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Showing page 1 of results 1 - 10 of about 29 pages

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Long-Term Honeymoon Period in Type 1 Diabetes: True Diagnosis MODY5; New Mutation of HNF1B | ESPE2019
Aysun Bideci; Zekiye Küpçü; Esra Döğer; Orhun Çamurdan; Peyami Cinaz
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-56
Published: 2019-08-22

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Evaluation of the Association of Glutamic Acid Decarboxylase Antibody and Limbic Encephalitis in Children with Type 1 Diabetes Mellitus | ESPE2019
Aylin Kilinç Ugurlu; Aysun Bideci; Ebru Arhan; Esra Döger; Ayse Serdaroglu; Orgun Leman Tekin; Acar Azime Sebnem Soysal; Orhun
http://abstracts.eurospe.org/hrp/0092/hrp0092P2-103
Published: 2019-08-22

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Cinacalcet Experience in Hypercalcemia Due to CaSR Mutation | ESPE2019
Esra Döger; Emine Demet Akbas; Ugurlu Aylin Kilinç; Zekiye Küpçü; Aysun Bideci; Orhun Çamurdan; Peyami Cinaz
http://abstracts.eurospe.org/hrp/0092/hrp0092P2-44
Published: 2019-08-22

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Congenital Generalized Lipodystrophy Type 4 - New Mutation in the CAVIN1 Gene | ESPE2019
Esra Döger; Abdullah Sezer; Aylin Kilinç Ugurlu; Emine Demet Akbas; Ferda Perçin; Aysun Bideci; Orhun Çamurdan; Peyami Cinaz
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-351
Published: 2019-08-22

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A Case of Panhipopituitarism with SOX3 Gene Deletion | ESPE2019
Peyami Cinaz; Gülsüm Kayhan; Esra Döğer; Aylin Kılınç Uğurlu; Emine Demet Akbaş; Zekiye Küpçü; Ferda Perçin; Aysun
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-103
Published: 2019-08-22

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Long-Term Honeymoon Period in Type 1 Diabetes: True Diagnosis MODY5; New Mutation of HNF1B | ESPE2019
Aysun Bideci; Zekiye Küpçü; Esra Döğer; Orhun Çamurdan; Peyami Cinaz
http://abstracts.eurospe.org/hrp/0092/hrp0092p3-56.html
Published: 2019-08-22

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34kb

Evaluation of the Association of Glutamic Acid Decarboxylase Antibody and Limbic Encephalitis in Children with Type 1 Diabetes Mellitus | ESPE2019
Aylin Kilinç Ugurlu; Aysun Bideci; Ebru Arhan; Esra Döger; Ayse Serdaroglu; Orgun Leman Tekin; Acar Azime Sebnem Soysal; Orhun
http://abstracts.eurospe.org/hrp/0092/hrp0092p2-103.html
Published: 2019-08-22

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2 hit(s)
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30kb

Cinacalcet Experience in Hypercalcemia Due to CaSR Mutation | ESPE2019
Esra Döger; Emine Demet Akbas; Ugurlu Aylin Kilinç; Zekiye Küpçü; Aysun Bideci; Orhun Çamurdan; Peyami Cinaz
http://abstracts.eurospe.org/hrp/0092/hrp0092p2-44.html
Published: 2019-08-22

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2 hit(s)
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31kb

Congenital Generalized Lipodystrophy Type 4 - New Mutation in the CAVIN1 Gene | ESPE2019
Esra Döger; Abdullah Sezer; Aylin Kilinç Ugurlu; Emine Demet Akbas; Ferda Perçin; Aysun Bideci; Orhun Çamurdan; Peyami Cinaz
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-351.html
Published: 2019-08-22

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2 hit(s)
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32kb

A Case of Panhipopituitarism with SOX3 Gene Deletion | ESPE2019
Peyami Cinaz; Gülsüm Kayhan; Esra Döğer; Aylin Kılınç Uğurlu; Emine Demet Akbaş; Zekiye Küpçü; Ferda Perçin; Aysun
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-103.html
Published: 2019-08-22

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