Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mahmoud Majeed"'
Autor:
Nagham Mahmoud Majeed
Publikováno v:
Tikrit Journal of Administrative and Economic Sciences, Vol 19, Iss 61, 2 (2023)
تتوانى أهداف الاصلاح الاقتصادي في العراق بكثرة يقابلها ارتفاع في البطالة في العراق مما يزيد من الفقر في العراق وبسبب هذه المشاكل الاقتصا
Externí odkaz:
https://doaj.org/article/257b521c18024462ad8ae1bc6fffb12f
Publikováno v:
مجلة العلوم السياسية, Iss 63 (2022)
في الخطابات المعاصرة سارَ النقاش عند اغلب المفكرين الغربيين في الجهود المبذولة لتوضيح الأسس المعيارية للديمقراطية. ومن ثم فقد تبنى بعض ا
Externí odkaz:
https://doaj.org/article/674fa44283974c59bfe420c568583b33
Publikováno v:
Journal of Tikrit University for Humanities. 29:292-311
بحثت هذه الدراسة بشكل موجز العلاقات العراقية المصرية من ثورة 23 تموز/يوليو 1952 إلى ثورة 25 كانون الثاني/يناير 2011 من خلال أبرز المحطات في تلك
Autor:
Muna Almutairi, Abeer Alrasheedi, Munira AlMarri, Hala M. Lotfy, Mabruka Zlenti, Khulood Khawaja, Reem Abdwani, Mahmoud Majeed, Abdulrahman Asiri, Safiya Al Abrawi, Nora Almutairi, Awatif Abushhaiwia, Wafa Alsewairi, Muatasem AlSuwaiti, Elsadeg M Sharif, Mohammed A. Muzaffer, Manal Alshaikh, Raed Alzyoud, Sulaiman M. Al-Mayouf, Soad Hashad, Ebtisam Kawaja
Publikováno v:
Arthritis Care & Research. 73:586-592
Objective To report the cumulative articular and extraarticular damage in Arab children with juvenile idiopathic arthritis (JIA) and to identify variables that correlate with disease damage. Methods We conducted a multicenter, cross-sectional study a
Publikováno v:
Journal of Tikrit University for Humanities; 2022, Vol. 29 Issue 10,part 2, p292-311, 20p
Publikováno v:
American Journal of Medical Genetics. 93:5-10
We describe 10 patients (6 females and 4 males) from 6 unrelated families with an autosomal recessive disease characterized by simultaneous presentation of nodulosis, arthropathy and osteolysis. They were followed up regularly at King Faisal Speciali
Publikováno v:
Clinical rheumatology. 21(3)
Pancreatitis is a rare complication of paediatric systemic lupus erythematosus (SLE). We describe a child with severe form of SLE who initially developed acute pancreatitis, subsequently complicated by extensive pancreatic pseudocyst. The treatment a
Autor:
Leftan Al-Otaibi, Mahmoud Majeed, Wea'am Al-Eid, S. Bahabri, Sulalman M. Al-Mayouf, Claes Hugosson
Publikováno v:
Pediatric radiology. 32(7)
Background: Diseases exhibiting osteolysis in children are rare hereditary conditions. Several types have been recognised with different clinical manifestations. One type includes subcutaneous nodules, arthropathy and osteolysis and has been termed N
Publikováno v:
Pediatric dermatology. 17(6)
We describe a girl who initially presented with linear scleroderma. Five and a half years later she developed systemic lupus erythematosus (SLE). Previous descriptions of the coexistence of linear scleroderma and SLE in childhood are reviewed.