Výsledky vyhledávání - "Hamdi E Tamimi"

Akademický článek

Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3.

Autor: Sezer Acar, Huda A BinEssa, Korcan Demir, Roua A Al-Rijjal, Minjing Zou, Gönül Çatli, Ahmet Anık, Anwar F Al-Enezi, Seçil Özışık, Manar S A Al-Faham, Ayhan Abacı, Bumin Dündar, Walaa E Kattan, Maysoon Alsagob, Salih Kavukçu, Hamdi E Tamimi, Brian F Meyer, Ece Böber, Yufei Shi

Publikováno v: PLoS ONE, Vol 13, Iss 3, p e0193388 (2018)

Hereditary hypophosphatemia is a group of rare renal phosphate wasting disorders. The diagnosis is based on clinical, radiological, and biochemical features, and may require genetic testing to be confirmed.Clinical features and mutation spectrum were

Externí odkaz: https://doaj.org/article/10b254c616884e3f832371affc2506e0

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Klinik Stajlarda Dikey Entegrasyon Oturumlarının Öğrenci Değerlendirmeleri

Autor: Ahlam AlShadoukhy, Akram Nurhussen, Sabri Kemahli, Dileep Kumar Rohra, Abdurrahman Ouban, Wael Al-Kattan, Hamdi E Tamimi

Publikováno v: Volume: 17, Issue: 52 27-34
Tıp Eğitimi Dünyası

Giriş ve Amaç: Çağdağ tıp eğitimindeki en önemli ilkelerden biri olan entegrasyonun eğitimin tüm evrelerinde sağlanması amaçtır. Klinik öncesi evrede yatay ve dikey entegrasyon sağlanması yaygın olarak uygulanmakta olup klinik evred

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce9a97301310c3f4d5a91541c27be9ef
https://doi.org/10.25282/ted.397608

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Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3

Autor: Bumin Dündar, Ayhan Abaci, Ece Böber, Secil Ozisik, Gönül Çatlı, Yufei Shi, Maysoon Alsagob, Minjing Zou, Huda A BinEssa, Brian F. Meyer, Roua A. Al-Rijjal, Sezer Acar, Salih Kavukçu, Korcan Demir, Walaa E Kattan, Anwar F Al-Enezi, Ahmet Anık, Hamdi E Tamimi, Manar S A Al-Faham

Publikováno v: PLoS ONE, Vol 13, Iss 3, p e0193388 (2018)
PLoS ONE

Background Hereditary hypophosphatemia is a group of rare renal phosphate wasting disorders. The diagnosis is based on clinical, radiological, and biochemical features, and may require genetic testing to be confirmed. Methodology Clinical features an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c13f29a24625f6662d5568007aa4372
https://avesis.deu.edu.tr/publication/details/f522beff-1661-4cf0-8a4d-9a07001aa2eb/oai

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