Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Khalid E. Ahmed"'
Autor:
Khaled Al Oweidat, Dana Marie, Ahmad A. Toubasi, Dunia Z. Jaber, Khalid E. Ahmed, Bayan O. Abu Alragheb, Asma S. Albtoosh
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract Bronchiectasis is a chronic lung disease characterized by recurrent respiratory symptoms. Several studies demonstrated that psychological comorbidities are common in patients with bronchiectasis. The aim of this study is to investigate the p
Externí odkaz:
https://doaj.org/article/d8c3fea704434b90b7493c6efcbd70e5
Autor:
M. Emad Al Madadha, Rama Rayyan, Khalid E. Ahmed, Nancy Al-Sanouri, Saddam Al Demour, Muayyad Ahmad
Publikováno v:
Cogent Public Health, Vol 9, Iss 1 (2022)
AbstractSince the beginning of the COVID-19 pandemic, catastrophic mortality and morbidity rates and unknown long-term ramifications were caused, leading to focused efforts on implementing effective vaccination. Nucleic acid-based vaccines (NBVs), an
Externí odkaz:
https://doaj.org/article/f4ce9eeda3cb4455866db1eda79eef60
Autor:
Muayyad Ahmad, Mamoun Ahram, M. Emad Al Madadha, Saddam Al Demour, Khalid E. Ahmed, Nancy Al-Sanouri, Rama Rayyan
Background With the implementation of nucleotide-based vaccines (NBVs) in the COVID-19 vaccination campaigns, a wide controversy surrounding NBVs has become a heated subject of debate, and it did not spare healthcare workers (HCW) and staff. HCW have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20866dfe220777947b53bb601c7b4358
https://doi.org/10.21203/rs.3.rs-871667/v1
https://doi.org/10.21203/rs.3.rs-871667/v1
Autor:
Mohammad Emad Al Madadha, Muayyad M. Ahmad, Khalid E. Ahmed, Saddam Al Demour, Mamoun Ahram, Nancy Al-Sanouri, Rama Rayyan
Background and objectives: With the implementation of nucleotide-based vaccines (NBVs) in the COVID-19 vaccination campaigns, a wide controversy surrounding NBVs has become a heated subject of debate, and it did not spare healthcare workers and staff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a637e72900e3df5db6f4beeeb6a069b
https://doi.org/10.21203/rs.3.rs-744975/v1
https://doi.org/10.21203/rs.3.rs-744975/v1
Autor:
Mohamed A. Yassin, Mohamed Abdelrazek, Shehab F. Mohamed, Deena Mudawi, Mona M Babikir, Abdulqadir J. Nashwan, Saleema C. Purayil, Khalid E. Ahmed
Publikováno v:
The American Journal of Case Reports
Patient: Male, 30-year-old Final Diagnosis: Acute myeloid leukemia Symptoms: Jaw numbness and pain Medication:— Clinical Procedure: None Specialty: Hematology Objective: Rare co-existance of disease or pathology Background: Numb chin syndrome is a
Autor:
Khalid E Ahmed
Publikováno v:
Haematology International Journal. 4
Autor:
Anas Hamad, Ahmed Atef Shible, Amna Gameil, Shehab F. Mohamed, Khalid E. Ahmed, Arshad Chanda, Marcus D. Lancé, Lubna Riaz
Publikováno v:
International Journal of Case Reports. :115
Haemophilia is a disorder that affects the ability of the blood to form clots. The congenital form of the disease is the most prevalent, is inherited as X-linked recessive and it causes deficiency of clotting Factor VIII or IX. clinically it presents
Autor:
Mohamed A. Yassin, Meshaal Alanzi, Khalid E. Ahmed, Mhd Baraa Habib, Shehab F. Mohamed, Bassel Mazen Dakkak, Ahmed Saleh
Publikováno v:
International Journal of Case Reports. :143
Thrombotic thrombocytopenic purpura (TTP) is a rare life-threatening hematologic disorder. It is mainly characterized by thrombocytopenia, microangiopathic hemolytic anemia (MAHA), fever, renal impairment and neurological abnormality. Plasmapheresis
Autor:
Khalid E. Ahmed, Amna Gameil, Dina Sameh Soliman, Mohamed A. Yassin, Aliaa Amer, Shehab F. Mohamed
Publikováno v:
International Journal of Case Reports. :118
Background: Combined factor V and factor VIII deficiency (F5F8D) is a rare autosomal recessive inherited coagulopathy. It has a higher prevalence in the Mediterranean region (1:100,000) compare to its prevalence in the general population which is est
Publikováno v:
International Journal of Case Reports. :119
Background: Factor XII is part of the intrinsic pathway. the activity of this pathway is assessed by measuring the activated partial thromboplastin time (aPTT). Deficiency of Factor XII is rare, often inherited as autosomal recessive, nevertheless au