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13 results on '"Sarenur Gokben"'

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1. The Histopathologic Examination of a Second Muscle Biopsy Specimen at a Later Date may Sometimes be the Best Approach to Make a Differential Diagnosis in Neuromuscular Disorders

2. Concomitant Alpha- and Gamma-Sarcoglycan Deficiencies in a Turkish Boy with a Novel Deletion in the Alpha-Sarcoglycan Gene

3. Continuous EEG Monitoring in Critically Ill Children and Prognostic Factors for Short-term Outcome: An Observational Study

4. Clinical and Molecular Spectrum of Tuberous Sclerosis Complex Patients: Identification of Three Novel Mutations

5. Necessity of Electroencephalography in High-risk Brief Resolved Unexplained Event

6. Acquired Demyelinating Syndrome: Single Center Experience

7. Determining Risk Factors of Epilepsy in Children with Cerebral Palsy: A Retrospective Study

8. De Novo CHRNE Mutation: Congenital Myasthenic Syndrome

9. Hereditary Neuropathy with Liability to Pressure Palsy: A Case Diagnosed with a Quick Multiplex Ligation-dependent Probe Amplification Test

10. The Effect of Vagal Nerve Stimulation on the Quality of Life in Pediatric Cases

11. Sturge-Weber Syndrome Type III

12. Polyneuropathy After Gastric By-pass Surgery

13. Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis.

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