194 results on '"Stewart, Gordon W."'
Search Results
2. Model systems in SDHx-related pheochromocytoma/paraganglioma
3. The cation‐leaky hereditary stomatocytosis syndromes: A tale of six proteins
4. A critical role for altered red cell cation permeability in pathogenesis of sickle cell disease and other haemolytic anaemias
5. Disorders of the Red Cell Membrane
6. Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
7. ‘The Hereditary Stomatocytosis and Allied Conditions’: Inherited Disorders Na+ and K+ Transport
8. Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome
9. The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein
10. Chloride-Activated Passive Potassium Transport in Human Erythrocytes
11. Letter to the Editor: A Further Possible Complication of Therapeutic Acetaminophen: Pyroglutamic Acidosis
12. Membrane raft actin deficiency and altered Ca 2+-induced vesiculation in stomatin-deficient overhydrated hereditary stomatocytosis
13. Familial pseudohyperkalemia in blood donors: a novel mutation with implications for transfusion practice
14. Stomatin immunoreactivity in ciliated cells of the human airway epithelium
15. Anaemia
16. Core Clinical Medicine
17. An MBPhD programme in the UK: the UCL experience
18. An Infant with Pseudohyperkalemia, Hemolysis, and Seizures: Cation-Leaky GLUT1-Deficiency Syndrome due to a SLC2A1 Mutation
19. South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects
20. Lessons of the month: Pyroglutamic acidosis: long-term paracetamol and a high anion gap
21. Mediterranean stomatocytosis/macrothrombocytopenia: update from Adelaide, Australia
22. Stomatin is mis-trafficked in the erythrocytes of overhydrated hereditary stomatocytosis, and is absent from normal primitive yolk sac-derived erythrocytes
23. Stomatocytic haemolysis and macrothrombocytopenia (Mediterranean stomatocytosis/macrothrombocytopenia) is the haematological presentation of phytosterolaemia
24. Eukaryotic and prokaryotic stomatins: the proteolytic link
25. Dehydrated hereditary stomatocytosis is associated with neonatal hepatitis
26. Four new cases of stomatin-deficient hereditary stomatocytosis syndrome: association of the stomatin-deficient cryohydrocytosis variant with neurological dysfunction
27. Cold storage of ‘cryohydrocytosis’ red cells: the osmotic susceptibility of the cold-stored erythrocyte
28. Familial pseudohyperkalaemia Cardiff: a mild version of cryohydrocytosis
29. A novel stomatocytosis variant showing marked abnormalities in intracellular [Na] and [K] with minimal haemolysis
30. Two further British families with the ‘cryohydrocytosis’ form of hereditary stomatocytosis
31. Familial pseudohyperkalaemia Chiswick: a novel congenital thermotropic variant of K and Na transport across the human red cell membrane
32. The “stomatin” gene and protein in overhydrated hereditary stomatocytosis
33. Temperature effects on cation transport in hereditary stomatocytosis and allied disorders
34. Two British families with variants with 'cryohydrocytosis' form of hereditary stomatocytosis
35. A variant of hereditary stomatocytosis with marked pseudohyperkalaemia
36. Absence of CD47 in protein 4.2–deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex: Presented at the 43rd Annual Meeting of the American Society of Hematology, Orlando, FL, December 7-11, 2001, and abstract published in Blood. 2001;98:(suppl1):10a.
37. Thrombo-embolic disease after splenectomy for hereditary stomatocytosis
38. Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24
39. The hereditary stomatocytoses and allied disorders: congenital disorders of erythrocyte membrane permeability to Na and K
40. Cyanosis Attributable To Right To Left Shunt In The Carcinoid Syndrome
41. Chloride-Dependent Cation Transport in Human Erythrocytes
42. Public drunkenness: no offence taken?
43. Disorders of the Red Cell Membrane
44. Statutes of limitation for Rule 10b-5.
45. Small issue industrial development bonds: the growing abuse.
46. Membrane raft actin deficiency and altered Ca2+-induced vesiculation in stomatin-deficient overhydrated hereditary stomatocytosis
47. Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man : an interaction between the Rh complex and the band 3 complex.
48. Membrane raft actin deficiency and altered Ca2+-induced vesiculation in stomatin-deficient overhydrated hereditary stomatocytosis
49. Characterization of red cell membrane proteins as a function of red cell density
50. 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
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