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RAFI SHAJI, M.D.
M.D.
Student in an Organized Health Care Education/Training Program
NPI: 1255125571Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Genotype phenotype correlation in Wilson's disease within families--a report on four south Indian families.
PMID 18698682·World J Gastroenterol·2008
8-other
Analysis of beta globin mutations in the Indian population: presence of rare and novel mutations and region-wise heterogeneity.
PMID 18294253·Clin Genet·2008
8-other
Screening for mutations in ATP7B gene using conformation-sensitive gel electrophoresis in a family with Wilson's disease.
PMID 17325640·Med Sci Monit·2007
8-other
Single-agent arsenic trioxide in the treatment of newly diagnosed acute promyelocytic leukemia: durable remissions with minimal toxicity.
PMID 16352810·Blood·2006
3-trial
Developing an algorithm of informative markers for evaluation of chimerism after allogeneic bone marrow transplantation.
PMID 16518431·Bone Marrow Transplant·2006
8-other
Compound heterozygosity for Hb E and Hb Lepore-Hollandia in India; first report and potential diagnostic pitfalls.
PMID 16114186·Hemoglobin·2005
5-case
Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.
PMID 16128892·Haemophilia·2005
8-other
Cytochrome P4501A1 and glutathione S transferase gene polymorphisms in patients with aplastic anemia in India.
PMID 16227674·Acta Haematol·2005
8-other
Fludarabine-based conditioning for allogeneic stem cell transplantation for multiply transfused patients with Fanconi's anemia.
PMID 15640819·Bone Marrow Transplant·2005
8-other
Hyperbilirubinemia in homozygous HbE disease is associated with the UGT1A1 gene polymorphism.
PMID 16114182·Hemoglobin·2005
8-other
Novel missense mutations in two patients with factor XI deficiency (Val271Leu and Tyr351Ser) and one patient with combined factor XI and factor IX deficiency (Phe349Val).
PMID 15842381·J Thromb Haemost·2005
8-other
Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.
PMID 15892853·J Thromb Haemost·2005
8-other
Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin.
PMID 15892863·J Thromb Haemost·2005
8-other
Hb Showa-Yakushiji [beta110(G12)Leu-->Pro] in four unrelated patients from west Bengal.
PMID 15768552·Hemoglobin·2005
8-other
Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India.
PMID 16270648·Thromb Haemost·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4802 10TH AVENUE MAIMONIDES MEDICAL CENTER
BROOKLYN, NY 11219 - Phone
- (718) 283-6000
Quick Facts
- NPI
- 1255125571
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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