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About 212 results

ALLMedicine™ Gray Platelet Syndrome Center

Research & Reviews  103 results

Gray Platelet Syndrome Presenting With Pancytopenia, Splenomegaly, and Bone Marrow Fibr...
https://doi.org/10.1093/ajcp/aqaa229
American Journal of Clinical Pathology; Tariq H, Perez Botero J et. al.

Feb 15th, 2021 - Gray platelet syndrome (GPS) is a rare platelet storage pool disorder associated with a marked decrease or absence of platelet α-granules and their contents. It is characterized clinically by mild to moderate bleeding; moderate macrothrombocytopen...

Incidence and risk factors of hepatic veno-occlusive disease/sinusoidal obstruction syn...
https://doi.org/10.1038/s41409-021-01215-y 10.1038/s41409-019-0492-6 10.1016/j.bbmt.2009.08.024 10.1038/bmt.2009.349 10.1038/bmt.2013.101 10.7326/0003-4819-118-4-199302150-00003 10.1097/00062752-200311000-00010 10.1016/S0140-6736(11)61938-7 10.1038/bmt.2017.161 10.1038/bmt.2014.168 10.1016/j.bbmt.2011.06.006 10.1038/sj.bmt.1705528 10.1200/JCO.1993.11.2.304 10.1016/j.bbmt.2019.04.020 10.1056/NEJMoa1509277 10.1038/sj.bmt.1702854 10.1038/sj.bmt.1705297 10.1111/j.1365-2141.1990.tb02583.x 10.1182/blood.V79.11.2834.bloodjournal79112834 10.1016/j.bbmt.2006.09.012 10.1182/blood-2014-01-552984 10.1002/cncr.31874 10.1007/s12185-010-0649-y 10.1111/j.1600-0609.2011.01697.x 10.1038/bmt.2016.171 10.1002/ajh.25257 10.1002/hep.1840040121 10.1097/00007890-198712000-00011 10.1038/bmt.2015.52 10.1038/bmt.2016.130 10.1182/blood-2015-10-676924 10.1182/bloodadvances.2017008375 10.1080/17512433.2018.1421943 10.1080/19371910903070333 10.1038/bmt.2015.283 10.7326/0003-4819-128-12_part_1-199806150-00002 10.1182/blood-2001-12-0159 10.1002/(SICI)1096-8652(200005)64:1<32::AID-AJH6>3.0.CO;2-N 10.1038/sj.bmt.1703342 10.1111/j.1600-0609.1991.tb01859.x 10.1097/00007890-199604150-00014 10.1111/j.1365-2141.1993.tb03152.x 10.3346/jkms.2006.21.5.897 10.1111/bjh.14727 10.1016/j.bbmt.2017.03.008
Bone Marrow Transplantation; Yoon JH, Min GJ et. al.

Feb 2nd, 2021 - NBEAL2 encodes a multidomain scaffolding protein with a putative role in granule ontogeny in human platelets. Mutations in NBEAL2 underlie gray platelet syndrome (GPS), a rare inherited bleeding disorder characterized by a lack of α-granules withi...

Neutrophil specific granule and NETosis defects in gray platelet syndrome.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7839360
Blood Advances; Aarts CEM, Downes K et. al.

Jan 26th, 2021 - Gray platelet syndrome (GPS) is an autosomal recessive bleeding disorder characterized by a lack of α-granules in platelets and progressive myelofibrosis. Rare loss-of-function variants in neurobeachin-like 2 (NBEAL2), a member of the family of be...

Gray platelet syndrome: NBEAL2 mutations are associated with pathology beyond megakaryo...
https://doi.org/10.1111/jth.15177
Journal of Thrombosis and Haemostasis : JTH; Pluthero FG, Kahr WHA

Dec 10th, 2020 - Gray platelet syndrome: NBEAL2 mutations are associated with pathology beyond megakaryocyte and platelet function defects.|2020|Pluthero FG,Kahr WHA,|

Gray platelet syndrome: immunity goes awry.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582557
Blood Rao AK, Rao DA

Oct 22nd, 2020 - Gray platelet syndrome: immunity goes awry.|2020|Rao AK,Rao DA,|

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Clinicaltrials.gov  107 results

Gray Platelet Syndrome Presenting With Pancytopenia, Splenomegaly, and Bone Marrow Fibr...
https://doi.org/10.1093/ajcp/aqaa229
American Journal of Clinical Pathology; Tariq H, Perez Botero J et. al.

Feb 15th, 2021 - Gray platelet syndrome (GPS) is a rare platelet storage pool disorder associated with a marked decrease or absence of platelet α-granules and their contents. It is characterized clinically by mild to moderate bleeding; moderate macrothrombocytopen...

Incidence and risk factors of hepatic veno-occlusive disease/sinusoidal obstruction syn...
https://doi.org/10.1038/s41409-021-01215-y 10.1038/s41409-019-0492-6 10.1016/j.bbmt.2009.08.024 10.1038/bmt.2009.349 10.1038/bmt.2013.101 10.7326/0003-4819-118-4-199302150-00003 10.1097/00062752-200311000-00010 10.1016/S0140-6736(11)61938-7 10.1038/bmt.2017.161 10.1038/bmt.2014.168 10.1016/j.bbmt.2011.06.006 10.1038/sj.bmt.1705528 10.1200/JCO.1993.11.2.304 10.1016/j.bbmt.2019.04.020 10.1056/NEJMoa1509277 10.1038/sj.bmt.1702854 10.1038/sj.bmt.1705297 10.1111/j.1365-2141.1990.tb02583.x 10.1182/blood.V79.11.2834.bloodjournal79112834 10.1016/j.bbmt.2006.09.012 10.1182/blood-2014-01-552984 10.1002/cncr.31874 10.1007/s12185-010-0649-y 10.1111/j.1600-0609.2011.01697.x 10.1038/bmt.2016.171 10.1002/ajh.25257 10.1002/hep.1840040121 10.1097/00007890-198712000-00011 10.1038/bmt.2015.52 10.1038/bmt.2016.130 10.1182/blood-2015-10-676924 10.1182/bloodadvances.2017008375 10.1080/17512433.2018.1421943 10.1080/19371910903070333 10.1038/bmt.2015.283 10.7326/0003-4819-128-12_part_1-199806150-00002 10.1182/blood-2001-12-0159 10.1002/(SICI)1096-8652(200005)64:1<32::AID-AJH6>3.0.CO;2-N 10.1038/sj.bmt.1703342 10.1111/j.1600-0609.1991.tb01859.x 10.1097/00007890-199604150-00014 10.1111/j.1365-2141.1993.tb03152.x 10.3346/jkms.2006.21.5.897 10.1111/bjh.14727 10.1016/j.bbmt.2017.03.008
Bone Marrow Transplantation; Yoon JH, Min GJ et. al.

Feb 2nd, 2021 - NBEAL2 encodes a multidomain scaffolding protein with a putative role in granule ontogeny in human platelets. Mutations in NBEAL2 underlie gray platelet syndrome (GPS), a rare inherited bleeding disorder characterized by a lack of α-granules withi...

Neutrophil specific granule and NETosis defects in gray platelet syndrome.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7839360
Blood Advances; Aarts CEM, Downes K et. al.

Jan 26th, 2021 - Gray platelet syndrome (GPS) is an autosomal recessive bleeding disorder characterized by a lack of α-granules in platelets and progressive myelofibrosis. Rare loss-of-function variants in neurobeachin-like 2 (NBEAL2), a member of the family of be...

Gray platelet syndrome: NBEAL2 mutations are associated with pathology beyond megakaryo...
https://doi.org/10.1111/jth.15177
Journal of Thrombosis and Haemostasis : JTH; Pluthero FG, Kahr WHA

Dec 10th, 2020 - Gray platelet syndrome: NBEAL2 mutations are associated with pathology beyond megakaryocyte and platelet function defects.|2020|Pluthero FG,Kahr WHA,|

Gray platelet syndrome: immunity goes awry.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582557
Blood Rao AK, Rao DA

Oct 22nd, 2020 - Gray platelet syndrome: immunity goes awry.|2020|Rao AK,Rao DA,|

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News  2 results

A Case of Chronic Thrombocytopenia in a 17-Year-Old Female
https://www.staging.medscape.com/viewarticle/920128

Abstract and Introduction Abstract Storage pool deficiency (SPD) is a group of rare platelet disorders that result from deficiencies in α-granules, δ-granules, or both. One type of α-SPD is gray platelet syndrome (GPS), caused by mutations in the ...

A Case of Chronic Thrombocytopenia in a 17-Year-Old Female
https://www.medscape.com/viewarticle/920128

Abstract and Introduction Abstract Storage pool deficiency (SPD) is a group of rare platelet disorders that result from deficiencies in α-granules, δ-granules, or both. One type of α-SPD is gray platelet syndrome (GPS), caused by mutations in the ...

see more →