Search Results - Atayar, Emine

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  1. 1
    An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues

    An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues by Akyol, Aytekin, Güner, Günes, Özşeker, Havva Solak, Işık, Aynur, Atcı, Özge, Uzun, Sarp, Atayar, Emine, Ozaltin, Fatih, Gedikoğlu, Gökhan, Sökmensüer, Cenk, Fearon, Eric R.

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  2. 2
    A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract

    A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract by Saygili, Seha, Atayar, Emine, Canpolat, Nur, Elicevik, Mehmet, Kurugoglu, Sebuh, Sever, Lale, Caliskan, Salim, Ozaltin, Fatih

    Published in Clinical genetics
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  3. 3
    Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Answers

    Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Answers by Saygili, Seha, Canpolat, Nur, Sever, Lale, Caliskan, Salim, Atayar, Emine, Ozaltin, Fatih

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  4. 4
    MO026CLINICAL AND MUTATIONAL SPECTRUM OF CHILDREN WITH AUTOSOMAL RECESSIVE AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

    MO026CLINICAL AND MUTATIONAL SPECTRUM OF CHILDREN WITH AUTOSOMAL RECESSIVE AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE by Tutal, Ozum, Gulhan, Bora, Atayar, Emine, Yuksel, Selcuk, Ozcakar, Z Birsin, Soylemezoglu, Oguz, Saygili, Seha, Inozu, Mihriban, Baskin, Esra, Duzova, Ali, Hayran, Mutlu, Topaloglu, Rezan, Ozaltin, Fatih

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  5. 5
    Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions

    Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions by Saygili, Seha, Canpolat, Nur, Sever, Lale, Caliskan, Salim, Atayar, Emine, Ozaltin, Fatih

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  6. 6
    COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome

    COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome by Ozdemir, Gulsah, Gulhan, Bora, Atayar, Emine, Saygılı, Seha, Soylemezoglu, Oguz, Ozcakar, Zeynep Birsin, Eroglu, Fehime Kara, Candan, Cengiz, Demir, Belde Kasap, Soylu, Alper, Yüksel, Selçuk, Alpay, Harika, Agbas, Ayse, Duzova, Ali, Hayran, Mutlu, Ozaltin, Fatih, Topaloglu, Rezan

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  7. 7
    P0063CLINICAL CHARACTERISTICS OF PATIENTS WITH GENETICALLY CONFIRMED ALPORT SYNDROME

    P0063CLINICAL CHARACTERISTICS OF PATIENTS WITH GENETICALLY CONFIRMED ALPORT SYNDROME by Ozdemir, Gulsah, Gulhan, Bora, Atayar, Emine, Canpolat, Nur, Soylemezoglu, Oguz, Ozcakar, Z Birsin, Kara Eroğlu, Fehime, Candan, Cengiz, Kasap Demir, Belde, Soylu, Alper, Yuksel, Selcuk, Alpay, Harika, Agbas, Ayse, Duzova, Ali, Hayran, Mutlu, Ozaltin, Fatih, Topaloglu, Rezan

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  8. 8
    A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome

    A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome by Canpolat, Nur, Liu, Dingxiao, Atayar, Emine, Saygili, Seha, Kara, Nazli Sila, Westfall, Trudi A., Ding, Qiong, Brown, Bartley J., Braun, Terry A., Slusarski, Diane, Karli Oguz, Kader, Ozluk, Yasemin, Tuysuz, Beyhan, Tastemel Ozturk, Tugba, Sever, Lale, Sezerman, Osman Ugur, Topaloglu, Rezan, Caliskan, Salim, Attanasio, Massimo, Ozaltin, Fatih

    Published in Clinical genetics
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