M. Chetty

发表

Dehydrated hereditary stomatocytosis is associated with neonatal hepatitis

B. Portmann, G. Mieli-Vergani, A. Nicolaou, 2004, British journal of haematology.

ATP‐dependent vesiculation in red cell membranes from different hereditary stomatocytosis variants

E. J. Turner, G. Stewart, Peter S. Rowley, 2003, British journal of haematology.

Low NADPH oxidase activity in Epstein-Barr-virus-immortalized B-lymphocytes is due to a post-transcriptional block in expression of cytochrome b558.

A. Abo, A. Thrasher, C. Casimir, 1995, The Biochemical journal.

Dehydrated hereditary stomatocytosis with transient perinatal ascites

A. Basu, A. Basu, G. Stewart, 2003, Archives of disease in childhood. Fetal and neonatal edition.

disease- derived B-cell line by retrovirus mediated gene transfer Restoration of superoxide generation to a chronic granulomatous

A. Segal, A. Thrasher, C. Casimir, 2011 .

Restoration of superoxide generation to a chronic granulomatous disease-derived B-cell line by retrovirus mediated gene transfer.

A. Segal, A. Thrasher, C. Casimir, 1992, Blood.

Nelson's Syndrome and Behavioural Changes Reversed by Selective Adenomectomy

D. Anderson, H. Freeman, M. Chetty, 1988, British Journal of Psychiatry.

Familial pseudohyperkalaemia Chiswick: a novel congenital thermotropic variant of K and Na transport across the human red cell membrane

A. Nicolaou, G. Stewart, S. E. Coles, 2001, British journal of haematology.

Cold storage of ‘cryohydrocytosis’ red cells: the osmotic susceptibility of the cold‐stored erythrocyte

G. Stewart, C. Briggs, D. Gore, 2003, British journal of haematology.

The relationship between chronic lymphocytic leukaemia and prolymphocytic leukaemia

S. Lewis, J. Melo, J. England, 1986, British journal of haematology.

Eukaryotic and prokaryotic stomatins: the proteolytic link.

G. Stewart, M. von Düring, M. Chetty, 2004, Blood cells, molecules & diseases.

Identification of the defective NADPH‐oxidase component in Chronic Granulomatous Disease: a study of 57 European families

A. Fischer, C. Griscelli, A. Segal, 1992, European journal of clinical investigation.

The "stomatin" gene and protein in overhydrated hereditary stomatocytosis.

E. J. Turner, A. Pizzey, A. Iolascon, 2003, Blood.

A family showing recessively inherited multisystem pathology with aberrant splicing of the erythrocyte Band 7.2b ('stomatin') gene

Y. Bertrand, M. von Düring, J. Delaunay, 2004, Journal of Inherited Metabolic Disease.

Allogeneic bone marrow transplantation for severe post‐splenectomy thrombophilic state in leaky red cell membrane haemolytic anaemia of the stomatocytosis class

G. Stewart, L. Brinch, M. Chetty, 2003, British journal of haematology.

Four new cases of stomatin‐deficient hereditary stomatocytosis syndrome: association of the stomatin‐deficient cryohydrocytosis variant with neurological dysfunction

A. Pizzey, S. Winter, M. Düring, 2004, British journal of haematology.

A variant of hereditary stomatocytosis with marked pseudohyperkalaemia

A. Nicolaou, G. Stewart, S. E. Coles, 1999, British journal of haematology.

Two further British families with the ‘cryohydrocytosis’ form of hereditary stomatocytosis

A. Nicolaou, G. Stewart, P. Hill, 2001, British journal of haematology.

Four pedigrees of the cation‐leaky hereditary stomatocytosis class presenting with pseudohyperkalaemia. Novel profile of temperature dependence of Na+–K+ leak in a xerocytic form

A. K. Sinha, A. Nicolaou, B. Vaidya, 2004, British journal of haematology.

Familial pseudohyperkalaemia Cardiff: a mild version of cryohydrocytosis

A. Nicolaou, G. Stewart, D. Gore, 2002, British journal of haematology.

A novel stomatocytosis variant showing marked abnormalities in intracellular [Na] and [K] with minimal haemolysis

A. Nicolaou, G. Stewart, M. Chetty, 2001, European journal of haematology.

Two British families with variants of the ‘cryohydrocytosis’ form of hereditary stomatocytosis

J. W. Kearney, A. Nicolaou, G. Stewart, 1999, British journal of haematology.