Kết quả tìm kiếm - Conca, Walter
- Đang hiển thị 1 - 13 kết quả của 13
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Recommendations for The Diagnosis and Management of Osteoporosis: A Local Perspective: The Osteoporosis Working Group, King Faisal Specialist Hospital and Research Center Bằng Raef, Hussein, Frayha, Husn H., El-Shaker, Mohamed, Al-Humaidan, Abdulla, Conca, Walter, Sieck, Ulla, Okane, Janine
Được phát hành 2004Text -
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Iacta Alea Est: The Inexorable Advance of Tofacitinib in the Treatment of Dermatomyositis-Associated Rapidly Progressive Interstitial Lung Disease. A Case Report Bằng Conca, Walter, Weheba, Ihab, Abouzied, Mohei-Eldin, Abdelsayed, Abeer, Aleyouni, Yousif, Al‐Mutairy, Eid, Bakshi, Nasir, Khalid, Mohammad
Được phát hành 2020Text -
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Serum β(2)-microglobulin levels in Coronavirus disease 2019 (Covid-19): Another prognosticator of disease severity? Bằng Conca, Walter, Alabdely, Mayyadah, Albaiz, Faisal, Foster, Michael Warren, Alamri, Maha, Alkaff, Morad, Al-Mohanna, Futwan, Nagelkerke, Nicolaas, Almaghrabi, Reem Saad
Được phát hành 2021Text -
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Data on hypoxia-induced VEGF, leptin and NF-kB p65 expression Bằng Al-Anazi, Azizah, Parhar, Ranjit, Saleh, Soad, Al-Hijailan, Reem, Inglis, Angela, Al-Jufan, Mansour, Bazzi, Mohammed, Hashmi, Sarwar, Conca, Walter, Collison, Kate, Al-Mohanna, Futwan
Được phát hành 2018Text -
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Induction of Hypergammaglobulinemia and Autoantibodies by Salmonella Infection in MyD88-Deficient Mice Bằng Issac, Jincy M., Mohamed, Yassir A., Bashir, Ghada Hassan, Al-Sbiei, Ashraf, Conca, Walter, Khan, Taj A., Iqbal, Asif, Riemekasten, Gabriela, Bieber, Katja, Ludwig, Ralf J., Cabral-Marques, Otavio, Fernandez-Cabezudo, Maria J., al-Ramadi, Basel K.
Được phát hành 2018Text -
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Identification of the Tetraspanin CD82 as a New Barrier to Xenotransplantation Bằng Saleh, Soad M., Parhar, Ranjit S., Al-Hejailan, Reem S., Bakheet, Razan H., Khaleel, Hala S., Khalak, Hanif G., Halees, Anason S., Zaidi, Marya Z., Meyer, Brian F., Yung, Gisella P., Seebach, Jörg D., Conca, Walter, Khabar, Khalid S., Collison, Kate S., Al-Mohanna, Futwan A.
Được phát hành 2013Text -
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An atypical pulmonary fibrosis is associated with co-inheritance of mutations in the calcium binding protein genes S100A3 and S100A13 Bằng Al-Mutairy, Eid A., Imtiaz, Faiga Ahmad, Khalid, Mohammed, Al Qattan, Somaya, Saleh, Soad, Mahmoud, Linah Mahmood, Al-Saif, Maher Mohammed, Al-Haj, Latifa, Al-Enazi, Azizah, AlJebreen, Abdullah M., Mohammed, Shamayel Faheem, Mobeireek, Abdullah Fahad, Alkattan, Khalid, Chisti, Muzamil Amin, Luzina, Irina G., Al-Owain, Mohammed, Weheba, Ihab, Abdelsayed, Abeer Mohamed, Ramzan, Khushnooda, Janssen, Luke J., Conca, Walter, Alaiya, Ayodele, Collison, Kate S., Meyer, Brian F., Atamas, Sergei P., Khabar, Khalid S., Hasday, Jeffrey D., Al-Mohanna, Futwan
Được phát hành 2019Text