Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Jankhah, A."'
Publikováno v:
Malaysian Journal of Microbiology, Vol 3, Iss 2, Pp 23-28 (2007)
Human cytomegalovirus (hCMV) has been described as an important etiological agent of intrauterine infection in women of childbearing age that causes congenital malformation. In the present study we examined 844 serum samples from women of child-beari
Externí odkaz:
https://doaj.org/article/4e3f6af48af4476596d353e0f4178f7b
Autor:
Hossein Jafari Khamirani, Sina Zoghi, Mehdi Dianatpour, Aria Jankhah, Seyed Sajjad Tabei, Sanaz Mohammadi, Seyed Alireza Dastgheib
Publikováno v:
Human Genome Variation, Vol 8, Iss 1, Pp 1-4 (2021)
Abstract PTRH2 deficiency is associated with an extremely rare disease, infantile-onset multisystem neurologic, endocrine, and pancreatic disease (IMNEPD). We report the first Iranian patient with IMNEPD. We detected a pathogenic variant in the PTRH2
Externí odkaz:
https://doaj.org/article/65d30e4d5ce041ababe457f0f3066f41
Autor:
Jankhah, Sepideh, Bérubé, Pierre R.
Publikováno v:
In Separation and Purification Technology 25 September 2014 134:58-65
Autor:
Jankhah, Sepideh, Bérubé, Pierre R.
Publikováno v:
In Water Research 1 November 2013 47(17):6516-6526
Autor:
Aria Jankhah, Mehdi Dianatpour, Hossein Jafari Khamirani, Seyed Sajjad Tabei, Sanaz Mohammadi, Seyed Alireza Dastgheib, Sina Zoghi
Publikováno v:
Human Genome Variation
Human Genome Variation, Vol 8, Iss 1, Pp 1-4 (2021)
Human Genome Variation, Vol 8, Iss 1, Pp 1-4 (2021)
PTRH2 deficiency is associated with an extremely rare disease, infantile-onset multisystem neurologic, endocrine, and pancreatic disease (IMNEPD). We report the first Iranian patient with IMNEPD. We detected a pathogenic variant in the PTRH2 gene (NM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30b382f9bf904e3bb90affefbb4bcbb0
https://doi.org/10.1038/s41439-021-00147-9
https://doi.org/10.1038/s41439-021-00147-9
Autor:
Blanchard, Jasmin, Oudghiri-Hassani, Hicham, Abatzoglou, Nicolas, Jankhah, Sepideh, Gitzhofer, François
Publikováno v:
In Chemical Engineering Journal 2008 143(1):186-194
Autor:
Jankhah, Sepideh, Abatzoglou, Nicolas, Gitzhofer, François, Blanchard, Jasmin, Oudghiri-Hassani, Hicham
Publikováno v:
In Chemical Engineering Journal 2008 139(3):532-539
Publikováno v:
In International Journal of Hydrogen Energy 2008 33(18):4769-4779
Autor:
Sepideh Jankhah
Publikováno v:
Membrane Technology. 2017:7-13
This article investigates the hydrodynamic conditions in a bench-scale membrane flow-cell. It looks at the way in which parameters such as the feed crossflow velocity, and geometry of the cell and feed-spacers, affect the system hydrodynamics. The fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::138cc30871b3c458dcba08dababaaf55
https://doi.org/10.1016/s0958-2118(17)30096-4
https://doi.org/10.1016/s0958-2118(17)30096-4
Autor:
Sarah Azimi, Leila Nouri Vahid, Krystyna Keleman, Pooneh Nikuei, Tara Akhtarkhavari, Thomas F. Wienker, Beate Albrecht, Hossein Khodaei, Mohammad Reza Ebrahimpour, Mohammad Javad Soltani Banavandi, Marzieh Mohseni, Vanessa Suckow, Aria Jankhah, Milad Bastami, Behzad Davarnia, Vera M. Kalscheuer, Farzaneh Larti, Saeide Akbari, Kimia Kahrizi, Jamileh Rezazadeh Varaghchi, Bettina Lipkowitz, Sanaz Arzhangi, Morteza Oladnabi, Monika Cohen, Sabine Otto, Zohreh Fattahi, Luciana Musante, Payman Jamali, Maryam Beheshtian, Masoumeh Hosseini, Maryam Taghdiri, Wei Chen, Seyedeh Sedigheh Abedini, Bernd Timmermann, Hans-Hilger Ropers, Andreas Tzschach, Gholamreza Bahrami, Birgit Zirn, Hossein Najmabadi, Dagmar Wieczorek, Ingrid Bader, Gabriele Gillessen-Kaesbach, Cornelia Oppitz, Elaheh Papari, Hao Hu, Ralf Herwig, Fatemeh Pourfatemi, Jutta Gärtner, Faezeh Mojahedi, Hossein Dehghani, Sepideh Mehvari, Seyed Hassan Tonekaboni
Publikováno v:
Molecular Psychiatry
Autosomal recessive (AR) gene defects are the leading genetic cause of intellectual disability (ID) in countries with frequent parental consanguinity, which account for about 1/7th of the world population. Yet, compared to autosomal dominant de novo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eda29e76af95f3244bac3fef885f1ad6
https://hdl.handle.net/21.11116/0000-0000-638A-5
https://hdl.handle.net/21.11116/0000-0000-638A-5
