Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Fahmida Ghaderibarmi"'
Publikováno v:
Acta Medica Iranica, Vol 53, Iss 10 (2015)
Migraine is a common and incapacitating neurologic disorder manifesting with episodic moderate to a severe headache and other symptoms such as photophobia, phonophobia, nausea, and vomiting. Triptans and ergot compounds have been used as treatment op
Externí odkaz:
https://doaj.org/article/e37b653098744bc09569d020f848c9c1
Autor:
Elaine F. Remmers, Ahmet Gül, Yohei Kirino, Sofia A. Oliveira, Fahmida Ghaderibarmi, Bahar Sadeghi Abdollahi, Daniel L. Kastner, Mary Blake, Masaki Takeuchi, Michael J. Ombrello, Nobuhisa Mizuki, Yilmaz Ozyazgan, Massimo Gadina, Fereydoun Davatchi, Atsuhisa Ueda, Burak Erer, Julie Le, Vânia Francisco, Ilknur Tugal-Tutkun, Abdolhadi Nadji, Niloofar Mojarad Shafiee, Akira Meguro, Colleen Satorius, Farhad Shahram, Tatsukata Kawagoe, Yoshiaki Ishigatsubo, Emire Seyahi, Shigeaki Ohno, Duran Ustek, Inês Sousa
Publikováno v:
Nature genetics
Daniel Kastner, Elaine Remmers and colleagues perform an association study of Behcet's disease based on dense genotyping of immune-related loci. They identify new association signals near genes involved in host response to microbial exposure and exte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af7a161df29da373b1983ab82f18f5c4
http://europepmc.org/articles/PMC5369770
http://europepmc.org/articles/PMC5369770
Autor:
Farhad Shahram, Fereydoun Davatchi, Abdolhadi Nadji, Sofia A. Oliveira, Niloofar Mojarad Shafiee, Fahmida Ghaderibarmi, Bahar Sadeghi Abdollahi, David Francisco, Inês Sousa, Joana M. Xavier
Publikováno v:
Arthritis & Rheumatology. 67:2742-2748
Objective To independently replicate the top findings from 4 published genome-wide association studies (GWAS) of susceptibility genes in Behcet's disease (BD). Methods We tested 14 single-nucleotide polymorphisms (SNPs) in 13 genomic loci (excluding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e8faa8922b4c2733eb982f56eb5fdf0
https://doi.org/10.1002/art.39240
https://doi.org/10.1002/art.39240
Autor:
Inês, Sousa, Farhad, Shahram, David, Francisco, Fereydoun, Davatchi, Bahar Sadeghi, Abdollahi, Fahmida, Ghaderibarmi, Abdolhadi, Nadji, Niloofar, Mojarad Shafiee, Joana M, Xavier, Sofia A, Oliveira
Publikováno v:
Arthritisrheumatology (Hoboken, N.J.). 67(10)
To independently replicate the top findings from 4 published genome-wide association studies (GWAS) of susceptibility genes in Behçet's disease (BD).We tested 14 single-nucleotide polymorphisms (SNPs) in 13 genomic loci (excluding the major histocom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::61702a070d20376ff8445dd817d5600f
https://pubmed.ncbi.nlm.nih.gov/26097239
https://pubmed.ncbi.nlm.nih.gov/26097239
Autor:
Hélder Trindade, Farhad Shahram, Fahmida Ghaderibarmi, Fereydoun Davatchi, Joana M. Xavier, Bahar Sadeghi Abdollahi, Sofia A. Oliveira, Dário Ligeiro, Abdolhadi Nadji, Vânia Francisco, Olga Abade, Niloofar Mojarad Shafiee
Publikováno v:
Arthritis Research & Therapy
© 2015 Xavier et al.; licensee BioMed Central. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9891170c8026b17c747df211fcc84ee3
https://hdl.handle.net/10451/53195
https://hdl.handle.net/10451/53195
Autor:
Manuel Salgado, Filipe Barcelos, Nádia Rei, Fereydoun Davatchi, Gorete Jesus, José Vaz Patto, Maria Francisca Moraes-Fontes, Farhad Shahram, Fahmida Ghaderibarmi, Jorge Crespo, Abdolhadi Nadji, Joana Vedes, Sofia A. Oliveira, Patrícia Abrantes, Niloofar Mojarad Shafiee, Joana M. Xavier, Inês Sousa, Bahar Sadeghi Abdollahi, Mafalda Matos
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
CIÊNCIAVITAE
Europe PubMed Central
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
CIÊNCIAVITAE
Europe PubMed Central
© 2014 Asia Pacific League of Associations for Rheumatology and Wiley Publishing Asia Pty Ltd.
Aim: To explain the missing heritability after the genome-wide association studies era, sequencing studies allow the identification of low-frequency
Aim: To explain the missing heritability after the genome-wide association studies era, sequencing studies allow the identification of low-frequency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95c1cd98359af6dcb1f113c980830045
https://pubmed.ncbi.nlm.nih.gov/24708170
https://pubmed.ncbi.nlm.nih.gov/24708170
Autor:
Fahmida Ghaderibarmi, Joana Vedes, Joana M. Xavier, Jorge Crespo, Bahar Sadeghi Abdollahi, Farhad Shahram, Sofia A. Oliveira, Benedita V. Fonseca, Gorete Jesus, Filipe Barcelos, Niloofar Mojarad Shafiee, Tiago Krug, Maria Francisca Moraes-Fontes, Manuel Salgado, Abdolhadi Nadji, Fereydoun Davatchi, José Vaz Patto
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
Europe PubMed Central
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
Europe PubMed Central
© Springer-Verlag Berlin Heidelberg 2013
Behçet's disease (BD) is a complex disease with genetic and environmental risk factors implicated in its etiology; however, its pathophysiology is poorly understood. To decipher BD's genetic underpinnin
Behçet's disease (BD) is a complex disease with genetic and environmental risk factors implicated in its etiology; however, its pathophysiology is poorly understood. To decipher BD's genetic underpinnin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4c90570ddf1aae940f3b503a540d9af
Autor:
Matos, Mafalda1,2, Xavier, Joana M.1,2, Abrantes, Patrícia1,2, Sousa, Inês1,2, Rei, Nádia1,2, Davatchi, Fereydoun3, Shahram, Farhad3, Jesus, Gorete4, Barcelos, Filipe5, Vedes, Joana6, Salgado, Manuel7, Abdollahi, Bahar Sadeghi3, Nadji, Abdolhadi3, Moraes ‐ Fontes, Maria Francisca2,8, Shafiee, Niloofar Mojarad3, Ghaderibarmi, Fahmida3, Vaz Patto, José5, Crespo, Jorge9, Oliveira, Sofia A.1,2 aaoliveira@fm.ul.pt
Publikováno v:
International Journal of Rheumatic Diseases. May2017, Vol. 20 Issue 5, p622-627. 6p.
Publikováno v:
Arthritis & Rheumatology; Dec2015, Vol. 67 Issue 12, p3336-3371, 36p
Autor:
Sousa, Inês, Shahram, Farhad, Francisco, David, Davatchi, Fereydoun, Abdollahi, Bahar Sadeghi, Ghaderibarmi, Fahmida, Nadji, Abdolhadi, Mojarad Shafiee, Niloofar, Xavier, Joana M., Oliveira, Sofia A.
Publikováno v:
Arthritis & Rheumatology; Oct2015, Vol. 67 Issue 10, p2742-2748, 7p, 1 Diagram, 2 Charts