Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Leenam Mota"'
Autor:
Bipin P Kulkarni, Sona B Nair, Manasi Vijapurkar, Leenam Mota, Sharda Shanbhag, Shehnaz Ali, Shrimati D Shetty, Kanjaksha Ghosh
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e108683 (2014)
BackgroundThough rare in occurrence, patients with rare bleeding disorders (RBDs) are highly heterogeneous and may manifest with severe bleeding diathesis. Due to the high rate of consanguinity in many caste groups, these autosomal recessive bleeding
Externí odkaz:
https://doaj.org/article/e4d25ae4a78646f6a6fc35a903eaf86b
Publikováno v:
Clinica Chimica Acta. 409:106-111
Background Congenital factor VII (FVII) deficiency is a rare coagulation deficiency caused due to defects in the FVII gene. Methods We analyzed 14 unrelated Indian patients with congenital FVII deficiency for mutations in FVII gene by conformation se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56e3a28541cd8ca0658ac408be22ecf1
https://doi.org/10.1016/j.cca.2009.09.007
https://doi.org/10.1016/j.cca.2009.09.007
Publikováno v:
Haemophilia. 15:1104-1108
The prevalence, cause and the impact of antiphospholipid antibodies (APAs) on the clinical severity in haemophilia patients is poorly studied. We studied 72 severe seronegative (negative for HIV, HBsAg, HCV) haemophilia patients for the presence of f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e537934d07669a2856bac45a7326a604
https://doi.org/10.1111/j.1365-2516.2009.02034.x
https://doi.org/10.1111/j.1365-2516.2009.02034.x
Autor:
Sonal Vora, Kanjaksha Ghosh, Leera Quadros, Manasi Vijapurkar, Bipin Kulkarni, Shrimati Shetty, Leenam Mota
Publikováno v:
British Journal of Haematology. 138:541-544
The role of natural anticoagulants, fibrinolytic cascade factors and common prothrombotic gene polymorphisms in modulating disease severity were studied in 35 'clinically mild' and 37 'clinically severe' haemophilia patients with severe factor VIII o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d816c9a379b79e11e9d9042e80e6d93
https://doi.org/10.1111/j.1365-2141.2007.06693.x
https://doi.org/10.1111/j.1365-2141.2007.06693.x
Publikováno v:
Blood Coagulation & Fibrinolysis. 19:324-326
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d78fe13df01a0399d8f54615757637b4
https://doi.org/10.1097/mbc.0b013e3282fa1a1f
https://doi.org/10.1097/mbc.0b013e3282fa1a1f
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4347017db2ec1120d4fed42048c908b
https://pubmed.ncbi.nlm.nih.gov/20331754
https://pubmed.ncbi.nlm.nih.gov/20331754
Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 15(1)
At this centre, 130 women with rare bleeding disorders (RBD) were investigated over the past 15 years. Fifty patients were above the age of menarche (age of menarche in India is 10 years). Of these 44 presented with menorrhagia. Other complications i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::652235a6dea0be6e33c9f66d23e04717
https://pubmed.ncbi.nlm.nih.gov/18803553
https://pubmed.ncbi.nlm.nih.gov/18803553
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 19(6)
The modern thrombin generation tests describe different phases of generation of thrombin that is initiation, amplification and inhibition of thrombin generation as well as the integral amount of generated thrombin. We investigated 55 patients with co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34c8c1996302132d4c620475e0093401
https://pubmed.ncbi.nlm.nih.gov/18685441
https://pubmed.ncbi.nlm.nih.gov/18685441
Publikováno v:
Journal of pediatric hematology/oncology. 29(3)
Prenatal diagnosis is sought after for those genetic disorders, whose management is not satisfactory either because of the outcome or owing to extreme cost involved in the management of the patients affected by a specific disorder. Severe hemophilia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bebd1e5acf9d8c38a83e9848bbd01f46
https://pubmed.ncbi.nlm.nih.gov/17356389
https://pubmed.ncbi.nlm.nih.gov/17356389
Autor:
Shrimati Shetty, Leenam Mota, Bipin Kulkarni, S. Shanbhag, S. Nair, Kanjaksha Ghosh, Shehnaz Ali, Manasi Vijapurkar
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e108683 (2014)
PLoS ONE
PLoS ONE
BackgroundThough rare in occurrence, patients with rare bleeding disorders (RBDs) are highly heterogeneous and may manifest with severe bleeding diathesis. Due to the high rate of consanguinity in many caste groups, these autosomal recessive bleeding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::015a50005a5736b878dca9f51e6f4298
https://doi.org/10.1371/journal.pone.0108683
https://doi.org/10.1371/journal.pone.0108683