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[1]
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Arab-Indian− 530 β-distal promoter haplotype and sickle/Hb D heterozygosis in Badagas of Nilgiris: is it suggestive of Harappan origin?
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Journal of Genetics,
2022 |
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[2]
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Demographic and Geographic Distribution of Sickle Cell Disease in Gondia District of Central India; A Hospital Based Study.
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2020 |
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[3]
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Spectrum of hemoglobinopathies in a tertiary care centre
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2020 |
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[4]
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Family Study a tool to diagnose variant haemoglobinopathies and ambivalent cases.
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IOSR Journal of Dental and Medical Sciences,
2019 |
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[5]
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Craniofacial and occlusal features of children with sickle cell disease compared to normal standards: a clinical and radiographic study of 50 paediatric patients
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2019 |
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[6]
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Establishment of cost effective screening method for hemoglobinopathies in undergraduate medical students
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International Journal of Clinical Biochemistry and Research,
2019 |
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[7]
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Assessment of the Factors Associated With Anaemia Status among Children Aged 6-59 Months in Acholi Region, Uganda
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2019 |
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[8]
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Prevalence of Thalassemia in Children of Adilabad District
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2018 |
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[9]
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Spectrum of hemoglobinopathies in the state of Madhya Pradesh, India
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Asian Pacific Journal of Health Sciences,
2018 |
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[10]
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Study on Prevalence and Severity of Thalassemia in Amravati District of Maharashtra
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International Journal of Pharmacy & Pharmaceutical Research,
2018 |
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[11]
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STUDY OF PREVALENCE AND PATTERNS OF SOME HEMOGLOBINOPATHIES IN CHANDRAPUR DISTRICT
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INDIAN JOURNAL OF APPLIED RESEARCH,
2018 |
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[12]
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Newborn screening for sickle cell disease: Indian experience
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2018 |
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[13]
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DETECTION OF RED CELL ALLOANTIBODY AMONG THE BLOOD TRANSFUSION RECIPIENTS
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2018 |
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[14]
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Candidate molecular markers for monoecy in dioecious tree spice nutmeg (Myristica fragrans Houtt.) and analysis of genetic variability in a core collection
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2018 |
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[15]
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The Prevalence and Severity of Sickle Cell Disease in Amravati District of Maharashtra
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2018 |
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[16]
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Candidate molecular markers for monoecy in dioecious tree spice nutmeg (Myristica fragrans Houtt.) and analysis of genetic variability in a core collection.
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2018 |
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[17]
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Detection of Compound Heterozygous Sickle Cell-β+ Thalassaemia in a Patient with Extreme Weakness, Mild Jaundice and Moderate Anaemia-A Case …
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Journal of clinical and diagnostic research: JCDR,
2017 |
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[18]
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UTILITY OF COMMUNITY GENETICS TOOLS IN ALLEVIATING HEALTH BURDEN FROM HAEMOGLOBINOPATHIES IN INDIA
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2017 |
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[19]
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SOCIO-DEMOGRAPHIC PROFILE OF SICKLE CELL DISEASE PATIENTS DIAGNOSED AT A TERTIARY CARE HOSPITAL IN CHANDRAPUR DISTRICT.
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2017 |
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[20]
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Spectrum of β - Thalassemia and Sickle Cell Anemia Diagnosed by Cation Exchange High Performance Liquid Chromatography in Different Communities of Mumbai District of Western India - A study from tertiary care hospital
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Saudi Journal of Medical and Pharmaceutical Sciences,
2017 |
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[21]
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Ethnicity of sickle cell anaemia: Study at Tertiary Care Hospital of Yavatmal
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2017 |
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[22]
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Optimization of DTT Buffer Volume in Dithionite Tube Test (DTT) With Respect to Hemoglobin Concentration Used for Field Screening of Sickle Hemoglobin (HbS)
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2016 |
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[23]
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Incidence of hemoglobinopathies and hemoglobin variants using HPLC as a diagnostic tool in 6500 anemic patients in a tertiary care center in Western India
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2016 |
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[24]
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β-Thalassaemia and its Co-existence with Haemoglobin E and Haemoglobin S in Upper Assam Region of North Eastern India: A Hospital Based Study
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Journal of clinical and diagnostic research: JCDR,
2016 |
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[25]
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CLINICO-PATHOLOGICAL CORRELATION OF SICKLE HEMOGLOBIN (HBS)
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Indian Journal of Medical Research and Pharmaceutical Sciences,
2016 |
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[26]
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MOLECULAR DIAGNOSIS OF SICKLE CELL ANEMIA IN CHOLANAICKAN TRIBALS
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2015 |
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[27]
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Profile of Genotype Hemoglobinopathies, Abo And Rhesus Blood Groups of Undergraduates of Federal University of Technology Owerri, Nigeria
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2015 |
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[28]
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Genotype and Sickle Cell Allele Frequency Distribution in a Tribal Population of India
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2015 |
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[29]
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Premarital screening of college students for carrier detection in thalassemia and sickle cell disease: need of the hour
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International Journal of Medical Science and Public Health,
2015 |
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[30]
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Sickle cell disease in tribal populations in India
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The Indian journal of medical research,
2015 |
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[31]
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Clinical Evaluation and Enhancement of Dithionite tube turbidity (DTT) test reagents used for field screening of Sickle Haemoglobin (HbS)
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INTERNATIONAL JOURNAL OF PHARMACY & LIFE SCIENCES,
2015 |
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[32]
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Tipping the balance: Haemoglobinopathies and the risk of diabetes
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World Journal of Diabetes,
2015 |
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[33]
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G-6-PD deficiency and Sickle cell anaemia in Badhiys Muslims of Purnia District (Bihar)
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International J. of Life Sciences,
2015 |
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[34]
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Int J Med Sci Public Health. 2015; 4 (3): 420-423
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Int J Med Sci,
2015 |
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[35]
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Incidence of Thalassemia and Sickle Cell Disease in Chhattisgarh, Central India: Using Hardy-Weinberg Equations
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2015 |
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[36]
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Premarital screening of college students for carrier detection in thalassemia and sickle cell disease
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2015 |
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[37]
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Sickle cell disease in India
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Current opinion in hematology,
2014 |
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[38]
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In Vitro Sickling Inhibitory Effects and Anti-Sickle Erythrocytes Hemolysis of Dicliptera colorata CB Clarke, Euphorbia hirta L. and Sorghum bicolor (L.) Moench
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2013 |
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[39]
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Haemoglobin S and βThal: Their Distribution in Maharashtra, India
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International journal of biomedical science: IJBS,
2013 |
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[40]
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Incidence of sickle cell trait among the Mahar of Raipur, Chattisgarh
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The Anthropologist,
2013 |
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[41]
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Burden of sickle cell disease among tribes of India: A burning problem
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International Research Journal of Pharmaceutical and Applied Sciences,
2013 |
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[42]
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In Vitro Sickling Inhibitory Effects and Anti-Sickle Erythrocytes Hemolysis of Dicliptera colorata CB Clarke, Euphorbia hirta L. and Sorghum bicolor (L.) …
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2013 |
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[43]
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Burden of sickle cell diseases among tribes of India-a burning problem
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2013 |
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[44]
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REVIEW ON SICKLE CELL ANEMIA: A CURRENT SCENARIO FROM DHULIA DISTRICT (MS), INDIA
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[45]
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Spectrum of β-Thalassemia and Sickle Cell Anemia Diagnosed by Cation Exchange High Performance Liquid Chromatography in Different Communities …
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SA Mujawar, SH Mulkutkar, SR Patil
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