2B or not 2B? A diagnosis of von Willebrand disease a lifetime of 86 years in the making.

Chapman, Kent; Prasad, Ritam; Mohammed, Soma; Favaloro, Emmanuel J

Chapman, Kent; Prasad, Ritam; Mohammed, Soma; Favaloro, Emmanuel J.

Affiliation

Chapman K; NSW Health Pathology North, John Hunter Hospital, Newcastle.
Prasad R; Calvary Mater Newcastle, Newcastle.
Mohammed S; NSW Health Pathology West, Institute of Clinical Pathology and Medical Research (ICPMR).
Favaloro EJ; NSW Health Pathology West, Institute of Clinical Pathology and Medical Research (ICPMR).

Blood Coagul Fibrinolysis ; 32(3): 229-233, 2021 Apr 01.

Article in En | MEDLINE | ID: mdl-33443930

Subject(s)

von Willebrand Disease, Type 2/diagnosis; Aged, 80 and over; Humans; Male; Mutation, Missense; Platelet Aggregation; Point Mutation; Polymorphism, Single Nucleotide; Protein Multimerization; von Willebrand Disease, Type 2/blood; von Willebrand Disease, Type 2/genetics; von Willebrand Factor/analysis; von Willebrand Factor/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Von Willebrand Disease, Type 2 Type of study: Diagnostic_studies Limits: Aged80 / Humans / Male Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 2021 Document type: Article Country of publication: United kingdom

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