Didem Tezen

Cerrahpasa, Turkey

Last Updated: 09/26/2026

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Found 10 publications

Early-onset Parkinson's disease: clinical findings and progression.

Early-onset Parkinson's disease: clinical findings and progression.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: January 29, 2026

Polysomnographic biomarkers for persisting (isolated) REM sleep without atonia in patients with obstructive sleep apnea.

Polysomnographic biomarkers for persisting (isolated) REM sleep without atonia in patients with obstructive sleep apnea.

Journal: Sleep medicine

Published: March 11, 2025

Correction to: Clinical, electrophysiological, and genetic analysis of a family with two rare neuromuscular disorders: congenital myasthenic syndrome and hereditary polyneuropathy.

Correction to: Clinical, electrophysiological, and genetic analysis of a family with two rare neuromuscular disorders: congenital myasthenic syndrome and hereditary polyneuropathy.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: October 10, 2024

Correlation between serum YKL-40 and VILIP 1 levels and brain volume in dementia patients.

Correlation between serum YKL-40 and VILIP 1 levels and brain volume in dementia patients.

Journal: Geriatrics & gerontology international

Published: July 31, 2024

Experience with salbutamol treatment in a family with congenital myasthenia due to CHRNE mutation.

Experience with salbutamol treatment in a family with congenital myasthenia due to CHRNE mutation.

Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology

Published: June 24, 2024

Clinical, electrophysiological, and genetic analysis of a family with two rare neuromuscular disorders: congenital myasthenic syndrome and hereditary polyneuropathy.

Clinical, electrophysiological, and genetic analysis of a family with two rare neuromuscular disorders: congenital myasthenic syndrome and hereditary polyneuropathy.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: April 03, 2024

Serum Sirtuin-1, HMGB1-TLR4, NF-KB and IL-6 Levels in Alzheimer's: The Relation Between Neuroinflammatory Pathway and Severity of Dementia.

Serum Sirtuin-1, HMGB1-TLR4, NF-KB and IL-6 Levels in Alzheimer's: The Relation Between Neuroinflammatory Pathway and Severity of Dementia.

Journal: Current Alzheimer research

Published: September 21, 2022

Four Turkish families with hyperekplexia: A missense mutation and the exon 1-7 deletion in the GLRA1 gene.

Four Turkish families with hyperekplexia: A missense mutation and the exon 1-7 deletion in the GLRA1 gene.

Journal: Parkinsonism & related disorders

Published: June 30, 2022

ADCY5 gene mutation: a case report.

ADCY5 gene mutation: a case report.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: March 05, 2022

Movement disorders in the early-diagnosed cerebrotendinous xanthomatosis: An electrophysiological study.

Movement disorders in the early-diagnosed cerebrotendinous xanthomatosis: An electrophysiological study.

Journal: Parkinsonism & related disorders

Published: August 08, 2020

Showing 1-10 of 10

Last Updated: 09/26/2026