Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Aruna Pawar"'
Publikováno v:
Indian Journal of Dermatology, Vol 56, Iss 5, Pp 497-500 (2011)
Background: Psoriasis, a common autoimmune disorder characterized by T cell-mediated keratinocyte hyperproliferation, is known to be associated with the presence of certain specific Human Leukocyte Antigen (HLA) alleles. Aim: To evaluate distribution
Externí odkaz:
https://doaj.org/article/bde991a591554bdbb5ceb5a6c550d510
Autor:
Kanjaksha Ghosh, Shankarkumar Umapathy, Deepak Khuperkar, U Khopkar, JP Devaraj, R Mitra, Aruna Pawar
Publikováno v:
Indian Journal of Dermatology
Indian Journal of Dermatology, Vol 56, Iss 5, Pp 497-500 (2011)
Indian Journal of Dermatology, Vol 56, Iss 5, Pp 497-500 (2011)
Background: Psoriasis, a common autoimmune disorder characterized by T cell-mediated keratinocyte hyperproliferation, is known to be associated with the presence of certain specific Human Leukocyte Antigen (HLA) alleles. Aim: To evaluate distribution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9727af65a7bc8a122b3586951890875f
http://europepmc.org/articles/PMC3221207
http://europepmc.org/articles/PMC3221207
Publikováno v:
Virus Adaptation and Treatment, Vol 2009, Iss default, Pp 1-4 (2009)
U Shankarkumar,A Pawar,K GhoshNational Institute of Immunohaematology (ICMR), KEM Hospital, Parel, Mumbai, Maharashtra, IndiaAbstract: A regimen with varied side effects and compliance is of paramount importance to prevent viral drug resistance. Most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::171dfac546cfb56d72a94c7aacbe62d2
http://www.dovepress.com/hiv-1-evolution-drug-resistance-and-host-genetics-the-indian-scenario-a2938
http://www.dovepress.com/hiv-1-evolution-drug-resistance-and-host-genetics-the-indian-scenario-a2938
Publikováno v:
Journal of Fluorescence. 14:459-463
Anti-neutrophil cytoplasmic antibodies (ANCA) are the immunodiagnostic markers for idiopathic necrotizing crescentic glomerulonephritis affecting mainly medium to small sized blood vessels. The diagnosis of ANCA associated vasculitis (AAV) is mainly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c80ea066efd375e2871d7f67fa13eb2
https://doi.org/10.1023/b:jofl.0000031827.75873.a4
https://doi.org/10.1023/b:jofl.0000031827.75873.a4
Publikováno v:
Transfusion. 42:317-320
BACKGROUND: Neonatal alloimmune thrombocytopenic purpura (NAITP) occurring because of fetomaternal incompatibility in the human platelet antigen-1 (HPA-1) system is increasingly being detected worldwide. Several studies have reported the frequency an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a78f46e2b4b04122bcb11f439897885d
https://doi.org/10.1046/j.1537-2995.2002.00048.x
https://doi.org/10.1046/j.1537-2995.2002.00048.x
Publikováno v:
Haemophilia. 8:51-55
Organizing services for haemophilia in developing countries with few resources is a formidable task. There is wide variation in haemophilia care and management between developing and developed countries. The management of a genetic disorder such as h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b15f676cf122958bbf52720991c2d035
https://doi.org/10.1046/j.1365-2516.2002.00576.x
https://doi.org/10.1046/j.1365-2516.2002.00576.x
Publikováno v:
Hepatology. 34:666-670
The inherited deficiencies of protein C, protein S, antithrombin III, factor V Leiden mutation, prothrombin gene polymorphism, and antiphospholipids were studied in 53 Budd-Chiari syndrome (BCS) and 33 portal vein thrombosis (PVT) cases and compared
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88e9927f8b24d7453b14b34acc6cd4a3
https://doi.org/10.1053/jhep.2001.27948
https://doi.org/10.1053/jhep.2001.27948
Autor:
Shrimati Shetty, Bipin Kulkarni, S. Nair, Dipika Mohanty, A. Khare, S. Baindur, Kanjaksha Ghosh, Aruna Pawar
Publikováno v:
Haemophilia. 7:273-278
Four hundred and seven patients (352 haemophilia A and 55 haemophilia B) were investigated for the presence of factor VIII and IX inhibitors. Twenty-four out of 292 severe and two out of 36 moderate haemophilia A patients showed the presence of inhib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1d2edb8496952ace55157685ca73351
https://doi.org/10.1046/j.1365-2516.2001.00505.x
https://doi.org/10.1046/j.1365-2516.2001.00505.x
Autor:
Anil Pathare, Aruna Pawar, A. Khare, Kanjaksha Ghosh, Shrimati Shetty, F. Jijina, S. Nair, Manisha Madkaikar, Dipika Mohanty
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 7:158-165
The goal of this article is to study the association of known markers of thrombophilia with venous thrombosis in young patients (< 45 years) from the Western part of India. A prospective study of 432 patients (252 males and 180 females, age 1-45 year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cab5b7b3d2eba5e150e6ad2bcd18c7a8
https://doi.org/10.1177/107602960100700214
https://doi.org/10.1177/107602960100700214
Autor:
Manisha Madkaikar, Dipika Mohanty, S. Nair, Shrimati Shetty, Anil Pathare, Aruna Pawar, S. Baindur, Kanjaksha Ghosh
Publikováno v:
Haemophilia. 6:504-507
The clinical and haematological heterogeneity in cases of the rare combined factor V and VIII deficiency has not been reported so far from India. Nine such cases belonging to five unrelated families have been analysed in the present study for the var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::793f4dbe781c477a09a7f93f635dd287
https://doi.org/10.1046/j.1365-2516.2000.00421.x
https://doi.org/10.1046/j.1365-2516.2000.00421.x