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Nihan Hande Akçakaya

Observed names: AKÇAKAYA, NİHAN HANDE, H. Akcakaya, Hande Akcakaya, N. Akcakaya, N. Akçakaya, N. H. Akcakaya, N.H. Akcakaya, N.H. Akçakaya, Nihade Akçakaya, Nihan H. Akçakaya, Nihan Hande Akcakaya, NİHAN HANDE AKÇAKAYA
Observed institutions: Koç University, Istanbul Florence Nightingale Hospital, Istanbul University-Cerrahpaşa, Ministry of Justice, Adli Tıp Kurumu, Turkish Ophthalmological Association, Maltepe University, Istanbul University
ORCID: 0000-0001-8414-4017
Observed ORCID: 0000-0001-8414-4017
OpenAlex ID: A5028482177
Psychological problems in turkish asthmatic children and their families
2003 · N. Akçakaya, M. Aydogğan, et al. · Allergologia et Immunopathologia · 27
Hypomyelinating spastic dyskinesia and ichthyosis caused by a homozygous splice site mutation leading to exon skipping in ELOVL1
2022 · Taiko Takahashi, Sevcan Mercan, et al. · Brain and Development · 25
Clinical and genetic features of PKAN patients in a tertiary centre in Turkey
2017 · Nihan Hande Akcakaya, Sibel Ugur Iseri, et al. · Clinical Neurology and Neurosurgery · 20
Early developmental support for preterm infants based on exploratory behaviors: A parallel randomized controlled study
2023 · Turgay Altunalan, Zübeyir Sarı, et al. · Brain and Behavior · 14
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A Novel and Mosaic WDR45 Nonsense Variant Causes Beta-Propeller Protein-Associated Neurodegeneration Identified Through Whole Exome Sequencing and X chromosome Heterozygosity Analysis
2019 · Nihan Hande Akçakaya, Barış Salman, et al. · NeuroMolecular Medicine · 10
Clinical and genetic spectrum of an orphan disease MPAN: a series with new variants and a novel phenotype
2019 · Nihan Hande Akçakaya, Garen Haryanyan, et al. · Neurologia i Neurochirurgia Polska · 9
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De novo 8p23.1 deletion in a patient with absence epilepsy
2017 · Nihan Hande Akcakaya, Özlem Yalcin Capan, et al. · Epileptic Disorders · 9
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A Case of Leukoencephalopathy and Small Vessels Disease Caused by a Novel HTRA1 Homozygous Mutation
2019 · Tuncay Gündüz, Yasemin Demirkol, et al. · Journal of Stroke and Cerebrovascular Diseases · 8
Idiopathic Intracranial Hypertension: Diagnosis and Therapeutic Approach
2017 · Nihan Hande Akçakaya, Mehmet Osman Akçakaya, et al. · Turkish Journal Of Neurology · 8
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A novel gene mutation in PANK2 in a patient with severe jaw-opening dystonia
2016 · Zuhal Yapici, Nihan Hande Akcakaya, et al. · Brain and Development · 8
Correlation of Prechtl Qualitative Assessment of General Movement Analysis with Neurological Evaluation: The Importance of Inspection in Infants
2019 · Nihan Hande Akcakaya, Turgay Altunalan, et al. · Turkish Journal Of Neurology · 7
Life-threatening parkinsonism-hyperpyrexia syndrome following bilateral deep brain stimulation of the subthalamic nucleus
2017 · Mehmet Osman Akçakaya, Nihan Hande Akçakaya, et al. · Neurologia i Neurochirurgia Polska · 7
Atypical enterovirus encephalitis causing behavioral changes and autism-like clinical manifestations: case report
2016 · Nihan Hande Akcakaya, Pinar Tekturk, et al. · Acta Neurologica Belgica · 6
Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey
2020 · Nihan H. Akçakaya, Burçak Özeş Ak, et al. · Neurologia i Neurochirurgia Polska · 5
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Quantitative Iron Measurements in the Basal Ganglia of NBIA Patients Using QSM : Insights From a Tertiary Center
2025 · Özge Uygun, Alpay Özcan, et al. · Annals of Clinical and Translational Neurology · 4
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A new splice-site mutation in SLC12A6 causing Andermann syndrome with motor neuronopathy
2017 · Nihan Hande Akçakaya, Zuhal Yapıcı, et al. · Journal of Neurology Neurosurgery & Psychiatry · 4
Primary Intracranial Abscess localized in the Basal Ganglia: A Case Report
2011 · O. Kilic, A. Kafadar, et al. · Journal of Tropical Pediatrics · 4
Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity
2022 · Sevcan Mercan, Nihan Hande Akcakaya, et al. · Genes & Genomics · 3
Two cases with mitochondrial membrane protein-associated neurodegeneration: genetic features and long-term clinical follow-up
2022 · Sevcan Mercan, Sibel Aylin Ugur Iseri, et al. · Neurocase · 3
The Differential Diagnosis of “Tigroid Pattern” on Brain Magnetic Resonance Imaging: A Case Report
2019 · Nihan Hande Akcakaya · Turkish Journal Of Neurology · 3
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Differential Diagnosis Approach to Bilateral Peripheral Facial Paralysis: A Case Report
2016 · Nihan Hande Akçakaya, Meltem Hale Alpsan Gökmen, et al. · Turkish Journal Of Neurology · 3
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P103 – 2340: Atypical enterovirus encephalitis causing behavioral changes and autism-like clinical manifestations: Case report
2015 · H. Akcakaya, P. Tekturk, et al. · European Journal of Paediatric Neurology · 3
Essential tremor: Family-based sequencing suggests involvement of neuronal and metabolic pathways
2026 · Agharza Aghayev, Melda Erdoğdu, et al. · Parkinsonism & Related Disorders · 2
From clinical observation to experimental validation: Investigating the neurotoxic impact of dimethylacetamide
2026 · Hizir Asliyuksek, Nihan Hande Akcakaya, et al. · NeuroToxicology · 2
A case with CMTX1 disease showing transient ischemic-attack-like episodes
2017 · Zehra Aktan, Nihan Hande Akcakaya, et al. · Neurologia i Neurochirurgia Polska · 2
Works count: 45
Citation count: 201
H-index: 8
I10-index: 5
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