D-bifunctional protein deficiency: A case report of a Turkish child

by Faruk Incecik, Neslihan O Mungan
Published 2019-01-01

Spinocerebellar ataxia-21 in a Turkish child

by Faruk Incecik, Ozlem M Herguner, Patrick Willems, Neslihan O Mungan
Published 2018-01-01

Dysarthria, ataxia, and dystonia associated with COX20 (FAM36A) gene mutation: A case report of a Turkish child

by Duygu G Ozcanyuz, Faruk Incecik, Ozlem M Herguner, Neslihan O Mungan, Sevcan T Bozdogan
Published 2020-01-01

Epilepsy and McArdle Disease in A Child

by Faruk incecik, Ozlem M Herguner, Gulen Mert, seyda Besen, Deniz Kor, Berna S. Yilmaz, Neslihan O. Mungan, sakir Altunbasak
Published 2015-03-01

Can untreated PKU patients escape from intellectual disability? A systematic review

by Danique van Vliet, Annemiek M. J. van Wegberg, Kirsten Ahring, Miroslaw Bik-Multanowski, Nenad Blau, Fatma D. Bulut, Kari Casas, Bozena Didycz, Maja Djordjevic, Antonio Federico, François Feillet, Maria Gizewska, Gwendolyn Gramer, Jozef L. Hertecant, Carla E. M. Hollak, Jens V. Jørgensen, Daniela Karall, Yuval Landau, Vincenzo Leuzzi, Per Mathisen, Kathryn Moseley, Neslihan Ö. Mungan, Francesca Nardecchia, Katrin Õunap, Kimberly K. Powell, Radha Ramachandran, Frank Rutsch, Aria Setoodeh, Maja Stojiljkovic, Fritz K. Trefz, Natalia Usurelu, Callum Wilson, Clara D. van Karnebeek, William B. Hanley, Francjan J. van Spronsen
Published 2018-08-01