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1
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17844403368
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Thalassemia minor associated with hemoglobin-Bi heterozygosity. A family report
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Huisman THJ, Punt K, Schaad JDG: Thalassemia minor associated with hemoglobin-Bi heterozygosity. A family report. Blood 1961; 17:747-757.
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(1961)
Blood
, vol.17
, pp. 747-757
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Huisman, T.1
Punt, K.2
Schaad, J.3
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3
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34547389999
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Study of a family possessing hemoglobin C, classical thalassemia and the abnormal minor hemoglobin component A2'
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Lee RC, Huisman THJ: Study of a family possessing hemoglobin C, classical thalassemia and the abnormal minor hemoglobin component A2'. Am J Hum Genet 1963;15:69-73.
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(1963)
Am J Hum Genet
, vol.15
, pp. 69-73
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Lee, R.C.1
Huisman, T.2
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4
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0025118721
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Observations on the levels of Hb A2 in patients with different p-thalassemia mutations and a 8 chain variant
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Codrington JF, Li H-W, Kutlar F. Gu L-H, Ramachandran M, Huisman THJ: Observations on the levels of Hb A2 in patients with different p-thalassemia mutations and a 8 chain variant. Blood 1990;76:1246-1249.
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(1990)
Blood
, vol.76
, pp. 1246-1249
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Codrington, J.F.1
Li, H.-W.2
Kutlar, F.L.-H.3
Ramachandran, M.4
Huisman, T.5
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5
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0025302542
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Fetal hemoglobin in normal adults and p-thalassemia heterozygotes
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Kutlar A, Kutlar F, Gu L.-G, Mayson SM, Huisman THJ: Fetal hemoglobin in normal adults and p-thalassemia heterozygotes. Hum Genet 1990;85:106-110.
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(1990)
Hum Genet
, vol.85
, pp. 106-110
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Kutlar, A.1
Kutlar, F.2
Gu, L.-G.3
Mayson, S.M.4
Huisman, T.5
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6
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0003909626
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New York, Dekker, The Hemoglobinopathies Techniques of Identification
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Huisman THJ, Jonxis JHP: Clinical and Biochemical Analysis. New York, Dekker, 1977, vol 6: The Hemoglobinopathies Techniques of Identification.
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(1977)
Clinical and Biochemical Analysis
, vol.6
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Huisman, T.1
Jonxis, J.2
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7
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0001441465
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Conventional isoelectric focusing and immobilized pH gradients for hemoglobin separation and identification
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Huisman THJ (ed):, Edinburgh, Churchill Livingstone, The Hemoglobinopathies
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Righetti PG, Gianazza E, Bianchi-Bosisio A, Cossu G: Conventional isoelectric focusing and immobilized pH gradients for hemoglobin separation and identification; in Huisman THJ (ed): Methods in Hematology. Edinburgh, Churchill Livingstone, 1986, vol 15: The Hemoglobinopathies.
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(1986)
Methods in Hematology
, vol.15
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Righetti, P.G.1
Gianazza, E.2
Bianchi-Bosisio, A.3
Cossu, G.4
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9
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0020573329
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A new high performance liquid chromatographic procedure for the separation and quantitation of various hemoglobin variants in adults and newborn babies
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Wilson JB, Headlee ME, Huisman THJ: A new high performance liquid chromatographic procedure for the separation and quantitation of various hemoglobin variants in adults and newborn babies. J Lab Clin Med 1983; 102:174-186.
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(1983)
J Lab Clin Med
, vol.102
, pp. 174-186
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Wilson, J.B.1
Headlee, M.E.2
Huisman, T.3
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10
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0024211736
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High-performance liquid chromatographic separation of human haemoglobins. Simultaneous quantitation of foetal and glycated haemoglobins
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Bisse E, Wieland H: High-performance liquid chromatographic separation of human haemoglobins. Simultaneous quantitation of foetal and glycated haemoglobins. J Chromatogr 1988;434:95-110.
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(1988)
J Chromatogr
, vol.434
, pp. 95-110
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Bisse, E.1
Wieland, H.2
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11
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0029294082
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The β- and 8-thalas-semia repository, cd 8
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Baysal E, Carver MFH: The β- and 8-thalas-semia repository, cd 8. Hemoglobin 1995:19: 213-216.
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(1995)
Hemoglobin
, vol.19
, pp. 213-216
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Baysal, E.1
Carver, M.2
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12
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0023789439
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HbS(C)-β‘-thalassemia: Different mutations are associated with different levels of normal Hb A
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Gonzalez-Redondo JM, Kutlar F, Kutlar A, Stoming TA, de Pablos JM, Kilin Y, Huisman THJ: HbS(C)-β‘-thalassemia: Different mutations are associated with different levels of normal Hb A. Br J Haematol 1988;70:85-89.
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(1988)
Br J Haematol
, vol.70
, pp. 85-89
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-
Gonzalez-Redondo, J.M.1
Kutlar, F.2
Kutlar, A.3
Stoming, T.A.4
De Pablos, J.M.5
Kilin, Y.6
Huisman, T.7
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13
-
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0023782895
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Clinical and genetic heterogeneity in Black patients with homozygous p-thalassemia from the southeastern United States
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Gonzalez-Redondo JM, Stoming TA, Lanclos KD, Gu YC, Kutlar A. Kutlar F, Nakatsuji T, Deng B, Han IS, McKie VC, Huisman THJ: Clinical and genetic heterogeneity in Black patients with homozygous p-thalassemia from the southeastern United States. Blood 1988;72: 1007-1014.
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(1988)
Blood
, vol.72
, pp. 1007-1014
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Gonzalez-Redondo, J.M.1
Stoming, T.A.2
Lanclos, K.D.3
Gu, Y.C.4
Kutlar, A.5
Kutlar, F.6
Nakatsuji, T.7
Deng, B.8
Han, I.S.9
McKie, V.C.10
Huisman, T.11
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14
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0028172737
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Y-mRNA and Hb F levels in 13-thalassemia
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Efremov DG, Dimovski AJ, Sukarova E, Schi-lird G, Zisovski N, Efremov GD. Burrone OR, Huisman THJ: y-mRNA and Hb F levels in 13-thalassemia. Br J Haematol 1994,88:311-317.
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(1994)
Br J Haematol
, vol.88
, pp. 311-317
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Efremov, D.G.1
Dimovski, A.J.2
Sukarova, E.3
Schi-Lird, G.4
Zisovski, N.5
Efremov, G.D.6
Burrone, O.R.7
Huisman, T.8
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15
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0016087442
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On the structure of the hemoglobins A, A1 and F in a Negro with homozygous β-thalasscmia
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Schroeder WA, Huisman THJ, Shelton JR, Apell G, Shelton JB, Brodie AR, Lutchcr CL, Blunt MH, Miller A: On the structure of the hemoglobins A, A1 and F in a Negro with homozygous β-thalasscmia. Biochem Med 1974;10:276-292.
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(1974)
Biochem Med
, vol.10
, pp. 276-292
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Schroeder, W.A.1
Huisman, T.2
Shelton, J.R.3
Apell, G.4
Shelton, J.B.5
Brodie, A.R.6
Lutchcr, C.L.7
Blunt, M.H.8
Miller, A.9
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16
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0020574451
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The distribution of fetal hemoglobin and the types of y chain in red cell fractions separated by gradient centrifugation from blood of patients with sickle cell anemia and other hemoglobinopathies
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Headlee ME, Gardiner MB. Reese AL, Huisman THJ: The distribution of fetal hemoglobin and the types of y chain in red cell fractions separated by gradient centrifugation from blood of patients with sickle cell anemia and other hemoglobinopathies. Biochem Med 1983;29: 337-354.
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(1983)
Biochem Med
, vol.29
, pp. 337-354
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Headlee, M.E.1
Gardiner, M.B.2
Reese, A.L.3
Huisman, T.4
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17
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0016338877
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Globin synthesis in the Jamaican Negro with beta-thalassaemia
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Friedman SH, Schwartz E, Ahem V, Ahem E: Globin synthesis in the Jamaican Negro with beta-thalassaemia. Br J Haematol 1974;28: 505-513.
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(1974)
Br J Haematol
, vol.28
, pp. 505-513
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Friedman, S.H.1
Schwartz, E.2
Ahem, V.3
Ahem, E.4
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18
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0025925290
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Hemoglobin A2: Origin, evolution, and aftermath
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Steinberg MH, Adams JG III: Hemoglobin A2: Origin, evolution, and aftermath. Blood 1991; 78:2165-2177.
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(1991)
Blood
, vol.78
, pp. 2165-2177
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Steinberg, M.H.1
Adams, J.G.2
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19
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0030909488
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Ideguchi 1: β-Thalassemia mutations in Japanese and Koreans
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Ohba Y, Hattori Y, Harano T, Harano K, Fukumaki Y, Ideguchi 1: β-Thalassemia mutations in Japanese and Koreans. Hemoglobin, 1997;21:191-200.
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Hemoglobin
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Ohba, Y.1
Hattori, Y.2
Harano, T.3
Harano, K.4
Fukumaki, Y.5
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