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au.\*:("PRASAD, Sai")

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Free-floating giant left atrial ball thrombus with aortic valve disease―a rare entity and a near missAGRAWAL, Dharmendra; SIMON, Ellis J; PRASAD, Sai et al.European journal of cardio-thoracic surgery. 2012, Vol 41, Num 3, pp 702-704, issn 1010-7940, 3 p.Article

Septic arthritis of the manubriosternal jointPENG, Edward W. K; MCKILLOP, Graham; PRASAD, Sai et al.The Annals of thoracic surgery. 2007, Vol 83, Num 3, pp 1190-1194, issn 0003-4975, 5 p.Article

Genotype-phenotype correlations for SLC26A4-related deafnessAZAIEZ, Hela; TAO YANG; PRASAD, Sai et al.Human genetics. 2007, Vol 122, Num 5, pp 451-457, issn 0340-6717, 7 p.Article

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locusWAYNE, Sigrid; ROBERTSON, Nahid G; SMITH, Richard J. H et al.Human molecular genetics (Print). 2001, Vol 10, Num 3, pp 195-200, issn 0964-6906Article

Efficacy of a monovalent human-bovine (116E) rotavirus vaccine in Indian children in the second year of lifeBHANDARI, Nita; RONGSEN-CHANDOLA, Temsunaro; JUVEKAR, Sanjay et al.Vaccine. 2014, Vol 32, issn 0264-410X, A110-A116, SUP1Article

Efficacy of a monovalent human-bovine (116E) rotavirus vaccine in Indian infants: a randomised, double-blind, placebo-controlled trialBHANDARI, Nita; RONGSEN-CHANDOLA, Temsunaro; JUVEKAR, Sanjay et al.Lancet (British edition). 2014, Vol 383, Num 9935, pp 2136-2143, issn 0140-6736, 8 p.Article

Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutationsPRASAD, Sai; KÖLLN, Karen A; CUCCI, Robert A et al.American journal of medical genetics. 2004, Vol 124A, Num 1, pp 1-9, issn 0148-7299, 9 p.Article

Sinus of Valsalva Aneurysm Masquerading as Coronary Artery DiseasePENG, Edward W. K; CODISPOTI, Max; VENUGOPAL, Prem et al.The Annals of thoracic surgery. 2007, Vol 84, Num 6, pp 2119-2119, issn 0003-4975, 1 p.Article

Development and preclinical testing of HNVAC, a cell culture-based H1N1 pandemic influenza vaccine from IndiaHEGDE, Nagendra R; KUMAR, Deepak; PANDURANGA RAO, P et al.Vaccine. 2014, Vol 32, Num 29, pp 3636-3643, issn 0264-410X, 8 p.Article

Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13)DE LEENHEER, Els M. R; KUNST, Henricus P. M; MCGUIRT, Wyman T et al.Archives of otolaryngology, head & neck surgery. 2001, Vol 127, Num 1, pp 13-17, issn 0886-4470Article

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