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Your search keyword '"Thrombocytosis genetics"' showing total 3 results
Start Over Descriptor "Thrombocytosis genetics" Publication Year Range More than 50 years ago
3 results on '"Thrombocytosis genetics"'

1. Thrombocythaemia. Familial occurrence and transition into blastic crisis.

Author

Fickers M and Speck B

Subjects
Alkaline Phosphatase blood, Anemia, Aplastic chemically induced, Blood Coagulation Tests, Bone Marrow Examination, Busulfan adverse effects, Busulfan therapeutic use, Chromosome Aberrations, Female, Fibrinogen analysis, Gastrointestinal Hemorrhage etiology, Humans, Inclusion Bodies, Leukemia drug therapy, Leukemia etiology, Leukocytes enzymology, Male, Phosphorus Radioisotopes therapeutic use, Prothrombin Time, Thiotepa therapeutic use, Thrombocytosis complications, Thrombocytosis drug therapy, Thrombocytosis genetics
Published
1974
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2. Specificity of the Ph1 chromosome.

Author

Nicoara S, Butoianu E, and Brosteanu R

Subjects
Humans, Leukemia, Myeloid genetics, Myeloproliferative Disorders genetics, Polycythemia Vera genetics, Primary Myelofibrosis genetics, Thrombocytosis genetics, Bone Marrow Diseases genetics, Chromosome Aberrations, Chromosome Disorders
Published
1967
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3. Acute manifestations of platelet dysfunction.

Author

Amorosi EL

Subjects
Acute Disease, Adenosine Diphosphate metabolism, Aspirin adverse effects, Blood Coagulation Factors, Blood Coagulation Tests, Blood Platelet Disorders chemically induced, Blood Platelet Disorders complications, Blood Platelet Disorders genetics, Blood Platelet Disorders pathology, Blood Platelets physiology, Clot Retraction, Disseminated Intravascular Coagulation etiology, Epinephrine pharmacology, Hemostasis, Humans, Liver Diseases complications, Phospholipids metabolism, Platelet Adhesiveness, Purpura, Thrombocytopenic etiology, Purpura, Thrombocytopenic genetics, Thrombocytosis genetics, Time Factors, Uremia etiology, von Willebrand Diseases etiology, Blood Platelet Disorders diagnosis
Published
1973
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