Search Results - "GURVIT, Hakan"

The interleukin 1 alpha, interleukin 1 beta, interleukin 6 and alpha-2-macroglobulin serum levels in patients with early or late onset Alzheimer's disease, mild cognitive impairment or Parkinson's disease by Dursun, Erdinç, Gezen-Ak, Duygu, Hanağası, Haşmet, Bilgiç, Başar, Lohmann, Ebba, Ertan, Sibel, Atasoy, İrem L, Alaylıoğlu, Merve, Araz, Ömür Selin, Önal, Burak, Gündüz, Ayşegül, Apaydın, Hülya, Kızıltan, Güneş, Ulutin, Turgut, Gürvit, Hakan, Yılmazer, Selma

“…Abstract Alzheimer's disease (EOAD, LOAD), mild cognitive impairment (MCI), Parkinson's disease (PD) and healthy controls were included to determine the serum…”
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Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement by Guerreiro, Rita João, Lohmann, Ebba, Brás, José Miguel, Gibbs, Jesse Raphael, Rohrer, Jonathan D, Gurunlian, Nicole, Dursun, Burcu, Bilgic, Basar, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat, Singleton, Andrew, Hardy, John

“…To identify new genes and risk factors associated with frontotemporal dementia (FTD). Several genes and loci have been associated with different forms of FTD,…”
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A novel PNPLA6 mutation in a Turkish family with intractable Holmes tremor and spastic ataxia by Emekli, Ahmed S., Samanci, Bedia, Şimşir, Gülşah, Hanagasi, Hasmet A., Gürvit, Hakan, Bilgiç, Başar, Başak, A. Nazlı

“…Autosomal recessive cerebellar ataxias are a group of rare neurological diseases with a genetic origin. Recently, the mutations in the PNPLA6 gene were…”
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BDNF, TNFα, HSP90, CFH, and IL-10 serum levels in patients with early or late onset Alzheimer's disease or mild cognitive impairment by Gezen-Ak, Duygu, Dursun, Erdinç, Hanağası, Haşmet, Bilgiç, Başar, Lohman, Ebba, Araz, Ömür Selin, Atasoy, Irem L, Alaylıoğlu, Merve, Önal, Burak, Gürvit, Hakan, Yılmazer, Selma

“…Identifying early-detection biomarkers have become an increasingly important approach in the treatment and prevention of Alzheimer's disease (AD). In this…”
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Cognitive deficits and cortical volume loss in COVID-19-related hyposmia by Gezegen, Haşim, Ay, Ulaş, Samancı, Bedia, Kurt, Elif, Yörük, Sanem Sultan, Medetalibeyoğlu, Alpay, Şen, Cömert, Şahin, Erdi, Barbüroğlu, Mehmet, Doğan, Faruk Uğur, Bilgiç, Başar, Hanağası, Haşmet, Gürvit, Hakan

“…Studies have found that up to 73% of COVID-19 patients experience hyposmia. It is unclear if the loss of smell in COVID-19 is due to damage to the peripheral…”
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Eating Difficulties and Relationship With Nutritional Status Among Patients With Dementia by CILIZ, Ozlem, TULEK, Zeliha, HANAGASI, Hasmet, BILGIC, Basar, GURVIT, I. Hakan

“…Background: One of the most common behavioral problems in patients with dementia is eating problems, which are known to increase the risk of malnutrition…”
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Resting-state fMRI analysis in apathetic Alzheimer's disease by Büyükgök, Deniz, Bayraktaroğlu, Zübeyir, Buker, H Seda, Kulaksızoğlu, M Işın Baral, Gurvit, İ Hakan

“…Diagnosis of comorbid psychiatric conditions are a significant determinant for the prognosis of neurodegenerative diseases. Apathy, which is a behavioral…”
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Elevated sTREM2 and NFL levels in patients with sepsis associated encephalopathy by Orhun, Günseli, Esen, Figen, Yilmaz, Vuslat, Ulusoy, Canan, Şanlı, Elif, Yıldırım, Elif, Gürvit, Hakan, Ergin Özcan, Perihan, Sencer, Serra, Bebek, Nerses, Tüzün, Erdem

“…Sepsis-associated encephalopathy (SAE) is a common manifestation of sepsis that may lead to cognitive decline. Our aim was to investigate whether the…”
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A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-Saguenay by Samanci, Bedia, Gokalp, Ebru Erzurumluoglu, Bilgic, Basar, Gurvit, Hakan, Artan, Sevilhan, Hanagasi, Hasmet A.

“…Loss-of-function mutations in the sacsin (SACS) gene lead to autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), impairing the function of…”
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Neurological features and outcomes of Wilson’s disease: a single-center experience by Samanci, Bedia, Sahin, Erdi, Bilgic, Basar, Tufekcioglu, Zeynep, Gurvit, Hakan, Emre, Murat, Demir, Kadir, Hanagasi, Hasmet A.

“…Wilson’s disease (WD) is an autosomal recessive genetic disorder of copper metabolism, and WD patients can present with neurologic symptoms. We aimed to report…”
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TREM2 variants as a possible cause of frontotemporal dementia with distinct neuroimaging features by Samanci, Bedia, Bilgiç, Başar, Gelişin, Özlem, Tepgeç, Fatih, Guven, Gamze, Tüfekçioğlu, Zeynep, Alaylıoğlu, Merve, Hanagasi, Hasmet A., Gürvit, Hakan, Guerreiro, Rita, Hardy, John, Emre, Murat

“…Background and purpose Nasu–Hakola disease (NHD) is a rare, autosomal recessive disorder characterized by skeletal and neurological symptoms. Behavioral…”
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Verbal and Nonverbal Memory in Neurodegenerative and Stroke Aphasia: Evidence From the Turkish Version of the Three Words Three Shapes Test by Seckin, Mustafa, Özbek, Begüm, Demir, İlayda, Kurt, Elif, Ay, Ulaş, Yildirim, Düzgün, Yeşilot, Nilüfer, Çoban, Oğuzhan, Öktem, Öget, Gürvit, Hakan

“…Although language impairment is the most salient feature of cognitive impairment in both primary progressive aphasia (PPA) and stroke aphasia (SA), memory can…”
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Peripheral TREM2 mRNA levels in early and late-onset Alzheimer disease’s patients by Guven, Gamze, Bilgic, Basar, Samanci, Bedia, Gurvit, Hakan, Hanagasi, Hasmet, Donmez, Cagla, Aslan, Rukiye, Lohmann, Ebba, Erginel-Unaltuna, Nihan

“…‘ Triggering receptor expressed on myeloid cells 2 ’ ( TREM2 ) gene is involved in Alzheimer’s disease (AD) and TREM2 mRNA expression is known to be increased…”
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Laboratory and clinical correlates of brain atrophy in Neuro-Behçet's disease by Gündüz, Tuncay, Kürtüncü, Murat, Matur, Zeliha, Tüzün, Erdem, Limon, Utku, Tanyıldız, Burak, İzgi, Belgin, Erdoğan, Nergis, Öge, Ali Emre, Gürvit, Hakan, Bilgiç, Başar, Akman-Demir, Gülşen

“…Diagnostic evaluation of patients with parenchymal Neuro-Behçet's disease (NBD) requires magnetic resonance imaging (MRI), neuro-ophthalmologic, and…”
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A new F-box protein 7 gene mutation causing typical Parkinson's disease by Lohmann, Ebba, Coquel, Anne-Sophie, Honoré, Aurélie, Gurvit, Hakan, Hanagasi, Hasmet, Emre, Murat, Leutenegger, Anne L., Drouet, Valérie, Sahbatou, Mourad, Guven, Gamze, Erginel-Unaltuna, Nihan, Deleuze, Jean-Francois, Lesage, Suzanne, Brice, Alexis

“…Background Recessive mutations in the F‐box protein 7 gene (FBXO7; PARK15) have been identified as a cause of the parkinsonian‐pyramidal syndrome. Here, we…”
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Genetic variants of vitamin D metabolism-related DHCR7/NADSYN1 locus and CYP2R1 gene are associated with clinical features of Parkinson's disease by Alaylıoğlu, Merve, Dursun, Erdinç, Genç, Gençer, Şengül, Büşra, Bilgiç, Başar, Gündüz, Ayşegül, Apaydın, Hülya, Kızıltan, Güneş, Gürvit, Hakan, Hanağası, Haşmet, Öztop Çakmak, Özgür, Ertan, Sibel, Yılmazer, Selma, Gezen-Ak, Duygu

“…Parkinson's disease (PD) is the second most common neurodegenerative disorder. Vitamin D deficiency is suggested to be related to PD. A genome-wide association…”
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The applicability of new screening instruments for cognitive impairment in parkinson's disease in turkey by Gurvit, Hakan I, Selvitop, Rabia

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Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review by Atasu, Burcu, Acarlı, Ayse Nur Ozdag, Bilgic, Basar, Baykan, Betül, Demir, Erol, Ozluk, Yasemin, Turkmen, Aydin, Hauser, Ann-Kathrin, Guven, Gamze, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat, Gasser, Thomas, Lohmann, Ebba

“…Biallelic pathogenic variants in the SCARB2 gene have been associated with action myoclonus-renal failure (AMRF) syndrome. Even though SCARB2 associated…”
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Comparison of epidural analgesia combined with general anesthesia and general anesthesia for postoperative cognitive dysfunction in elderly patients by Orhun, Günseli, Sungur, Zerrin, Koltka, Kemalettin, Savran Karadeniz, Meltem, Yavru, Hacer Ayşe, Gürvit, Hakan, Şentürk, Mert

“…Cognitive dysfunction in the early postoperative course is common for the elderly population. Anesthetic management may affect postoperative cognitive decline…”
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Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients by Guven, Gamze, Lohmann, Ebba, Bras, Jose, Gibbs, J Raphael, Gurvit, Hakan, Bilgic, Basar, Hanagasi, Hasmet, Rizzu, Patrizia, Heutink, Peter, Emre, Murat, Erginel-Unaltuna, Nihan, Just, Walter, Hardy, John, Singleton, Andrew, Guerreiro, Rita

“…'Microtubule-associated protein tau' (MAPT), 'granulin' (GRN) and 'chromosome 9 open reading frame72' (C9ORF72) gene mutations are the major known genetic…”
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