1. A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (MTCYB) in a Patient with Prader Willi Syndrome. (March 2015) Authors: Yiş, Uluç; Ezgü, Fatih Süheyl; Karakaya, Pakize; Polat, İpek; Arslan, Nur; Çankaya, Tufan; Bozkaya, Özlem Giray; Kurul, Semra Hız Journal: Journal of child neurology Issue: Volume 30:Number 3(2015:Mar.) Page Start: 378 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Acute flaccid myelitis outbreak through 2016–2018: A multicenter experience from Turkey. (January 2021) Authors: Ünver, Olcay; Türkdoğan, Dilşad; Güler, Serhat; Kipoğlu, Osman; Güngör, Mesut; Paketçi, Cem; Çarman, Kürşat Bora; Öztürk, Gülten; Genç, Hülya Maraş; Özkan, Mehpare; Dündar, Nihal Olgaç; Işık, Uğur; Karatoprak, Elif; Kılıç, Betül; Özkale, Murat; Bayram, Erhan; Yarar, Coşkun; Sözen, Hatice Gülhan; ... Journal: European journal of paediatric neurology Issue: Volume 30(2021) Page Start: 113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Alternative medications for epilepsy of infancy with migrating focal seizures; Potassium bromide and ketogenic diet. (June 2017) Authors: Polat, İpek; Ayanoglu, Muge; Okur, Derya; Edem, Pinar; Paketci, Cem; Bayram, Erhan; Yiş, Uluç; Kurul, Semra Hız Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e36 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Capillary Malformation–Arteriovenous Malformation Syndrome with Spinal Involvement. Issue 6 (14th July 2014) Authors: Yiş, Uluç; Kurul, Semra H.; Güleryüz, Handan; Men, Süleyman Journal: Pediatric dermatology Issue: Volume 31:Issue 6(2014) Page Start: 744 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database. (November 2017) Authors: Yaramış, Ahmet; Cansu, Ali; Ünalp, Aycan; Aksoy, Ayşe; Bayram, Ayşe Kaçar; Kartal, Ayşe; Tosun, Ayşe; Serdaroğlu, Ayşe; Konuşkan, Bahadır; Sarıoğlu, Berrak; Yüzbaşı, Beste Kıpçak; Kılıç, Betül; Taşkın, Birce Dilge; Bulut, Cahide; Yılmaz, Cahide; Yarar, Coşkun; Okuyaz, Çetin; Gençsel, Çigdem; Yüks... Journal: European journal of paediatric neurology Issue: Volume 21:Number 6(2017:Nov.) Page Start: 864 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Expression Patterns of Micro-RNAs 146a, 181a, and 155 in Subacute Sclerosing Panencephalitis. (January 2015) Authors: Yiş, Uluç; Tüfekçi, Uğur Kemal; Genç, Şermin; Çarman, Kürşat Bora; Bayram, Erhan; Topçu, Yasemin; Kurul, Semra Hız Journal: Journal of child neurology Issue: Volume 30:Number 1(2015:Jan.) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy. Issue 8 (17th March 2016) Authors: Mignot, Cyril; von Stülpnagel, Celina; Nava, Caroline; Ville, Dorothée; Sanlaville, Damien; Lesca, Gaetan; Rastetter, Agnès; Gachet, Benoit; Marie, Yannick; Korenke, G Christoph; Borggraefe, Ingo; Hoffmann-Zacharska, Dorota; Szczepanik, Elżbieta; Rudzka-Dybała, Mariola; Yiş, Uluç; Çağlayan, Hande... Other Names: author non-byline.; Craiu Dana author non-byline.; De Jonghe Peter author non-byline.; Helbig Ingo author non-byline.; Guerrini Renzo author non-byline.; Lehesjoki Anna-Elina author non-byline.; Marini Carla author non-byline.; Muhle Hiltrud author non-byline.; Møller Rikke S author non-byline.;... Journal: Journal of medical genetics Issue: Volume 53:Issue 8(2016) Page Start: 511 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genetic Landscape of Congenital Myasthenic Syndromes From Turkey: Novel Mutations and Clinical Insights. (July 2017) Authors: Yiş, Uluç; Becker, Kerstin; Kurul, Semra Hız; Uyanik, Gökhan; Bayram, Erhan; Haliloğlu, Göknur; Polat, Ayşe İpek; Ayanoğlu, Müge; Okur, Derya; Tosun, Ayşe Fahriye; Serdaroğlu, Gül; Yilmaz, Sanem; Topaloğlu, Haluk; Anlar, Banu; Cirak, Sebahattin; Engel, Andrew G. Journal: Journal of child neurology Issue: Volume 32:Number 8(2017:Aug.) Page Start: 759 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?. Issue 2 (16th November 2020) Authors: Pennisi, Alessandra; Rötig, Agnès; Roux, Charles-Joris; Lévy, Raphaël; Henneke, Marco; Gärtner, Jutta; Teke Kisa, Pelin; Sarioglu, Fatma Ceren; Yiş, Uluç; Konczal, Laura L; Burkardt, Deepika D; Wu, Sulin; Gaignard, Pauline; Besmond, Claude; Hubert, Laurence; Rio, Marlène; Barcia, Giulia; Munnich,... Journal: Journal of medical genetics Issue: Volume 59:Issue 2(2022) Page Start: 204 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Impact of next‐generation sequencing panels in the evaluation of limb‐girdle muscular dystrophies. (7th May 2019) Authors: Özyilmaz, Berk; Kirbiyik, Özgür; Özdemir, Taha R.; Kaya Özer, Özge; Kutbay, Yaşar B.; Erdogan, Kadri M.; Güvenç, Merve Saka; Kale, Murat Yildirim; Gazeteci, Hande; Kiliç, Betül; Sertpoyraz, Filiz; Diniz, Gulden; Baydan, Figen; Gençpinar, Pinar; Dündar, Nihal Olgaç; Yiş, Uluç Journal: Annals of human genetics Issue: Volume 83:Number 5(2019:Sep.) Page Start: 331 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗