- hand
binds to
purinergic receptors on the
platelet surface.
Since the
thrombocytic purinergic receptor P2Y12 is
coupled to Gi proteins, ADP
reduces platelet...
-
anomaly Lanza F (2006). "Bernard-Soulier
syndrome (hemorrhagiparous
thrombocytic dystrophy)".
Orphanet J Rare Dis. 1: 46. doi:10.1186/1750-1172-1-46....
-
Immune thrombocytopenic purpura (ITP), also
known as
idiopathic thrombocytopenic purpura or
immune thrombocytopenia, is an
autoimmune primary disorder...
-
Hematologic anemia,
hemostasis disorders, granulocytic,
lymphocytic and
thrombocytic dysfunction Cardiovascular hypertension, atherosclerosis,
coronary artery...
- (low
platelet count) is
mediated by the
immune system, and may lead to
thrombocytic purpura.
Quinidine intoxication can lead to a
collection of symptoms...
- megakaryocyte,
platelets are formed. The
megakaryoblast is the
beginning of the
thrombocytic series or
platelet forming series.
Megakaryoblasts typically have a large...
-
Hemorrhagic proctocolitis Hemorrhagic thrombocythemia Hemorrhagiparous thrombocytic dystrophy Hemosiderosis Hemothorax Hennekam–Beemer
syndrome Hennekam–Koss–de...
-
bleeding if used
simultaneously with
anticoagulants and
inhibitors of
thrombocytic aggregation due to
modulation of the
arachidonate cascade"
Psyllium seed...
- 93 (7): 659. PMID 16873073. Bernard, J (December 2000). "[Congential
thrombocytic hemorrhagic dystrophy]". La
Revue du praticien. 50 (20): 2213–5. PMID 11217121...
- PMID 21908432.
Lanza F (2006). "Bernard-Soulier
syndrome (hemorrhagiparous
thrombocytic dystrophy)".
Orphanet J Rare Dis. 1: 46. doi:10.1186/1750-1172-1-46....
