1. 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) ↗
2. Coenzyme Q10 deficiency; A treatable autosomal recessive cerebellar ataxias. (June 2017) Authors: Kaya Ozcora, Gül Demet; Basak, Nazlı; Canpolat, Mehmet; Acer, Hamit; Kumandas, Sefer Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e136 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Fibromuscular Dysplasia Complicated With Cerebral Stroke in a Child With Congenital Dyserythropoietic Anemia Type II. Issue 8 (November 2016) Authors: Ozcan, Alper; Patiroglu, Turkan; Acer, Hamit; Gumus, Hakan; Senol, Serkan; Karakukcu, Musa; Ozdemir, Mehmet A.; Unal, Ekrem Journal: Journal of pediatric hematology/oncology Issue: Volume 38:Issue 8(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Neuroblastoma in a Child With Wolf-Hirschhorn Syndrome. Issue 4 (May 2017) Authors: Ozcan, Alper; Acer, Hamit; Ciraci, Saliha; Gumus, Hakan; Karakukcu, Musa; Patiroglu, Turkan; Ozdemir, Mehmet A.; Unal, Ekrem Journal: Journal of pediatric hematology/oncology Issue: Volume 39:Issue 4(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. PEX10 mutation; Autosomal recessive cerebellar ataxia. (June 2017) Authors: Canpolat, Mehmet; Kaya Ozcora, Gül Demet; Erdoğan, Murat; Acer, Hamit; Kumandaş, Sefer Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e135 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes. (November 2022) Authors: Yılmaz, Ünsal; Gücüyener, Kıvılcım; Yavuz, Merve; Öncel, İbrahim; Canpolat, Mehmet; Saltık, Sema; Ünver, Olcay; Çıtak Kurt, Ayşegül Neşe; Tosun, Ayşe; Yılmaz, Sanem; Özgör, Bilge; Erol, İlknur; Öztoprak, Ülkühan; Elitez, Duygu Aykol; Direk, Meltem Çobanoğulları; Bodur, Muhittin; Teber, Serap; Anl... Journal: European journal of paediatric neurology Issue: Volume 41(2022) Page Start: 8 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice. Issue 7 (24th February 2021) Authors: Vural, Atay; Şimşir, Gülşah; Tekgül, Şeyma; Koçoğlu, Cemile; Akçimen, Fulya; Kartal, Ece; Şen, Nesli E.; Lahut, Suna; Ömür, Özgür; Saner, Nazan; Gül, Tuğçe; Bayraktar, Elif; Palvadeau, Robin; Tunca, Ceren; Pirkevi Çetinkaya, Caroline; Gündoğdu Eken, Aslı; Şahbaz, Irmak; Kovancılar Koç, Müge; Özto... Journal: Movement disorders Issue: Volume 36:Issue 7(2021) Page Start: 1676 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗