Idiopathic Intracranial Hypertension: Diagnosis and Therapeutic Approach
Akçakaya, Nihan Hande, Akçakaya, Mehmet Osman, Sencer, Altay, Yapıcı, Zuhal
Published in Türk nöroloji dergisi (01.01.2017)
Published in Türk nöroloji dergisi (01.01.2017)
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Journal Article
Correlation of Prechtl Qualitative Assessment of General Movement Analysis with Neurological Evaluation: The Importance of Inspection in Infants
Akcakaya, Nihan Hande, Altunalan, Turgay, Doğan, Tuba Derya, Yılmaz, Arzu, Yapıcı, Zuhal
Published in Türk nöroloji dergisi (01.01.2019)
Published in Türk nöroloji dergisi (01.01.2019)
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Journal Article
Hypomyelinating spastic dyskinesia and ichthyosis caused by a homozygous splice site mutation leading to exon skipping in ELOVL1
Takahashi, Taiko, Mercan, Sevcan, Sassa, Takayuki, Akçapınar, Günseli Bayram, Yararbaş, Kanay, Süsgün, Seda, İşeri, Sibel Aylin Uğur, Kihara, Akio, Akçakaya, Nihan Hande
Published in Brain & development (Tokyo. 1979) (01.06.2022)
Published in Brain & development (Tokyo. 1979) (01.06.2022)
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Journal Article
Early developmental support for preterm infants based on exploratory behaviors: A parallel randomized controlled study
Altunalan, Turgay, Sarı, Zübeyir, Doğan, Tuba Derya, Hacıfazlıoğlu, Nilüfer Eldeş, Akman, İpek, Altıntaş, Tuğba, Uzer, Sevil, Akçakaya, Nihan Hande
Published in Brain and behavior (01.11.2023)
Published in Brain and behavior (01.11.2023)
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Journal Article
A new splice-site mutation in SLC12A6 causing Andermann syndrome with motor neuronopathy
Akçakaya, Nihan Hande, Yapıcı, Zuhal, Tunca, Ceren İskender, Tektürk, Pınar, Akçimen, Fulya, Başak, Ayşe Nazlı
Published in Journal of neurology, neurosurgery and psychiatry (01.10.2018)
Published in Journal of neurology, neurosurgery and psychiatry (01.10.2018)
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Journal Article
Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity
Mercan, Sevcan, Akcakaya, Nihan Hande, Salman, Baris, Yapici, Zuhal, Ozbek, Ugur, Ugur Iseri, Sibel Aylin
Published in Genes & genomics (2023)
Published in Genes & genomics (2023)
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Journal Article
A novel gene mutation in PANK2 in a patient with severe jaw-opening dystonia
Yapici, Zuhal, Akcakaya, Nihan Hande, Tekturk, Pinar, Iseri, Sibel Aylin Ugur, Ozbek, Ugur
Published in Brain & development (Tokyo. 1979) (01.09.2016)
Published in Brain & development (Tokyo. 1979) (01.09.2016)
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Journal Article
A Novel and Mosaic WDR45 Nonsense Variant Causes Beta-Propeller Protein-Associated Neurodegeneration Identified Through Whole Exome Sequencing and X chromosome Heterozygosity Analysis
Akçakaya, Nihan Hande, Salman, Barış, Görmez, Zeliha, Tarkan Argüden, Yelda, Çırakoğlu, Ayşe, Çakmur, Raif, Dönmez Çolakoğlu, Berril, Hacıhanefioğlu, Seniha, Özbek, Uğur, Yapıcı, Zuhal, Uğur İşeri, Sibel Aylin
Published in Neuromolecular medicine (01.03.2019)
Published in Neuromolecular medicine (01.03.2019)
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Journal Article
Clinical and genetic spectrum of an orphan disease MPAN: a series with new variants and a novel phenotype
Akçakaya, Nihan Hande, Haryanyan, Garen, Mercan, Sevcan, Sozer, Nejla, Ali, Asuman, Tombul, Temel, Ozbek, Ugur, Uğur İşeri, Sibel Aylin, Yapıcı, Zuhal
Published in Neurologia i neurochirurgia polska (01.01.2019)
Published in Neurologia i neurochirurgia polska (01.01.2019)
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Journal Article
Combined thalamic and pallidal deep brain stimulation in diabetic hemiballism/hemichorea
Ozturk, Onur, Akcakaya, Nihan Hande, Akcakaya, Mehmet Osman
Published in Neurocirugía (Asturias, Spain) (01.09.2024)
Published in Neurocirugía (Asturias, Spain) (01.09.2024)
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Journal Article