical & Experimental Immunology, 1997, v. 110, n. 3, p. 479, doi. 10.1046/j.1365-2249.1997.4091423.x
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- Article
Cardiac alterations in 36 consecutive patients with idiopathic haemochromatosis: polygraphic and echocardiographic evaluation.
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- European Heart Journal, 1991, v. 12, n. 2, p. 224, doi. 10.1093/oxfordjournals.eurheartj.a059873
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- Article
Genetic interactions in thalassemia intermedia: Analysis of β-Mutations, α-Genotype, γ-Promoters, and β-LCR hypersensitive sites 2 and 4 in Italian patients.
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- American Journal of Hematology, 1995, v. 48, n. 2, p. 82, doi. 10.1002/ajh.2830480203
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- Article
Effect of estrogens and progesterone on human peripheral erythroid burst-forming unit (BFU-E) growth.
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- American Journal of Hematology, 1991, v. 38, n. 2, p. 81, doi. 10.1002/ajh.2830380202
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- Article
Electrophoresis of Glucose-6-phosphate Dehydrogenase: a New Technique.
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- Nature, 1967, v. 213, n. 5071, p. 79, doi. 10.1038/213079b0
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- Article
Red blood cell antioxidant and iron status in alcoholic and nonalcoholic cirrhosis.
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- European Journal of Clinical Investigation, 2002, v. 32, p. 21, doi. 10.1046/j.1365-2362.2002.0320s1021.x
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- Article
Oxidative status and malondialdehyde in β-thalassaemia patients.
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- European Journal of Clinical Investigation, 2002, v. 32, p. 55, doi. 10.1046/j.1365-2362.2002.0320s1055.x
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- Article
Erythrocyte Ferritin in Thalassemia Syndromes.
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- Acta Haematologica, 1984, v. 71, n. 4, p. 251, doi. 10.1159/000206596
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- Article
The Iron Status of Italian Subjects with Beta-Thalassemia Trait.
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- Acta Haematologica, 1982, v. 68, n. 2, p. 109, doi. 10.1159/000206961
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- Article
Chronic Liver Disease in Transfusion-Dependent Thalassemia: Liver Iron Quantitation and Distribution.
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- Acta Haematologica, 1981, v. 65, n. 1, p. 32, doi. 10.1159/000207146
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- Article
The Relevance of Immune Reactions in Acute Favism.
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- Acta Haematologica, 1974, v. 51, n. 4, p. 211, doi. 10.1159/000208296
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- Article
G-6-PD-Mangel mit Hämoglobinopathie und alpha-Thalassämie.
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- Acta Haematologica, 1968, v. 39, n. 3, p. 167, doi. 10.1159/000208957
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- Article
Role for autocrine TGF-β1 in regulating differentiation of a human leukemic cell line toward osteoclast-like cells.
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- Journal of Cellular Physiology, 1994, v. 160, n. 3, p. 482, doi. 10.1002/jcp.1041600311
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- Article
Alternative splicing of human G6PD messenger RNA in K562 cells but not in cultured erythroblasts.
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- European Journal of Clinical Investigation, 1993, v. 23, n. 3, p. 188, doi. 10.1111/j.1365-2362.1993.tb00760.x
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- Article
Venous thromboembolism and hypercoagulability in splenectomized patients with thalassaemia intermedia.
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- British Journal of Haematology, 2000, v. 111, n. 2, p. 467, doi. 10.1046/j.1365-2141.2000.02376.x
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- Article
Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f-PCT).
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- Human Mutation, 2001, v. 17, n. 4, p. 350, doi. 10.1002/humu.35
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- Article
Lecithin-cholesterol-acyltransferase deficiency: autosomal recessive transmission in a large kindred.
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- Clinical Genetics, 1981, v. 19, n. 6, p. 448, doi. 10.1111/j.1399-0004.1981.tb02063.x
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- Article
α.
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- Clinical Genetics, 1981, v. 19, n. 2, p. 134, doi. 10.1111/j.1399-0004.1981.tb00684.x
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- Article
Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia.
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- British Journal of Haematology, 1994, v. 87, n. 1, p. 148, doi. 10.1111/j.1365-2141.1994.tb04885.x
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- Article
HEREDITARY SPHEROCYTOSIS CHARACTERIZED BY INCREASED SPECTRIN/BAND 3 RATIO.
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- British Journal of Haematology, 1992, v. 80, n. 1, p. 133, doi. 10.1111/j.1365-2141.1992.tb06417.x
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- Article
Association of thalassaemia intermedia with a beta-globin gene haplotype.
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- British Journal of Haematology, 1987, v. 65, n. 3, p. 367, doi. 10.1111/j.1365-2141.1987.tb06870.x
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- Article
Alpha thalassaemia in an Italian population.
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- British Journal of Haematology, 1986, v. 63, n. 3, p. 497, doi. 10.1111/j.1365-2141.1986.tb07526.x
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- Article
Feasibility of prenatal diagnosis of β thalassaemia by DNA polymorphisms in an Italian population.
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- British Journal of Haematology, 1986, v. 62, n. 3, p. 495, doi. 10.1111/j.1365-2141.1986.tb02961.x
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- Article
FACTORS AFFECTING ERYTHROCYTE FERRITIN CONTENT IN THALASSAEMIA INTERMEDIA.
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- British Journal of Haematology, 1984, v. 56, n. 1, p. 173, doi. 10.1111/j.1365-2141.1984.tb01285.x
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- Article
THE TRIPLICATED ALPHA-GENE LOCUS AND HETEROZYGOUS BETA THALASSAEMIA: A CASE OF THALASSAEMIA INTERMEDIA.
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- British Journal of Haematology, 1983, v. 55, n. 4, p. 709, doi. 10.1111/j.1365-2141.1983.tb02854.x
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- Article
Interaction between Homozygous β<sup>0</sup> Thalassaemia and the Swiss Type of Hereditary Persistence of Fetal Haemoglobin.
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- British Journal of Haematology, 1981, v. 48, n. 4, p. 561, doi. 10.1111/j.1365-2141.1981.tb02753.x
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- Article