about
External fixation versus volar locking plate for displaced intra-articular distal radius fractures: a prospective randomized comparative study of the functional outcomesAssociation between fetal weight and amniotic fluid index in women of Central India.Profiling β Thalassemia Mutations in Consanguinity and Nonconsanguinity for Prenatal Screening and Awareness Programme.Serum Total Sialic Acid and Highly Sensitive C-reactive Protein: Prognostic Markers for the Diabetic Nephropathy.BMP15 and GDF9 Gene Mutations in Premature Ovarian FailureMaternal and perinatal outcome of women with sickle cell disease of a tribal population in Central India.Predicators for weight gain in children treated for severe acute malnutrition: a prospective study at nutritional rehabilitation centerAmoebic liver abscess: a report from central India.Chronic pancreatitis: A new pathophysiology.Non-HFE iron overload as a surrogate marker of disease severity in patients of liver cirrhosis.Prevalence of hypothyroidism in rheumatoid arthritis and its correlation with disease activity.Serum interleukin 8 and 12 levels predict severity and mortality in patients with alcoholic hepatitis.Post-partum acute kidney injury.Genetic Heterogeneity of Beta Globin Mutations among Asian-Indians and Importance in Genetic Counselling and Diagnosis.Characterization of the ligand binding functionality of the extracellular domain of activin receptor type IIb.Influence of Xmn 1(G)γ (HBG2 c.-211 C → T) Globin Gene Polymorphism on Phenotype of Thalassemia Patients of North India.Epidemiology and risk factors for surgical site infections in patients requiring orthopedic surgery.Species distribution and drug susceptibility of candida in clinical isolates from a tertiary care centre at Indore.Genetic predisposition for development of nephropathy in type 2 diabetes mellitus.Prevention of homozygous beta thalassemia by premarital screening and prenatal diagnosis in India.Investigation of OPG/RANK/RANKL Genes as a Genetic Marker for Cardiac abnormalities in Thalassemia Major Patients.Rare hemoglobin variant Hb I Philadelphia in North Indian family.Outcome of Total Knee Replacement via Two Approaches in Indian Scenario.Status of 25-hydroxyvitamin D deficiency and effect of vitamin D receptor gene polymorphisms on bone mineral density in thalassemia patients of North India.Nonsense mutation of β-globin gene at codon 82 (AAG→TAG) or HBB:C247 A→T with polymorphism: cause of thalassemia intermedia?Sickle cell anemia--molecular diagnosis and prenatal counseling: SGPGI experienceAcute kidney injury in severe acute pancreatitis: an experience from a tertiary care centerNovel Mutations in a Patient with Triple A SyndromeSpectrum and hematological profile of hereditary anemia in North Indians: SGPGI experienceAssociation of GSTT1/GSTM1 and ApoE variants with left ventricular diastolic dysfunction in thalassaemia major patientsClinico-Hematological Presentation of Rare Hemoglobin Variant (HB-O Indonesia) in 3 Families
P50
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P50
description
researcher
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հետազոտող
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name
Ravindra Kumar
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Ravindra Kumar
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Ravindra Kumar
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Ravindra Kumar
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Ravindra Kumar
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রবীন্দ্র কুমার
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type
label
Ravindra Kumar
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Ravindra Kumar
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Ravindra Kumar
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Ravindra Kumar
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Ravindra Kumar
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রবীন্দ্র কুমার
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prefLabel
Ravindra Kumar
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Ravindra Kumar
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Ravindra Kumar
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Ravindra Kumar
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Ravindra Kumar
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রবীন্দ্র কুমার
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P1053
C-7455-2013
P106
P1153
55492127100
55780060900
P31
P3829
P496
0000-0001-9469-8080