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Abdullah Kutlar

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Chemicals & Drugs

Disorders

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High Pressure Liquid Chromatography

Physiology

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Amino Acid Sequence

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Turkey

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Co-Publications
Name
75
Kutlar, Ferdane
44
Huisman, TH
14
Aksoy, Cemalettin
14
McKie, Virgil
11
Altay, Cigdem
10
Gurgey, Aytemiz
9
Holley, Leslie
8
Adams, Robert
7
Dinçol, Günçag
7
Efremov, Georgi
6
Woods, Kristy
5
Prchal, Josef
5
Elam, Dedrey
5
Clair, Betsy
5
Brambilla, Donald

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Publications

TOP 3
Kutlar F; Hilliard L M; Zhuang L; Patel N; Eroglu B; Meiler S E; Carmichael H; Russell R B; Kutlar A
Hb M Dothan [beta 25/26 (B7/B8)/(GGT/GAG-->GAG//Gly/Glu-->Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics.
Hughes Heather Yaun; McKie Kathleen; Carmichael Harris; Bora Komal; Kutlar Abdullah; Kutlar Ferdane
Diagnostic complication and molecular characteristics of Hb SC-Chicago disease with alpha-thal-2 (-alpha3.7 deletion): effects of multiple variant on patient's phenotype.
Subbannan Karthi; Ustun Celalettin; Natarajan Kavita; Clair Betsy; Daitch Lisa; Fields Sabine; Kutlar Ferdane; Kutlar Abdullah
Acute splenic complications and implications of splenectomy in hemoglobin SC disease.

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All Publications

2009: Kutlar F; Hilliard L M; Zhuang L; Patel N; Eroglu B; Meiler S E; Carmichael H; Russell R B; Kutlar A
Hb M Dothan [beta 25/26 (B7/B8)/(GGT/GAG-->GAG//Gly/Glu-->Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics.
Blood cells, molecules & diseases 2009;43(3):235-8.
2009: Hughes Heather Yaun; McKie Kathleen; Carmichael Harris; Bora Komal; Kutlar Abdullah; Kutlar Ferdane
Diagnostic complication and molecular characteristics of Hb SC-Chicago disease with alpha-thal-2 (-alpha3.7 deletion): effects of multiple variant on patient's phenotype.
Annals of hematology 2009;88(11):1151-3.
2009: Subbannan Karthi; Ustun Celalettin; Natarajan Kavita; Clair Betsy; Daitch Lisa; Fields Sabine; Kutlar Ferdane; Kutlar Abdullah
Acute splenic complications and implications of splenectomy in hemoglobin SC disease.
European journal of haematology 2009;83(3):258-60.
2009: McKeown Sean M; Carmichael Harris; Markowitz Rhea-Beth; Kutlar Abdullah; Holley Leslie; Kutlar Ferdane
Rare occurrence of Hb Lepore-Baltimore in African Americans: molecular characteristics and variations of Hb Lepores.
Annals of hematology 2009;88(6):545-8.
2008: Fung Ellen B; Harmatz Paul R; Milet Meredith; Balasa Vinod; Ballas Samir K; Casella James F; Hilliard Lee; Kutlar Abdullah; McClain Kenneth L; Olivieri Nancy F; Porter John B; Vichinsky Elliott P;
Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions.
Transfusion 2008;48(9):1971-80.
2008: Ataga Kenneth I; Smith Wally R; De Castro Laura M; Swerdlow Paul; Saunthararajah Yogen; Castro Oswaldo; Vichinsky Elliot; Kutlar Abdullah; Orringer Eugene P; Rigdon Greg C; Stocker Jonathan W;
Efficacy and safety of the Gardos channel blocker, senicapoc (ICA-17043), in patients with sickle cell anemia.
Blood 2008;111(8):3991-7.
2008: Perry Rodney T; Gearhart Debra A; Wiener Howard W; Harrell Lindy E; Barton James C; Kutlar Abdullah; Kutlar Ferdane; Ozcan Ozan; Go Rodney C P; Hill William D
Hemoglobin binding to A beta and HBG2 SNP association suggest a role in Alzheimer's disease.
Neurobiology of aging 2008;29(2):185-93.
2008: Dainer Erin; Shell Richard; Miller Randy; Atkin Joan F; Pastore Matt; Kutlar Abdullah; Zhuang Lina; Holley Leslie; Davis Debra H; Kutlar Ferdane
Neonatal cyanosis due to a novel fetal hemoglobin: Hb F-Circleville [Ggamma63(E7)His-->Leu, CAT>CTT].
Hemoglobin 2008;32(6):596-600.
2008: Dainer Erin; Wenk Robert E; Luddy Ruth; Elam Dedrey; Holley Leslie; Kutlar Abdullah; Kutlar Ferdane
Two new hemoglobin variants: Hb Sinai-Greenspring [beta34(B16)Val-->Ile, GTC > ATC] and Hb Sinai-Bel Air [beta53(D4)Ala-->Asp, GCT > GAT].
Hemoglobin 2008;32(6):588-91.
2007: Agarwal Neeraj; Kutlar Ferdane; Mojica-Henshaw Mariluz P; Ou Ching N; Gaikwad Amos; Reading N Scott; Bailey Lakeia; Kutlar Abdullah; Prchal Josef T
Missense mutation of the last nucleotide of exon 1 (G->C) of beta globin gene not only leads to undetectable mutant peptide and transcript but also interferes with the expression of wild allele.
Haematologica 2007;92(12):1715-6.
2007: Ma Q; Wyszynski D F; Farrell J J; Kutlar A; Farrer L A; Baldwin C T; Steinberg M H
Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.
The pharmacogenomics journal 2007;7(6):386-94.
2007: Kutlar Abdullah
Sickle cell disease: a multigenic perspective of a single gene disorder.
Hemoglobin 2007;31(2):209-24.
2006: Valadi N; Silva G S; Bowman L S; Ramsingh D; Vicari P; Filho A C; Massaro A R; Kutlar A; Nichols F T; Adams R J
Transcranial Doppler ultrasonography in adults with sickle cell disease.
Neurology 2006;67(4):572-4.
2006: Lezcano Nelson E; Odo Nadine; Kutlar Abdullah; Brambilla Donald; Adams Robert J
Regular transfusion lowers plasma free hemoglobin in children with sickle-cell disease at risk for stroke.
Stroke; a journal of cerebral circulation 2006;37(6):1424-6.
2006: Dinçol Gunçag; Güvenç Serkan; Elam Dedrey; Kutlar Abdullah; Kutlar Ferdane
Hb J- Meerut [alpha 120 (H3) Ala ->Glu (alpha1)] in a Turkish male.
International journal of medical sciences 2006;3(1):26-7.
2005: Adekile A; Kutlar F; McKie K; Addington A; Elam D; Holley L; Clair B; Kutlar A
The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.
European journal of haematology 2005;75(2):150-5.
2005: Kutlar F; Mirmow D; Glendenning M; Holley L; Kutlar A
Postmortem molecular diagnosis of sickle beta thalassaemia.
Journal of clinical pathology 2005;58(5):548-9.
2005: Yan Jing-He; Ataga Kenneth; Kaul Sanjeev; Olson Jeffery S; Grasela Dennis M; Gothelf Samantha; Kutlar Abdulah; Orringer Eugene
The influence of renal function on hydroxyurea pharmacokinetics in adults with sickle cell disease.
Journal of clinical pharmacology 2005;45(4):434-45.
2005: Bakanay Sule M; Dainer Erin; Clair Betsy; Adekile Adekunle; Daitch Lisa; Wells Leigh; Holley Leslie; Smith David; Kutlar Abdullah
Mortality in sickle cell patients on hydroxyurea therapy.
Blood 2005;105(2):545-7.
2005: Kutlar Abdullah
Sickle cell disease: a multigenic perspective of a single gene disorder.
Hematology (Amsterdam, Netherlands) 2005;10 Suppl 1():92-9.
2005: Kutlar Abdullah
Sickle cell disease: a multigenic perspective of a single-gene disorder.
Medical principles and practice : international journal of the Kuwait University, Health Science Centre 2005;14 Suppl 1():15-9.
2004: Bergeron Michael F; Cannon Joseph G; Hall Elaina L; Kutlar Abdullah
Erythrocyte sickling during exercise and thermal stress.
Clinical journal of sport medicine : official journal of the Canadian Academy of Sport Medicine 2004;14(6):354-6.
2004: Ergul Sitki; Brunson Chris Y; Hutchinson Jim; Tawfik Amany; Kutlar Abdullah; Webb R Clinton; Ergul Adviye
Vasoactive factors in sickle cell disease: in vitro evidence for endothelin-1-mediated vasoconstriction.
American journal of hematology 2004;76(3):245-51.
2004: Wyszynski D F; Baldwin C T; Cleves M A; Amirault Y; Nolan V G; Farrell J J; Bisbee A; Kutlar A; Farrer L A; Steinberg M H
Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia.
Cellular and molecular biology (Noisy-le-Grand, France) 2004;50(1):23-33.
2004: Vinson Amy E; Walker Aisha; Elam Dedrey; Glendenning Michele; Kutlar Ferdane; Clair Betsy; Harbin Jeanette; Kutlar Abdullah
A novel approach to rapid determination of betaS-globin haplotypes: sequencing of the Agamma-IVS-II region.
Hemoglobin 2004;28(4):317-23.
2003: Dinçol Gunçag; Elam Dedrey; Kutlar Abdullah; Kutlar Ferdane
Hb Setif [alpha94(G1)Asp --> Tyr (alpha2)] detected in a Turkish family.
Hemoglobin 2003;27(4):249-52.
2003: Hsu Lewis L; Miller Scott T; Wright Elizabeth; Kutlar Abdullah; McKie Virgil; Wang Winfred; Pegelow Charles H; Driscoll Catherine; Hurlet Anne; Woods Gerald; Elsas Louis; Embury Stephen; Adams Robert J;
Alpha Thalassemia is associated with decreased risk of abnormal transcranial Doppler ultrasonography in children with sickle cell anemia.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2003;25(8):622-8.
2003: Adams Gaye T; Snieder Harold; McKie Virgil C; Clair Betsy; Brambilla Donald; Adams Robert J; Kutlar Ferdane; Kutlar Abdullah
Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen.
BMC medical genetics 2003;4():6.
2003: Jillella Anand P; Ustun Celalettin; Robach Eric; Sertkaya Durdu; DiPiro Cecily; Kallab Andre M; Brick Wendy G; Dainer Paul M; Kutlar Abdullah; Townsend Andrea R; Burgess Russell E
Infectious complications in patients receiving mobilization chemotherapy for autologous peripheral blood stem cell collection.
Journal of hematotherapy & stem cell research 2003;12(2):155-60.
2003: Steinberg Martin H; Barton Franca; Castro Oswaldo; Pegelow Charles H; Ballas Samir K; Kutlar Abdullah; Orringer Eugene; Bellevue Rita; Olivieri Nancy; Eckman James; Varma Mala; Ramirez Gloria; Adler Brian; Smith Wally; Carlos Timothy; Ataga Kenneth; DeCastro Laura; Bigelow Carolyn; Saunthararajah Yogen; Telfer Margaret; Vichinsky Elliott; Claster Susan; Shurin Susan; Bridges Kenneth; Waclawiw Myron; Bonds Duane; Terrin Michael
Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment.
JAMA : the journal of the American Medical Association 2003;289(13):1645-51.
2003: Steinberg Martin H; Voskaridou Ersi; Kutlar Abdullah; Loukopoulos Dimitris; Koshy Mabel; Ballas Samir K; Castro Oswaldo; Barton Franca
Concordant fetal hemoglobin response to hydroxyurea in siblings with sickle cell disease.
American journal of hematology 2003;72(2):121-6.
2003: Ustun Celatettin; Kutlar Ferdane; Holley Leslie; Seigler Maree; Burgess Russell; Kutlar Abdullah
Interaction of sickle cell trait with hereditary spherocytosis: splenic infarcts and sequestration.
Acta haematologica 2003;109(1):46-9.
2002: Redding-Lallinger Rupa; Tankut Gaye; Holley Leslie; Wright Frances; Kutlar Abdullah; Kutlar Ferdane
Molecular characterization of Hb D-Ibadan [beta87(F3)Thr-->Lys] in combination with Hb S [beta6(A3)Glu-->Val] and with beta+-Thalassemia: report of two cases.
Hemoglobin 2002;26(2):129-34.
2002: Files Beatrice; Brambilla Don; Kutlar Abdullah; Miller Scott; Vichinsky Elliott; Wang Winfred; Granger Suzanne; Adams Robert J
Longitudinal changes in ferritin during chronic transfusion: a report from the Stroke Prevention Trial in Sickle Cell Anemia (STOP).
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2002;24(4):284-90.
2001: Araten D J; Swirsky D; Karadimitris A; Notaro R; Nafa K; Bessler M; Thaler H T; Castro-Malaspina H; Childs B H; Boulad F; Weiss M; Anagnostopoulos N; Kutlar A; Savage D G; Maziarz R T; Jhanwar S; Luzzatto L
Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria.
British journal of haematology 2001;115(2):360-8.
2001: Orringer E P; Casella J F; Ataga K I; Koshy M; Adams-Graves P; Luchtman-Jones L; Wun T; Watanabe M; Shafer F; Kutlar A; Abboud M; Steinberg M; Adler B; Swerdlow P; Terregino C; Saccente S; Files B; Ballas S; Brown R; Wojtowicz-Praga S; Grindel J M
Purified poloxamer 188 for treatment of acute vaso-occlusive crisis of sickle cell disease: A randomized controlled trial.
JAMA : the journal of the American Medical Association 2001;286(17):2099-106.
2001: Kutlar A; Kutlar F; Turker I; Tural C
The methylene tetrahydrofolate reductase (C677T) mutation as a potential risk factor for avascular necrosis in sickle cell disease.
Hemoglobin 2001;25(2):213-7.
2001: Adekile A D; Kutlar F; Haider M Z; Kutlar A
Frequency of the 677 C-->T mutation of the methylenetetrahydrofolate reductase gene among Kuwaiti sickle cell disease patients.
American journal of hematology 2001;66(4):263-6.
2001: Barbeau P; Woods K F; Ramsey L T; Litaker M S; Pollock D M; Pollock J S; Callahan L A; Kutlar A; Mensah G A; Gutin B
Exercise in sickle cell anemia: effect on inflammatory and vasoactive mediators.
Endothelium : journal of endothelial cell research 2001;8(2):147-55.
2001: Woods K F; Ramsey L T; Callahan L A; Mensah G A; Litaker M S; Kutlar A; Barbeau P; Gutin B
Body composition in women with sickle cell disease.
Ethnicity & disease 2001;11(1):30-5.
2000: Jillella A P; Kallab A M; Kutlar A
Autoimmune thrombocytopenia following autologous hematopoietic cell transplantation: review of literature and treatment options.
Bone marrow transplantation 2000;26(8):925-7.
2000: Woods K F; Onuoha A; Schade R R; Kutlar A
Helicobacter pylori infection in sickle cell disease.
Journal of the National Medical Association 2000;92(7):361-5.
2000: Valafar H; Valafar F; Darvill A; Albersheim P; Kutlar A; Woods K F; Hardin J
Predicting the effectiveness of hydroxyurea in individual sickle cell anemia patients.
Artificial intelligence in medicine 2000;18(2):133-48.
2000: Woods K F; Johnson J A; Kutlar A; Daitch L; Stachura M E
Sickle cell disease telemedicine network for rural outreach.
Journal of telemedicine and telecare 2000;6(5):285-90.
1999: Tadmouri G O; Bilenoglu O; Kutlar F; Markowitz R B; Kutlar A; Basak A N
Identification of the Chinese IVS-II-654 (C-->T) beta-thalassemia mutation in an immigrant Turkish family: recurrence or migration?
Human biology; an international record of research 1999;71(2):295-302.
1999: Woods K F; Kutlar A; Johnson J A; Waller J L; Grigsby R K; Stachura M E; Rahn D W
Sickle cell telemedicine and standard clinical encounters: a comparison of patient satisfaction.
Telemedicine journal : the official journal of the American Telemedicine Association 1999;5(4):349-56.
1998: Tuohy A M; McKie V C; Sabio H; Kutlar F; Kutlar A; Wilson J B
Hb Hammersmith [beta 42(CD1) Phe-->Ser]: occurrence as a de novo mutation in black monozygotic twins with multiple congenital anomalies.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 1998;20(6):563-6.
1998: Bagasra O; Steiner R M; Ballas S K; Castro O; Dornadula G; Embury S; Jungkind D; Bobroski L; Kutlar A; Burchott S
Viral burden and disease progression in HIV-1-infected patients with sickle cell anemia.
American journal of hematology 1998;59(3):199-207.
1998: Thomas J J; Kutlar A; Scott D F; Lanclos K D
Inhibition of gene expression by the Ggamma 5' flanking region of the Bantu beta(s) chromosome.
American journal of hematology 1998;59(1):51-6.
1998: Carroll J E; McKie V; Kutlar A
Are sickle cell disease patients with stroke genetically predisposed to the event by inheriting a tendency to high tumor necrosis factor levels?
American journal of hematology 1998;58(3):250.
1998: Adams R J; McKie V C; Hsu L; Files B; Vichinsky E; Pegelow C; Abboud M; Gallagher D; Kutlar A; Nichols F T; Bonds D R; Brambilla D
Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography.
The New England journal of medicine 1998;339(1):5-11.
1998: Kutlar F; Adamkiewicz T V; Markowitz R B; Holley L; Kutlar A
An alpha-2 globin gene initiation codon mutation in a Vietnamese patient with Hb H disease.
Annals of the New York Academy of Sciences 1998;850():398-400.
1998: Adams R J; McKie V C; Brambilla D; Carl E; Gallagher D; Nichols F T; Roach S; Abboud M; Berman B; Driscoll C; Files B; Hsu L; Hurlet A; Miller S; Olivieri N; Pegelow C; Scher C; Vichinsky E; Wang W; Woods G; Kutlar A; Wright E; Hagner S; Tighe F; Waclawiw M A
Stroke prevention trial in sickle cell anemia.
Controlled clinical trials 1998;19(1):110-29.
1998: Woods K; Kutlar A; Grigsby R K; Adams L; Stachura M E
Primary-care delivery for sickle cell patients in rural Georgia using telemedicine.
Telemedicine journal : the official journal of the American Telemedicine Association 1998;4(4):353-61.
1995: Sutcharitchan P; Saiki R; Huisman T H; Kutlar A; McKie V; Erlich H; Embury S H
Reverse dot-blot detection of the African-American beta-thalassemia mutations.
Blood 1995;86(4):1580-5.
1995: Cürük M A; Howard S C; Kutlar A; Huisman T H
A newly discovered beta O-thalassemia (IVS-II-850, G-->A) mutation in a north European family.
Hemoglobin 1995;19(3-4):207-11.
1994: Adams R J; Kutlar A; McKie V; Carl E; Nichols F T; Liu J C; McKie K; Clary A
Alpha thalassemia and stroke risk in sickle cell anemia.
American journal of hematology 1994;45(4):279-82.
1993: Gürgey A; Beksaç S; Mesci L; Cakar N; Karakas U; Kutlar A; Altay C
Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I.
The Turkish journal of pediatrics 1993;35(3):159-62.
1993: Prchal J T; Kutlar A; Hall K; Robinson C A; Scott C W
Case report: alpha G-Philadelphia, beta O-Arab, and beta C globins present in a single patient.
The American journal of the medical sciences 1993;305(5):307-11.
1993: Kutlar F; Kutlar A; Nuguid E; Prchal J; Huisman T H
Usefulness of HPLC methodology for the characterization of combinations of the common beta chain variants Hbs S, C, and O-Arab, and the alpha chain variant Hb G-Philadelphia.
Hemoglobin 1993;17(1):55-66.
1992: Cürük M A; Kutlar A; Huisman T H
Hb Shelby [alpha 2 beta 2(131)(H9)Gln----Lys]-beta zero-thalassemia [codon 15 (TGG----TGA)] identified by DNA sequencing.
Hemoglobin 1992;16(5):417-9.
1991: Gonzalez-Redondo J M; Kutlar A; Kutlar F; McKie V C; McKie K M; Baysal E; Huisman T H
Molecular characterization of Hb S(C) beta-thalassemia in American blacks.
American journal of hematology 1991;38(1):9-14.
1991: Huisman T H; Harris H F; Stewart A; Kutlar A; Gardner R J; Green C
The frequencies of Hbs S and C in Georgia and South Carolina.
Human genetics 1991;87(1):102-5.
1991: Kutlar F; Felice A E; Grech J L; Bannister W H; Kutlar A; Wilson J B; Webber B B; Hu H Y; Huisman T H
The linkage of Hb Valletta [alpha 2 beta 287(f3)Thr----Pro] and Hb F-Malta-I [alpha 2G gamma 2117(G19)His----Arg] in the Maltese population.
Human genetics 1991;86(6):591-4.
1991: Altay C; Gurgey A; Oner R; Kutlar A; Kutlar F; Huisman T H
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation site.
Hemoglobin 1991;15(4):327-30.
1990: George-Kodiseri E; Yang K G; Kutlar F; Wilson J B; Kutlar A; Stoming T A; Gonzales-Redondo J M; Huisman T H
Chinese in west Malaysia: the geography of beta thalassaemia mutations.
Singapore medical journal 1990;31(4):374-7.
1990: Kutlar A; Ozcan O; Brisco J T; Ansley M C; Huisman T H
The detection of hemoglobin variants by isoelectrofocusing using EDTA-collected and filter paper-dried cord blood specimens.
American journal of clinical pathology 1990;94(2):199-202.
1990: Kutlar A; Kutlar F; Gu L G; Mayson S M; Huisman T H
Fetal hemoglobin in normal adults and beta-thalassemia heterozygotes.
Human genetics 1990;85(1):106-10.
1990: Wilson J B; Webber B B; Hu H; Kutlar A; Kutlar F; Codrington J F; Prchal J T; Hall K M; de Pablos J M; Rodriguez I
Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions.
Blood 1990;75(9):1883-7.
1990: Kattamis C; Hu H; Cheng G; Reese A L; Gonzalez-Redondo J M; Kutlar A; Kutlar F; Huisman T H
Molecular characterization of beta-thalassaemia in 174 Greek patients with thalassaemia major.
British journal of haematology 1990;74(3):342-6.
1990: Jankovic L; Efremov G D; Josifovska O; Juricic D; Stoming T A; Kutlar A; Huisman T H
An initiation codon mutation as a cause of a beta-thalassemia.
Hemoglobin 1990;14(2):169-76.
1990: Masala B; Manca L; Wilson J B; Webber B B; Kutlar A; Huisman T H
Hb Lepore-Baltimore in a north Sardinian family.
Hemoglobin 1990;14(3):241-6.
1990: Petkov G H; Efremov G D; Efremov D G; Dimovski A; Tchaicarova P; Tchaicarov R; Rogina B; Agarwal S; Kutlar A; Kutlar F
Beta-thalassemia in Bulgaria.
Hemoglobin 1990;14(1):25-33.
1990: Oner R; Altay C; Gurgey A; Aksoy M; Kilinç Y; Stoming T A; Reese A L; Kutlar A; Kutlar F; Huisman T H
Beta-thalassemia in Turkey.
Hemoglobin 1990;14(1):1-13.
1990: Harkness M; Harkness D R; Kutlar F; Kutlar A; Wilson J B; Webber B B; Codrington J F; Huisman T H
Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2, a new unstable variant occurring in low quantities.
Hemoglobin 1990;14(5):479-89.
1990: Zhao W; Wilson J B; Webber B B; Kutlar A; Tamagnini G P; Kuam B; Huisman T H
Hb Hekinan observed in three Chinese from Macau; identification of the GAG----GAT mutation in the alpha 1-globin gene.
Hemoglobin 1990;14(6):627-35.
1990: Plaseska D; Li H J; Wilson J B; Kutlar F; Kutlar A; Huisman T H; Kulpa J
Hb F-Brooklyn or alpha 2G gamma 2(66)(E10)Lys----Gln.
Hemoglobin 1990;14(2):213-6.
1989: George E; Huisman T H; Yang K G; Kutlari F; Wilson J B; Kutlar A; Storming T A; Gonzales-Redondo J M; Faridah K; Khalid A K
First observation of haemoglobin Malay alpha 2B2 26 (B1) Asn----Ser--a case report.
The Medical journal of Malaysia 1989;44(3):259-62.
1989: Ojwang P J; Ogada T; Gonzalez-Redondo J M; Kutlar A; Kutlar F; Huisman T H
beta S-haplotypes and alpha-thalassemia along the coastal belt of Kenya.
East African medical journal 1989;66(6):377-80.
1989: Yang K G; Kutlar F; George E; Wilson J B; Kutlar A; Stoming T A; Gonzalez-Redondo J M; Huisman T H
Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia major.
British journal of haematology 1989;72(1):73-80.
1989: Gonzalez-Redondo J M; Stoming T A; Kutlar A; Kutlar F; Lanclos K D; Howard E F; Fei Y J; Aksoy M; Altay C; Gurgey A
A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with "silent" beta-thalassemia.
Blood 1989;73(6):1705-11.
1989: Kutlar F; Gonzalez-Redondo J M; Kutlar A; Gurgey A; Altay C; Efremov G D; Kleman K; Huisman T H
The levels of zeta, gamma, and delta chains in patients with Hb H disease.
Human genetics 1989;82(2):179-86.
1989: Fei Y J; Stoming T A; Kutlar A; Huisman T H; Stamatoyannopoulos G
One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain.
Blood 1989;73(4):1075-7.
1989: Prchal J T; Scott C W; Rahbar S; Nagel R L; Kutlar A; Galla J H; Hall K
Mild sickle cell anemia associated with alpha globin mutant alpha Montgomery.
The American journal of medicine 1989;86(2):232-6.
1989: Gonzalez-Redondo J M; Stoming T A; Kutlar F; Kutlar A; McKie V C; McKie K M; Huisman T H
Severe Hb S-beta zero-thalassaemia with a T----C substitution in the donor splice site of the first intron of the beta-globin gene.
British journal of haematology 1989;71(1):113-7.
1989: Martins M C; Rosado L; Wilson J B; Kutlar A; Hu H; Huisman T H
Hb Himeji or alpha 2 beta 2(140)(H18)Ala----Asp in a Portuguese family.
Hemoglobin 1989;13(4):411-5.
1989: Bird A R; Elliott T; Wilson J B; Webber B B; Hu H; Kutlar A; Kutlar F; Huisman T H
Two rare unstable beta chain variants, Hb Mozhaisk or alpha 2 beta 292(F8)His----Arg and Hb Djelfa or alpha 2 beta 298(Fg5)Val----Ala, each being observed for the second time.
Hemoglobin 1989;13(2):193-7.
1989: Prior J F; Raven J L; Wilson J B; Kutlar A; Kutlar F; Huisman T H
Hb J-Lome or alpha 2 beta 259(E3)Lys----Asn in a Vietnamese family.
Hemoglobin 1989;13(1):79-81.
1989: Dash S; Wilson J B; Webber B B; Kutlar A; Huisman T H
Hb Chandigarh or alpha 2 beta 2(94)(FG1)Asp----Gly observed in an Indian family.
Hemoglobin 1989;13(7-8):749-52.
1989: Wilson J B; Webber B B; Kutlar A; Reese A L; McKie V C; Lutcher C L; Felice A E; Huisman T H
Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia.
Hemoglobin 1989;13(6):557-66.
1989: Ulukutlu L; Ozsahin H; Wilson J B; Webber B B; Hu H; Kutlar A; Kutlar F; Huisman T H
Hb Brockton [alpha 2 beta 2138(H16)Ala----Pro] observed in a Turkish girl.
Hemoglobin 1989;13(5):509-13.
1989: Villegas A; Martín G; Wilson J B; Webber B B; Hu H; Kutlar A; Kutlar F; Huisman T H
Hb Extremadura or alpha 2 beta 2133 (H11)Val----Leu, a new mildly unstable hemoglobin in a Spanish female.
Hemoglobin 1989;13(5):505-8.
1989: Gonzalez-Redondo J M; Stoming T A; Kutlar F; Kutlar A; Hu H; Wilson J B; Huisman T H
Hb Monroe or alpha 2 beta 230(B12)Arg----Thr, a variant associated with beta-thalassemia due to A G----C substitution adjacent to the donor splice site of the first intron.
Hemoglobin 1989;13(1):67-74.
1989: Glader B E; Zwerdling D; Kutlar F; Kutlar A; Wilson J B; Huisman T H
Hb F-M-Osaka or alpha 2G gamma 2(63)(E7)His----Tyr in a Caucasian male infant.
Hemoglobin 1989;13(7-8):769-73.
1989: Wilson J B; Webber B B; Kutlar A; Huisman T H
Hb Gainesville-GA or alpha 2 beta 2(46)(CD5)Gly----Arg; second report.
Hemoglobin 1989;13(6):623-4.
1989: Kutlar A; Kutlar F; Aksoy M; Gurgey A; Altay C; Wilson J B; Diaz-Chico J C; Hu H; Huisman T H
Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemia.
Hemoglobin 1989;13(1):7-16.
1989: Gurgey A; Altay C; Diaz-Chico J C; Kutlar F; Kutlar A; Huisman T H
Molecular heterogeneity of beta-thalassemia intermedia in Turkey.
Acta haematologica 1989;81(1):22-7.
1988: Jogessar V B; Westermeyer K; Webber B B; Wilson J B; Hu H; Gonzalez-Redondo J M; Kutlar A; Huisman T H
Hb natal or alpha 2(minus Tyr-Arg) beta 2: a high oxygen affinity alpha chain variant with a deleted carboxy-terminus resulting from a TAC----TAA (Tyr----terminating codon) mutation in codon alpha 140.
Biochimica et biophysica acta 1988;951(1):36-41.
1988: Gonzalez-Redondo J M; Kutlar F; Kutlar A; Stoming T A; de Pablos J M; Kilinç Y; Huisman T H
Hb S(C)-beta+-thalassaemia: different mutations are associated with different levels of normal Hb A.
British journal of haematology 1988;70(1):85-9.
1988: Gonzalez-Redondo J M; Stoming T A; Lanclos K D; Gu Y C; Kutlar A; Kutlar F; Nakatsuji T; Deng B; Han I S; McKie V C
Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States.
Blood 1988;72(3):1007-14.
1988: Beris P; Miescher P A; Diaz-Chico J C; Han I S; Kutlar A; Hu H; Wilson J B; Huisman T H
Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114.
Blood 1988;72(2):801-5.
1988: Moscoso H; Kiefer C R; Kutlar A; Garver F A
Quantification of hemoglobins S, C, and F by a magnetic affinity immunoassay.
Clinical chemistry 1988;34(5):902-5.
1988: Efremov D G; Efremov G D; Zisovski N; Stojanovski N; Kutlar F; Diaz-Chico J C; Kutlar A; Yang K G; Stoming T A; Huisman T H
Variation in clinical severity among patients with Hb Lepore-Boston-beta-thalassaemia is related to the type of beta-thalassaemia.
British journal of haematology 1988;68(3):351-5.
1988: Diaz-Chico J C; Yang K G; Stoming T A; Efremov D G; Kutlar A; Kutlar F; Aksoy M; Altay C; Gurgey A; Kilinc Y
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes.
Blood 1988;71(1):248-51.
1988: Malcorra-Azpiazu J J; Balda-Aguirre M I; Diaz-Chico J C; Kutlar F; Kutlar A; Wilson J B; Hu H; Huisman T H
Hb Le Lamentin or alpha 2 20(B1)His----GLN beta 2 found in a Spanish family.
Hemoglobin 1988;12(2):201-5.
1988: Malcorra-Azpiazu J J; Balda-Aguirre M I; Diaz-Chico J C; Hu H; Wilson J B; Webber B B; Kutlar F; Kutlar A; Huisman T H
Hb Las Palmas or alpha 2 beta 2(49)(CD8)Ser----Phe, a mildly unstable hemoglobin variant.
Hemoglobin 1988;12(2):163-70.
1988: Ali M A; Pinkerton P; Chow S W; Zaetz S D; Wilson J B; Webber B B; Hu H; Kutlar A; Kutlar F; Huisman T H
Some rare hemoglobin variants with altered oxygen affinities; Hb linkoping [beta 36(C2)Pro----Thr], Hb Caribbean [beta 91(F7)Leu----Arg], and Hb Sunnybrook [beta 36(C2)Pro----Arg]
Hemoglobin 1988;12(2):137-48.
1988: Kutlar A; Kutlar F; Wilson J B; Webber B B; Hu H; Huisman T H
Hb F-Austell or alpha 2G gamma (2)40(C6)Arg----Lys.
Hemoglobin 1988;12(4):409-11.
1987: Felice A E; McKie K M; Cleek M P; Marino E M; Kutlar A; McKie V C
Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from Georgia.
American journal of hematology 1987;25(4):389-400.
1987: Diaz-Chico J C; Yang K G; Kutlar A; Reese A L; Aksoy M; Huisman T H
An approximately 300 bp deletion involving part of the 5' beta-globin gene region is observed in members of a Turkish family with beta-thalassemia.
Blood 1987;70(2):583-6.
1987: Kutlar F; Fei Y J; Wilson J B; Kutlar A; Huisman T H
Detection of the embryonic zeta chain in blood from newborn babies by reversed-phase high-performance liquid chromatography.
Journal of chromatography 1987;394(2):333-43.
1987: Beris P; Huber P; Miescher P A; Wilson J B; Kutlar A; Chen S S; Huisman T H
HB Q-Thailand-HB H disease in a Chinese living in Geneva, Switzerland: characterization of the variant and identification of the two alpha-thalassemic chromosomes.
American journal of hematology 1987;24(4):395-400.
1987: Ojwang P J; Ogada T; Beris P; Hattori Y; Lanclos K D; Kutlar A; Kutlar F; Huisman T H
Haplotypes and alpha globin gene analyses in sickle cell anaemia patients from Kenya.
British journal of haematology 1987;65(2):211-5.
1987: Huisman T H; Kutlar F; Kutlar A; Wilson J B; Harris H F
The M gamma chain of human fetal hemoglobin; its identification and occurrence.
Journal of chromatography 1987;388(2):429-39.
1987: Kleman K; Lubin B; Kutlar A; Wilson J B; Webber B B; Huisman T H
A second family with Hb Minneapolis-Laos or alpha 2 beta (2)118(GH1)Phe----Tyr.
Hemoglobin 1987;11(4):401-2.
1987: Altay C; Kutlar A; Wilson J B; Webber B B; Huisman T H
Hb P-Nilotic or alpha 2(beta delta)2 in a Turkish family.
Hemoglobin 1987;11(4):395-9.
1987: Masala B; Manca L; Stangoni A; Cuccuru G B; Wilson J B; Webber B B; Kutlar A; Huisman T H
Hb Sassari or alpha (2)126(H9)Asp---His beta 2 observed in a family from Northern Sardinia.
Hemoglobin 1987;11(4):373-8.
1987: Kutlar A; Lanclos K D
The thalassemia repository.
Hemoglobin 1987;11(2):191-8.
1987: Landman H; Wilson J B; Kutlar A; Gonzalez Redondo J M; Huisman T H
Hb G-Taipei or beta 22(B4)Glu----Gly in a Chinese family living in The Netherlands.
Hemoglobin 1987;11(2):169-71.
1987: Bird A R; Elliot T E; Wilson J B; Webber B B; Kutlar F; Kutlar A; Huisman T H
Hb Borås or alpha 2 beta 2(88)(F4)Leu----Arg in a South African female.
Hemoglobin 1987;11(2):157-60.
1987: Indrak K; Wiedermann B F; Batek F; Wilson J B; Webber B B; Kutlar A; Huisman T H
Hb Olomouc or alpha 2 beta 2(86)(F2)Ala----Asp, a new high oxygen affinity variant.
Hemoglobin 1987;11(2):151-5.
1987: Gonzalez Redondo J M; Wilson J B; Kutlar A; Huisman T H; Sicilia A; Romero C; Fernandes Fuertes I
Hb J-Pontoise or alpha 2(63)(E12)Ala----Asp beta 2 in four members of a Spanish family.
Hemoglobin 1987;11(1):47-50.
1987: de Pablos J M; Kutlar A; Wilson J B; Webber B B; Hu H; Huisman T H
Hb D-Granada or alpha 2 beta 2 22(B4)Glu----Val.
Hemoglobin 1987;11(6):563-5.
1987: Efremov G D; Jankovic L; Juricic D; Stojancov A; Wilson J B; Webber B B; Kutlar F; Kutlar A; Hu H; Huisman T H
Hb Bushwick [beta 74(E18)Gly----Val] heterozygotes in a Yugoslavian family have 35 to 40% of the unstable variant.
Hemoglobin 1987;11(6):557-62.
1987: Kutlar F; Kutlar A; Gu Y C; Huisman T H
Adult hemoglobin levels in newborn babies from different countries and in babies with some significant hemoglobinopathies.
Acta haematologica 1987;78(1):28-32.
1987: Gonzalez Redondo J M; Sicilia A; Murga M J; Kutlar A; Wilson J B; Huisman T H
Hb E-Saskatoon or alpha 2 beta 2(22)(B4)Glu----Lys in a Spanish family.
Hemoglobin 1987;11(1):35-8.
1987: Huisman T H; Kutlar F; Kutlar A; Wilson J B; Harris H F
The M gamma chain of human fetal hemoglobin.
Progress in clinical and biological research 1987;251():507-17.
1987: de Pablos J M; Wilson J B; Kutlar A; Kutlar F; Webber B B; Huisman T H
Hb F-Kingston or alpha 2G gamma 2(55)(D6)Met----Arg in a Spanish newborn.
Hemoglobin 1987;11(5):513-6.
1987: Kutlar A; Kutlar F; Wilson J B; Webber B B; Gonzalez Redondo J M; Huisman T H
Hb F-Clarke or alpha 2G gamma 2(65)(E9)Lys----Asn.
Hemoglobin 1987;11(2):185-8.
1987: Kleman K; Lubin B; Wilson J B; Kutlar A; Webber B B; Huisman T H
Hb F-Oakland or alpha 2G gamma I2(26)(B8)Glu----Lys.
Hemoglobin 1987;11(2):181-3.
1986: Yang K G; Liu J Z; Kutlar F; Kutlar A; Altay C; Gurgey A; Huisman T H
Beta zero-thalassemia in association with a gamma-globin gene quadruplication.
Blood 1986;68(6):1394-7.
1986: Aluoch J R; Kilinç Y; Aksoy M; Yüregir G T; Bakioglu I; Kutlar A; Kutlar F; Huisman T H
Sickle cell anaemia among Eti-Turks: haematological, clinical and genetic observations.
British journal of haematology 1986;64(1):45-55.
1986: Nakatsuji T; Kutlar A; Kutlar F; Huisman T H
Haplotypes among Vietnamese hemoglobin E homozygotes including one with a gamma-globin gene triplication.
American journal of human genetics 1986;38(6):981-3.
1986: Huisman T H; Wilson J B; Kutlar A; Yang K G; Chen S S; Webber B B; Altay C; Martinez A V
Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identification.
Biochimica et biophysica acta 1986;871(2):229-31.
1986: Efremov G D; Filipce V; Gjorgovski I; Juricic D; Stojanovski N; Harano T; Nakatsuji T; Kutlar A; Kutlar F; Bakioglu I
G gamma A gamma(delta beta)zero-thalassaemia and a new form of gamma globin gene triplication identified in the Yugoslavian population.
British journal of haematology 1986;63(1):17-28.
1986: Kutlar F; Kutlar A; Huisman T H
Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography.
Journal of chromatography 1986;357(1):147-53.
1986: Miller D R; Wilson J B; Kutlar A; Huisman T H
Hb Bicêtre or alpha 2 beta(2)63(E7)His----Pro in a white male: clinical observations over a period of 25 years.
American journal of hematology 1986;21(2):209-14.
1986: Bakioglu I; Kutlar A; Huisman T H
Differences between the levels of G gamma chain in the fetal hemoglobin in two types of hereditary persistence of fetal hemoglobin are linked with a variation in the DNA sequence.
Biochemical genetics 1986;24(1-2):149-51.
1986: Wilson J B; Chen S S; Webber B B; Kutlar A; Kutlar F; Villegas A; Huisman T H
The identification of five rare beta-chain abnormal hemoglobins by high performance liquid chromatographic procedures.
Hemoglobin 1986;10(1):49-63.
1986: Bowman J E; Bloom R; Chen S S; Webber B B; Wilson J B; Kutlar F; Kutlar A; Huisman T H
HB Chicago or alpha (2)136 (H19) Leu----Met beta 2 and a -G gamma-G gamma-globin gene arrangement in a black family.
Hemoglobin 1986;10(5):495-505.
1986: Aksoy M; Gurgey A; Altay C; Kilinc Y; Carstairs K C; Kutlar A; Chen S S; Webber B B; Wilson J B; Huisman T H
Some notes about Hb Q-India and Hb Q-Iran.
Hemoglobin 1986;10(2):215-9.
1986: Wiedermann B F; Indrak K; Wilson J B; Webber B B; Yang K G; Kutlar F; Kutlar A; Huisman T H
Hb Saint Louis or alpha 2 beta 2(28)(B10)Leu----Gln in a Czechoslovakian male.
Hemoglobin 1986;10(6):673-6.
1986: de Pablos J M; Wilson J B; Kutlar A; Chen S S; Huisman T H
Hb F-Albaicin or G gamma 8(A5)Lys----Glu or Gln.
Hemoglobin 1986;10(6):655-9.
1986: Hattori Y; Kutlar F; Kutlar A; McKie V C; Huisman T H
Haplotypes of beta S chromosomes among patients with sickle cell anemia from Georgia.
Hemoglobin 1986;10(6):623-42.
1986: Lanclos K D; Kutlar A; Kutlar F; Ojwang P J; Reese A L; Huisman T H
The effect of alpha-thalassemia on the level of hybrid hemoglobin variants in heterozygotes.
Hemoglobin 1986;10(4):401-16.
1985: Bakioglu I; Hattori Y; Kutlar A; Mathew C; Huisman T H
Five adults with mild sickle cell anemia share a beta S chromosome with the same haplotype.
American journal of hematology 1985;20(3):297-300.
1985: Kamel K; el-Najjar A; Webber B B; Chen S S; Wilson J B; Kutlar A; Huisman T H
Hb Doha or alpha 2 beta 2[X-N-Met-1(NA1)Val----Glu]; a new beta-chain abnormal hemoglobin observed in a Qatari female.
Biochimica et biophysica acta 1985;831(2):257-60.
1985: Aksoy M; Kutlar A; Efremov G D; Nikolov N; Petkov G; Reese A L; Harano T; Chen S S; Huisman T H
Haplotypes and levels of fetal hemoglobin and G gamma to A gamma ratios in Mediterranean patients with thalassemia minor and major.
American journal of hematology 1985;20(1):7-16.
1985: Aksoy M; Kutlar A; Kutlar F; Dinçol G; Erdem S; Bastesbihçi S
Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace.
Journal of medical genetics 1985;22(4):288-90.
1985: Chen S S; Wilson J B; Webber B B; Kutlar A; Huisman T H
HB G-Copenhagen or alpha 2 beta 2(47) (CD6) Asp----Asn observed in a black newborn.
Hemoglobin 1985;9(4):405-8.
1985: de Weinstein B I; Kutlar A; Webber B B; Wilson J B; Huisman T H
Hemoglobin Daneshgah-Tehran or alpha 2(72) (EF1) His----Arg beta 2 in an Argentinean family.
Hemoglobin 1985;9(4):409-11.
1985: Carstairs K C; Raulfs A; Kutlar A; Chen S S; Webber B B; Wilson J B; Huisman T H
Hb Fort Worth or alpha2 27(B8)Glu----Gly beta2 in a black family from Canada.
Hemoglobin 1985;9(2):201-5.
1985: Aksoy M; Kutlar A; Kutlar F; Harano T; Chen S S; Huisman T H
Hemoglobin H disease in two Turkish females and one Iranian newborn.
Hemoglobin 1985;9(4):373-84.
1985: Kilinç Y; Kumi M; Gurgey A; Altay C; Webber B B; Wilson J B; Kutlar A; Huisman T H
Hemoglobin O-Padova or alpha(2)30(B11)Glu----Lys beta 2 observed in members of a Turkish family.
Hemoglobin 1985;9(6):621-5.
1985: Chen S S; Webber B B; Kutlar A; Wilson J B; Huisman T H
Hb F-Cobb or alpha(2)A gamma(2)37(C3)Trp----Gly.
Hemoglobin 1985;9(6):617-9.
1985: Kutlar A; Hattori Y; Bakioglu I; Kutlar F; Kamel K; Huisman T H
Hematological observations on Arabian SS patients with a homozygosity or heterozygosity for a beta S chromosome with haplotype #31.
Hemoglobin 1985;9(6):545-57.
1985: Chen S S; Wilson J B; Webber B B; Kutlar A; Huisman T H
Hb F-Auckland [alpha 2G gamma 2(7)(A4)Asp----Asn] observed in a Caucasian newborn from Alabama.
Hemoglobin 1985;9(5):531-3.
1984: Aksoy M; Erdem S; Dinçol G; Bakioglu I; Kutlar A
Aplastic anemia due to chemicals and drugs: a study of 108 patients.
Sexually transmitted diseases 1984;11(4 Suppl):347-50.
1984: Kutlar A; Kutlar F; Wilson J B; Headlee M G; Huisman T H
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 1984;17(1):39-53.
1984: Kutlar A; Gardiner M B; Headlee M G; Reese A L; Cleek M P; Nagle S; Sukumaran P K; Huisman T H
Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G gamma and A gamma types of gamma chain.
Biochemical genetics 1984;22(1-2):21-35.
1984: Dinçol G; Aksoy M; Dinçol K; Kutlar A; Wilson J B; Huisman T H
Hemoglobin Hamadan or alpha 2 beta 256(D7)Gly----Arg in a Turkish family.
Hemoglobin 1984;8(4):423-5.
1984: Aksoy M; Kutlar A; Kutlar F; Dinçol G; Erdem S; Wilson J B; Huisman T H
Hb Beograd-beta zero thalassemia in a Turkish family from Yugoslavia.
Hemoglobin 1984;8(4):417-21.
1984: Aksoy M; Erdem S; Dinçol G; Kutlar A; Bakioglu I; Hepyüksel T
Clinical observations showing the role of some factors in the etiology of multiple myeloma. A study in 7 patients.
Acta haematologica 1984;71(2):116-20.
1982: Aksoy M; Bermek E; Almis G; Kutlar A
beta-Thalassemia intermedia homozygous for normal hemoglobin A2 beta-thalassemia. Study in four families.
Acta haematologica 1982;67(1):57-61.
1979: Bermek E; Aksoy M; Almis G; Kutlar A
Further data on one of the first examples of sickle cell alpha-thalassemia disease.
Hemoglobin 1979;3(6):471-4.

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