A case of Roberts syndrome: its ultrasonographic characteristics and genetic diagnosis

Autor: Ayaz, Reyhan, Göktaş, Emine, Balasar, Mine

Publikováno v: Perinatal Journal, Vol 28, Iss 3, Pp 212-216 (2020)

Objective: Roberts syndrome is a very rare genetic disease, and it has an autosomal recessive inheritance pattern. It develops as a result of the mutation in ESCO2 gene located in the 8th chromosome. In our study, we aimed to present a case which was

Externí odkaz: https://doaj.org/article/86df266f7a9b4a6f893dfd759b9089cb

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A snapshot of geriatric infections in Turkey: ratio of geriatric inpatients in hospitals and evaluation of their infectious diseases: A multicenter point prevalence study

Autor: Aslaner, Hande, Ulu, Aslıhan, Sehmen, Emine, Erol, Serpil, Kızmaz, Yeşim Uygun, Durmuş, Gül, Işık, M Emirhan, Solay, Aslı Haykır, Komur, Suheyla, Azak, Emel, Yavuz, İlknur, Karagöz, Ergenekon, Sayar, Merve Sefa, Naz, Hasan, Demirbaş, Zehra, İnce, Nevin, Korkmaz, Fatime, Armağan, Şule Özdemir, Savaşçı, Ümit, Aktaş, Sabahat, Tigen, Elif Tükenmez, Şengel, Buket Ertürk, Gürsul, Nur Cancan, Acar, Ali, Sarı, Sema, Turan, Sema, Kostakoğlu, Uğur, Evik, Güliz, Arslan, Kader, Kılıç, Esra Kaya, Atilla, Aynur, Ağalar, Canan, Ateş, Selma, Uğurlu, Kenan, Doğan, Mustafa, Bilman, Funda, Kılıçaslan, Nirgül, Okay, Gülay, Altunal, Nilsun, Balkan, Yasemin, Yetik, Mevliye, Uysal, Serhat, Baran, A İrfan, Erben, Nurettin, Aydemir, Hande, Sezer, B Ergüt, Daldal, Abdulkadir, Kadanalı, Ayten, Tartar, Ayşe Sağmak, Şener, Alper, Harman, Rezan, Ceylan, M Reşat, Ürgüdücü, Hatice, Dökmetaş, İlyas, Hamidi, Ahmet, Yıldırım, A Altunçekiç, Kaygusuz, Sedat, Yılmaz, Esmeray Mutlu, Esen, Şaban, Nazik, Selçuk, Koç, Filiz, Özden, Hale Turan, Demirel, Aslıhan, Kürekçi, Yeşim, Erdoğan, Haluk, Göktaş, Emine Fırat, Uluğ, Mehmet, Kuşoğlu, Hülya, Gözüküçük, Ramazan, Elmaslar Mert, Habibe Tülin, Erdem, İlknur, Şahintürk, Hüseyin, Aliravcı, Işıl Deniz, Ali, Rıdvan Kara, Koçak, Funda, Yıldız, İE, Aslan, Emel, Karadağ, Fatma Yılmaz, Inal, A Seza, Tasova, Yesim, Kurtaran, Behice, Kuscu, Ferit, Korkmaz, Pinar, Ozdemir, Burcu, Inan, Dilara, Oztoprak, Nefise, Ozatag, Duru Mistanoglu, Daglı, Ozgur, Birengel, Serhat, Ozdemir, Kevser

Publikováno v: In International Journal of Infectious Diseases November 2020 100:337-342

TARİH BURADA DERGİSİ

Autor: Uygun, Sadık, Düzgün, Akın, Hüzmeli, Süleyman, Hüzmeli, Mena, Bozkır, Mustafa Ertan, Oflazoğlu, Nurcan, Yılmaz, Ali, Demirli, İbrahim Hakkı, Çörtük, Gökhan, Gün, Mehmet, Bakal, Ahmet, Yılmaz, Şükrü, Aşkar, Nizam, Arslantaş, Mustafa Barış, Arslantaş, Sevil, Pehlivan, Murat, Ateş, Bilal, Karagözlü, Hüseyin Serdar, Yaylacı, Halit, Yaylacı, Esra, Göktaş, Emine Kaya, Çetin, Remzi, Çaparoğlu, Abdullah, Kaya, Hanifi, Turunç, Günay, Yaylacı, Mehmet, Danacı, İrfan, Danacı, Songül, Ekinci, Adem, Aydın, Mehmet, Sakman, Murat, Yücel, Ercan, Doğan, Mehmet Metin, Köseoğlu, Osman, Köseoğlu, Habibe, Göktürk, Mehmet, Akkaya, Başer, Bulgurcu, Meriç, Aydoğan, Ümit, Urhan, Gökhan, Doğru, Ekrem, Tuncer, Asif, Akgül, Kubilay, Akgül, Belma, Ardıç, Hüseyin, Açıkyol, Volkan, Duran, Meral

In this issue (Volume: 2023-1-1) of the Journal of History, articles prepared in the social and human fields are published. Most of the articles contain the memories of the institutions, social areas and touristic places of Hatay Antakya, which was l

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3e2531834806380f01a5890e09fc851

Roberts sendromu olgusu: Ultrasonografik özellikleri ve genetik tanısı.

Autor: Ayaz, Reyhan¹, Göktaş, Emine², Balasar, Mine³

Publikováno v: Perinatal Journal / Perinatoloji Dergisi. Dec2020, Vol. 28 Issue 3, p212-216. 5p.