Rajagopal Krishnamoorthy

Rajagopal Krishnamoorthy

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Publications by authors named "Rajagopal Krishnamoorthy"

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The HLA 8.1 Ancestral Haplotype in schizophrenia: dual implication in neuro-synaptic pruning and autoimmunity?

Acta Psychiatr Scand 2019 Nov 9. Epub 2019 Nov 9.

Department of Psychiatry, Psychotherapy and Psychosomatics, Martin-Luther-University Halle-Wittenberg, Halle, Germany.

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http://dx.doi.org/10.1111/acps.13125DOI Listing
November 2019

Obsessive-Compulsive Disorder: Autoimmunity and Neuroinflammation.

Curr Psychiatry Rep 2019 Aug 1;21(8):78. Epub 2019 Aug 1.

Inserm U955, Team 15, Genetic Psychiatry, 94000, Creteil, France.

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http://dx.doi.org/10.1007/s11920-019-1062-8DOI Listing
August 2019

Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single-Patient Data Meta-Analysis in More Than 15,000 Individuals.

Clin Pharmacol Ther 2019 Jun 17;105(6):1477-1491. Epub 2019 Feb 17.

General Medicine and Hypertension Unit, Department of Medicine, University of Verona, Verona, Italy.

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http://doi.wiley.com/10.1002/cpt.1323
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http://dx.doi.org/10.1002/cpt.1323DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542461PMC
June 2019

Association of MICA-129 polymorphism and circulating soluble MICA level with rheumatoid arthritis in a south Indian Tamil population.

Int J Rheum Dis 2018 Mar 27;21(3):656-663. Epub 2017 Jul 27.

Department of Clinical Immunology, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry, India.

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http://doi.wiley.com/10.1111/1756-185X.13138
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http://dx.doi.org/10.1111/1756-185X.13138DOI Listing
March 2018

The scientific legacy of Ronald L. Nagel (1936-2016), a true renaissance man.

Am J Hematol 2016 Sep 4;91(9):865-6. Epub 2016 Jul 4.

INSERM, Paris.

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http://dx.doi.org/10.1002/ajh.24444DOI Listing
September 2016

[Immunogenetics of nasopharyngeal carcinoma].

Ann Biol Clin (Paris) 2014 May-Jun;72(3):281-91

Laboratoire Jean Dausset d'immunologie et d'histocompatibilité, CIB-HOG, AP-HP et IUH, Inserm U940 Hôpital Saint-Louis, Paris, France.

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http://www.john-libbey-eurotext.fr/medline.md?doi=10.1684/ab
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http://dx.doi.org/10.1684/abc.2014.0958DOI Listing
May 2016

Dectin-1 Polymorphism: A Genetic Disease Specifier in Autism Spectrum Disorders?

PLoS One 2015 9;10(9):e0137339. Epub 2015 Sep 9.

INSERM, U1160, Hôpital Saint Louis, Paris, France; Fondation FondaMental, Créteil, France; Laboratoire Jean Dausset and LabEx Transplantex, Hôpital Saint Louis, Paris, France; Université Paris Diderot, Sorbonne Paris-Cité, Paris, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0137339PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4564239PMC
May 2016

Functional polymorphisms of Monocyte Chemoattractant Protein-1 gene and Pott's disease risk.

Immunobiology 2016 Mar 18;221(3):462-7. Epub 2015 Nov 18.

INSERM, UMRS 1160, Hôpital Saint Louis, Paris 75010, France; Laboratoire Jean Dausset et LabEx Transplantex, Hôpital Saint Louis, Paris 75010, France; Université Paris Diderot, Sorbonne Paris-Cité, Paris 75013, France. Electronic address:

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http://dx.doi.org/10.1016/j.imbio.2015.11.004DOI Listing
March 2016

Combined effect of TLR2 gene polymorphism and early life stress on the age at onset of bipolar disorders.

PLoS One 2015 19;10(3):e0119702. Epub 2015 Mar 19.

INSERM, U1160, Hôpital Saint Louis, Paris, France; Laboratoire Jean Dausset and LabEx Transplantex, Hôpital Saint Louis, Paris, France; Fondation FondaMental, Créteil, France; Université Paris Diderot, Sorbonne Paris-Cité, Paris, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0119702PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366110PMC
February 2016

Resolution of a manic episode treated with activated charcoal: Evidence for a brain-gut axis in bipolar disorder.

Aust N Z J Psychiatry 2015 Dec 24;49(12):1221-3. Epub 2015 Jul 24.

FondaMental Foundation, Créteil, France Jean Dausset Laboratory, LabEx Transplantex & INSERM, UMRS 1160 Hôpital Saint Louis, Université Paris Diderot, Paris, France.

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http://journals.sagepub.com/doi/10.1177/0004867415595873
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http://dx.doi.org/10.1177/0004867415595873DOI Listing
December 2015

Cognitive deterioration among bipolar disorder patients infected by Toxoplasma gondii is correlated to interleukin 6 levels.

J Affect Disord 2015 Jul 1;179:161-6. Epub 2015 Apr 1.

Inserm U955, Equipe 15 « Psychiatrie Génétique », Créteil F-94000, France; AP-HP, DHU Pe-PSY, Université Paris Est Créteil, Groupe Henri Mondor - Albert Chenevier, Pôle de psychiatrie et d׳Addictologie, Créteil F-94000, France; Fondation Fondamental, Fondation de coopération scientifique, Créteil F94000, France.

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http://dx.doi.org/10.1016/j.jad.2015.03.038DOI Listing
July 2015

Treatment with anti-toxoplasmic activity (TATA) for toxoplasma positive patients with bipolar disorders or schizophrenia: a cross-sectional study.

J Psychiatr Res 2015 Apr 24;63:58-64. Epub 2015 Feb 24.

INSERM U955, Équipe de Psychiatrie Translationnelle, Université Paris-Est Créteil, DHU Pe-psy, Pôle de psychiatrie des hôpitaux universitaire H Mondor, Créteil, France; Fondation FondaMental Fondation de coopération scientifique en santé mentale, France.

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http://dx.doi.org/10.1016/j.jpsychires.2015.02.011DOI Listing
April 2015

Polymorphisms in oxidative stress-related genes are associated with nasopharyngeal carcinoma susceptibility.

Immunobiology 2015 Jan;220(1):20-5

Department of Clinical Biology, Salah Azaiz Institut of Cancer, Tunis, Tunisia; INSERM, U940, Saint-Louis Hospital, Paris, France; Biochemistry Department, ISBAT, Science University of Tunis, Tunisia.

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http://dx.doi.org/10.1016/j.imbio.2014.09.021DOI Listing
January 2015

Cytokine expression and cytokine-based T cell profiling in South Indian rheumatoid arthritis.

Immunobiology 2014 Oct 27;219(10):772-7. Epub 2014 Jun 27.

Department of Clinical Immunology, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Pondicherry 605006, India. Electronic address:

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http://dx.doi.org/10.1016/j.imbio.2014.06.004DOI Listing
October 2014

Genetic association between a 'standing' variant of NOD2 and bipolar disorder.

Immunobiology 2014 Oct 9;219(10):766-71. Epub 2014 Jul 9.

INSERM, U1160, Hôpital Saint Louis, Paris F75010, France; Laboratoire Jean Dausset, LabEx Transplantex, Hôpital Saint Louis, Paris F75010, France; Fondation FondaMental, Créteil F94000, France; Université Paris Diderot, Sorbonne Paris-Cité, Paris F75013, France. Electronic address:

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http://dx.doi.org/10.1016/j.imbio.2014.06.003DOI Listing
October 2014

Association between toll-like receptor 2 gene diversity and early-onset bipolar disorder.

J Affect Disord 2014 Aug 4;165:135-41. Epub 2014 May 4.

INSERM, U1160, Hôpital Saint Louis, Paris F75010, France; Laboratoire Jean Dausset and LabEx Transplantex, Hôpital Saint Louis, Avenue Claude Vellefaux, Paris F75010, France; Fondation FondaMental, Créteil F94000 France; Université Paris Diderot, Sorbonne Paris-Cité, Paris F75013, France.

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http://dx.doi.org/10.1016/j.jad.2014.04.059DOI Listing
August 2014

Polymorphism of Toll-like receptor 4 gene in bipolar disorder.

J Affect Disord 2014 Jan 17;152-154:395-402. Epub 2013 Oct 17.

INSERM, UMRS 940, Hôpital Saint-Louis, Paris F75010, France; INSERM, U 955, IMRB, Psychiatrie Génétique, Créteil F94000, France; Fondation FondaMental, fondation de coopération scientifique, Créteil, France.

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http://dx.doi.org/10.1016/j.jad.2013.09.043DOI Listing
January 2014

The association of CD81 polymorphisms with alloimmunization in sickle cell disease.

Clin Dev Immunol 2013 22;2013:937846. Epub 2013 May 22.

Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Medical Center, 111 Michigan Avenue NW, Washington, DC 20010-2970, USA.

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http://dx.doi.org/10.1155/2013/937846DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674646PMC
December 2013

A stepwise α-thalassemia screening strategy in high-prevalence areas.

Eur J Haematol 2013 Aug 15;91(2):164-9. Epub 2013 Jun 15.

Sultan Qaboos University and Hospital, Muscat, Oman.

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http://dx.doi.org/10.1111/ejh.12136DOI Listing
August 2013

Molecular spectrum of β-thalassemia mutations in the admixed Venezuelan population, and their linkage to β-globin gene haplotypes.

Hemoglobin 2012 ;36(3):209-18

Laboratorio de Investigación de Hemoglobinas Anormales, Hospital Universitario de Caracas and Instituto Anatómico José Izquierdo, Universidad Central de Venezuela , Caracas , Venezuela.

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http://dx.doi.org/10.3109/03630269.2012.674997DOI Listing
October 2012

Warfarin pharmacogenetics: development of a dosing algorithm for Omani patients.

J Hum Genet 2012 Oct 2;57(10):665-9. Epub 2012 Aug 2.

Department of Haematology, Sultan Qaboos University Hospital, Muscat, Oman.

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http://dx.doi.org/10.1038/jhg.2012.94DOI Listing
October 2012

Relative Copy Number Variations of CYP2C19 in South Indian Population.

Mol Biol Int 2012 25;2012:643856. Epub 2012 Jun 25.

Pharmacogenomics Laboratory, Department of Pharmacology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry 605006, India.

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http://dx.doi.org/10.1155/2012/643856DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3389726PMC
August 2012

The β-globin promoter -71 C>T mutation is a β+ thalassemic allele.

Eur J Haematol 2011 Nov 15;87(5):457-60. Epub 2011 Sep 15.

Sultan Qaboos University Hospital, Muscat, Oman.

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http://dx.doi.org/10.1111/j.1600-0609.2011.01687.xDOI Listing
November 2011

Neonatal Screening: Mean haemoglobin and red cell indices in cord blood from Omani neonates.

Sultan Qaboos Univ Med J 2011 Nov 25;11(4):462-9. Epub 2011 Oct 25.

Department of Haematology, College of Medicine & Health Sciences, Sultan Qaboos University, Muscat, Oman;

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206748PMC
November 2011

Hb A2' (Hb B2) in the Omani population and diagnostic significance.

Hemoglobin 2011 ;35(2):117-24

Department of Hematology, Sultan Qaboos University, Muscat, Oman.

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http://dx.doi.org/10.3109/03630269.2011.553557DOI Listing
August 2011

Influence of the genetic polymorphisms in the 5' flanking and exonic regions of CYP2C19 on proguanil oxidation.

Drug Metab Pharmacokinet 2009 ;24(6):537-48

Pharmacogenomics Laboratory, Department of Pharmacology, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Pondicherry 605006, India.

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http://dx.doi.org/10.2133/dmpk.24.537DOI Listing
April 2010

A novel deletional beta-thalassemic variant in an ethnic Qatari patient.

Hemoglobin 2009 ;33(3):214-9

Biological and Environmental Sciences Department, Qatar University, Doha, Qatar.

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http://dx.doi.org/10.1080/03630260903081398DOI Listing
February 2010

Isotopic biomarker discovery and application in translational medicine.

Drug Discov Today 2010 Feb 28;15(3-4):127-36. Epub 2009 Dec 28.

Department of Structural & Molecular Biology, University College London, Gower Street, London WC1E 6BT, United Kingdom.

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http://dx.doi.org/10.1016/j.drudis.2009.12.005DOI Listing
February 2010

MICA-129 genotype, soluble MICA, and anti-MICA antibodies as biomarkers of chronic graft-versus-host disease.

Blood 2009 Dec;114(25):5216-24

Laboratoire d'Immunologie et d'Histocompatibilité, Centre d'Innovations Biomédicales-Hématologie/Oncologie/Greffe (CIB-HOG), Institut Universitaire d'Hématologie (IUH), and Inserm, UMRS, 940, Hôpital Saint-Louis, Paris, France.

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http://www.bloodjournal.org/content/114/25/5216.full.pdf
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http://www.bloodjournal.org/cgi/doi/10.1182/blood-2009-04-21
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http://dx.doi.org/10.1182/blood-2009-04-217430DOI Listing
December 2009

Present day inbreeding does not forbid the forensic utility of commonly explored STR loci: a case study of native Qataris.

Forensic Sci Int Genet 2009 Dec 1;4(1):e11-3. Epub 2009 Feb 1.

Biological Science Department, Qatar University, Doha, Qatar.

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http://dx.doi.org/10.1016/j.fsigen.2008.12.005DOI Listing
December 2009

Genetic variations and haplotypes of the 5' regulatory region of CYP2C19 in South Indian population.

Drug Metab Pharmacokinet 2009 ;24(2):185-93

Pharmacogenomics laboratory, Department of Pharmacology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India.

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http://dx.doi.org/10.2133/dmpk.24.185DOI Listing
November 2009

Haematological and clinical features of beta-thalassaemia associated with Hb Dhofar.

Eur J Haematol 2008 Jan;80(1):67-70

Department of Haematology, College of Medicine & Health Sciences, Sultan Qaboos University, Muscat, Sultanate of Oman.

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http://doi.wiley.com/10.1111/j.1600-0609.2007.00989.x
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http://dx.doi.org/10.1111/j.1600-0609.2007.00989.xDOI Listing
January 2008

HLA-E*0101 allele in homozygous state favors severe bacterial infections in sickle cell anemia.

Hum Immunol 2007 Oct 19;68(10):849-53. Epub 2007 Sep 19.

Immunology and Histocompatibility Department, CIB-HOG, AP-HP/GHU-Nord, IUh and INSERM U662, Saint-Louis Hospital, Paris, France.

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http://dx.doi.org/10.1016/j.humimm.2007.08.260DOI Listing
October 2007

Molecular basis of thalassemia in Qatar.

Hemoglobin 2007 ;31(2):121-7

Biological Sciences Department, Qatar University, Doha, Qatar.

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http://dx.doi.org/10.1080/03630260701288815DOI Listing
July 2007

Homozygous status for HLA-E*0103 confers protection from acute graft-versus-host disease and transplant-related mortality in HLA-matched sibling hematopoietic stem cell transplantation.

Transplantation 2006 Dec;82(11):1436-40

Assistance publique- Hôpitaux de Paris/Groupement Hôspitalier et Universitaire Nord, Institut Universitaire d'Hématologie, et Institut National de la Santé et de la Recherche Médicale U662, Hôpital Saint-Louis, Paris, France.

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http://dx.doi.org/10.1097/01.tp.0000244598.92049.ddDOI Listing
December 2006

Implications of the genetic epidemiology of globin haplotypes linked to the sickle cell gene in southern Iran.

Hum Biol 2006 Dec;78(6):719-31

Medical Biology Research Center, Medical School, Kermanshah University of Medical Sciences, Daneshgah Avenue, P.O. Box 67148-69914, Kermanshah, Iran.

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http://muse.jhu.edu/content/crossref/journals/human_biology/
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http://dx.doi.org/10.1353/hub.2007.0016DOI Listing
December 2006

CYP2D6 genetic polymorphism in South Indian populations.

Biol Pharm Bull 2006 Aug;29(8):1655-8

Pharmacogenomics Laboratory, Department of Pharmacology, JIPMER, India.

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http://dx.doi.org/10.1248/bpb.29.1655DOI Listing
August 2006

UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia.

Am J Hematol 2006 May;81(5):377-9

UMR S-458 INSERM/Université des Antilles et de la Guyane, CHU de Pointe-à-Pitre, Guadeloupe, French West Indies.

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http://doi.wiley.com/10.1002/ajh.20574
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http://dx.doi.org/10.1002/ajh.20574DOI Listing
May 2006

Early-onset ankylosing spondylitis is associated with a functional MICA polymorphism.

Hum Immunol 2005 Oct 2;66(10):1057-61. Epub 2005 Nov 2.

Laboratoire d'Immunologie et d'Histocompatibilité CIB-HOB, AP-HP, IUH and INSERM U662, Hôpital Saint-Louis, Paris, France.

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http://dx.doi.org/10.1016/j.humimm.2005.09.004DOI Listing
October 2005

CYP2C9 and CYP2C19 genetic polymorphisms: frequencies in the south Indian population.

Fundam Clin Pharmacol 2005 Feb;19(1):101-5

Pharmacogenomics Laboratory, Department of Pharmacology, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Pondicherry, India.

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http://dx.doi.org/10.1111/j.1472-8206.2004.00307.xDOI Listing
February 2005

Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia.

Haematologica 2005 Feb;90(2):188-99

UMR S-458 INSERM/Université des Antilles et de la Guyane, France.

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February 2005

An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expression.

Am J Hematol 2005 Jan;78(1):59-63

Department of Child Health, Hematology, and Biochemistry, Sultan Qaboos University Hospital, Al-Khoud, Oman.

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http://dx.doi.org/10.1002/ajh.20256DOI Listing
January 2005

Glutathione S-transferase M1 polymorphism: a risk factor for hepatic venoocclusive disease in bone marrow transplantation.

Blood 2004 Sep 13;104(5):1574-7. Epub 2004 May 13.

Department of Haematology, Christian Medical College, Vellore 632 004, India.

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http://dx.doi.org/10.1182/blood-2003-11-3778DOI Listing
September 2004

A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene (GAG-->TAG) in a Tunisian family.

Hemoglobin 2004 Aug;28(3):249-54

Laboratoire de Biochimie, Clinique-Hôpital d'Enfants, Tunis, Tunisia.

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http://dx.doi.org/10.1081/hem-120040258DOI Listing
August 2004

A new high A2-beta-thalassemia due to a 468 bp deletion (-475 to -8) in the beta-globin gene promoter of the intact beta-globin structural gene.

Hemoglobin 2004 Feb;28(1):69-72

Laboratoire de Biochimie Génétique, Federation de Génétique, Hôpital Robert Debré, Paris, France.

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http://dx.doi.org/10.1081/hem-120028890DOI Listing
February 2004

Beta-globin-like gene cluster haplotypes in hemoglobinopathies.

Methods Mol Med 2003 ;82:195-211

Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.

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http://dx.doi.org/10.1385/1-59259-373-9:195DOI Listing
November 2003

Origin of Hb A2' (Hb B2) [delta16(A13)Gly --> Arg (GGC --> CGC)].

Hemoglobin 2003 May;27(2):105-10

Laboratory of Molecular Genetics, Department of Life Sciences, Faculty of Science and Technology of Tangier, Tangier, Morocco.

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http://dx.doi.org/10.1081/hem-120021543DOI Listing
May 2003

Hb Lepore in the Indian population.

Hemoglobin 2003 Feb;27(1):7-14

Department of Hematology, Christian Medical College, Vellore, India.

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http://dx.doi.org/10.1081/hem-120018431DOI Listing
February 2003

Human genetic polymorphisms and asymptomatic Plasmodium falciparum malaria in Gabonese schoolchildren.

Am J Trop Med Hyg 2003 Feb;68(2):186-90

Centre International de Recherches Médicales de Franceville, Franceville, Gabon.

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February 2003

Origin of Hb S Antilles.

Am J Hematol 2002 Aug;70(4):331-2

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http://dx.doi.org/10.1002/ajh.10121DOI Listing
August 2002

Coexistence of a novel beta-globin gene deletion (codons 81-87) with the codon 30 (G-->C) mutation in an Indian patient with beta0-thalassemia.

Hemoglobin 2002 Aug;26(3):237-43

Department of Haematology, Christian Medical College Hospital, Vellore, India.

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http://dx.doi.org/10.1081/hem-120015027DOI Listing
August 2002

Foetal haemoglobin in normal healthy adults: relationship with polymorphic sequences cis to the beta globin gene.

Eur J Hum Genet 2002 May;10(5):320-6

Institut National de la Santé et de la Recherche Médicale, Unité 458, Hôpital Robert Debré, 48 boulevard Sérurier, 75019 Paris, France.

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http://dx.doi.org/10.1038/sj.ejhg.5200809DOI Listing
May 2002

A novel beta-thalassemia mutation in an Asian Indian.

Hemoglobin 2002 Feb;26(1):49-57

Department of Haematology, Christian Medical College Hospital, Vellore, India.

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http://dx.doi.org/10.1081/hem-120002940DOI Listing
February 2002