Matches in DBpedia 2016-04 for { ?s ?p "Bernard–Soulier syndrome (BSS), also called hemorrhagiparous thrombocytic dystrophy, is a rare autosomal recessive coagulopathy (bleeding disorder) that causes a deficiency of glycoprotein Ib (GpIb), the receptor for von Willebrand factor, an important glycoprotein involved in hemostasis.The incidence of BSS is estimated to be less than 1 case per million persons, based on cases reported from Europe, North America, and Japan.BSS is a giant platelet disorder, meaning that it is characterized by abnormally large platelets."@en }
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- Bernard–Soulier_syndrome abstract "Bernard–Soulier syndrome (BSS), also called hemorrhagiparous thrombocytic dystrophy, is a rare autosomal recessive coagulopathy (bleeding disorder) that causes a deficiency of glycoprotein Ib (GpIb), the receptor for von Willebrand factor, an important glycoprotein involved in hemostasis.The incidence of BSS is estimated to be less than 1 case per million persons, based on cases reported from Europe, North America, and Japan.BSS is a giant platelet disorder, meaning that it is characterized by abnormally large platelets.".
- Q822228 abstract "Bernard–Soulier syndrome (BSS), also called hemorrhagiparous thrombocytic dystrophy, is a rare autosomal recessive coagulopathy (bleeding disorder) that causes a deficiency of glycoprotein Ib (GpIb), the receptor for von Willebrand factor, an important glycoprotein involved in hemostasis.The incidence of BSS is estimated to be less than 1 case per million persons, based on cases reported from Europe, North America, and Japan.BSS is a giant platelet disorder, meaning that it is characterized by abnormally large platelets.".
- Bernard–Soulier_syndrome comment "Bernard–Soulier syndrome (BSS), also called hemorrhagiparous thrombocytic dystrophy, is a rare autosomal recessive coagulopathy (bleeding disorder) that causes a deficiency of glycoprotein Ib (GpIb), the receptor for von Willebrand factor, an important glycoprotein involved in hemostasis.The incidence of BSS is estimated to be less than 1 case per million persons, based on cases reported from Europe, North America, and Japan.BSS is a giant platelet disorder, meaning that it is characterized by abnormally large platelets.".
- Q822228 comment "Bernard–Soulier syndrome (BSS), also called hemorrhagiparous thrombocytic dystrophy, is a rare autosomal recessive coagulopathy (bleeding disorder) that causes a deficiency of glycoprotein Ib (GpIb), the receptor for von Willebrand factor, an important glycoprotein involved in hemostasis.The incidence of BSS is estimated to be less than 1 case per million persons, based on cases reported from Europe, North America, and Japan.BSS is a giant platelet disorder, meaning that it is characterized by abnormally large platelets.".