Gordon W. Stewart

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1

Immacolata Andolfo, Seth L. Alper, Lucia De Franceschi et al. · Blood · 2013 · 322 citations

Life Sciences, Genetics, Molecular Genetics +5

Chloride-activated passive potassium transport in human erythrocytes.

Philip B. Dunham, Gordon W. Stewart, J. C. Ellory · Proceedings of the National Academy of Sciences · 1980 · 246 citations · Full text

Life Sciences, Biochemistry, Physiology +17

THROMBO‐EMBOLIC DISEASE AFTER SPLENECTOMY FOR HEREDITARY STOMATOCYTOSIS

Gordon W. Stewart, John Amess, Stefan Eber et al. · British Journal of Haematology · 1996 · 208 citations

Medicine, Hematology, Surgery +14

<scp>ICSH</scp> guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders

M.‐J. King, Loïc Garçon, J. D. Hoyer et al. · International Journal of Laboratory Hematology · 2015 · 175 citations · Full text

Medicine, Biochemistry, Hematology +16

Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1

Lesley J. Bruce, Hannah C Robinson, Hélène Guizouarn et al. · Nature Genetics · 2005 · 164 citations

Life Sciences, Biochemistry, Physiology +16