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<title>Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi, C12/S1-2 (1998)</title>
<link href="http://hdl.handle.net/20.500.12397/2809" rel="alternate"/>
<subtitle/>
<id>http://hdl.handle.net/20.500.12397/2809</id>
<updated>2026-05-07T17:58:15Z</updated>
<dc:date>2026-05-07T17:58:15Z</dc:date>
<entry>
<title>A CASE OF BEALS' SYNDROME (CONGENİTAL CONTRACTURAL ARACHNODACTYLY)</title>
<link href="http://hdl.handle.net/20.500.12397/3376" rel="alternate"/>
<author>
<name>ÖZKAN, HASAN</name>
</author>
<author>
<name>ÖREN, HALE</name>
</author>
<author>
<name>ÖREN, Bahattin </name>
</author>
<author>
<name>Akçoral, Adnan</name>
</author>
<author>
<name>KARAOĞLAN, OSMAN</name>
</author>
<author>
<name>ALICI, EMİN</name>
</author>
<id>http://hdl.handle.net/20.500.12397/3376</id>
<updated>2020-06-16T12:44:40Z</updated>
<published>1998-01-01T00:00:00Z</published>
<summary type="text">A CASE OF BEALS' SYNDROME (CONGENİTAL CONTRACTURAL ARACHNODACTYLY)
ÖZKAN, HASAN; ÖREN, HALE; ÖREN, Bahattin ; Akçoral, Adnan; KARAOĞLAN, OSMAN; ALICI, EMİN
BEALS' SYNDROME, ALSO KNOWN AS CONGENİTAL CONTRACTURAL ARACHNODACTYLY, IS A RECENT RECOGNİZED DİSORDER CHARACTERİZED BY MULTİPLE JOİNT CONTRACTURES.
</summary>
<dc:date>1998-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>RİNOORBİTAL MUKORMİKOZİS</title>
<link href="http://hdl.handle.net/20.500.12397/3374" rel="alternate"/>
<author>
<name>PINAR, Ercan</name>
</author>
<author>
<name>TOPAK, Murat</name>
</author>
<author>
<name>ŞAHİN, Serap Eren</name>
</author>
<author>
<name>TATAR, Bekir</name>
</author>
<author>
<name>AKACUN, Kaan</name>
</author>
<id>http://hdl.handle.net/20.500.12397/3374</id>
<updated>2020-06-16T12:44:40Z</updated>
<published>1998-01-01T00:00:00Z</published>
<summary type="text">RİNOORBİTAL MUKORMİKOZİS
PINAR, Ercan; TOPAK, Murat; ŞAHİN, Serap Eren; TATAR, Bekir; AKACUN, Kaan
MUKORMİKOZİS NADİR GÖRÜLEN BİR OPORTUNİSTİK ENFEKSİYON OLUP GENELLİKLE DİYABETİK İMMÜNOSÜPRESİF TEDAVİ GÖREN HASTALARDA VE KANSER HASTALARINDA GÖRÜLÜR.
</summary>
<dc:date>1998-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>KONJENİTAL PULMONER KAPAK YOKLUKLU BEŞ OLGU</title>
<link href="http://hdl.handle.net/20.500.12397/3373" rel="alternate"/>
<author>
<name>UĞURLU, ŞEVKET BARAN</name>
</author>
<author>
<name>Yunus, Şemsettin</name>
</author>
<author>
<name>OTO, ÖZTEKİN</name>
</author>
<author>
<name>Hüdaoğlu, Suphi</name>
</author>
<author>
<name>Meşe, Timur</name>
</author>
<author>
<name>Akçoral, Adnan</name>
</author>
<author>
<name>ÜNAL, NURETTİN</name>
</author>
<id>http://hdl.handle.net/20.500.12397/3373</id>
<updated>2020-06-16T12:44:40Z</updated>
<published>1998-01-01T00:00:00Z</published>
<summary type="text">KONJENİTAL PULMONER KAPAK YOKLUKLU BEŞ OLGU
UĞURLU, ŞEVKET BARAN; Yunus, Şemsettin; OTO, ÖZTEKİN; Hüdaoğlu, Suphi; Meşe, Timur; Akçoral, Adnan; ÜNAL, NURETTİN
DOĞUMSAL PULMONER KAPAK YOKLUĞU NADİR GÖRÜLEN BİR ANOMALİ OLUP OLGULARIN BÜYÜK KISMI FALLOT TETRALOJİSİ İLE BİRLİKTE GÖRÜLDÜĞÜNDEN FALLOT TETRALOJİSİNİN BİR VARİANTI OLARAK DA TANIMLANMAKTADIR.
</summary>
<dc:date>1998-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>LUTEAL FAZ DEFEKTLERİ</title>
<link href="http://hdl.handle.net/20.500.12397/3372" rel="alternate"/>
<author>
<name>GÜLEKLİ, BÜLENT</name>
</author>
<id>http://hdl.handle.net/20.500.12397/3372</id>
<updated>2020-06-16T12:44:40Z</updated>
<published>1998-01-01T00:00:00Z</published>
<summary type="text">LUTEAL FAZ DEFEKTLERİ
GÜLEKLİ, BÜLENT
KIRK YIL ÖNCE LİTARATÜRE İLK GİRDİĞİNDEN BERİ LUTEAL FAZ YETMEZLİĞİ (LFD) GEREK TANISI GEREKSE TEDAVİSİ BAKIMINDAN ÇELİŞKİLER İÇERMEKTEDİR.
</summary>
<dc:date>1998-01-01T00:00:00Z</dc:date>
</entry>
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