S. Kulkarni

发表

Flow cytometric quantification of antigen D sites on red blood cells of partial D and weak D variants in India

S. Kulkarni, D. Mohanty, S. Gupte, 2006, Transfusion medicine.

Changes in platelet glycoprotein receptors after smoking – a flow cytometric study

S. Kulkarni, D. Mohanty, K. Ghosh, 2001, Platelets.

Frequency of partial D in Western India

S. Kulkarni, D. Mohanty, K. Vasantha, 2008, Transfusion medicine.

First report of Rhnull individuals in the Indian population and characterization of the underlying molecular mechanisms

C. Férec, Y. Fichou, S. Kulkarni, 2017, Transfusion.

Para-Bombay phenotype: A case report from a tertiary care hospital from South Gujarat

S. Kulkarni, Jitendra N. Patel, A. Pandya, 2018, Asian journal of transfusion science.

Molecular organization of ‘Rh’ gene is likely to be heterogeneous across the world

S. Kulkarni, K. Ghosh, A. Gorakshakar, 2013, Asian journal of transfusion science.

A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population.

S. Kulkarni, K. Ghosh, Vasantha Kasiviswanathan, 2013, Blood transfusion = Trasfusione del sangue.

Molecular Characterization of FUT1(H) Gene in the Bombay Phenotypes Detected in India

S. Kulkarni, D. Mohanty, K. Vasantha, 2008 .

Varied distribution of RhD epitopes in the Indian population.

S. Kulkarni, D. Mohanty, K. Vasantha, 2007, The National medical journal of India.

Partial matching of blood group antigens to reduce alloimmunization in Western India.

S. Kulkarni, K. Vasantha, K. Ghosh, 2016, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Molecular genotyping of clinically important blood group antigens in patients with thalassaemia

S. Kulkarni, M. Madkaikar, M. Manglani, 2018, The Indian journal of medical research.

Red cell antigen phenotypes in blood donors & thalassaemia patients for creation of red cell antigen-matched inventory

S. Kulkarni, M. Madkaikar, Bhavika Choudhary, 2020, The Indian journal of medical research.

Antigen negative red blood cell inventory of Indian blood donors.

S. Kulkarni, K. Vasantha, K. Ghosh, 2016, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Usefulness of prenatal detection of Usefulness of prenatal detection of

S. Kulkarni, D. Mohanty, S. Gupte, 2007 .

Iron deficiency as a risk factor for first febrile seizure

S. Kulkarni, K. Ghosh, R. Vaswani, 2010, Indian pediatrics.

An Improved Flow Cytometric Approach for Isolation of Fetal Cells from Maternal Blood for Non Invasive Prenatal Diagnosis of Hemoglobinopathies

Swati Kulkarni, S. Kulkarni, D. Mohanty, 2007, Hemoglobin.

Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.

S. Kulkarni, D. Mohanty, K. Ghosh, 2003, Clinical and laboratory haematology.

Phenotyping and Genotyping of HNA: Prevalence, Risk of Alloimmunization, and HNA Incompatibilities in Indians

S. Kulkarni, M. Madkaikar, A. Gorakshakar, 2022, Transfusion Medicine and Hemotherapy.

Functional and fibrinogen receptor studies in platelets in pre-eclamptic toxaemia of pregnancy.

S. Kulkarni, D. Mohanty, K. Ghosh, 1999, Platelets.

Oral

Rajkumar, S. Prakash, B. Meena, 2016, Journal of Medical Physics.

Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele

C. Férec, Y. Fichou, S. Kulkarni, 2018, Transfusion.

Molecular characterization of RhD variant phenotypes among blood donors: A study from the coastal region of India.

G. Mishra, S. Kulkarni, S. Shastry, 2021, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Characterising Indian RhD variants by serological and molecular methods.

G. Mishra, S. Kulkarni, M. Madkaikar, 2020, Transfusion medicine.

RHD-Positive Alleles among D- C/E+ Individuals from India

C. Férec, G. Mishra, Y. Fichou, 2018, Transfusion Medicine and Hemotherapy.

Studies on the ABH-Iso-Agglutinins in serum, saliva and milk from mothers with “Bombay” (Oh) phenotype

S. Kulkarni, K. Vasantha, S. Joshi, 2009, Asian journal of transfusion science.

Experience with intrauterine transfusions for severe Rh alloimmunization in a developing country.

S. Kulkarni, S. Gupte, R. Merchant, 1998, The Journal of maternal-fetal medicine.

Noninvasive fetal RHD genotyping from maternal plasma

S. Kulkarni, D. Parchure, 2016 .

Incidence of Rh immunization between 1981 and 1992.

S. Kulkarni, S. Gupte, 1994, The National medical journal of India.

Molecular genotyping of Indian blood group system antigens in Indian blood donors.

S. Kulkarni, M. Madkaikar, Harita Gogri, 2018, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Fetal Loss Due to Anti-Hro in a Lady Having Rare Genotype of Rh (D--/D--)

S. Kulkarni, D. Mohanty, K. Vasantha, 2008 .

Molecular characterization of rare D--/D-- variants in individuals of Indian origin.

C. Férec, G. Mishra, Y. Fichou, 2020, Blood transfusion = Trasfusione del sangue.

D‐‐phenotype due to RHD‐RHCE hybrid transcript in a case of severe haemolytic disease of newborn with anti‐Rh 17(Hrₒ) antibodies

G. Mishra, S. Kulkarni, Debasish Gupta, 2021, Transfusion medicine.

Molecular characterization of a rare Rh phenotype Dc-from the Indian subcontinent.

G. Mishra, S. Kulkarni, M. Madkaikar, 2021, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Oral N-acetylcysteine as an adjunct to standard medical therapy improved heart function in cases with stable class II and III systolic heart failure

Rajkumar, S. Prakash, B. Meena, 2021, Irish Journal of Medical Science (1971 -).