 Prabhakar S Kedar
| Title | Research Fellow in Medicine (EXT) |
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| Institution | Beth Israel Deaconess Medical Center |
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| Department | Medicine |
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| Address | Beth Israel Deaconess Medical Center
Medicine - RW 763
330 Brookline Ave
Boston MA 02215
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| Phone | 617/667-2930 |
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| Fax | 617/667-8040 |
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 Bibliographic
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications.
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Warang P, Kedar P, Kar R, Ghosh K, Colah R. New missense homozygous mutation (Q270Ter) in the pyrimidine 5' nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia. Ann Hematol. 2013 May; 92(5):715-7.
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Kedar P, Warang P, Ghosh K, Colah R. Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family. Ann Hematol. 2012 Dec; 91(12):1985-6.
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Warang P, Kedar P, Ghosh K, Colah RB. Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene. Int J Hematol. 2012 Aug; 96(2):263-7.
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Kedar PS, Warang P, Ghosh K, Colah RB. Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: compound heterozygous for NADH-cytochrome b5 reductase gene mutations. Am J Hematol. 2011 Mar; 86(3):327-9.
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Warang P, Gupta M, Kedar P, Ghosh K, Colah R. Flow cytometric osmotic fragility--an effective screening approach for red cell membranopathies. Cytometry B Clin Cytom. 2011 May; 80(3):186-90.
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Stewart AK, Kedar PS, Shmukler BE, Vandorpe DH, Hsu A, Glader B, Rivera A, Brugnara C, Alper SL. Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis. Am J Physiol Cell Physiol. 2011 May; 300(5):C1034-46.
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Shmukler BE, Kedar PS, Warang P, Desai M, Madkaikar M, Ghosh K, Colah RB, Alper SL. Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D. Am J Hematol. 2010 Oct; 85(10):824-8.
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Kedar PS, Warang P, Nadkarni AH, Colah RB, Ghosh K. A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia. Blood Cells Mol Dis. 2008 May-Jun; 40(3):323-7.
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Gupta N, Bianchi P, Fermo E, Kabra M, Warang P, Kedar P, Gupta N, Colah R. Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family. Prenat Diagn. 2007 Feb; 27(2):117-8.
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Kedar PS, Warang P, Colah RB, Mohanty D. Red cell pyruvate kinase deficiency in neonatal jaundice cases in India. Indian J Pediatr. 2006 Nov; 73(11):985-8.
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Kedar PS, Nadkarni AH, Phanasgoankar S, Madkaikar M, Ghosh K, Gorakshakar AC, Colah RB, Mohanty D. Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian family. Am J Hematol. 2005 Jun; 79(2):168-70.
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Kedar PS, Colah RB, Ghosh K, Mohanty D. Hereditary spherocytosis in association with severe G6PD deficiency: report of an unusual case. Clin Chim Acta. 2004 Jun; 344(1-2):221-4.
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Kedar PS, Ghosh K, Colah RB, Mohanty D. Chronic persistent hemolysis in an infant: can we afford to forget malaria as a cause? Hematol J. 2002; 3(2):114-5.
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Kedar PS, Colah RB, Ghosh K, Mohanty D. Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families. Haematologia (Budap). 2002; 32(4):543-9.
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