Zobrazeno 1 - 10
of 449
pro vyhledávání: '"Ss, Bhattacharya"'
Publikováno v:
Asian Pacific Journal of Health Sciences. 5:21-24
Objectives: To compare the antimicrobial sensitivity patterns in neonatal infections in the year 2011 and 2014 in a Tertiary care Hospital in east India. Methodology: A retrospective study was done by collecting data from medical records of 150 neona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb72d6355692ff0645a95079ffd4ae95
https://doi.org/10.21276/apjhs.2018.5.3.3
https://doi.org/10.21276/apjhs.2018.5.3.3
Autor:
SS Bhattacharya, Aadhar M
Publikováno v:
International Journal of Innovative Research in Science, Engineering and Technology. :1046-1053
PP/nanoclay nonwoven composites were prepared by spun bond technology on spunbonding machine. The prepared nonwoven composites were characterized by SEM and EDX techniques. The thermal properties were analyzed using DSC, revels lower Tg inflection po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4817f196d9f59bc5fc33efe143c04fe7
https://doi.org/10.15680/ijirset.2015.0403048
https://doi.org/10.15680/ijirset.2015.0403048
Autor:
Soraya Bardien, Jacquie Greenberg, Neil D. Ebenezer, Peter Beighton, L. Bartmann, C F Inglehearn, Ss Bhattacharya, Rajkumar Ramesar, Rene Goliath
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Scopus-Elsevier
instname
Scopus-Elsevier
Retinitis pigmentosa is one of the most common causes of severe visual handicap in middle to late life. Prior to this report, seven loci had previously been mapped for the autosomal dominant form of this disorder (adRP). We now report the identificat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::433e6558e80398e4b886aee5c869091f
https://pubmed.ncbi.nlm.nih.gov/7581389
https://pubmed.ncbi.nlm.nih.gov/7581389
Autor:
SA Carter, AM Stephenson, Ss Papiha, A Jackson, C. F. Inglehearn, T J Keen, Ss Bhattacharya, U Atif, A C Bird, Janet C. Lindsey, R. Bashir, Marcelle Jay
Publikováno v:
Genomics. 14(1)
Genetic studies have revealed that 25 to 30% of autosomal dominant retinitis pigmentosa (adRP) families have mutations in the rhodopsin gene, while the remainder do not. More recently linkage data and mutation detection have demonstrated two further
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd2e8b09f422adabdd90706229c744d9
https://pubmed.ncbi.nlm.nih.gov/1427827
https://pubmed.ncbi.nlm.nih.gov/1427827
Autor:
Usha Dash, SS Bhattacharya
Publikováno v:
Indian Journal of Medical Microbiology. 25:78
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::575a7b46d59eb9b4f0ad469462e5ad7c
https://doi.org/10.4103/0255-0857.31077
https://doi.org/10.4103/0255-0857.31077
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3685d28687c23b79b864629fa0f72749
http://hdl.handle.net/10261/270048
http://hdl.handle.net/10261/270048
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 121(1)
(1) Results were presented of an investigation of the relationship between ionic strength and PK'1 (negative logarithmic form of the apparent overall first dissociation constant of carbonic acid in plasma) in separated human plasma at constant PCO2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45c12758a346e6bc9b90953f7dc21b60
https://pubmed.ncbi.nlm.nih.gov/6805986
https://pubmed.ncbi.nlm.nih.gov/6805986
Publikováno v:
Europe PubMed Central
X-linked retinitis pigmentosa (XLRP) is a degenerative disease of the retina characterized in the early stages of disease by night blindness as a result of rod photoreceptor loss, progressing to severe disease with loss of central vision by the third
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::be879b24d387260d16c82fb6c64b894b
http://europepmc.org/abstract/med/10892847
http://europepmc.org/abstract/med/10892847
Publikováno v:
Europe PubMed Central
Proximal Xp harbors many inherited retinal disorders, including retinitis pigmentosa (RP) and congenital stationary night blindness, both of which display genetic heterogeneity. X-linked congenital stationary night blindness (CSNBX) is a nonprogressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::111e540a9efafff64a7a363138594ebf
http://europepmc.org/abstract/med/9418727
http://europepmc.org/abstract/med/9418727
Autor:
Ss, Bhattacharya, Dev Borman A, Gandra M, Rh, Henderson, Ge, Holder, Li Z, Donna Mackay, At, Moore, Moradi P, Da, Thompson, Waseem N, Ar, Webster, Ga, Wright
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9b238730bcfe1209c77c0f46b04c8920
http://europepmc.org/abstract/med/22065924
http://europepmc.org/abstract/med/22065924