167 related articles for article (PubMed ID: 6462777)
21. Studies on a large kindred with hemolytic anemia and low erythrocyte 2,3-DPG.
Harkness DR; Roth S; Goldman P; Kim C; Isaacks RE
Prog Clin Biol Res; 1978; 21():251-74. PubMed ID: 208085
[No Abstract] [Full Text] [Related]
22. [Five cases of hereditary high red cell membrane phosphatidylcholine hemolytic anemia in three families].
Wakita M; Matsui T; Tsuzuki M; Nomura T; Miyazaki H; Kojima H; Maruyama F; Okamoto M; Ino T; Ezaki K; Sugihara T; Kanzaki A; Yawata Y; Hirano M
Rinsho Ketsueki; 1996 Mar; 37(3):265-70. PubMed ID: 8727354
[TBL] [Abstract][Full Text] [Related]
23. Stomatocytosis in 7 related Standard Schnauzers.
Bonfanti U; Comazzi S; Paltrinieri S; Bertazzolo W
Vet Clin Pathol; 2004; 33(4):234-9. PubMed ID: 15570561
[TBL] [Abstract][Full Text] [Related]
24. Mild erythrocytosis as a presenting manifestation of
Knight T; Zaidi AU; Wu S; Gadgeel M; Buck S; Ravindranath Y
Pediatr Hematol Oncol; 2019 Aug; 36(5):317-326. PubMed ID: 31298594
[TBL] [Abstract][Full Text] [Related]
25. Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis).
Andolfo I; Russo R; Manna F; Shmukler BE; Gambale A; Vitiello G; De Rosa G; Brugnara C; Alper SL; Snyder LM; Iolascon A
Am J Hematol; 2015 Oct; 90(10):921-6. PubMed ID: 26178367
[TBL] [Abstract][Full Text] [Related]
26. 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.
Gore DM; Layton M; Sinha AK; Williamson PJ; Vaidya B; Connolly V; Mannix P; Chetty MC; Nicolaou A; Stewart GW
Br J Haematol; 2004 May; 125(4):521-7. PubMed ID: 15142123
[TBL] [Abstract][Full Text] [Related]
27. Hereditary stomatocytosis and cation-leaky red cells--recent developments.
Bruce LJ
Blood Cells Mol Dis; 2009; 42(3):216-22. PubMed ID: 19261491
[TBL] [Abstract][Full Text] [Related]
28. Two British families with variants of the 'cryohydrocytosis' form of hereditary stomatocytosis.
Coles SE; Chetty MC; Ho MM; Nicolaou A; Kearney JW; Wright SD; Stewart GW
Br J Haematol; 1999 Jun; 105(4):1055-65. PubMed ID: 10554820
[TBL] [Abstract][Full Text] [Related]
29. [Familial erythrocyte ATP: pyruvate phosphotransferase deficiency].
Torliński L; Karoń H; Czech A; Michalewska D; Duczmal B
Acta Haematol Pol; 1982; 13(3-4):157-63. PubMed ID: 7184297
[No Abstract] [Full Text] [Related]
30. [NONSPHEROCYTIC CONGENITAL HEMOLYTIC ANEMIA WITH INCREASED INTRA-ERYTHROCYTIC CONCENTRATION OF 2,3-DIPHOSPHOGLYCERATE].
BIOERCK G; BOETTIGER LE; ORINIUS E
Nord Med; 1963 Sep; 70():1054-6. PubMed ID: 14050375
[No Abstract] [Full Text] [Related]
31. A novel stomatocytosis variant showing marked abnormalities in intracellular [Na] and [K] with minimal haemolysis.
Jarvis HG; Chetty MC; Nicolaou A; Fisher J; Miller A; Stewart GW
Eur J Haematol; 2001 Jun; 66(6):412-4. PubMed ID: 11488942
[No Abstract] [Full Text] [Related]
32. Two cases of red cell aldolase deficiency associated with hereditary hemolytic anemia in a Japanese family.
Miwa S; Fujii H; Tani K; Takahashi K; Takegawa S; Fujinami N; Sakurai M; Kubo M; Tanimoto Y; Kato T; Matsumoto N
Am J Hematol; 1981 Dec; 11(4):425-37. PubMed ID: 7331996
[TBL] [Abstract][Full Text] [Related]
33. Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis).
Iolascon A; Stewart GW; Ajetunmobi JF; Perrotta S; Delaunay J; Carella M; Zelante L; Gasparini P
Blood; 1999 May; 93(9):3120-3. PubMed ID: 10216110
[TBL] [Abstract][Full Text] [Related]
34. Exclusion of the stomatin, alpha-adducin and beta-adducin loci in a large kindred with dehydrated hereditary stomatocytosis.
Innes DS; Sinard JH; Gilligan DM; Snyder LM; Gallagher PG; Morrow JS
Am J Hematol; 1999 Jan; 60(1):72-4. PubMed ID: 9883810
[TBL] [Abstract][Full Text] [Related]
35. Hereditary leaky red cell syndrome in a Swiss family.
Fey MF; Bischof M; Zahler P; Schatzmann HJ; Bucher U
Acta Haematol; 1986; 75(2):70-8. PubMed ID: 3090825
[TBL] [Abstract][Full Text] [Related]
36. Hereditary high-adenosine triphosphate syndrome: study of a new variant.
Bapat JP; Baxi AJ
Biochem Genet; 1981 Oct; 19(9-10):1017-22. PubMed ID: 6460500
[TBL] [Abstract][Full Text] [Related]
37. The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations.
Delaunay J
Semin Hematol; 2004 Apr; 41(2):165-72. PubMed ID: 15071792
[TBL] [Abstract][Full Text] [Related]
38. ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.
King MJ; Garçon L; Hoyer JD; Iolascon A; Picard V; Stewart G; Bianchi P; Lee SH; Zanella A;
Int J Lab Hematol; 2015 Jun; 37(3):304-25. PubMed ID: 25790109
[TBL] [Abstract][Full Text] [Related]
39. Köln haemoglobinopathy. Further data and a comparison with other hereditary Heinz body anaemias.
Jones RV; Grimes AJ; Carrell RW; Lehmann H
Br J Haematol; 1967 May; 13(3):394-408. PubMed ID: 6067323
[No Abstract] [Full Text] [Related]
40. [Congenital stomatocytosis associated with aplastic anemia].
Takigawa A; Kajigaya Y; Funabiki T; Fukazawa K; Ikuta K; Sasaki H; Matsuyama S; Terasawa T; Shichishima T; Kanzaki A
Rinsho Ketsueki; 1989 May; 30(5):713-8. PubMed ID: 2795885
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]