53 related articles for article (PubMed ID: 2386513)
1. Heterogeneity of glucose-6-phosphate dehydrogenase enzymopathies in the CSSR.
Jacobasch G; Sakalova A; Brabec V
Biomed Biochim Acta; 1990; 49(2-3):S247-50. PubMed ID: 2386513
[TBL] [Abstract][Full Text] [Related]
2. Heterogeneity of glucose-6-phosphate dehydrogenase enzymopathies in the GDR.
Jacobasch G; Buckwitz D; Jurowski R; Gerth C; Plonka A; Kuckelkorn U
Biomed Biochim Acta; 1987; 46(2-3):S177-81. PubMed ID: 3593296
[TBL] [Abstract][Full Text] [Related]
3. [Electrophoretic and kinetic properties of the erythrocyte glucose-6-phosphate dehydrogenase of patients with hemolytic anemia related to a deficit in the activity of that enzyme].
Cherniak NB; Batishchev AI; Lamzina NV; Tokarev IuN; Alekseev GA
Vopr Med Khim; 1977; 23(2):166-71. PubMed ID: 18839
[TBL] [Abstract][Full Text] [Related]
4. Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency.
Pietrapertosa A; Palma A; Campanale D; Delios G; Vitucci A; Tannoia N
Haematologica; 2001 Jan; 86(1):30-5. PubMed ID: 11146567
[TBL] [Abstract][Full Text] [Related]
5. Marked decrease in specific activity contributes to disease phenotype in two human glucose 6-phosphate dehydrogenase mutants, G6PD(Union) and G6PD(Andalus).
Wang XT; Lam VM; Engel PC
Hum Mutat; 2005 Sep; 26(3):284. PubMed ID: 16088936
[TBL] [Abstract][Full Text] [Related]
6. Classification of glucose-6-phosphate dehydrogenase variants by multivariate statistical analysis.
Buckwitz D; Jacobasch G; Post A
Biomed Biochim Acta; 1990; 49(2-3):S251-4. PubMed ID: 2386514
[TBL] [Abstract][Full Text] [Related]
7. New stable mutant (Gd(-) variants: G6PD Tashkent and G6PD Nucus. Molecular basis of hereditary enzyme deficiency.
Yermakov N; Tokarev Ju; Chernjak N; Schönian G; Grieger M; Guckler A; Jacobasch G; Mahmudova M; Bahramov S
Acta Biol Med Ger; 1981; 40(4-5):559-62. PubMed ID: 7315103
[TBL] [Abstract][Full Text] [Related]
8. A new glucose 6-phosphate dehydrogenase variant (GDTrinacria) in two unrelated families of Sicilian ancestry.
Sansone G; Perroni L; Yoshida A; Dave V
Ital J Biochem; 1977; 26(1):44-50. PubMed ID: 16832
[TBL] [Abstract][Full Text] [Related]
9. Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism.
Jablonska-Skwiecinska E; Lewandowska I; Plochocka D; Topczewski J; Zimowski JG; Klopocka J; Burzynska B
Hum Mutat; 1999; 14(6):477-84. PubMed ID: 10571945
[TBL] [Abstract][Full Text] [Related]
10. A glucose-6-phosphate dehydrogenase variant, Gd(-) Santamaria found in Costa Rica.
Sáenz GF; Chaves M; Berrantes A; Elizondo J; Montero AG; Yoshida A
Acta Haematol; 1984; 72(1):37-40. PubMed ID: 6433630
[TBL] [Abstract][Full Text] [Related]
11. Red cell enzymopathies as a model of inborn errors of metabolism.
Miwa S; Kanno H; Hirono A; Fujii H
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():112-9. PubMed ID: 8629088
[TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of a German variant of glucose-6-phosphate dehydrogenase deficiency (G6PD Aachen).
Efferth T; Osieka R; Beutler E
Blood Cells Mol Dis; 2000 Feb; 26(1):101-4. PubMed ID: 10772881
[TBL] [Abstract][Full Text] [Related]
13. Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.
Miwa S; Fujii H
Am J Hematol; 1996 Feb; 51(2):122-32. PubMed ID: 8579052
[TBL] [Abstract][Full Text] [Related]
14. Gd(-) Rennes, a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia found in France.
Picat C; Etiemble J; Boivin P; Le Prise PY
Hum Genet; 1980; 55(1):125-7. PubMed ID: 7450748
[TBL] [Abstract][Full Text] [Related]
15. Red cell glucose-6-phosphate dehydrogenase phenotypes in Iraq.
Hilmi FA; Al-Allawi NA; Rassam M; Al-Shamma G; Al-Hashimi A
East Mediterr Health J; 2002 Jan; 8(1):42-8. PubMed ID: 15330559
[TBL] [Abstract][Full Text] [Related]
16. Molecular biology of G 6 PD variants.
Beutler E; Lisker R; Kuhl W
Biomed Biochim Acta; 1990; 49(2-3):S236-41. PubMed ID: 2386511
[TBL] [Abstract][Full Text] [Related]
17. Three new G6PD variants, G6PD Adana, G6PD Samandağ, and G6PD Balcali in Cukurova, Turkey.
Aksoy K; Yüregir GT; Dikmen N; Unlükurt I
Hum Genet; 1987 Jun; 76(2):199-201. PubMed ID: 3610149
[TBL] [Abstract][Full Text] [Related]
18. Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutation.
Sukumar S; Mukherjee MB; Colah RB; Mohanty D
Blood Cells Mol Dis; 2005; 35(2):193-5. PubMed ID: 15996881
[TBL] [Abstract][Full Text] [Related]
19. The role of enzyme variants, polymorphisms and enzyme hybrids in enzyme deficiency conditions.
Aebi H; Wyss SR
Acta Biol Med Ger; 1981; 40(4-5):537-41. PubMed ID: 7315100
[TBL] [Abstract][Full Text] [Related]
20. A new glucose-6-phosphate dehydrogenase variant (G6PD Tsukui) associated with congenital hemolytic anemia.
Ogura H; Morisaki T; Tani K; Kanno H; Tsutsumi H; Takahashi K; Miyamori T; Fujii H; Miwa S
Hum Genet; 1988 Apr; 78(4):369-71. PubMed ID: 3360447
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
