Search Results - "Nair, S. C"

Vascular Anomalies of the Head and Neck Region by Nair, S. C.

“…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…”
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Knee Joint Distraction Compared to Total Knee Arthroplasty for Treatment of End Stage Osteoarthritis: Simulating Long-Term Outcomes and Cost-Effectiveness by van der Woude, J A D, Nair, S C, Custers, R J H, van Laar, J M, Kuchuck, N O, Lafeber, F P J G, Welsing, P M J

“…In end-stage knee osteoarthritis the treatment of choice is total knee arthroplasty (TKA). An alternative treatment is knee joint distraction (KJD), suggested…”
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A Personalized Approach to Biological Therapy Using Prediction of Clinical Response Based on MRP8/14 Serum Complex Levels in Rheumatoid Arthritis Patients by Nair, S C, Welsing, P M J, Choi, I Y K, Roth, J, Holzinger, D, Bijlsma, J W J, van Laar, J M, Gerlag, D M, Lafeber, F P J G, Tak, P P

“…Measurement of MRP8/14 serum levels has shown potential in predicting clinical response to different biological agents in rheumatoid arthritis (RA). We aimed…”
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Repeat voluntary non-remunerated blood donor is the best quality indicator for blood safety by Nair, S C, Mammen, J J

“…The landmark judgement in 1996 by the Supreme Court of India in the "Common cause versus Union of India", brought to the fore, the then predominant practice of…”
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Molecular basis of quantitative fibrinogen disorders in 27 patients from India by Sumitha, E., Jayandharan, G. R., Arora, N., Abraham, A., David, S., Devi, G. S., Shenbagapriya, P., Nair, S. C., George, B., Mathews, V., Chandy, M., Viswabandya, A., Srivastava, A.

“…Summary Congenital fibrinogen deficiency is an extremely rare (1:1 000 000) hereditary bleeding disorder caused by defects in genes coding for fibrinogen Aα‐,…”
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Surgical management of vascular lesions of the head and neck: a review of 115 cases by Nair, S.C, Spencer, N.J, Nayak, K.P, Balasubramaniam, K

“…Abstract Vascular anomalies are amongst the most common congenital abnormalities observed in infants and children. Their occurrence in the head and neck region…”
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Hemostatic abnormalities in severe renal failure: Do they bark or bite? by Mohapatra, A, Valson, A, Gopal, B, Singh, S, Nair, S, Viswabandya, A, Varughese, S, Tamilarasi, V, John, G

“…Abnormal primary hemostasis is believed to be the most significant contributor to uremic bleeding. This study aimed to describe the prevalence and profile of…”
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Dacryo salivary fistula. Unusual case of salivary fistula draining into the inferior fornix of the eye by Nair, S.C, Prabhu, R, Nayak, K.P

“…Abstract Salivary fistula after a traumatic injury in the buccal region is not common. It is most commonly encountered in injuries involving the pre auricular…”
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Underlying prothrombotic states in pregnancy associated cerebral venous thrombosis by Aaron, S, Alexander, M, Maya, T, Mathew, V, Goel, M, Nair, S. C, Mammen, J, Vikram, M

“…Background : The exact pathogenesis of pregnancy associated cerebral venous thrombois is still unsettled. Aims : To identify possible inherited and acquired…”
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Targeting raised von Willebrand factor levels and macrophage activation in severe COVID-19: Consider low volume plasma exchange and low dose steroid by Zachariah, U., Nair, S.C., Goel, A., Balasubramanian, K.A., Mackie, I., Elias, E., Eapen, C.E.

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Re: Gorham–Stout disease with involvement of the jaws: a systematic review by Chandra, S.R., Nair, S.C.

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Hexamoll DINCH plasticised PVC containers for the storage of platelets by Nair, C S Bhaskaran, Vidya, R, Ashalatha, P M

“…Containers for the storage of platelets are made using polyvinyl chloride plasticised with di, (2-ethyl hexyl) phthalate, n-butyryl, tri (n-hexyl) citrate and…”
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Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions by Jayandharan, G., Shaji, R. V., Baidya, S., Nair, S. C., Chandy, M., Srivastava, A.

“…Haemophilia A (HA) is an X‐linked bleeding disorder caused by diverse mutations in the human coagulation factor VIII (FVIII) gene. We have analysed DNA from…”
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Towards standardization of clot waveform analysis and recommendations for its clinical applications by Shima, M., Thachil, J., Nair, S. C., Srivastava, A.

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Laboratory issues in bleeding disorders by LILLICRAP, D., NAIR, S. C., SRIVASTAVA, A., RODEGHIERO, F., PABINGER, I., FEDERICI, A. B.

“…The clinical history of the patient and of his/her relatives is the most important tool for making correct diagnosis of inherited or acquired bleeding…”
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Personalised treatment using serum drug levels of adalimumab in patients with rheumatoid arthritis: an evaluation of costs and effects by Krieckaert, C L M, Nair, S C, Nurmohamed, M T, van Dongen, C J J, Lems, W F, Lafeber, F P J G, Bijlsma, J W J, Koffijberg, H, Wolbink, G, Welsing, P M J

“…To evaluate the cost-effectiveness of personalised treatment for rheumatoid arthritis (RA) using clinical response and serum adalimumab levels. A personalised…”
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Tests of global haemostasis and their applications in bleeding disorders by NAIR, S. C., DARGAUD, Y., CHITLUR, M., SRIVASTAVA, A.

“…There is a potential for significant paradigm shift in the assessment of haemostasis from the conventional plasma recalcification times, such as prothrombin…”
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Ahead to 100% of voluntary nonremunerated blood donation at a tertiary referral hospital blood bank in South India by Siromani, Umakanth, Rajaiah, Molly, Daniel, Dolly, Mammen, Joy J, Nair, S C

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Progesterone receptor structure and function altered by geldanamycin, an hsp90-binding agent by Smith, David F., Whitesell, Luke, Nair, Satish C., Chen, Shiying, Prapapanich, Viravan, Rimerman, Ronald A.

“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Principles of haemophilia care: The Asia‐Pacific perspective by Dunkley, S., Lam, J. C. M., John, M. J., Wong, R. S. M., Tran, H., Yang, R., Nair, S. C., Shima, M., Street, A., Srivastava, A.

“…Optimal haemophilia care is best established and implemented through a well‐coordinated plan guided by clearly defined principles and priorities. A document…”
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