Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Fadi Busaleh"'
Autor:
Hussain A Al Ghadeer, Fadi Busaleh, Hassan M Albahrani, Alla M Albisher, Abdulaziz AlHassan, Hassan M AlAmer, Hassan M Alibrahim, Ahmed H Alherz, Abdullah F Al Muaibid, Tawfiq M Aljubran
Publikováno v:
Cureus.
Autor:
Murtadha Alrashed, Fadi Busaleh, Fatimah Al-Hajji, Heba Alameer, Mohammed Ali Nasser Ali, Mahdi Alsuwailem, Abdullah Al Muaibid, Ali Hassan Saleh, Sajjad M AlKadhem, Mohammed Alnasser
Publikováno v:
International Journal of Medicine in Developing Countries. :2023-2026
Autor:
Fadi Busaleh, Omkolthoom A Alasmakh, Fatimah Almohammedsaleh, Maram F Almutairi, Juwdaa S Al Najjar, Abbas Alabdulatif
Publikováno v:
Cureus
Vitamin B12 is an essential water-soluble vitamin that mediates multiple coenzymes needed for cell synthesis, mainly the red blood cells. Its deficiency is characterized by megaloblastic anemia and neuropsychiatric symptoms. Macrocytosis is the class
Autor:
Hussain A. Al Ghadeer, Jumanah Alatiya, Fatimah A. Albahrani, Ahmed M. Alhamrani, Fadi Busaleh, Walaa Hassan, Hibah A. Alatiyyah, Haider Alnofaily, Jawad H Alnaqaa, Salwa B. Alshaikh
Publikováno v:
Cureus
Microcephalic primordial dwarfism is a group of disorders that result in growth restriction and multiple morbidities. The condition is subdivided into three categories, with microcephalic osteodysplastic primordial dwarfism type II (MOPDII) being the
Autor:
Zahra A. AlGhadeer, Zahra Alhashim, Fatimah Y. AlHejji, Hashem A. AlOmran, Yasen Alsaleh, Manal AlHelal, Aida AlJabri, Abdulelah M. Al dandan, Mousa AlMazeedi, Fadi Busaleh
Publikováno v:
Cureus
Allgrove syndrome or Triple-A syndrome is a triad of achalasia, alacrimia, and adrenal insufficiency. It is a rare disease that’s only described in the literature with no known incidence rate. Atypical presentation of some cases is rarely seen, esp
Autor:
Zakariya Aldandan, Latifah A. Alhashim, Salsabeel AlSultan, Hussain Albaqshi, Nawal Alfarhan, Fadi Busaleh, Sarah Alateeq
Publikováno v:
Cureus
Inflammatory bowel disease (IBD) is a debilitating chronic disorder that is classified into Crohn’s disease, ulcerative colitis, and unspecified which are marked by recurrent gastrointestinal inflammatory episodes. Anti-tumor necrosis agents, espec
Autor:
Fadi Busaleh, Jaber A Al Habeeb, Mishael M Aldawood, Murtadha M Bin Abd, Abdullah E Almutahhar, Rabab M Alaithan, Hussain A. Al Ghadeer
Publikováno v:
Cureus
Chronic granulomatous disease (CGD) is an inherited primary immunodeficiency disease caused by a genetic defect in the nicotinamide adenine dinucleotide phosphate oxidase (NADPH) complex that affects phagocytes. This leads to recurrent severe bacteri
Autor:
Mahmoud M Aldandan, Luay F Almulaifi, Fadi Busaleh, Jumanah M. Almajed, Abdullah A Almubarak, Mujtaba A Alabdullah, Sajjad M AlKadhem, Aymen Albarrak
Publikováno v:
Cureus
Kawasaki disease (KD) is a treatable medium-sized vasculitis in the pediatric population consisting of a myriad of specific signs and symptoms. A new entity of the disease, Kawasaki disease shock syndrome (KDSS), is defined as a KD patient presenting
Autor:
Heba H Al Ameer, Sajjad M AlKadhem, Osama Kattih, Zainab A Almoosa, Fadi Busaleh, Fatimah A AlMuhanna
Publikováno v:
Cureus
Fortunately, coronavirus disease 2019 (COVID-19) infection in pediatric populations exhibits a mild course of disease. However, a small number have recently been identified who develop a significant systemic inflammatory response, a new disease entit
Publikováno v:
Cureus
The World Health Organization is still revising the epidemiology of multi-system inflammatory syndrome in children (MIS-C) and the preliminary case definition, although there is a dearth of robust evidence regarding the clinical presentations, severi