ristocetin and Albinism

ristocetin has been researched along with Albinism* in 2 studies

Other Studies

2 other study(ies) available for ristocetin and Albinism

Article	Year
Hermansky-Pudlak syndrome and factor VIII ristocetin cofactor. British journal of haematology, 1979, Volume: 41, Issue:3 Topics: Adult; Albinism; Factor VIII; Female; Hemorrhage; Hemorrhagic Disorders; Humans; Platelet Aggregation; Postoperative Complications; Ristocetin; Syndrome	1979
Hereditary thrombocytopathies with abnormal release reaction (author's transl). Nouvelle revue francaise d'hematologie, 1976, Volume: 16, Issue:3 The authors have examined 8 cases with Hermansky-Pudlak syndrome in whom besides the usual abnormalities of abnormal aggregation with collagen, absence of second wave of aggregation, reduction of the 5-HT uptake, presence of 5-HIAA in the platelets, two new abnormalities are described: the presence of a large amount of an unidentified metabolite after 5-HT incorporation which differs from 5-HT and 5 hydroxytryptophol and an abnormal incorporation of labelled glycerol in the triglycerides. Correlation between abnormal lipid metabolism and defective 5-HT incorporation is discussed. Topics: Adenosine Diphosphate; Albinism; Bone Marrow; Bone Marrow Cells; Clot Retraction; Collagen; Cytoplasmic Granules; Epinephrine; Glycerol; Hemorrhagic Disorders; Humans; Macrophages; Platelet Aggregation; Ristocetin; Serotonin; Syndrome; Triglycerides	1976

Article

Year

Hermansky-Pudlak syndrome and factor VIII ristocetin cofactor.

British journal of haematology, 1979, Volume: 41, Issue:3

Topics: Adult; Albinism; Factor VIII; Female; Hemorrhage; Hemorrhagic Disorders; Humans; Platelet Aggregation; Postoperative Complications; Ristocetin; Syndrome

1979

Hereditary thrombocytopathies with abnormal release reaction (author's transl).

Nouvelle revue francaise d'hematologie, 1976, Volume: 16, Issue:3

The authors have examined 8 cases with Hermansky-Pudlak syndrome in whom besides the usual abnormalities of abnormal aggregation with collagen, absence of second wave of aggregation, reduction of the 5-HT uptake, presence of 5-HIAA in the platelets, two new abnormalities are described: the presence of a large amount of an unidentified metabolite after 5-HT incorporation which differs from 5-HT and 5 hydroxytryptophol and an abnormal incorporation of labelled glycerol in the triglycerides. Correlation between abnormal lipid metabolism and defective 5-HT incorporation is discussed.

Topics: Adenosine Diphosphate; Albinism; Bone Marrow; Bone Marrow Cells; Clot Retraction; Collagen; Cytoplasmic Granules; Epinephrine; Glycerol; Hemorrhagic Disorders; Humans; Macrophages; Platelet Aggregation; Ristocetin; Serotonin; Syndrome; Triglycerides

1976