Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Soheila Sotudeh"'
Autor:
Amir Hossein Saeidian, Hassan Vahidnezhad, Leila Youssefian, Soheila Sotudeh, Meisam Sargazi, Sirous Zeinali, Jouni Uitto
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 11, Pp n/a-n/a (2019)
Abstract Background Hypotrichosis with juvenile macular dystrophy (HJMD) is an autosomal recessive disorder characterized by abnormal growth of scalp hair and juvenile macular degeneration leading to blindness. We have explored the genetic basis of H
Externí odkaz:
https://doaj.org/article/2883c06dec16426990e5322d9434a131
Autor:
Marzieh Maddah, Mohammad Reza Fazlollahi, Reza Shiari, Farhad Shahram, Setareh Mamishi, Delara Babaie, Maryam Monajemzadeh, Soheila Sotudeh, Amir Ali Hamidieh, Mohsen Badalzadeh, Shaghayegh Tajik, Leila Sedighipour, Zahra Pourpak
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 18, Iss 4 (2019)
Chronic granulomatous disease (CGD) is a rare genetic disorder of neutrophil activity, resulting in increased rate of recurrent infections with catalase–positive bacteria and fungi, as well as various autoimmune diseases such as sarcoidosis, rheuma
Externí odkaz:
https://doaj.org/article/a15f81fe1d2840ddab146a221b2044bb
Autor:
Leila Youssefian, Soheila Sotudeh, Sirous Zeinali, Meisam Sargazi, Jouni Uitto, Hassan Vahidnezhad, Amir Hossein Saeidian
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 11, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Hypotrichosis with juvenile macular dystrophy (HJMD) is an autosomal recessive disorder characterized by abnormal growth of scalp hair and juvenile macular degeneration leading to blindness. We have explored the genetic basis of HJMD in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3bae6e524c9a381100ee64693187197
https://doi.org/10.1002/mgg3.975
https://doi.org/10.1002/mgg3.975
Autor:
Zahra Pourpak, Mohammad Reza Fazlollahi, Maryam Monajemzadeh, Farhad Shahram, Setareh Mamishi, Soheila Sotudeh, Delara Babaie, Marzieh Maddah, Leila Sedighipour, Amir Ali Hamidieh, Mohsen Badalzadeh, Reza Shiari, Shaghayegh Tajik
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 18, Iss 4 (2019)
Chronic granulomatous disease (CGD) is a rare genetic disorder of neutrophil activity, resulting in increased rate of recurrent infections with catalase–positive bacteria and fungi, as well as various autoimmune diseases such as sarcoidosis, rheuma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5a6641ea88117904e6fca9da0c197ed
https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1671
https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1671