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au.\*:("ELAHI, Elahe")

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Discovery of single nucleotide polymorphisms and mutations by PyrosequencingRONAGHI, Mostafa; ELAHI, Elahe.Comparative and functional genomics. 2002, Vol 3, Num 1, pp 51-56, issn 1531-6912, 6 p.Article

Pyrosequencing for microbial typingRONAGHI, Mostafa; ELAHI, Elahe.Journal of chromatography. B, Biomedical sciences and applications. 2002, Vol 782, Num 1-2, pp 67-72, issn 1387-2273, 6 p.Article

Neural differentiation of mouse embryonic stem cells on conductive nanofiber scaffoldsKABIRI, Mahboubeh; SOLEIMANI, Masoud; SHABANI, Iman et al.Biotechnology letters. 2012, Vol 34, Num 7, pp 1357-1365, issn 0141-5492, 9 p.Article

Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucomaNAROOIE-NEJAD, Mehrnaz; SEYED HASSAN PAYLAKHI; ELAHI, Elahe et al.Human molecular genetics (Print). 2009, Vol 18, Num 20, pp 3969-3977, issn 0964-6906, 9 p.Article

Variable Expressivity and High Penetrance of CYP1B1 Mutations Associated with Primary Congenital GlaucomaSURI, Fatemeh; YAZDANI, Shahin; NAROOIE-NEJHAD, Mehrnaz et al.Ophthalmology (Rochester, MN). 2009, Vol 116, Num 11, pp 2101-2109, issn 0161-6420, 9 p.Article

Four mutations (three novel, one founder) in TACSTD2 among iranian GDLD patientsALAVI, Afagh; ELAHI, Elahe; AMINI, Seyed S. H et al.Investigative ophthalmology & visual science. 2007, Vol 48, Num 10, pp 4490-4497, issn 0146-0404, 8 p.Article

A Clinic-Based Screening of Mutations in Exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's Disease PatientsSHOJAEE, Seyedmehdi; SINA, Farzad; ELAHI, Elahe et al.Movement disorders. 2009, Vol 24, Num 7, pp 1023-1027, issn 0885-3185, 5 p.Article

Genome-wide Linkage Analysis of a Parkinsonian-Pyramidal Syndrome Pediqree by 500 K SNP ArraysSHOJAEE, Seyedmehdi; SINA, Farzad; SADAT BANIHOSSEINI, Setareh et al.American journal of human genetics. 2008, Vol 82, Num 6, pp 1375-1384, issn 0002-9297, 10 p.Article

Concentrations of nitric oxide metabolites in the serum of Iranian multiple sclerosis patientsROGHANI, Mehrzad; MAHBOUDI, Fereidoun; MOHAMMAD ALI SAHARIAN et al.Journal of the neurological sciences. 2010, Vol 294, Num 1-2, pp 92-94, issn 0022-510X, 3 p.Article

Determination of hepatitis C virus genotype by PyrosequencingELAHI, Elahe; POURMAND, Nader; CHAUNG, Ramsey et al.Journal of virological methods. 2003, Vol 109, Num 2, pp 171-176, issn 0166-0934, 6 p.Article

PRKN, DJ-1, and PINK1 Screening Identifies Novel Splice Site Mutation in PRKN and Two Novel DJ-1 MutationsGHAZAVI, Farzaneh; FAZLALI, Zeinab; SHAHIDI, Gholam-Ali et al.Movement disorders. 2011, Vol 26, Num 1, pp 80-89, issn 0885-3185, 10 p.Article

Identification of four novel potentially Parkinson's disease associated LRRK2 variations among Iranian patientsSHOJAEE, Seyedmehdi; FAZLALI, Zeinab; ELAHI, Elahe et al.Neuroscience letters. 2009, Vol 467, Num 2, pp 53-57, issn 0304-3940, 5 p.Article

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