Ardicli, D. Et Al. 2017. Neonatal-Onset Recurrent Guillain-Barre Syndrome-Like Disease: Clues for Inherited CD59 Deficiency. NEUROPEDIATRICS , vol.48, no.6 , 477-481.

Ardicli, D., TASKIRAN, E. Z., KOŞUKCU, C., Temucin, Ç. M., OGUZ, K. K., HALILOGLU, G., ... ALİKAŞİFOĞLU, M.(2017). Neonatal-Onset Recurrent Guillain-Barre Syndrome-Like Disease: Clues for Inherited CD59 Deficiency. NEUROPEDIATRICS , vol.48, no.6, 477-481.

Ardicli, DİDEM Et Al. "Neonatal-Onset Recurrent Guillain-Barre Syndrome-Like Disease: Clues for Inherited CD59 Deficiency," NEUROPEDIATRICS , vol.48, no.6, 477-481, 2017

Ardicli, DİDEM Et Al. "Neonatal-Onset Recurrent Guillain-Barre Syndrome-Like Disease: Clues for Inherited CD59 Deficiency." NEUROPEDIATRICS , vol.48, no.6, pp.477-481, 2017

Ardicli, D. Et Al. (2017) . "Neonatal-Onset Recurrent Guillain-Barre Syndrome-Like Disease: Clues for Inherited CD59 Deficiency." NEUROPEDIATRICS , vol.48, no.6, pp.477-481.

@article{article, author={DİDEM ARDIÇLI Et Al. }, title={Neonatal-Onset Recurrent Guillain-Barre Syndrome-Like Disease: Clues for Inherited CD59 Deficiency}, journal={NEUROPEDIATRICS}, year=2017, pages={477-481} }