Sharda Shanbhag
Sharda Shanbhag
National Institute of Immunohaematology
Verified email at gov.in
Title
Cited by
Cited by
Year
Rare coagulation factor deficiencies: a countrywide screening data from India
BKKG S. Shetty, T. Shelar, D. Mirgal, V. Nawadkar, P. Pinto, S. Shanbhag, A ...
Haemophilia 20 (4), 575–581, 2014
312014
Molecular pathology of rare bleeding disorders (RBDs) in India: a systematic review
BP Kulkarni, SB Nair, M Vijapurkar, L Mota, S Shanbhag, S Ali, SD Shetty, ...
PloS one 9 (10), e108683, 2014
162014
The epidemiology of FVIII inhibitors in Indian haemophilia A patients
P Pinto, T Shelar, V Nawadkar, D Mirgal, A Mukaddam, P Nair, P Kasatkar, ...
Indian Journal of Hematology and Blood Transfusion 30 (4), 356-363, 2014
152014
Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected
S Shanbhag, S Shetty, K Ghosh
Haemophilia 17 (5), e843-e845, 2011
102011
An improved, semi quantitative clot based assay for factor XIII
S Shanbhag, S Shetty, B Kulkarni, K Ghosh
Haemophilia 17 (4), 718-720, 2011
92011
Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: identification of fourteen novel mutations
S Shanbhag, K Ghosh, S Shetty
Blood Cells, Molecules, and Diseases 57, 81-84, 2016
72016
First trimester prenatal diagnosis of severe FXIII deficiency.
S Shanbhag, K Ghosh, S Shetty
Haemophilia: the official journal of the World Federation of Hemophilia 22 …, 2016
32016
A de novo factor VIII mutation in a haemophilia B family leading to combined deficiency of factor VIII and IX.
A Prabhudesai, S Shanbhag, D Mirgal, N Kawankar, S Shetty
Haemophilia: the official journal of the World Federation of Hemophilia 23 …, 2017
22017
A rare case of Glanzmann's thrombasthenia and factor VII deficiency due to a combination of pathogenic and non-pathogenic gene variants.
R Deshpande, S Shanbhag, A Jadli, S Shetty
Haemophilia: the official journal of the World Federation of Hemophilia 26 …, 2019
12019
Somatic mosaicism in a severe haemophilia B family detected by allele specific PCR: An alert to the genetic diagnostic laboratories.
S Shanbhag, K Ghosh, S Shetty
Thrombosis research 158, 138-139, 2017
12017
Prenatal diagnosis in a haemophilia carrier with triplet pregnancy
S Shanbhag, C Lulla, K Ghosh, S Shetty
Haemophilia: the official journal of the World Federation of Hemophilia 21 …, 2015
2015
Prenatal diagnosis in a family with purfura fulminans
S Shanbhag, N Pai, K Ghosh, S Shetty
Blood Coagulation & Fibrinolysis 26 (3), 350, 2015
2015
Molecular basis of 21 severe FXIIIA deficiency cases: 11 novel mutations detected: PB 4.74–4
S Shanbhag, K Ghosh, S Shetty
Journal of Thrombosis and Haemostasis 11, 2013
2013
A SEMIQUANTITAIVE ASSAY FOR DIAGNOSIS OF FACTOR XIII DEFICIENCY
K Ghosh, S Shanbhag, S Shetty, B Kulkarni
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL 95, 754-754, 2010
2010
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