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ABDULLAH KUTLAR, MD
MD
Hematology & Oncology Physician
NPI: 1780793349IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hematology & Oncology PhysicianPrimary
Internal Medicine — Hematology & Oncology
Code: 207RH0003X
034751(GA)
Education
OTHER
Class of 1971
Research & Publications (20)
Sickle cell disease: a multigenic perspective of a single gene disorder.
PMID 17486504·Hemoglobin·2007
6-review
Sickle cell disease: a multigenic perspective of a single-gene disorder.
PMID 16103709·Med Princ Pract·2005
6-review
Sickle cell disease: a multigenic perspective of a single gene disorder.
PMID 16188647·Hematology·2005
6-review
The methylene tetrahydrofolate reductase (C677T) mutation as a potential risk factor for avascular necrosis in sickle cell disease.
PMID 11480782·Hemoglobin·2001
8-other
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.
PMID 19373463·Ann Hematol·2009
8-other
Acute splenic complications and implications of splenectomy in hemoglobin SC disease.
PMID 19459924·Eur J Haematol·2009
8-other
Rare occurrence of Hb Lepore-Baltimore in African Americans: molecular characteristics and variations of Hb Lepores.
PMID 18989669·Ann Hematol·2009
5-case
Hemoglobin binding to A beta and HBG2 SNP association suggest a role in Alzheimer's disease.
PMID 17157413·Neurobiol Aging·2008
8-other
Neonatal cyanosis due to a novel fetal hemoglobin: Hb F-Circleville [Ggamma63(E7)His-->Leu, CAT>CTT].
PMID 19065339·Hemoglobin·2008
5-case
Efficacy and safety of the Gardos channel blocker, senicapoc (ICA-17043), in patients with sickle cell anemia.
PMID 18192510·Blood·2008
2-rct
Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions.
PMID 18513257·Transfusion·2008
4-observational
Two new hemoglobin variants: Hb Sinai-Greenspring [beta34(B16)Val-->Ile, GTC > ATC] and Hb Sinai-Bel Air [beta53(D4)Ala-->Asp, GCT > GAT].
PMID 19065337·Hemoglobin·2008
5-case
Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.
PMID 17299377·Pharmacogenomics J·2007
4-observational
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.
PMID 18056002·Haematologica·2007
5-case
Regular transfusion lowers plasma free hemoglobin in children with sickle-cell disease at risk for stroke.
PMID 16627796·Stroke·2006
2-rct
Transcranial Doppler ultrasonography in adults with sickle cell disease.
PMID 16924006·Neurology·2006
2-rct
Hb J- Meerut [alpha 120 (H3) Ala ->Glu (alpha1)] in a Turkish male.
PMID 16575421·Int J Med Sci·2006
8-other
The influence of renal function on hydroxyurea pharmacokinetics in adults with sickle cell disease.
PMID 15778424·J Clin Pharmacol·2005
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1120 15TH ST
AUGUSTA, GA 30912 - Phone
- (706) 721-2505
Quick Facts
- NPI
- 1780793349
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 55
- Publications
- 20
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