Zobrazeno 1 - 10 of 23 pro vyhledávání: '"S C Nair"'
1
Akademický článek
A Personalized Approach to Biological Therapy Using Prediction of Clinical Response Based on MRP8/14 Serum Complex Levels in Rheumatoid Arthritis Patients.
Autor: S C Nair, P M J Welsing, I Y K Choi, J Roth, D Holzinger, J W J Bijlsma, J M van Laar, D M Gerlag, F P J G Lafeber, P P Tak
Publikováno v: PLoS ONE, Vol 11, Iss 3, p e0152362 (2016)
Measurement of MRP8/14 serum levels has shown potential in predicting clinical response to different biological agents in rheumatoid arthritis (RA). We aimed to develop a treatment algorithm based on a prediction score using MRP8/14 measurements and
Externí odkaz: https://doaj.org/article/244baf6716a743a3939bbbc47b15a0cc
Zobrazit plný text záznamu
2
Akademický článek
Knee Joint Distraction Compared to Total Knee Arthroplasty for Treatment of End Stage Osteoarthritis: Simulating Long-Term Outcomes and Cost-Effectiveness.
Autor: J A D van der Woude, S C Nair, R J H Custers, J M van Laar, N O Kuchuck, F P J G Lafeber, P M J Welsing
Publikováno v: PLoS ONE, Vol 11, Iss 5, p e0155524 (2016)
OBJECTIVE:In end-stage knee osteoarthritis the treatment of choice is total knee arthroplasty (TKA). An alternative treatment is knee joint distraction (KJD), suggested to postpone TKA. Several studies reported significant and prolonged clinical impr
Externí odkaz: https://doaj.org/article/a34c44bcba404f56a4ef1d4035fd9d24
Zobrazit plný text záznamu
4
Vascular Anomalies of the Head and Neck Region
Autor: S. C. Nair
Publikováno v: Journal of Maxillofacial and Oral Surgery. 17:1-12
Vascular anomalies of the head and neck region are a complex group of lesions that challenge the head and neck physicians. From the very understanding of the difference between its two distinct forms, hemangiomas and vascular malformations to its man
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17705373272bd3b6b0dd0cfc30ef5042
https://doi.org/10.1007/s12663-017-1063-2
Zobrazit plný text záznamu
6
THU0523 CLINICAL UTILITY OF TESTING CONVENTIONAL AND NON-CONVENTIONAL ANTI-PHOSPHOLIPID ANTIBODIES IN SUSPECTED OBSTETRIC ANTI-PHOSPHOLIPID SYNDROME
Autor: A. Ganapati, J. K, A. Nair, A. Mathew, R. Goel, J. Mathew, J. A. J. Prakash, S. C. Nair, D. Danda
Publikováno v: Annals of the Rheumatic Diseases. 79:500.1-501
Background:Anti-phospholipid syndrome (APS) is an important cause for recurrent pregnancy losses (RPL). Conventional APS antibodies (aPLs) like lupus anti-coagulant (LA), anti-cardiolipin(ACL) and anti-beta 2 glycoprotein I (anti-β2 GP I) are not pr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1f6d4b96946f1d78eb4704e76b7c62fc
https://doi.org/10.1136/annrheumdis-2020-eular.3466
Zobrazit plný text záznamu
8
Laboratory issues in bleeding disorders
Autor: F, Rodeghiero, A, Ruiz-Sáez, P H B, Bolton-Maggs, C P M, Hayward, S C, Nair, A, Srivastava
Publikováno v: Haemophilia. 14:93-103
Selected laboratory issues critical for the appropriate diagnosis of haemophilia A and B, von Willebrand's disease (VWD) and more rare bleeding disorders (RBD) are discussed from a worldwide perspective. The overall picture that emerges is on the who
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f42828ac1a10cfb49937d9c9e010eeea
https://doi.org/10.1111/j.1365-2516.2008.01716.x
Zobrazit plný text záznamu
9
Evaluation of primary haemostasis in people with neurofibromatosis type 1
Autor: M. Zafer, M. Hertzberg, Emmanuel J. Favaloro, Kathryn N. North, S. C. Nair
Publikováno v: Clinical and Laboratory Haematology. 26:341-345
Assessment of haemostasis in people with neurofibromatosis type 1 (NF-1) is essentially lacking, despite case reports of an association with von Willebrand disorder (VWD) and reported excessive bleeding post-surgery. We assessed routine blood haemato
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2baf33e558104fc06f16cd58fdda71e
https://doi.org/10.1111/j.1365-2257.2004.00632.x
Zobrazit plný text záznamu
10
A novel β-globin gene mutation HBB.c.22 GC produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC
Autor: E S, Edison, M, Sathya, S V, Rajkumar, S C, Nair, A, Srivastava, R V, Shaji
Publikováno v: International journal of laboratory hematology. 34(5)
Hemoglobinopathies are highly prevalent in Indian population. DNA analysis to detect causative mutations is required for identifying rare hemoglobin variants or when hematological results are discordant with the clinical phenotype. In this report, we
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ff10954ad8f1d71583cb27cadb3d280e
https://pubmed.ncbi.nlm.nih.gov/22471768
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje