Haemopoietic stem cell transplantation is a curative treatment option with minimal transplant-related complications for patients with severe Glanzmann's …
C Crone, B James - Clinical Medicine, 2019 - ncbi.nlm.nih.gov
Aims Glanzmann's thrombasthenia is a rare autosomal recessive bleeding disorder of
platelet function caused by a qualitative or quantitative defect of the platelet membrane …
platelet function caused by a qualitative or quantitative defect of the platelet membrane …
Stem Cell Transplant in Severe Glanzmann Thrombasthenia in an Adult Patient.
Glanzmann thrombasthenia is an inherited auto-somal recessive disorder characterized by
normal platelet count but lack of platelet aggregation due to absence of platelet glycoprotein …
normal platelet count but lack of platelet aggregation due to absence of platelet glycoprotein …
Bone marrow transplantation in severe Glanzmann's thrombasthenia with antiplatelet alloimmunization
S Bellucci, G Damaj, B Boval, V Rocha… - Bone Marrow …, 2000 - nature.com
Glanzmann's thrombasthenia is an autosomal recessive disorder characterized by a lack of
platelet aggregation due to the absence of platelet glycoprotein IIb and IIIa. Usually, the …
platelet aggregation due to the absence of platelet glycoprotein IIb and IIIa. Usually, the …
Sibling allogeneic bone marrow transplantation in a patient with type I Glanzmann's thrombasthenia
MD McColl, BES Gibson - British journal of haematology, 1997 - Wiley Online Library
Glanzmann's thrombasthenia is a rare inherited bleeding disorder caused by either
quantitative or qualitative abnormalities of the platelet membrane glycoprotein (Gp) IIb/IIIa …
quantitative or qualitative abnormalities of the platelet membrane glycoprotein (Gp) IIb/IIIa …
Indication for allogeneic stem cell transplantation in Glanzmann's thrombasthenia
V Wiegering, K Sauer, B Winkler, M Eyrich… - …, 2013 - thieme-connect.com
Glanzmann's thrombasthenia (GT) is an autosomal recessive disorder characterized by a
lack of thrombocyte aggregation due to the absence of thrombocyte glycoproteins IIb and …
lack of thrombocyte aggregation due to the absence of thrombocyte glycoproteins IIb and …
Sustained engraftment and resolution of bleeding phenotype after unrelated cord blood hematopoietic stem cell transplantation for severe Glanzmann thrombasthenia
Glanzmann thrombasthenia is a rare, autosomal recessive, qualitative platelet disorder
resulting from abnormal platelet surface glycoprotein IIb/IIIa. In phenotypically severe cases …
resulting from abnormal platelet surface glycoprotein IIb/IIIa. In phenotypically severe cases …
Bone marrow transplantation for Glanzmann's thrombasthenia.
A Johnson, AH Goodall, CJ Downie… - Bone marrow …, 1994 - europepmc.org
Allogeneic matched bone marrow transplantation (BMT) was performed in a patient with
type I Glanzmann's thrombasthenia, a rare, inherited bleeding disorder caused by a …
type I Glanzmann's thrombasthenia, a rare, inherited bleeding disorder caused by a …
Allogeneic stem cell transplantation for Glanzmann thrombasthenia
MK Ishaqi, M El‐Hayek, A Gassas… - Pediatric Blood & …, 2009 - Wiley Online Library
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding disorder
characterized by normal platelet count, but lack of platelet aggregation. The molecular basis …
characterized by normal platelet count, but lack of platelet aggregation. The molecular basis …
Use of allogeneic stem cell transplantation for moderate–severe Glanzmann thrombasthenia
A Walz, A Lenzen, B Curtis, J Canner, J Schneiderman - Platelets, 2015 - Taylor & Francis
Glanzmann thrombasthenia (GT) is a rare, autosomal recessive coagulopathy characterized
by either qualitative or quantitative abnormalities of the membrane glycoprotein αIIbβ3 …
by either qualitative or quantitative abnormalities of the membrane glycoprotein αIIbβ3 …
Successful use of hematopoietic stem cell transplantation for 2 pediatric cases of Glanzmann thrombasthenia and review of the literature
BD Friend, GD Roach, PH Kempert… - Journal of Pediatric …, 2020 - journals.lww.com
Glanzmann thrombasthenia is a rare platelet disorder characterized by an abnormal integrin
receptor on the surface of platelets that results in the failure of platelets to aggregate …
receptor on the surface of platelets that results in the failure of platelets to aggregate …