Search Results - "Gökhan Çetin"

Gyroscopic precession control for maneuvering two‐wheeled robot recoil stabilization by Çetin, Gökhan, Ünker, Faruk

“…A two‐wheeled robot has high maneuverability and can spin around with a high velocity but is prone to roll over under a recoil force. Because the wheels are…”
Get full text

A novel mutation in SLURP1 in patients with Mal de Meleda from Turkey by İmren, Işıl Göğem, Ertürk, Sevilay, Çetin, Gökhan Ozan, Kaçar, Nida

Get full text

Early onset disease, anarthria, areflexia, and dystonia can be the distinctive features of SPG64, a very rare form of hereditary spastic paraplegias by Ölmez, Akgün, Çetin, Gökhan Ozan, Karaer, Kadri

“…Hereditary spastic paraplegias (HSP) are a group of inherited, neurodegenerative disorders characterized by progressive gait impairment, lower extremity…”
Get full text

Resilient active seismic response control of structural systems by Çetin, Gökhan, Fadali, Mohammed S, Pekcan, Gökhan

“…This paper proposes a dissipative resilient observer and controller (DROC) design for a network controlled system (NCS) that handles faults, implementation…”
Get full text

Expanding the clinical and molecular features of tricho-rhino-phalangeal syndrome with a novel variant by Öztürk, Nuray, Karamık, Gökcen, Mutlu, Hatice, Bayer, Öznur Yılmaz, Mıhçı, Ercan, Çetin, Gökhan Ozan, Nur, Banu

“…Tow bone mineral density (BMD) was identified in two TRPS2 family members presenting with bone fracture, and growth hormone deficiency was detected in two…”
Get full text

Expanding the clinical and molecular features of trichorhino- phalangeal syndrome with a novel variant by Öztürk, Nuray, Karamık, Gökcen, Mutlu, Hatice, Bayer, Öznur Yılmaz, Mıhçı, Ercan, Çetin, Gökhan Ozan, Nur, Banu

“…Background. Tricho-rhino-phalangeal syndrome (TRPS) is a rare, autosomal dominant disorder characterized by typical craniofacial features, ectodermal and…”
Get full text

Diagnostic and Management Strategies of Bietti Crystalline Dystrophy: Current Perspectives by Saatci, Ali Osman, Ataş, Ferdane, Çetin, Gökhan Ozan, Kayabaşı, Mustafa

“…Bietti crystalline dystrophy (BCD) is a rare, genetically determined chorioretinal dystrophy presenting with intraretinal crystalline deposits and varying…”
Get full text

Analyzing Peak Clipping for Load Factor Improvement: Real Case Studies of a Solar Power Plant in a University Campus by Osman Demirci, Emir Kaan Tutuş, Sezai Taşkın, Gökhan Çetin, Macit Tozak

Get full text

A novel nonsense mutation in CHST3 in a Turkish patient with spondyloepiphyseal dysplasia, Omani type by Albuz, Burcu, Çetin, Gökhan Ozan, Özhan, Bayram, Sarikepe, Bilge, Anlaş, Özlem, Öztürk, Menekşe, Zeybek, Selcan, Sabir, Nuran, Bağci, Gülseren, Semerci Gündüz, Cavidan Nur

Get full text

Terminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocation by Bağcı, Gülseren, Çetin, Gökhan Ozan, Semerci, Nur, Toruner, Gokce A., Cinbiş, Mine

“…Terminal deletions of chromosome 14q are very rarely reported. Schneider et al. (2008) reviewed about 20 cases of 14q32 region deletion in a previous article…”
Get full text

An unusual cause of OptiVol alarm: increased intra-abdominal pressure associated with irritable bowel syndrome by Türkoğlu, Cengizhan, Aliyev, Farid, Celiker, Cengiz, Cetin, Gökhan

“…Monitoring intrathoracic impedance has become an integral part of follow-up of patients with implantable cardioverter defibrillator (ICD) or cardiac…”
Get full text

OTEL YÖNETİCİLERİNİN KARAR VERME YAKLAŞIMLARININ İNCELENMESİ: DÜZCE VE BOLU İLİ OTELLERİNE YÖNELİK BİR ARAŞTIRMA by Ağraş, Süleyman, Çetin, Gökhan

“…Bu çalışmanın amacı, otel yöneticilerinin karar verme yaklaşımlarının incelenmesidir. Araştırma kapsamını Bolu ve Düzce illerinde faaliyet gösteren 3, 4 ve 5…”
Get full text

A case of recombinant chromosome 4: further delineation of the clinical features by ANLAŞ, Özlem, ÇETİN, Gökhan Ozan, YARARBAŞ, Kanay, DÜZCAN, Füsun, Cavidan Nur SEMERCİ GÜNDÜZ, AYAZ, Akif, BAĞCI, Gülseren

“…Recombinant chromosome 4 is a very rare chromosomal aberration with eleven cases reported in the literature up to date. Here we report a five years old male…”
Get full text

Optimization of Repolarization during Biventricular Pacing: A New Target in Patients with Biventricular Devices? by Türkoğlu, Cengizhan, Aliyev, Farid, Çeliker, Cengiz, Çetin, Gökhan, Alici, Gökhan, Uzunhasan, Işil, Firatli, Inci

“…Background: Evaluation of repolarization during sequentional biventricular pacing. Methods: Patients with biventricular devices, and left ventricular leads…”
Get full text

Optimal resource allocation in networked control systems by Cetin, Gokhan, Fadali, M. Sami, Xu, Hao

“…This study proposes an optimal bandwidth allocation algorithm for a Networked Control System (NCS) that includes a time‐driven sensor, event‐driven controller…”
Get full text

Face and Speech Recognition on Field Programmable Gate Array by Çetin, Gökhan

“…Biometric recognition can be defined as automatic recognition of person based on one or more personal traits. Face and speech recognition occupies an important…”
Get full text

Expanding the clinical and molecular features of trichorhino- phalangeal syndrome with a novel variant by Öztürk, Nuray, Karamık, Gökcen, Mutlu, Hatice, Bayer, Öznur Yılmaz, Mıhçı, Ercan, Çetin, Gökhan Ozan, Nur, Banu

“…Tricho-rhino-phalangeal syndrome (TRPS) is a rare, autosomal dominant disorder characterized by typical craniofacial features, ectodermal and skeletal…”
Get more information

Early onset disease, anarthria, areflexia, and dystonia can be the distinctive features of SPG64, a very rare form of hereditary spastic paraplegias by Ölmez, Akgün, Çetin, Gökhan Ozan, Karaer, Kadri

Get full text

Vascular endothelial growth factor gene polymorphisms in age-related macular degeneration in a Turkish population by Bulgu, Yunus, Cetin, Gokhan Ozan, Caner, Vildan, Cetin, Ebru Nevin, Yaylali, Volkan, Yildirim, Cem

“…AIM:To assess the association between age-related macular degeneration(AMD) and three single nucleotide polymorphisms(SNPS) related to the vascular endothelial…”
Get full text

Vascular endothelial growth factor gene polymorphisms in age-related macular degeneration in a Turkish population by Bulgu, Yunus, Cetin, Gokhan Ozan, Caner, Vildan, Cetin, Ebru Nevin, Yaylali, Volkan, Yildirim, Cem

“…AIMTo assess the association between age-related macular degeneration (AMD) and three single nucleotide polymorphisms (SNPs) related to the vascular…”
Get full text