Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Mofareh AlZahrani"'
Autor:
Manar Abdulaziz Bin Obaid, Sahar Abdulaziz AlSedairy, Hamza Ali Alghamdi, Ghzail M. Aljameel, Eman Alidrissi, Mofareh AlZahrani, Manal Abdulaziz Binobead
Publikováno v:
Children, Vol 10, Iss 9, p 1468 (2023)
With a variety of symptoms that can impede children’s development, food allergies are an important public health concern. With the help of information from the King Fahad Medical City Hospital in Riyadh, we looked at how restricting certain foods a
Externí odkaz:
https://doaj.org/article/1823e5d5d0804c44b6fff5c22633477a
Autor:
Mofareh AlZahrani, Eman AlIdrissi, Hamza Ali Alghamdi, Suha A. Tashkandi, Enas S. Alharbi, Murad K. Habazi, Khelad A. AlSaidi, Rawan D. Aledielah
Publikováno v:
Journal of Clinical Immunology. 38:847-853
Autor:
Arts, Peer, Simons, Annet, Mofareh AlZahrani, Elanur Yilmaz, AlIdrissi, Eman, Aerde, Koen, Njood Alenezi, AlGhamdi, Hamza, Hadeel AlJubab, Abdulrahman Al-Hussaini, AlManjomi, Fahad, Alsaad, Alaa, Alsaleem, Badr, Abdulrahman Andijani, Asery, Ali, Ballourah, Walid, Bleeker-Rovers, Chantal, Deuren, Marcel, Flier, Michiel, Gerkes, Erica, Gilissen, Christian, Habazi, Murad, Hehir-Kwa, Jayne, Henriet, Stefanie, Hoppenreijs, Esther, Hortillosa, Sarah, Kerkhofs, Chantal, Keski-Filppula, Riikka, Lelieveld, Stefan, Lone, Khurram, MacKenzie, Marius, Mensenkamp, Arjen, Moilanen, Jukka, Nelen, Marcel, Oever, Jaap, Potjewijd, Judith, Paassen, Pieter, Schuurs-Hoeijmakers, Janneke, Simon, Anna, Stokowy, Tomasz, Vorst, Maartje, Vreeburg, Maaike, Wagner, Anja, Well, Gijs, Zafeiropoulou, Dimitra, Zonneveld-Huijssoon, Evelien, Veltman, Joris, Zelst-Stams, Wendy, Faqeih, Eissa, Veerdonk, Frank, Netea, Mihai, Hoischen, Alexander
Additional material and references. (DOCX 31 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6196a48a5805b7de46c86b18879dbd0f
Autor:
Jayne Y. Hehir-Kwa, Njood Alenezi, Stefan H. Lelieveld, Badr Alsaleem, Arjen R. Mensenkamp, Marcel van Deuren, Christian Gilissen, Mofareh AlZahrani, Murad K. Habazi, Eman AlIdrissi, Mihai G. Netea, Alaa B. Alsaad, Pieter van Paassen, Wendy A. G. van Zelst-Stams, Hadeel A. AlJubab, Maartje van de Vorst, Sarah Hortillosa, Joris A. Veltman, Abdulrahman Al-Hussaini, Stefanie S. V. Henriet, Anja Wagner, Hamza A. AlGhamdi, Fahad AlManjomi, Maaike Vreeburg, Annet Simons, Walid Ballourah, Esther P A H Hoppenreijs, Chantal P. Bleeker-Rovers, Jukka S. Moilanen, M.A. MacKenzie, Dimitra Zafeiropoulou, Abdulrahman A. Andijani, Michiel van der Flier, Peer Arts, Judith Potjewijd, Eissa Faqeih, Koen J. van Aerde, Gijs Th. J. van Well, Frank L. van de Veerdonk, Erica H. Gerkes, Anna Simon, Tomasz Stokowy, Evelien Zonneveld-Huijssoon, Ali Asery, Khurram Lone, Chantal Kerkhofs, Janneke H M Schuurs-Hoeijmakers, Marcel R. Nelen, Riikka Keski-Filppula, Jaap ten Oever, Alexander Hoischen, Elanur Yilmaz
Publikováno v:
Genome Medicine, 11, 1
Genome Medicine
Genome medicine, 11:38. BMC
Genome Medicine, 11:38, 1-15. BioMed Central Ltd
Genome Medicine, 11:38. BioMed Central Ltd.
Genome Medicine, 11
Genome Medicine, Vol 11, Iss 1, Pp 1-15 (2019)
Genome Medicine
Genome medicine, 11:38. BMC
Genome Medicine, 11:38, 1-15. BioMed Central Ltd
Genome Medicine, 11:38. BioMed Central Ltd.
Genome Medicine, 11
Genome Medicine, Vol 11, Iss 1, Pp 1-15 (2019)
Background Diagnosis of primary immunodeficiencies (PIDs) is complex and cumbersome yet important for the clinical management of the disease. Exome sequencing may provide a genetic diagnosis in a significant number of patients in a single genetic tes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e04ce74acbb094de4102667590f55cd7
https://hdl.handle.net/2066/204759
https://hdl.handle.net/2066/204759
Autor:
Scott Hackett, Daniela Siegmund, Sergey Nejentsev, Delphine Cuchet-Lourenço, Changxin Wu, Emma Goss, Harald Wajant, Chris M. Bacon, Miguel B. Gaspar, Mofareh AlZahrani, Peter D. Arkwright, Ali Alisaac, Rainer Doffinger, Olivier Papapietro, Lourdes Ceron-Gutierrez, Davide Eletto, Dinakantha S. Kumararatne, Vincent Plagnol, Eman AlIdrissi, Badr AlSaleem, Mario Abinun, Mailis Maes, James Curtis
Publikováno v:
Cuchet-Lourenço, D, Eletto, D, Wu, C, Plagnot, V, Papapietro, O, Curtis, J, Ceron-Gutierrez, L, Bacon, C M, Hackett, S, Alsaleem, B, Maes, M, Gaspar, M, Alisaac, A, Goos, E, Alidrissi, E, Siegmund, D, Wajant, H, Kumararatne, D, AlZahrani, M S, Arkwright, P, Abinun, M, Doffinger, R & Nejentsev, S 2018, ' Biallelic RIPK1 mutations in humans cause severe immunodeficiency, arthritis and intestinal inflammation ', Science, vol. 361, no. 6404, pp. 810-813 . https://doi.org/10.1126/science.aar2641
Humans as models of human disease Mice are a convenient model for exploring the functions of cellular signaling pathways. Occasionally, however, an “experiment of nature” highlights the perils of overreliance on mice. RIPK1 is a well studied prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff4907946e07f00a22725a9c3066251f
https://doi.org/10.1126/science.aar2641
https://doi.org/10.1126/science.aar2641
Autor:
Catherine Sodroski, Rodrigo Hoyos-Bachiloglu, Abdallah Beano, Fahd Almanjomi, Magdalena Angelova, Mohamed Al Shehri, Raif S. Geha, Janet Chou, Murad K. Habazi, Eman Al Idrissi, Wayne Bainter, Morsi Alaa Eldin, Mofareh AlZahrani, Hamza Ali Alghamdi, Nagi Elsidig, David M. Knipe
Primary immunodeficiencies are often monogenic disorders characterized by vulnerability to specific infectious pathogens. Here, we performed whole-exome sequencing of a patient with disseminated Mycobacterium abscessus, Streptococcus viridians bacter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02af3471a45965ea485c5fd6e7cc1c48
https://europepmc.org/articles/PMC5707159/
https://europepmc.org/articles/PMC5707159/
Publikováno v:
Journal of Gastroenterology. 48:1205-1212
To our knowledge, in Asia, data on utility of allergy tests in management of eosinophilic esophagitis are lacking. The objective of our study was to determine the role of allergy evaluation in management of Saudi children with eosinophilic esophagiti
Autor:
Satoshi Okada, Mohammed A. Al Shehri, Takuji Murata, Motoaki Ohtsubo, Miyuki Tsumura, Geyhad ElGhazali, Yoshihiro Takihara, Takahiro Yasumi, Ryuta Nishikomori, Masao Kobayashi, Jean-Laurent Casanova, Avinash Abhyankar, Shin'ichiro Yasunaga, Xiao-Fei Kong, Hideto Obata, Saleh Al-Muhsen, Tatsutoshi Nakahata, Toshio Heike, Mofareh AlZahrani, Hidemasa Sakai, Stéphanie Boisson-Dupuis
Publikováno v:
Human Mutation. 33:1377-1387
Patients carrying two loss-of-function (or hypomorphic) alleles of STAT1 are vulnerable to intracellular bacterial and viral diseases. Heterozygosity for loss-of-function dominant-negative mutations in STAT1 is responsible for autosomal dominant (AD)
Autor:
Amal Jaber, Hasan Al-Dhekri, Saleh Al-Muhsen, Bandar Al-Saud, Afaf Al-Otaibi, Safa Alhissi, Muna M. Al Breacan, Nazema Ades, Maryam Al-Helale, Rana Kattan, Nada Al-Tassan, Mofareh AlZahrani, Shazia Subhani, Lina El-Baik, Rand Arnaout, Farrukh Sheikh, Brian F. Meyer, Salma M. Wakil, Mohamed El-Kalioby, Mohamed Abouelhoda, Tariq Faquih, Noukha Alnader, Majed Dasouki, Haya Al-Dusery, Khalid Al Abdelrahman, Eman Al Idrissi, Tanzeil Elamin, Abbas Hawwari, Dorota Monies, Fadi Alzayer, Sulaiman Al Gazlan, Faisal S. Bin Humaid, Sahar Elshorbagi, A. Al-Ghonaium, Omnia Kheir, Hamoud Al-Mousa
Publikováno v:
The Journal of allergy and clinical immunology. 137(6)
Background Molecular genetics techniques are an essential diagnostic tool for primary immunodeficiency diseases (PIDs). The use of next-generation sequencing (NGS) provides a comprehensive way of concurrently screening a large number of PID genes. Ho
Autor:
Galila F. Zaher, Salwa Hindawi, Ashraf Dallol, Mamdooh Gari, Mofareh AlZahrani, Adeel G. Chaudhary, Ghazi A. Damanhouri, Faten Al-Sayes, Mohammed H. Al-Qahtani, Adel M. Abuzenadah
Publikováno v:
Journal of thrombosis and thrombolysis. 36(4)
We describe in this report a case of a 6-years-old female who presented at the age of 1 month with a mucocutaneous bleeding and suspected thrombocytopenia. The patient’s condition was refractory to the known idiopathic thrombocytopenic purpura trea