Search Results - "Karasoy, Hatice"

Stock Market's Assessment of Monetary Policy Transmission: The Cash Flow Effect by GÜRKAYNAK, REFET, KARASOY‐CAN, HATİCE GÖKÇE, LEE, SANG SEOK

“…ABSTRACT We show that firm liability structure and associated cash flows matter for firm behavior and that financial market participants price stocks…”
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The Explanatory Power and the Forecast Performance of Consumer Confidence Indices for Private Consumption Growth in Turkey by Karasoy Can, Hatice Gökçe, Yüncüler, Çağlar

“…In this study, we assess empirically whether consumer confidence indices contain information about future private consumption growth in Turkey. To this end, we…”
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Vestibular impairment in Charcot–Marie–Tooth disease by Akdal, Gülden, Koçoğlu, Koray, Tanrıverdizade, Tural, Bora, Elçin, Bademkıran, Fikret, Yüceyar, Ayşe Nur, Ekmekçi, Özgül, Şengün, İhsan Şükrü, Karasoy, Hatice

“…Objective To find out if Charcot–Marie–Tooth (CMT) patients, who have peripheral vestibular as well as peripheral somatosensory impairment, have worse postural…”
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Presence of Concomitant Depression and its Effect on Clinical Course in Patients Diagnosed with Myasthenia Gravis by Çetin, Fatma Ece, Karasoy, Hatice

“…Objective: Myasthenia gravis (MG) is a chronic autoimmune disease with fluctuating non-specific symptoms, and symptoms are exacerbated by stress. Many…”
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Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy by Böhm, Johann, Biancalana, Valérie, DeChene, Elizabeth T., Bitoun, Marc, Pierson, Christopher R., Schaefer, Elise, Karasoy, Hatice, Dempsey, Melissa A., Klein, Fabrice, Dondaine, Nicolas, Kretz, Christine, Haumesser, Nicolas, Poirson, Claire, Toussaint, Anne, Greenleaf, Rebecca S., Barger, Melissa A., Mahoney, Lane J., Kang, Peter B., Zanoteli, Edmar, Vissing, John, Witting, Nanna, Echaniz-Laguna, Andoni, Wallgren-Pettersson, Carina, Dowling, James, Merlini, Luciano, Oldfors, Anders, Bomme Ousager, Lilian, Melki, Judith, Krause, Amanda, Jern, Christina, Oliveira, Acary S. B., Petit, Florence, Jacquette, Aurélia, Chaussenot, Annabelle, Mowat, David, Leheup, Bruno, Cristofano, Michele, Poza Aldea, Juan José, Michel, Fabrice, Furby, Alain, Llona, Jose E. Barcena, Van Coster, Rudy, Bertini, Enrico, Urtizberea, Jon Andoni, Drouin-Garraud, Valérie, Béroud, Christophe, Prudhon, Bernard, Bedford, Melanie, Mathews, Katherine, Erby, Lori A. H., Smith, Stephen A., Roggenbuck, Jennifer, Crowe, Carol A., Brennan Spitale, Allison, Johal, Sheila C., Amato, Anthony A., Demmer, Laurie A., Jonas, Jessica, Darras, Basil T., Bird, Thomas D., Laurino, Mercy, Welt, Selman I., Trotter, Cynthia, Guicheney, Pascale, Das, Soma, Mandel, Jean-Louis, Beggs, Alan H., Laporte, Jocelyn

“…Centronuclear myopathy (CNM) is a genetically heterogeneous disorder associated with general skeletal muscle weakness, type I fiber predominance and atrophy,…”
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Mitochondrial Membrane Protein-associated Neurodegeneration: Two Adult Cases with Different Clinical Presentation by Aykaç, Şeyma, Karakaya, Hanife, Uludağ, Burhanettin, Karasoy, Hatice

“…Neurodegeneration with brain iron accumulation is a clinically and genetically heterogeneous group of diseases. Mitochondrial membrane protein-associated…”
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Corporate debt, repayment and maturity structure, and monetary policy transmission by Karasoy Can, Hatice Gökçe

“…Abstract This article develops a stylized New Keynesian Dynamic Stochastic General Equilibrium model and explores the function of the repayment and maturity…”
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An integrated diagnosis strategy for congenital myopathies by Böhm, Johann, Vasli, Nasim, Malfatti, Edoardo, Le Gras, Stéphanie, Feger, Claire, Jost, Bernard, Monnier, Nicole, Brocard, Julie, Karasoy, Hatice, Gérard, Marion, Walter, Maggie C, Reilich, Peter, Biancalana, Valérie, Kretz, Christine, Messaddeq, Nadia, Marty, Isabelle, Lunardi, Joël, Romero, Norma B, Laporte, Jocelyn

“…Congenital myopathies are severe muscle disorders affecting adults as well as children in all populations. The diagnosis of congenital myopathies is…”
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Effects of comorbid diseases on clinical outcomes in patients with myasthenia gravis by Ozdemir, Huseyin Nezih, Karasoy, Hatice, Yuceyar, Ayse Nur, Ekmekci, Ozgul

“…Background This cross-sectional study was undertaken to evaluate the existence and distribution of comorbid disorders among myasthenia gravis (MG) patients…”
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Presence of Concomitant Depression and its Effect on Clinical Course in Patients Diagnosed with Myasthenia Gravis/Myastenia Gravis Tanili Hastalarda Hastaliga Eslik Eden Depresyonun Varligi ve Klinik Seyre Etkisi by Cetin, Fatma Ece, Karasoy, Hatice

“…Objective: Myasthenia gravis (MG) is a chronic autoimmune disease with fluctuating non-specific symptoms, and symptoms are exacerbated by stress. Many…”
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DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability by Köroğlu, Çiğdem, Baysal, Leyla, Cetinkaya, Murat, Karasoy, Hatice, Tolun, Aslhan

“…Abstract Familial parkinson's disease is both clinically and genetically heterogeneous. By mapping the disease locus with a lod score of 5.13 to a  < 3.5 Mbp…”
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Mitochondrial Membrane Protein-associated Neurodegeneration: Two Adult Cases with Different Clinical Presentation/Mitokondriyal Membran Protein-iliskili Nörodejenerasyon; Farkli Klinik Prezentasyonlu Iki Yetiskin Olgu by Aykaç, Seyma, Karakaya, Hanife, Uludag, Burhanettin, Karasoy, Hatice

“…Neurodegeneration with brain iron accumulation is a clinically and genetically heterogeneous group of diseases. Mitochondrial membrane protein-associated…”
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Homozygous MYH7 R1820W mutation results in recessive myosin storage myopathy: Scapuloperoneal and respiratory weakness with dilated cardiomyopathy by Yüceyar, Nur, Ayhan, Özgecan, Karasoy, Hatice, Tolun, Aslıhan

“…Highlights • Our research family with MSM is the second family with recessive MYH7 mutation. • We identified a homozygous missense mutation in MYH7 exon 37. •…”
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Turkish Neurology Board Examinations: 2004-2008 by Ayhan Çalışkan, Tülay Kansu, Şerefnur Öztürk, Nilgun Araç, Sevin Balkan, İbrahim Bora, Canan Aykut Bingöl, Ufuk Can, Feza Deymeer, Muhteşem Gedizlioglu, Zeki Gökçil, Hatice Karasoy

“…This study aims to describe planning, application and the results of Turkish Neurology Board Examinations. Data was collected from five Board Examination…”
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Juvenile myasthenia gravis: Comparison of pre and postpubertal cases by Ekmekci, Ozgul, Karasoy, Hatice, Yuceyar, Ayse Nur

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Genotype–phenotype correlation in seven motor neuron disease families with novel ALS2 mutations by Sprute, Rosanne, Jergas, Hannah, Ölmez, Akgün, Alawbathani, Salem, Karasoy, Hatice, Dafsari, Hormos Salimi, Becker, Kerstin, Daimagüler, Hülya‐Sevcan, Nürnberg, Peter, Muntoni, Francesco, Topaloglu, Haluk, Uyanik, Gökhan, Cirak, Sebahattin

“…Autosomal‐recessive mutations in the Alsin Rho guanine nucleotide exchange factor (ALS2) gene may cause specific subtypes of childhood‐onset progressive…”
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Vestibular impairment in chronic inflammatory demyelinating polyneuropathy by Akdal, Gülden, Tanrıverdizade, Tural, Şengün, İhsan, Bademkıran, Fikret, Koçoğlu, Koray, Yüceyar, Ayşe Nur, Ekmekçi, Özgül, Karasoy, Hatice, Halmágyi, G. Michael

“…Chronic inflammatory demyelinating polyneuropathy (CIDP) is a common, treatable, autoimmune peripheral neuropathy considered to produce imbalance by weakness…”
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The decision-making levels of urine tetrasaccharide for the diagnosis of Pompe disease in the Turkish population by Canbay, Erhan, Vural, Melisa, Kalkan Uçar, Sema, Sezer, Ebru Demirel, Karasoy, Hatice, Yüceyar, Ayşe Nur, Çoker, Mahmut, Sözmen, Eser Yildirim

“…Background Recently, urinary excretion of the tetrasaccharide 6-α-D-glucopyranosyl-maltotriose (Glc4) has been proposed as a marker for the diagnosis and…”
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Myasthenia gravis and thymoma coexisting with myotonic dystrophy type 1 by Ekmekci, Ozgul, Karasoy, Hatice, Bademkiran, Fikret, Akkus, Dilek Evyapan, Yuceyar, Nur

“…Abstract We describe a 34-year old man presenting with subacute generalized myasthenic symptoms. His clinical features and laboratory investigations…”
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Idiopathic Hypereosinophilic Syndrome as a Rare Cause of Stroke: A Case Report/Inmenin Nadir Bir Nedeni, Idiyopatik Hipereozinofilik Sendrom: Olgu Sunumu by Aykaç, Seyma, Karakaya, Hanife, Uludag, Burhanettin, Turgut, Hatice Karasoy Esra, Alpua, Murat, Yalçin, Selim, Coskun, Oya, Bilgili, Mirace Yasemin Karadeniz, Açikgöz, Ergin Ayaslioglu, Coskun, Özlem

“…Hypereosinophilic syndrome (HES) is a rare hematological disease that causes organ damage by eosinophil infiltration in the tissue with increased eosinophil…”
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