Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Amal Al-Naamani"'
Autor:
Mohamed-Rachid Boulassel, Amal Al-Naamani, Abeer Al-Zubaidi, Zahra Al-Qarni, Hammad Khan, Amar Oukil, Amira Al-Badi, Juma Al-Kaabi, Jalila Al-Shekaili, Sulaiman Al-Hashmi, Fahad Zadjali, Rizwan Nabi Qureshi, Vinodh Panjwani, Salam Al-Kindi
Publikováno v:
Human immunology. 83(12)
The incidence of connective tissue diseases such as systemic lupus erythematous (SLE), in adult patients with sickle cell disease (SCD), appears to be increasing. The exact causes underlying this increased risk are still unknown, but a link with B re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dad093769e6cf51f8e85d052e2caa06
https://pubmed.ncbi.nlm.nih.gov/36184367
https://pubmed.ncbi.nlm.nih.gov/36184367
Autor:
Mohamed Rachid Boulassel, Hanan F. Nazir, Zahra Al-Qarni, Doaa Khater, Maryam Al-Ghonimi, Badriya Al-Balushi, Amal Al-Naamani, Salam Alkindi, Maryam Al-Shezawi, Mohamed Elshinawy, Yasser Wali, Anil Pathare, Hamad Khan
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 24:618-624
Development of inhibitors remains a major clinical complication in patients with hemophilia A receiving replacement therapy with factor VIII (FVIII). Understanding the immune mechanisms involved in the development of inhibitors can provide valuable i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3fb2e64aa8109076cc51579350c5692
https://doi.org/10.1177/1076029617702244
https://doi.org/10.1177/1076029617702244
Autor:
Amal Al-Naamani, Nasra Al-Obaidani, Sulaiman Al-Hashmi, Salam Alkindi, Mohammed Al-Huneini, Hamad Khan, Ahmed Al-Yarabi, Nasser Ambu-Ali, Alya Al-Ansari, Mohamed Rachid Boulassel, Zahra Al-Qarni, Amar Oukil, Khalil Al-Farsi, Murtadha Al-Khabori, Juma K. Alkaabi, Jalila Alshekaili, Tahar Al-Shabibi, Fahad Al-Zadjali, Yasser Wali
Publikováno v:
Blood. 128:3641-3641
Recent observational cohort studies indicated that the incidence of connective tissue diseases such as systemic lupus erythematous (SLE), in adult patients with sickle cell disease (SCD), appears to be increasing. The exact causes underlying this inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d78d49740d8cba0b685a77c88d3f22ab
https://doi.org/10.1182/blood.v128.22.3641.3641
https://doi.org/10.1182/blood.v128.22.3641.3641