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Results: 1-25/52
Authors:
Beutler, E
Gelbart, T
West, C
Citation: E. Beutler et al., Synergy between TLR2 and TLR4: A safety mechanism, BL CELL M D, 27(4), 2001, pp. 728-730
Authors:
Lee, PL
Halloran, C
Beutler, E
Citation: Pl. Lee et al., Polymorphisms in the transferrin 5 ' flanking region associated with differences in total iron binding capacity: Possible implications in iron homeostasis, BL CELL M D, 27(2), 2001, pp. 539-548
Authors:
Lee, PL
Halloran, C
West, C
Beutler, E
Citation: Pl. Lee et al., Mutation analysis of the transferrin receptor-2 gene in patients with ironoverload, BL CELL M D, 27(1), 2001, pp. 285-289
Authors:
Beutler, E
Citation: E. Beutler, Commentary: Mutations of transferrin receptor 2 (Trf-2) and iron storage disease, BL CELL M D, 27(1), 2001, pp. 294-295
Authors:
Beutler, E
West, C
Speir, JA
Wilson, IA
Worley, M
Citation: E. Beutler et al., The HFE gene of browsing and grazing rhinoceroses: A possible site of adaptation to a low-iron diet, BL CELL M D, 27(1), 2001, pp. 342-350
Authors:
Beutler, E
Citation: E. Beutler, The treatment of acute leukemia: past, present, and future, LEUKEMIA, 15(4), 2001, pp. 658-661
Authors:
Suzuki, M
West, C
Beutler, E
Citation: M. Suzuki et al., Large-scale molecular screening for galactosemia alleles in a pan-ethnic population, HUM GENET, 109(2), 2001, pp. 210-215
Authors:
Kaplan, M
Hammerman, C
Beutler, E
Citation: M. Kaplan et al., Hyperbilirubinaemia, glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome, EUR J PED, 160(3), 2001, pp. 195-195
Authors:
Kaplan, M
Hammerman, C
Beutler, E
Citation: M. Kaplan et al., Heterozygosity for a polymorphism in the promoter region of the UGT1A1 gene, J HEPATOL, 35(1), 2001, pp. 148-149
Authors:
Beutler, E
Felitti, V
Gelbart, T
Ho, N
Citation: E. Beutler et al., Genetics of iron storage and hemochromatosis, DRUG META D, 29(4), 2001, pp. 495-499
Authors:
Beutler, E
Citation: E. Beutler, Subunit structure of the hexosaminidase isozymes, ADV GENETIC, 44, 2001, pp. 93-100
Authors:
Kaplan, M
Hammerman, C
Vreman, HJ
Stevenson, DK
Beutler, E
Citation: M. Kaplan et al., Acute hemolysis and severe neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes, J PEDIAT, 139(1), 2001, pp. 137-140
Authors:
Koziol, JA
Ho, NJ
Felitti, VJ
Beutler, E
Citation: Ja. Koziol et al., Reference centiles for serum ferritin and percentage of transferrin saturation, with application to mutations of the HFE gene, CLIN CHEM, 47(10), 2001, pp. 1804-1810
Authors:
Waalen, J
Beutler, E
Citation: J. Waalen et E. Beutler, Comment on "Frequency of elevated serum transferrin saturation in elderly subjects", CLIN CHIM A, 306(1-2), 2001, pp. 145-146
Authors:
Lee, PL
Halloran, C
Trevino, R
Felitti, V
Beutler, E
Citation: Pl. Lee et al., Human transferrin G277S mutation: a risk factor for iron deficiency anaemia, BR J HAEM, 115(2), 2001, pp. 329-333
Authors:
Corrons, JLV
Alvarez, R
Pujades, A
Zarza, R
Oliva, E
Lasheras, G
Callis, M
Ribes, A
Gelbart, T
Beutler, E
Citation: Jlv. Corrons et al., Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinicaland molecular studies, BR J HAEM, 112(2), 2001, pp. 475-482
Authors:
Beutler, E
Citation: E. Beutler, Discrepancies between genotype and phenotype in hematology: an important frontier, BLOOD, 98(9), 2001, pp. 2597-2602
Authors:
Beutler, E
Citation: E. Beutler, DNA-based diagnosis of red cell enzymopathies: how we threw out the baby with the bathwater, BLOOD, 97(11), 2001, pp. 3325-3325
Authors:
Beutler, E
Citation: E. Beutler, Introduction - Hemochromatosis population screening, GENET TEST, 4(2), 2000, pp. 95-96
Authors:
Beutler, E
Gelbart, T
Citation: E. Beutler et T. Gelbart, Large-scale screening for HFE mutations: Methodology and cost, GENET TEST, 4(2), 2000, pp. 131
Authors:
Iancovici-Kidon, M
Sthoeger, D
Abrahamov, A
Volach, B
Beutler, E
Gelbart, T
Barak, Y
Citation: M. Iancovici-kidon et al., A new exon 9 glucose-6-phosphate dehydrogenase mutation (G6PD "Rehovot") in a Jewish Ethiopian family with variable phenotypes, BL CELL M D, 26(6), 2000, pp. 567-571
Authors:
Beutler, E
Citation: E. Beutler, Commentary: Dosage-response in the treatment of Gaucher disease by enzyme replacement therapy, BL CELL M D, 26(4), 2000, pp. 303-306
Authors:
Beutler, E
Gelbart, T
Citation: E. Beutler et T. Gelbart, A common intron 3 mutation (IVS3-48c -> g) leads to misdiagnosis of the c.845G -> A (C282Y) HFE gene mutation, BL CELL M D, 26(3), 2000, pp. 229-233
Authors:
Beutler, E
Citation: E. Beutler, Message from the editor, BL CELL M D, 26(1), 2000, pp. 1-1
Authors:
Efferth, T
Osieka, R
Beutler, E
Citation: T. Efferth et al., Molecular characterization of a German variant of glucose-6-phosphate dehydrogenase deficiency (G6PD Aachen), BL CELL M D, 26(1), 2000, pp. 101-104