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of 10
pro vyhledávání: '"Nermin Ahmad"'
Autor:
nermin ahmad, Lama Esber
Publikováno v:
مجلة جامعة تشرين للدراسات والبحوث العلمية، سلسلة العلوم الاقتصادية والقانونية, Vol 44, Iss 4 (2022)
هدف البحث إلى تقييم مدى إمكانية تنفيذ الرقابة الاستراتيجية في الجامعات الخاصة، وتحديداً في الأكاديمية العربية للعلوم والتكنولوجيا والن
Externí odkaz:
https://doaj.org/article/7aea34fe822f4b8ebad3843e00786b29
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 52, Iss 1, Pp 1-10 (2021)
Abstract Background Phase contrast MR imaging is a rapid and non-invasive technique which is sensitive in diagnosis and follow-up of different neurological diseases that cause CSF flow abnormality. MRI CSF flowmetry will be currently assessed in diff
Externí odkaz:
https://doaj.org/article/b45f99346e024249af6c15308b24feb7
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 46, Iss 2, Pp 449-454 (2015)
Aim of the study: To evaluate role of fiber tractography in the assessment of white matter (WM) fiber tract affection in patient with multiple sclerosis (MS). Patient and methods: Using fiber tractography, WM tract fibers were evaluated in 12 patient
Externí odkaz:
https://doaj.org/article/145acad27b754096a59fe173e8eaab85
Autor:
Mohammad Al-Haggar, Nermin Ahmad, Sohier Yahia, Amany Shams, Bothina Hasaneen, Rasha Hassan Hassan, Yahya Wahba, Nanees Abdel-Badie Salem, Dina Abdel-Hady
Publikováno v:
Case Reports in Genetics, Vol 2013 (2013)
Fibrodysplasia ossificans progressiva (FOP) is an autosomal dominant severe musculoskeletal disease characterized by extensive new bone formation within soft connective tissues and unique skeletal malformations of the big toes which represent a birth
Externí odkaz:
https://doaj.org/article/165127ac9c494a308f5c8aa7c6f85b91
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 46, Iss 2, Pp 449-454 (2015)
Aim of the study: To evaluate role of fiber tractography in the assessment of white matter (WM) fiber tract affection in patient with multiple sclerosis (MS). Patient and methods: Using fiber tractography, WM tract fibers were evaluated in 12 patient
Autor:
Yahya Wahba, Nermin Ahmad, Nanees Salem, Amira Kamal El-Hawary, Dina Abdel-Hady, Mohammad Al-Haggar, Ashraf A. Elsharkawy, Amany El-Hawary, Abdel-Rhman Eid, Laurence Jonard
Publikováno v:
Pediatric Diabetes. 16:305-316
Objectives H syndrome and pigmented hypertrichosis with insulin-dependent diabetes mellitus (PHID) had been described as two autosomal recessive disorders. We aim to screen for pathogenic SLC29A3 mutations in two unrelated Egyptian families with affe
Publikováno v:
British Journal of Medicine and Medical Research. 3:1918-1928
Aims: To screen cases of infantile cystinosis among different forms of proximal renal tubular acidosis (RTA). Study Design: Cross sectional. Place and Duration of Study: From a total of 25 families of RTA followed up in Nephrology unit of Mansoura Un
Autor:
Yahya Wahba, Nanees Salem, Sohier Yahia, Nermin Ahmad, Bothina Hasaneen, Amany Shams, Rasha H. Hassan, Mohammad Al-Haggar, Dina Abdel-Hady
Publikováno v:
Case Reports in Genetics
Case Reports in Genetics, Vol 2013 (2013)
Case Reports in Genetics, Vol 2013 (2013)
Fibrodysplasia ossificans progressiva (FOP) is an autosomal dominant severe musculoskeletal disease characterized by extensive new bone formation within soft connective tissues and unique skeletal malformations of the big toes which represent a birth
Autor:
Lukasz P. Kozlowski, Nermin Ahmad, Agnieszka Madej-Pilarczyk, Amany Shams, Sohier Yahia, Mohammad Al-Haggar, Monika Puzianowska-Kuznicka, Sahar Hamed, Dina Abdel-Hadi, Janusz M. Bujnicki
Mandibuloacral dysplasia (MAD) is a rare disease resulting from a mutation of LMNA gene encoding lamins A and C. The most common mutation associated with this disease is a homozygous arginine 527 replacement by histidine. Three female patients origin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17475ec739303fc3eb5767fb9c7efb64
https://europepmc.org/articles/PMC3476705/
https://europepmc.org/articles/PMC3476705/
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