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Browsing Makale Koleksiyonu by Author "Asli Aksoy Gundogdu"

Now showing items 1-7 of 7

Autosomal Recessive Parkinson's Disease with Early-Onset in a Turkish Family

Zeynep Ozozen Ayas; Kotan Dündar, Dilcan; Asli Aksoy Gundogdu (GAZI UNIV, FAC MED, 2019)

Parkinson disease is a progressive, neurodegenerative disease with an increasing incidence of age. It is thought that genetic factors in etiology may be the underlying cause together with environmental factors. Sporadic ...
Diaphragm pacing system implanted in a patient with ALS

Kotan Dündar, Dilcan; Kamil Kaymak; Asli Aksoy Gundogdu (IOS PRESS, 2016)

The diaphragm pacing system (DPS) is a life quality improving operation in amyotrophic lateral sclerosis (ALS) patients who need mechanical ventilation or have chronic respiratory insufficiency. This procedure is gaining ...
Fabry Disease Diagnosis in a Young Stroke Patient: A Case Report

Asli Aksoy Gundogdu; Kotan Dündar, Dilcan; Murat Alemdar; Zeynep Ozozen Ayas (AVES, 2018)
Paroxysmal posterior variant alien hand syndrome associated with parietal lobe infarction: case presentation

Bekir Enes Demiryurek; Asli Aksoy Gundogdu; Acar, Bilgehan Atılgan; Alagöz, Aybala Neslihan (SPRINGER, 2016)

Alien hand syndrome (AHS) is an involuntary and rare neurological disorder emerges at upper extremity. AHS is a disconnection syndrome with the symptoms of losing sense of agency and sense of ownership, and presence of ...
Resolving speech disorders in Parkinson disease: our clinical experience with voice therapy.

Asli Aksoy Gundogdu; Ayse Oznur Akidil; Kotan Dündar, Dilcan (ALLIED ACAD, 2017)

Conclusions: We aimed to improve our understanding of the importance of non-motor symptoms of the PD such as voice and speech problems. Consistent with the literature, the current study suggests that LSVT is an effective ...
The Frequency of Fabry Disease among Young Cryptogenic Stroke Patients in the City of Sakarya

Asli Aksoy Gundogdu; Kotan Dündar, Dilcan; Murat Alemdar (ELSEVIER SCIENCE BV, 2017)

Background: Fabry disease (FD) is known as a rare cause of stroke. Recent studies suggested that FD is an underdiagnosed entity among young stroke patients. We aimed to investigate the frequency of FD in young cryptogenic ...
The spectrum of neurological manifestations of Fabry disease in alarge Turkish family with c.[680G > A] p.[R227Q]mutation

Asli Aksoy Gundogdu; Zeynep Ozozen Ayas; Murat Alemdar; Kotan Dündar, Dilcan (ASEAN NEUROLOGICAL ASSOC, 2017)

Conclusion: The clinical and genetic features of this large Turkish family with FD support an association between the neurological phenotype and the c.[680G> A] p.[R227Q] mutation. Since FD is treatable, it is recommended ...