Found: 14
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Pulmonary tumour thrombotic microangiopathy in a young man: clinical and immunohistochemical characterisation of a rare complication of gastric signet-ring cell carcinoma.
- Published in:
- Blood Transfusion (17232007), 2021, v. 19, n. 6, p. 506, doi. 10.2450/2021.0016-21
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- Publication type:
- Article
Muscle expression of glucose-6-phosphate dehydrogenase deficiency in different variants.
- Published in:
- Clinical Genetics, 1995, v. 48, n. 5, p. 232, doi. 10.1111/j.1399-0004.1995.tb04095.x
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- Publication type:
- Article
Adenine and Pyridine Nucleotides in Erythroid Cell Development.
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- Cellular Physiology & Biochemistry (Karger AG), 1995, v. 5, n. 2, p. 96, doi. 10.1159/000154744
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- Publication type:
- Article
Population-based prevalence and mutational landscape of von Willebrand disease using large-scale genetic databases.
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- NPJ Genomic Medicine, 2023, v. 8, n. 1, p. 1, doi. 10.1038/s41525-023-00375-8
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- Publication type:
- Article
Interaction of ATP with erythroblast glucose-6-phosphate dehydrogenase.
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- IUBMB Life, 1996, v. 39, n. 2, p. 377, doi. 10.1080/15216549600201411
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- Publication type:
- Article
Molecular characterization, recombinant protein expression, and mRNA analysis of type 3 von Willebrand disease: Studies of an Italian cohort of 10 patients.
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- American Journal of Hematology, 2012, v. 87, n. 9, p. 870, doi. 10.1002/ajh.23265
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- Publication type:
- Article
Molecular characterization of the PK-LR gene in sixteen pyruvate kinase-deficient patients.
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- British Journal of Haematology, 2001, v. 113, n. 1, p. 43, doi. 10.1046/j.1365-2141.2001.02711.x
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- Publication type:
- Article
The dominant p.Thr274Pro mutation in the von Willebrand factor propeptide causes the von Willebrand disease type 1 phenotype in two unrelated patients.
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- Haemophilia, 2022, v. 28, n. 2, p. 292, doi. 10.1111/hae.14494
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- Publication type:
- Article
Evaluation of a fully automated von Willebrand factor assay panel for the diagnosis of von Willebrand disease.
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- Haemophilia, 2020, v. 26, n. 2, p. 298, doi. 10.1111/hae.13929
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- Article
Severe acquired von Willebrand syndrome secondary to systemic lupus erythematosus.
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- 2019
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- Publication type:
- Letter to the Editor
Mutations in pyruvate kinase.
- Published in:
- Human Mutation, 1996, v. 7, n. 1, p. 1, doi. 10.1002/(SICI)1098-1004(1996)7:1<1::AID-HUMU1>3.0.CO;2-H
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- Publication type:
- Article
G6PD 'campinas:' A deficient enzyme with a mutation at the far 3′ end of the gene.
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- Human Mutation, 1993, v. 2, n. 1, p. 77, doi. 10.1002/humu.1380020115
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- Publication type:
- Article
Pro-coagulant imbalance in patients with community acquired pneumonia assessed on admission and one month after hospital discharge.
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- Clinical Chemistry & Laboratory Medicine, 2021, v. 59, n. 10, p. 1699, doi. 10.1515/cclm-2021-0538
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- Publication type:
- Article
A variant of the EPB3 gene of the anti-Lepore type in hereditary spherocytosis.
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- British Journal of Haematology, 1997, v. 98, n. 2, p. 283, doi. 10.1046/j.1365-2141.1997.1983013.x
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- Publication type:
- Article