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Your search keyword '"Soheila Alyasin"' showing total 3 results
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3 results on '"Soheila Alyasin"'

1. An unusual case of cystic fibrosis with pancytopenia due to copper deficiency and blindness caused by vitamin A deficiency: A case-report

Author

Hesamedin Nabavizadeh, Leila Johari, Rafat Noeiaghdam, Soheila Alyasin, Hossein Esmaeilzadeh, Zahra Kanannejad, and Maryam Emaminia

Subjects
Cystic fibrosis, Blindness, Pancytopenia, Diseases of the respiratory system, RC705-779
Abstract

Cystic fibrosis (CF) is a multi-systemic autosomal recessive disease which mostly involves the respiratory, digestive, and reproductive systems, but it can present with various clinical presentations, especially in adulthood. We describe a 19-year-old boy, a known case of CF who presented with less known clinical presentations of CF, blindness, liver cirrhosis, vitamin A deficiency, and pancytopenia.

Published
2022
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2. Defects in intrinsic and innate immunity

Author

Mohamed-Ridha Barbouche, Hassan Abolhassani, Morteza Fallahpour, Aziz Bousfiha, Peter Olbrich, Farhad Seif, Soheila Alyasin, and Alireza Mahdaviani

Subjects
Respiratory Mucosa, Innate immune system, business.industry, Immunology, Pattern recognition receptor, Medicine, Disease, Acquired immune system, business, Receptor, medicine.disease, Immunodeficiency, Complement system
Abstract

Innate immunity consists of phagocytic cells such as neutrophils, macrophages, dendritic cells, or intermediate cells (penumbra between innate and adaptive immunity) such as natural killer (NK) cells, and NK-T cells accompanied by natural barriers (skin epithelial layers and antimicrobial secretions and gastrointestinal and respiratory mucosa), and cytokines. Innate Immunity receptors that are called pattern recognition receptors (PRRs) are either cell-associated (e.g., Toll-like Receptor) or soluble (e.g., complement proteins) that can recognize numerous pathogen-associated molecular patterns or damage-associated molecular patterns. Some defects in each part of this integrated system involved in bacterial defense may result in pyogenic infections. We have provided in this chapter an appropriate or timely diagnosis and management guideline of innate immunodeficiency which can enhance the outcome of the disease treatment and provide more insight into introducing cost-effective and accurate predictive, diagnostic, and prognostic approaches to lessen the burden of the disease for patients, their families, and healthcare systems in the future.

Published
2021
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3. Contributors

Author

Hassan Abolhassani, Asghar Aghamohammadi, Pilar Llobet Agulló, Hamid Ahanchian, Soheila Alyasin, Saba Arshi, Gholamreza Azizi, Mohamed-Ridha Barbouche, Mohammad Hassan Bemanian, Aziz Bousfiha, Zahra Chavoshzadeh, Taher Cheraghi, Romina Dieli Crimi, Charlotte Cunningham-Rundles, Abbas Dabbaghzadeh, Sepideh Darougar, Rainer Doffinger, Anne Durandy, Mohammad Ehlayel, Hermann Eibel, Mohammad Hossein Eslamian, Hossein Esmaeilzadeh, Teresa Espanol, Morteza Fallahpour, Saba Fekrvand, Andrew R Gennery, Javad Ghaffari, Negar Ghaffari, Sudhir Gupta, Lennart Hammarström, Marzieh Heydrzadeh, Arash Kalantari, Rasoul Nasiri Kalmarzi, Hirokazu Kanegane, Negar Khalighi, Abbas Khalili, Martin Lavin, Alireza Mahdaviani, Tooba Momen, Mohammad Nabavi, Tim Niehues, Hans D. Ochs, Peter Olbrich, Alessandro Plebani, Nima Rezaei, Farhad Seif, Mikko Seppänen, Mahnaz Sadeghi Shabestari, Alireza Shafiei, Mansoureh Shariat, Deepti Suri, Marzieh Tavakol, Mirjam van der Burg, Menno van Zelm, Ahmad Vosoughi Motlagh, and Reza Yazdani

Published
2021
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