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Last Updated: 10/31/2025

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Found 33 publications

Transient presence of stomatocytes: A clue to the diagnosis of overhydrated hereditary stomatocytosis in a child with beta-thalassemia.

Transient presence of stomatocytes: A clue to the diagnosis of overhydrated hereditary stomatocytosis in a child with beta-thalassemia.

Journal: Journal of clinical laboratory analysis
Published: July 12, 2023

Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to SLC4A1 variants.

Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to SLC4A1 variants.

Journal: Pediatric blood & cancer
Published: March 03, 2023

Mechanosensitive Pannexin 1 Activity Is Modulated by Stomatin in Human Red Blood Cells.

Mechanosensitive Pannexin 1 Activity Is Modulated by Stomatin in Human Red Blood Cells.

Journal: International journal of molecular sciences
Published: July 22, 2022

Reticulocyte Maturation and Variant Red Blood Cells.

Reticulocyte Maturation and Variant Red Blood Cells.

Journal: Frontiers in physiology
Published: December 13, 2021

Rh-null phenotype and stomatocytosis.

Rh-null phenotype and stomatocytosis.

Journal: British journal of haematology
Published: April 26, 2021

Previously misdiagnosed red cell membrane disorder and familial consequences.

Previously misdiagnosed red cell membrane disorder and familial consequences.

Journal: British journal of haematology
Published: June 09, 2020

Advances in understanding the pathogenesis of red cell membrane disorders.

Advances in understanding the pathogenesis of red cell membrane disorders.

Journal: British journal of haematology
Published: August 01, 2019

PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood Cells.

PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood Cells.

Journal: Frontiers in physiology
Published: December 03, 2018

Hereditary stomatocytosis: an unusual cause of severe neonatal jaundice.

Hereditary stomatocytosis: an unusual cause of severe neonatal jaundice.

Journal: Singapore medical journal
Published: October 13, 2018

Overhydrated stomatocytosis associated with a complex RHAG genotype including a novel de novo mutation.

Overhydrated stomatocytosis associated with a complex RHAG genotype including a novel de novo mutation.

Journal: Journal of clinical pathology
Published: January 17, 2018

Band 3, the human red cell chloride/bicarbonate anion exchanger (AE1, SLC4A1), in a structural context.

Band 3, the human red cell chloride/bicarbonate anion exchanger (AE1, SLC4A1), in a structural context.

Journal: Biochimica et biophysica acta
Published: December 14, 2015

The structure of a conserved piezo channel domain reveals a topologically distinct β sandwich fold.

The structure of a conserved piezo channel domain reveals a topologically distinct β sandwich fold.

Journal: Structure (London, England : 1993)
Published: July 01, 2014
Showing 1-12 of 33

Last Updated: 10/31/2025