Literature DB >> 36258725

Gray Platelet Syndrome with Severe Thrombocytopenia: A Novel NBEAL2 Gene Variant from India.

Archana Mevalegire Venkatagiri1, Kalasekhar Vijayasekharan1, K Vasudeva Bhat1, Sindhura Lakshmi Koulmane Laxminarayana2, Sushma Belurkar2, Vishwapriya Mahadev Godkhindi2.   

Abstract

Entities:  

Year:  2022        PMID： 36258725      PMCID： PMC9569258          DOI： 10.1007/s12288-022-01531-3

Source DB:  PubMed          Journal:  Indian J Hematol Blood Transfus        ISSN： 0971-4502            Impact factor:   0.915


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  4 in total

1.  Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency.

Authors:  Roberta Bottega; Alessandro Pecci; Erica De Candia; Nuria Pujol-Moix; Paula G Heller; Patrizia Noris; Daniela De Rocco; Gian Marco Podda; Ana C Glembotsky; Marco Cattaneo; Carlo L Balduini; Anna Savoia
Journal:  Haematologica       Date:  2012-10-25       Impact factor: 9.941

Review 2.  NBEAL2 mutations and bleeding in patients with gray platelet syndrome.

Authors:  Fred G Pluthero; Jorge Di Paola; Manuel D Carcao; Walter H A Kahr
Journal:  Platelets       Date:  2018-06-05       Impact factor: 3.862

Review 3.  Inherited thrombocytopenias: history, advances and perspectives.

Authors:  Alan T Nurden; Paquita Nurden
Journal:  Haematologica       Date:  2020-06-11       Impact factor: 9.941
  4 in total

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