Genetic background of supernumerary teeth von Subasioglu, Aslı, Savas, Selcuk, Kucukyilmaz, Ebru, Kesim, Servet, Yagci, Ahmet, Dundar, Munis

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Mitochondrial Mutations in Multiple Sclerosis Patients with Atypical Optic Neuropathy von Beckmann, Yesim, Uzunköprü, Cihat, Subaşıoğlu, Aslı

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IL-1 blocking experience in a case with Majeed syndrome diagnosed in adulthood von Güleç Yazır, Merve, Durak Ediboğlu, Elif, Kabadayı, Gökhan, Subaşıoğlu, Aslı, Akar, Servet

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Treatment of three hereditary leiomyomatosis patients with cryotherapy von Uyar, Belkız, Acar, Emine M., Subaşıoğlu, Aslı

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A Rare Neuromuscular Disease: Limb-girdle Muscular Dystrophy-R18 Case Report von Yılmaz Çakan, Gülce Coşku, Bölük, Ebru, Seçil, Yaprak, Subaşıoğlu, Aslı, Tosun, Özgür

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Genetic, Surgical and Oncological Approach to Breast Cancer, with BRCA1, BRCA2, CDH1, PALB2, PTEN and TP53 Variants von Subaşıoğlu, Aslı, Güç, Zeynep Gülsüm, Gür, Emine Özlem, Tekindal, Mustafa Agah, Atahan, Murat Kemal

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Radixin modulates the function of outer hair cell stereocilia von Prasad, Sonal, Vona, Barbara, Diñeiro, Marta, Costales, María, González-Aguado, Rocío, Fontalba, Ana, Diego-Pérez, Clara, Subasioglu, Asli, Bademci, Guney, Tekin, Mustafa, Cabanillas, Rubén, Cadiñanos, Juan, Fridberger, Anders

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FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing von Diaz-Horta, Oscar, Subasioglu-Uzak, Asli, Grati, M'hamed, DeSmidt, Alexandra, Foster, Joseph, Cao, Lei, Bademci, Guney, Tokgoz-Yilmaz, Suna, Duman, Duygu, Cengiz, F. Basak, Abad, Clemer, Mittal, Rahul, Blanton, Susan, Liu, Xue Z., Farooq, Amjad, Walz, Katherina, Lu, Zhongmin, Tekin, Mustafa

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Research of genetic bases of hereditary non-syndromic hearing loss von Subaşıoğlu, Aslı, Duman, Duygu, Sırmacı, Aslı, Bademci, Güney, Carkıt, Fehime, Somdaş, Mehmet Akif, Erkan, Mustafa, Tekin, Mustafa, Dündar, Munis

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A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia von Mastushita, Masaki, Kitoh, Hiroshi, Subasioglu, Asli, Kurt Colak, Fatma, Dundar, Munis, Mishima, Kenichi, Nishida, Yoshihiro, Ishiguro, Naoki

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ATP6V1B1 mutations in distal renal tubular acidosis and sensorineural hearing loss: clinical and genetic spectrum of five families von Subasioglu Uzak, Asli, Cakar, Nilgun, Comak, Elif, Yalcinkaya, Fatos, Tekin, Mustafa

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Emopamil binding protein mutation in conradi-hünermann-happle syndrome representing plaque-type psoriasis von Ozyurt, Kemal, Subasioglu, Asli, Ozturk, Perihan, Inci, Rahime, Ozkan, Fuat, Bueno, Elena, Cañueto, Javier, González Sarmiento, Rogelio

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Healthcare in overview of Turkey von Dundar, Munis, Uzak, Aslı Subasioglu, Karabulut, Yesim

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Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort von Bademci, Guney, Foster, Joseph, Mahdieh, Nejat, Bonyadi, Mortaza, Duman, Duygu, Cengiz, F.Basak, Menendez, Ibis, Diaz-Horta, Oscar, Shirkavand, Atefeh, Zeinali, Sirous, Subasioglu, Asli, Tokgoz-Yilmaz, Suna, Huesca-Hernandez, Fabiola, de la Luz Arenas-Sordo, Maria, Dominguez-Aburto, Juan, Hernandez-Zamora, Edgar, Montenegro, Paola, Paredes, Rosario, Moreta, Germania, Vinueza, Rodrigo, Villegas, Franklin, Mendoza-Benitez, Santiago, Guo, Shengru, Bozan, Nazim, Tos, Tulay, Incesulu, Armagan, Sennaroglu, Gonca, Blanton, Susan H., Ozturkmen-Akay, Hatice, Yildirim-Baylan, Muzeyyen, Tekin, Mustafa

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Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss von Duman, Duygu, Ramzan, Memoona, Subasioglu, Asli, Mutlu, Ahmet, Peart, LéShon, Seyhan, Serhat, Guo, Shengru, Ila, Kadri, Balta, Burhan, Kalcioglu, Mahmut Tayyar, Bademci, Guney, Tekin, Mustafa

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A Rare Neuromuscular Disease: Limb-girdle Muscular Dystrophy-R18 Case Report/Nadir Bir Noromuskuler Hastalik: Limb-girdle Muskuler Distrofi-R18 Olgu Sunumu von Cakan, Gulce Cosku Yilmaz, Boluk, Ebru, Secil, Yaprak, Subasioglu, Asli, Tosun, Ozgur

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Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss von Li, Chong, Bademci, Guney, Subasioglu, Asli, Diaz-Horta, Oscar, Zhu, Yi, Liu, Jiaqi, Mitchell, Timothy Gavin, Abad, Clemer, Seyhan, Serhat, Duman, Duygu, Cengiz, Filiz Basak, Tokgoz-Yilmaz, Suna, Blanton, Susan H., Farooq, Amjad, Walz, Katherina, Zhai, R. Grace, Tekin, Mustafa

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A novel homozygous GALC mutation: Very early onset and rapidly progressive Krabbe disease von Kardas, Fatih, Uzak, Asli Subasioglu, Hossain, Mohammad Arif, Sakai, Norio, Canpolat, Mehmet, Yıkılmaz, Ali

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De Novo BETA-2 adrenergic receptor gene variant associated with obesity von Yaman Kalender, Derya Sema, Ertürk, Mehmet Sercan, Subaşıoğlu, Aslı, Gasımlı, Roya, Örük, Güzide Gonca, Gölbaşı, Murat, Önder Pamuk, Barış

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Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency von Fasano, Tommaso, Zanoni, Paolo, Rabacchi, Claudio, Pisciotta, Livia, Favari, Elda, Adorni, Maria Pia, Deegan, Patrick B., Park, Adrian, Hlaing, Thinn, Feher, Michael D., Jones, Ben, Uzak, Asli Subasioglu, Kardas, Fatih, Dardis, Andrea, Sechi, Annalisa, Bembi, Bruno, Minuz, Pietro, Bertolini, Stefano, Bernini, Franco, Calandra, Sebastiano

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