Suchergebnisse - "Sarigecili, Esra"

PubPharm (27)

1

Optic neuritis in Turkish children and adolescents : A multicenter retrospective study

enthalten in: Multiple sclerosis and related disorders | 2024

von Direk, M. | Besen, �. | Öncel, �. | +55

2

A Rare Cause of Paroxysmal Movement Disorder Associated with TBC1D24 Gene Mutation in Two Siblings

enthalten in: Annals of Indian Academy of Neurology | 2023

von Sarıgecılı, E. | Anlas, O.

3

Acute necrotizing encephalopathy associated with RANBP2 mutation : value of MRI findings for diagnosis and intervention

enthalten in: Acta neurologica Belgica | 2023

von Sarigecili, E. | Ucar, H. | Havali, C. | +2

4

Short-Term and Long-Term Effects of Levetiracetam Monotherapy On Hematological Parameters in Children with Idiopathic Epilepsy

enthalten in: Sisli Etfal Hastanesi tip bulteni | 2023

von Ucar, H. | Sarigecili, E. | Bilen, S. | +1

5

Acute necrotizing encephalopathy associated with RANBP2 mutation: value of MRI findings for diagnosis and intervention

enthalten in: Acta neurologica Belgica | 2022

von Sarigecili, E. | Ucar, H. | Havali, C. | +2

6

Acute necrotizing encephalopathy associated with RANBP2 mutation: value of MRI findings for diagnosis and intervention

enthalten in: Acta neurologica Belgica | 2022

von Sarigecili, E. | Ucar, H. | Havali, C. | +2

7

Acute necrotizing encephalopathy associated with RANBP2 mutation: value of MRI findings for diagnosis and intervention

enthalten in: Acta neurologica Belgica | 2022

von Sarigecili, E. | Ucar, H. | Havali, C. | +2

8

The PURPLE N study : objective and perceived nutritional status in children and adolescents with cerebral palsy

enthalten in: Disability and rehabilitation | 2022

von Fogarasi, A. | Fazzi, E. | Smorenburg, A. | +71

9

Optic nerve ultrasonography in the evaluation of the relationship between arachnoid cyst and headache

enthalten in: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery | 2022

von Sarigecili, E. | Bilen, S. | Gokay, S. | +2

10

A rare cause of microcephaly, thin corpus callosum and refractory epilepsy due to a novel SLC1A4 gene mutation

enthalten in: Clinical neurology and neurosurgery | 2022

von Sarigecili, E. | Bulut, F. | Anlas, O.