Citations (51)
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Georgi D. Efremov. (2001) FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999). Hemoglobin 25:2, pages 125-168.
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H. Landman & T. H. J. Huisman. (1998) Persistent Iron and Folate Deficiency in a Patient with Deletional Hereditary Persistence of Fetal Hemoglobin; the Effect on the Relative Levels of HB F and Gγ Chains and the Corresponding mRNAS. Hemoglobin 22:1, pages 53-63.
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S. El-Kalla & A. R. Mathews. (1997) A Novel β-Thalassemia Mutation [Codon 45 (-T)] in a Pakistani Family. Hemoglobin 21:6, pages 499-503.
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S. El-kalla & A. R. Mathews. (1995) A Novel Frameshift Mutation Causing β-Thalassemia in a Sikh. Hemoglobin 19:3-4, pages 183-189.
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E. Baysal, S. Sharma, S. C. Wong, V. B. Jogessar & T. H.J. Huisman. (1994) Distribution of β-thalassemia mutations in three asian indian populations with distant geographical locations. Hemoglobin 18:3, pages 201-209.
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R. Öner, S. Agarwal, A. J. Dimovski, G. D. Efremov, G. H. Petkov, C. Altay, A. Gurgey & T. H.J. Huisman. (1991) The G→A Mutation at Position +22 31 to the Cap Site of the β-Globin Gene as a Possible Cause for a β-Thalassemia. Hemoglobin 15:1-2, pages 67-76.
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C. Altay, A. Gurgey, R. Öner, A. Kutlar, F. Kutlar & T. H. J. Huisman. (1991) A Mild Thalassemia Major Resulting from a Compound Heterozygosity for the IVS-11-1 (G→A) Mutation and the Rare T→C Mutation at the Polyadenylation Site. Hemoglobin 15:4, pages 327-330.
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L. Jankovic, G. D. Efremov, O. Josifovska, D. Juricic, T. A. Stomingl, A. Kutlar & T. H. J. Huisman. (1990) An Initiation Codon Mutation as a Cause of a β-Thalassemia. Hemoglobin 14:2, pages 169-176.
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D. Corso, B. Cognata, C. Ciaccio, T. Piazza, S. P. Dibenedetto, P. Samperi, G. Russo Mancuso & G. Schiliro. (1990) Hb Agenogi [β90(F6)Glu → Lys] and β°-Thalassa in A Sicilian Family. Hemoglobin 14:5, pages 549-553.
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M. Harkness, D. R. Harkness, F. Kutlar, A. Kutlar, J. B. Wilson, B. B. Webber, J. F. Codrington & T. H.J. Huisman. (1990) Hb Sun Prae or α213o(H13)Ala → Proβ2 A New Unstable Variant Occurring In Low Quantities. Hemoglobin 14:5, pages 479-489.
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R. Öner, C. Altay, A. Gurgey, M. Aksoy, Y. Kilinc, T. A. Stoming, A. L. Reese, A. Kutlar, F. Kutlar & T. H. J. Huisman. (1990) β-Thalassemia in Turkey. Hemoglobin 14:1, pages 1-13.
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S. Dash, B. B. Webber, A. Kutlar, T. H. J. Huisman & J. B. Wilson. (1989) HB Chandigarh or α2β294(FGl)ASP→GLY Observed in an Indian Family. Hemoglobin 13:7-8, pages 749-752.
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L. Ulukutlu, H. Ozsahin, J. B. Wilson, B. B. Webber, H. Hu, A. Kutlar, F. Kutlar & T. H. J. Huisman. (1989) HB Brockton [α2β2138(H16)ALA→PRO] Observed in a Turkish Girl. Hemoglobin 13:5, pages 509-513.
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J. M. Gonzalez-Redondo, T. A. Stoming, F. Kutlar, A. Kutlar, H. Hu, J. B. Wilson & T. H. J. Huisman. (1989) HB Monroe or α2β230(B12)ARG→THR, a Variant Associated with β-Thalassemia due to a G→C Substitution Adjacent to the Donor Splice Site of the First Intron. Hemoglobin 13:1, pages 67-74.
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A. Kutlar, F. Kutlar, M. Aksoy, A. Gurgey, Ç. Altay, J. B. Wilson, J. C. Diaz-Chico, H. Hu & T. H. J. Huisman. (1989) β-Thalassemia Intermedia in Two Turkish Families is Caused by the Interaction of HB Knossos [β27(B9)ALA→SER] and of HB City of hope [β69(E13)Gly→Ser] with B°-Thalassemia. Hemoglobin 13:1, pages 7-16.
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B.H. Al-Awamy, G. A. Niazi, M.I. El-Mouzan, M.T. Altorki & M.A. Naeem. (1986) Relationship of haemoglobin F and alpha thalassaemia to severity of sickle-cell anaemia in the Eastern Province of Saudi Arabia. Annals of Tropical Paediatrics 6:4, pages 261-265.
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Y. Hattori, F. Kutlar, A. Kutlar, V. C. McKie & T. H. J. Huisman. (1986) Haplotypes of βS Chromosomes Among Patients with Sickle Cell Anemia from Georgia. Hemoglobin 10:6, pages 623-642.
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William L. Marsh & Harold M. Koenig. (1982) The Laboratory Evaluation of Microcytic Red Blood Cells. CRC Critical Reviews in Clinical Laboratory Sciences 16:3, pages 195-254.
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T. H. J. Huisman. (1980) Chromatographic Methods for the Separation of Normal and Abnormal Hemoglobins. Hemoglobin 4:3-4, pages 527-539.
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T. H. J. Huisman, B. L. Abraham, H. F. Harris, M. E. Gravely, J. Henson, D. Williams, J. B. Wilson, A. Miller, S. Mayson, R. N. Wrightstone, E. Moss, B. Joseph, L. Walker, J. Brisco & L. Brisco. (1980) Hemoglobinopathies Observed in the Population of the Southeastern United States (SE-USA). Hemoglobin 4:3-4, pages 373-386.
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R. O. Schneider. (1978) Methods for Detection of Hemoglobin Variants and Hemoglobinopathies in the Routine Clinical Laboratory. CRC Critical Reviews in Clinical Laboratory Sciences 9:3, pages 243-271.
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Articles from other publishers (30)
Anju Gupta, Yukio Hattori, Usha R. Gupta, Swati Sarwai, Nitu Nigam, Pragya Singhal & Sarita Agarwal. (2003) Molecular Genetic Testing of β-Thalassemia Patients of Indian Origin and a Novel 8-bp Deletion Mutation at Codons 36/37/38/39. Genetic Testing 7:2, pages 163-168.
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Anju Gupta, Yukio Hattori & Sarita Agarwal. (2002) Initiation codon mutation in an Asian Indian family. American Journal of Hematology 71:2, pages 134-136.
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Xiao-Dong Huang, Xuexian O. Yang, Rui-Bin Huang, Hong-Yuan Zhang, Hua-Lu Zhao, Yan-Jun Zhao, Cheng-Le Huang, Chun-Jiang Hou & Jun-Wu Zhang. (2000) A novel four base-pair deletion within the A?-GLOBin gene promoter associated with slight increase of A? expression in adult. American Journal of Hematology 63:1, pages 16-19.
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Sarita Agarwal, Li Wei, Yukio Hattori & S. S. Agarwal. (1997) Codon 4 ACT→ACA, codon 5 CCT→TCT, and codon 6 GAG→TAG mutations in cis position: A form of thalassemia trait. American Journal of Hematology 56:3, pages 187-188.
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Natalia S. Smetanina, Cihan Öner, Erol Baysal, Reyhan Öner, Gülsen Bozkurt, Çigdem Altay, Aytemiz Gürgey, Adekunle D. Adekile, Li-Hao Gu & Titus H.J. Huisman. (1996) The relative levels of α2-, α1-, and ζ-mRNA in HB H patients with different deletional and nondeletional α-thalassemia determinants. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1316:3, pages 176-182.
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A. J. Dimovski, A. D. Adekile & T. H. J. Huisman. (1994) The in vivo expression of the globin genes of theβ cistron in γ-,δ-, andδβ-thalassemia heterozygotes. Experientia 50:2, pages 167-170.
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Cihan �ner, AleksandarJ. Dimovski, NancyF. Olivieri, Gino Schiliro, JohnF. Codrington, Sladdehine Fattoum, AdekunleD. Adekile, Reyhan �ner, GunesT. Y�regir, C. Altay, A. Gurgey, RashikB. Gupta, VinodB. Jogessar, MichaelN. Kitundu, Dimitris Loukopoulos, GabrielP. Tamagnini, M.LeticiaS. Ribeiro, Ferdane Kutlar, Li-Hao Gu, KennethD. Lanclos & TitusH.J. Huisman. (1992) ?s Haplotypes in various world populations. Human Genetics 89:1, pages 99-104.
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Karel Indrak, Vaclav Brabec, Jarmila Indrakova, Ladislav Chrobak, Adriana Sakalova, Marie Jarosova, Jaroslav Cermak, You-jun Fei, Ferdane Kutlar, Yuan-chao Gu, Erol Baysal & Titus H. J. Huisman. (1992) Molecular characterization of β-thalassemia in Czechoslovakia. Human Genetics 88:4, pages 399-404.
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Ph. Beris, R. Darbellay, A. Hochmann, E. Pradervand & P. Pugin. (1991) Interaction of heterozygous β0-thalassemia and triplicated alpha globin loci in a Swiss-Spanish family. Klinische Wochenschrift 69:15, pages 710-714.
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K. Indrak, J. Indrakova, F. Kutlar, D. Pospisilova, I. Sulovska, E. Baysal & T. H. J. Huisman. (1991) Compound heterozygosity for a β∘-thalassemia (frameshift codons 38/39; -C) and a nondeletional swiss type of HPFH (A→C at NT -110, Gγ) in a Czechoslovakian family. Annals of Hematology 63:2, pages 111-115.
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Photis Beris, Regis Darbellay, Catherine Dornier, Agnes Hochmann & Peter Miescher. (2009) Prenatal diagnosis of thalassemia and hemoglobinopathies in Switzerland. European Journal of Haematology 46:3, pages 163-171.
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G. D. Efremov, O. Josifovska, N. Nikolov, J. F. Codrington, C. Oner, J. M. Gonzalez‐Redondo & T. H. J. Huisman. (2008) Hb Icaria–Hb H disease: identification of the Hb Icaria mutation through analysis of amplified DNA. British Journal of Haematology 75:2, pages 250-253.
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K. G. Yang, F. Kutlar, E. George, J. B. Wilson, A. Kutlar, T. A. Stoming, J. M. Gonzalez Redondo & T. H. J. Huisman. (2008) Molecular characterization of β‐globin gene mutations in Malay patients with Hb E‐β‐thalassaemia and thalassaemia major. British Journal of Haematology 72:1, pages 73-80.
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Ferdane Kutlar, Jose M. Gonzalez-Redondo, Abdullah Kutlar, Aytemiz Gurgey, �igdem Altay, Georgi D. Efremov, Klara Kleman & Titus H. J. Huisman. (1989) The levels of ?, ?, and ? chains in patients with Hb H disease. Human Genetics 82:2, pages 179-186.
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Ferdane Kutlar, Li Hao Gu, Huaiyu Hu & Titus H.J. Huisman. (1989) Quantitation of hemoglobins Bart's, H, Portland-I, Portland-II and constant spring by anion-exchange high-performance liquid chromatography. Journal of Chromatography B: Biomedical Sciences and Applications 487, pages 265-274.
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J. M. Gonzalez‐Redondo, J. C. Diaz‐Chico, J. J. Malcorra‐Azpiazu, M. I. Balda‐Aguirre & T. H. J. Huisman. (2008) Characterization of a newly discovered α‐thalassaemia‐1 in two Spanish patients with Hb H disease. British Journal of Haematology 70:4, pages 459-463.
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J.L. Mahu, D. Valteau, J.P. Suquet, C. Meskens, J.C. Saly, J. Lebas, H. Isautier, G. Gerard, H. Caillens, J.P. Christides, G. Potier de Courcy, F. Galacteros & M. Turquet. (1988) Prevalence and etiology of anemia in reuntion: Comparative study of hematological, biochemical and anthropometric parameters, parasitic and clinical status of anemic and non-anemic children. Nutrition Research 8:7, pages 733-744.
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H. J. Huang, T. A. Stoming, H. F. Harris, F. Kutlar & T. H. J. Huisman. (2006)
The greek
a
γβ
+
‐hpfh observed in a large black family
. American Journal of Hematology 25:4, pages 401-408.
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Y. C. Gu, H. Landman & T. H. J. Huisman. (1987) Two different quadruplicated α globin gene arrangements. British Journal of Haematology 66:2, pages 245-250.
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T.H.J. Huisman, F. Kutlar, A. Kutlar, J.B. Wilson & H.F. Harris. (1987) The Mγ chain of human fetal hemoglobin; its identification and occurrence. Journal of Chromatography A 388, pages 429-439.
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F Kutlar, A Kutlar & T.H.J Huisman. (1986) Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography. Journal of Chromatography A 357, pages 147-153.
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M. Aksoy, A. Kutlar, G. D. Efremov, N. Nikolov, G. Petkov, A. L. Reese, T. Harano, S. S. Chen & T. H. J. Huisman. (2006)
Haplotypes and levels of fetal hemoglobin and
G
γ to
A
γ ratios in mediterranean patients with thalassemia minor and major
. American Journal of Hematology 20:1, pages 7-16.
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P. S. Henthorn, O. Smithies, T. Nakatsuji, A. E. Felice, M. B. Gardiner, A. L. Reese & T. H. J. Huisman. (2008)
(
A
γδβ)°‐Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA
. British Journal of Haematology 59:2, pages 343-356.
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T. Harano, A. L. Reese, R. Ryan, B. L. Abraham & T. H. J. Huisman. (2008)
Five haplotypes in Black β‐thalassaemia heterozygotes: three are associated with high and two with low
G
γ values in fetal haemoglobin
. British Journal of Haematology 59:2, pages 333-342.
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T. Nakatsuji, K. Shimizu & T.H.J. Huisman. (1984) Hb F-LA grange or α2γ2101(G3)Glu → Lys; 75IIe; 136Gly: A high affinity fetal hemoglobin variant observed in a caucasian newborn. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology 789:2, pages 224-228.
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Abdullah Kutlar, Ferdane Kutlar, Jerry B. Wilson, Marsha G. Headlee & Titus H. J. Huisman. (2006) Quantitation of hemoglobin components by high‐performance cation‐exchange liquid chromatography: Its use in diagnosis and in the assessment of cellular distribution of hemoglobin variants. American Journal of Hematology 17:1, pages 39-53.
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RANDHIR S. SANDHU & STEVEN J. FISCHMAN. 1984. Clinical Biochemistry. Clinical Biochemistry
215
260
.
G. Saglio, C. Camaschella, A. Guerrasio, G. Rege Cambrin, A. Capaldi, P. G. Pich, M. Trento & U. Mazza. (2008)
G
Γ and
A
Γ globin chain synthesis in bone marrow and peripheral blood of β‐thalassaemia homozygotes
. British Journal of Haematology 52:2, pages 225-231.
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P. Basset, F. Braconnier & J. Rosa. (1982) An update on electrophoretic and chromatographic methods in the diagnosis of hemoglobinopathies. Journal of Chromatography B: Biomedical Sciences and Applications 227:2, pages 267-304.
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Haewon C. Kim. (2016) Laboratory Identification of Inherited Hemoglobinopathies in Children. Clinical Pediatrics 20:3, pages 161-171.
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