Výsledky vyhledávání - "Fahmida Ghaderibarmi"

Akademický článek

Intravenous Valproate versus Subcutaneous Sumatriptan in Acute Migraine Attack

Autor: Fahmida Ghaderibarmi, Nader Tavakkoli, Mansoureh Togha

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

Zobrazit plný text záznamu

Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet’s disease susceptibility

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

Zobrazit plný text záznamu

Brief Report: Association ofCCR1,KLRC4,IL12A-AS1,STAT4, andERAP1With Behçet's Disease in Iranians

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

Zobrazit plný text záznamu

Brief report: association of CCR1, KLRC4, IL12A-AS1, STAT4, and ERAP1 With Behçet's disease in Iranians

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

Zobrazit plný text záznamu

Characterization of the major histocompatibility complex locus association with Behçet’s disease in Iran

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

Zobrazit plný text záznamu

IL10 low-frequency variants in Behçet's disease patients

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

© 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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95c1cd98359af6dcb1f113c980830045
https://pubmed.ncbi.nlm.nih.gov/24708170

Zobrazit plný text záznamu

Gene expression profiling and association studies implicate the neuregulin signaling pathway in Behçet's disease susceptibility

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

© 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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4c90570ddf1aae940f3b503a540d9af

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání