D-bifunctional Protein Deficiency: A Case Report of a Turkish Child

por Incecik, Faruk, Mungan, Neslihan O.
Publicado 2019

Clinical Features and Molecular Genetics of Autosomal Recessive Ataxia in the Turkish Population

por Incecik, Faruk, Herguner, Ozlem M, Mungan, Neslihan O
Publicado 2020

Spinocerebellar Ataxia-21 in a Turkish Child

por Incecik, Faruk, Herguner, Ozlem M., Willems, Patrick, Mungan, Neslihan O.
Publicado 2018

Late-Onset Leigh Syndrome due to NDUFV1 Mutation in a 10-Year-Old Boy Initially Presenting with Ataxia

por Incecik, Faruk, Herguner, Ozlem M., Besen, Seyda, Bozdoğan, Sevcan T., Mungan, Neslihan O.
Publicado 2018

Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child

por Ozcanyuz, Duygu G., Incecik, Faruk, Herguner, Ozlem M., Mungan, Neslihan O., Bozdogan, Sevcan T.
Publicado 2020

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

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