M Fiore, X Pillois, P Nurden, AT Nurden… - European Journal of …, 2011 - nature.com The c.1544+1G>A substitution at the 5′ splice donor site of intron 15 of the ITGA2B gene, called the French Gypsy mutation, causes Glanzmann thrombasthenia, an inherited hemorrhagic disorder transmitted as an autosomal recessive trait and characterized by an altered synthesis of ... All 3 versions
AT Nurden, M Fiore, P Nurden, R Heilig… - Platelets, 2011 - informahealthcare.com The question as to whether Glanzmann thrombasthenia patients with ITGB3 defects and deficiencies of both αIIbβ3 and αvβ3 show phenotypic differences to those with abnormalities exclusive to αIIbβ3 is unresolved. Studies on β3-deficient mice have shown an increased bone mass. ... Related articles - All 2 versions
H Kashiwagi, K Kiyomizu, T Kamae… - International …, 2011 - ingentaconnect.com Abstract The occurrence of transfusion-related alloim- munization against aIIbb3 is a major concern in patients with Glanzmann thrombasthenia (GT). However, few data are available about molecular defects of GT patients with anti-aIIbb3 alloantibodies as well as clinical impact of these ... Related articles
V Wiegering, B Winkler, F Langhammer… - Klinische …, 2011 - thieme-connect.com Case report: We report the case of a 13-month-old boy, presenting with a severe course of GT, who was successfully treated with an HLA-identical sibling bone marrow transplant. SCT was complicated by anti-platelet alloimmunization after platelet transfusion successfully ... Related articles - All 2 versions
W Mansour, Y Einav, H Hauschner… - … of Thrombosis and …, 2011 - Wiley Online Library Summary. Background: Studies of Glanzmann thrombasthenia (GT)-causing mutations has generated invaluable information on the formation and function of integrin αIIbβ 3 . Objective: To characterize the mutation in four siblings of an Israeli Arab family affected by GT, and to analyze the ... Related articles - All 2 versions
M Fiore, X Pillois, P Nurden, AT Nurden… - European Journal of …, 2011 - nature.com The c.1544+1G>A substitution at the 5′ splice donor site of intron 15 of the ITGA2B gene, called the French Gypsy mutation, causes Glanzmann thrombasthenia, an inherited hemorrhagic disorder transmitted as an autosomal recessive trait and characterized by an altered synthesis of ... All 3 versions
AT Nurden, M Fiore, P Nurden, R Heilig… - Platelets, 2011 - informahealthcare.com The question as to whether Glanzmann thrombasthenia patients with ITGB3 defects and deficiencies of both αIIbβ3 and αvβ3 show phenotypic differences to those with abnormalities exclusive to αIIbβ3 is unresolved. Studies on β3-deficient mice have shown an increased bone mass. ... Related articles - All 2 versions
H Kashiwagi, K Kiyomizu, T Kamae… - International …, 2011 - ingentaconnect.com Abstract The occurrence of transfusion-related alloim- munization against aIIbb3 is a major concern in patients with Glanzmann thrombasthenia (GT). However, few data are available about molecular defects of GT patients with anti-aIIbb3 alloantibodies as well as clinical impact of these ... Related articles
V Wiegering, B Winkler, F Langhammer… - Klinische …, 2011 - thieme-connect.com Case report: We report the case of a 13-month-old boy, presenting with a severe course of GT, who was successfully treated with an HLA-identical sibling bone marrow transplant. SCT was complicated by anti-platelet alloimmunization after platelet transfusion successfully ... Related articles - All 2 versions
W Mansour, Y Einav, H Hauschner… - … of Thrombosis and …, 2011 - Wiley Online Library Summary. Background: Studies of Glanzmann thrombasthenia (GT)-causing mutations has generated invaluable information on the formation and function of integrin αIIbβ 3 . Objective: To characterize the mutation in four siblings of an Israeli Arab family affected by GT, and to analyze the ... Related articles - All 2 versions
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