Macrothrombocytes
National Institutes of Health
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BACKGROUND
The diagnosis of 22q11.2 deletion syndrome depends on a time-consuming and expensive method, fluorescence in situ…
Harris platelet syndrome (HPS), also known as asymptomatic constitutional macrothrombocytopenia (ACMT), is an autosomal dominant…
Summary Congenital thrombocytopenia in childhood and adolescence requires an extensive diagnostic workup to find the underlying…
We report a 37-year-old renal transplanted patient with thrombocytopaenia. He had May–Hegglin anomaly (MHA) inherited from his…
An X-linked mutation in the GATA-1 transcription factor, G208S, causes macrothrombocytopenia and serious bleeding problems in…
Germline mutations in the X-linked transcription factor, GATA-1, cause several hematopoietic disorders resulting in anemia and/or…
OBJECTIVE
The purpose of this study was to compare platelet concentration in cavalier King Charles spaniels (CKCS) measured by…
Previous investigations from our laboratory have characterized the ultrastructural and cytochemical pathology of platelets in…
This is a report of Fechtner syndrome in two Japanese families. Six members of family I and three members of family II were…