Search Results - Caylan, Ahmet E

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  1. 1
    Isolated Penile Fournier's Gangrene: A Rare Case

    Isolated Penile Fournier's Gangrene: A Rare Case by Batmaz, Orkun, Ucar, Murat, Caylan, Ahmet E, Gök, İsmail B, Vural, Veli

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  2. 2
    Does The Learning Curve Affect the Surgical, Functional, and Oncologic Outcomes in Bilateral Nerve-Sparing Robot Assisted Laparoscopic Prostatectomy?

    Does The Learning Curve Affect the Surgical, Functional, and Oncologic Outcomes in Bilateral Nerve-Sparing Robot Assisted Laparoscopic Prostatectomy? by Ucar, Murat, Varol, Alkim T, Gülkesen, Kemal H, Caylan, Ahmet E, Kutlu, Ömer, Güntekin, Erol

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  3. 3
    Isolated Penile Fournier's Gangrene: A Rare Case

    Isolated Penile Fournier's Gangrene: A Rare Case by Batmaz, Orkun, Ucar, Murat, Caylan, Ahmet E, Gök, İsmail B, Vural, Veli

    Published in Cureus
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  4. 4
    Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35

    Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35 by Collin, Rob W.J., Kalay, Ersan, Tariq, Muhammad, Peters, Theo, van der Zwaag, Bert, Venselaar, Hanka, Oostrik, Jaap, Lee, Kwanghyuk, Ahmed, Zubair M., Çaylan, Refik, Li, Yun, Spierenburg, Henk A., Eyupoglu, Erol, Heister, Angelien, Riazuddin, Saima, Bahat, Elif, Ansar, Muhammad, Arslan, Selcuk, Wollnik, Bernd, Brunner, Han G., Cremers, Cor W.R.J., Karaguzel, Ahmet, Ahmad, Wasim, Cremers, Frans P.M., Vriend, Gert, Friedman, Thomas B., Riazuddin, Sheikh, Leal, Suzanne M., Kremer, Hannie

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  5. 5
    GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutations

    GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutations by Kalay, Ersan, Caylan, Refik, Kremer, Hannie, de Brouwer, Arjan P.M., Karaguzel, Ahmet

    Published in Hearing research
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  6. 6
    A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein

    A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein by WATTENHOFER, Marie, SAHIN-CALAPOGLU, Nilüfer, ANTONARAKIS, Stylianos E, ANDREASEN, Ditte, KALAY, Ersan, CAYLAN, Refik, BRAILLARD, Bastien, FOWLER-JAEGER, Nicole, REYMOND, Alexandre, ROSSIER, Bernard C, KARAGUZEL, Ahmet

    Published in Human genetics
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