Search Results - "Kurt,Can Ebru"

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    Functional exercise capacity evaluated by timed walk tests in myasthenia gravis by Salci, Yeliz, Karanfil, Ecem, Balkan, Ayla Fil, Kütükçü, Ebru Çalik, Ceren, Ali Naim, Ayvat, Fatma, Bekircan‐Kurt, Can Ebru, Armutlu, Kadriye

    Published in Muscle & nerve (01-02-2019)
    “…ABSTRACT Introduction: We sought to evaluate the test–retest reliability and construct validity of the 6‐ and 2‐minute walk tests (6mWT and 2mWT, respectively)…”
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    Journal Article
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    Cellular infiltrates in skin and sural nerve of patients with polyneuropathies by Üçeyler, Nurcan, Braunsdorf, Silvia, Kunze, Ekkehard, Riediger, Nadja, Scheytt, Sarah, Divisova, Šarka, Bekircan‐kurt, Can Ebru, Toyka, Klaus Viktor, Sommer, Claudia

    Published in Muscle & nerve (01-06-2017)
    “…ABSTRACT Introduction The aim of this study was to determine the diagnostic usefulness of skin punch biopsies with emphasis on visualization and quantification…”
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    Identifying A Cut-Off Point for Timed Up and Go Test in Neuromuscular Diseases by Savcun Demirci, Cevher, Sütçü, Gülşah, Ayvat, Fatma, Onursal Kılınç, Özge, Doğan, Mert, Ayvat, Ender, Bekircan-Kurt, Can Ebru, Erdem-Özdamar, Sevim, Yıldırım, Sibel Aksu, Kılınç, Muhammed, Tan, Ersin

    Published in Türk nöroloji dergisi (01-03-2022)
    “…Objective: Balance problems and falls due to a progressive loss of muscle strength in neuromuscular diseases (NMD) negatively affect the activities of daily…”
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    Recent therapeutic developments in spinal muscular atrophy by Bora, Gamze, Ayşe, Yeşbek-Kaymaz, Can Ebru, Bekircan Kurt, Vildan Göknur, Haliloğlu, Haluk Aydın, Topaloğlu, Hayat, Erdem Yurter, Sevim, Erdem Özdamar

    Published in Turkish journal of medical sciences (30-04-2018)
    “…Proximal spinal muscular atrophy (SMA) is an inherited neurodegenerative disease with a heterogeneous clinical phenotype. Although there is no cure for SMA,…”
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    Dysferlinopathy: A Case Report and Literature Update by Orkide Kutlu, Can Ebru Bekircan Kurt, İbrahim Ünsal, Zeynep Arıbaş, Bilge Renkliyıldız, Hasan Eruzun, Ayşe Duran Karagülmez, Sevim Erdem Özdamar

    Published in İstanbul Medical Journal (01-12-2016)
    “…Dysferlinopathy is a rare autosomal recessive myopathy, resulting in the lack or absence of dysferlin production caused by mutations in the encoding gene…”
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    Cutaneous activation of rage in nonsystemic vasculitic and diabetic neuropathy by Bekircan-Kurt, Can Ebru, Üçeyler, Nurcan, Sommer, Claudia

    Published in Muscle & nerve (01-09-2014)
    “…ABSTRACT Introduction: We asked whether the receptor of advanced glycation end products (RAGE) is related to dermal inflammation in nonsystemic vasculitic…”
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    Organelle Positioning in Neurons and Skeletal Muscle Cells by Aksu Mengeş,Evrim, Kural Mangıt,Ecem, Kurt,Can Ebru, Bora,Gamze

    Published in Gazi tıp dergisi (22-05-2021)
    “…Organelles are dynamic compartments, whose spatial positions are tightly regulated for cellular functions. An increasing number of studies have shown…”
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    Psychosocial Adjustment and Adherence to Medication in Patients with Myasthenia Gravis by Aşiret,Güler Duru, Kapucu,Sevgisun, Türten Kaymaz,Tuğçe, Kurt,Can Ebru

    Published in Gazi tıp dergisi (01-07-2021)
    “…Objective: This descriptive study was conducted to determine psychosocial adjustment and adherence to medication of myasthenia gravis (MG) patients in two…”
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    ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree by Tunca, Ceren, Akçimen, Fulya, Coşkun, Cemre, Gündoğdu-Eken, Aslı, Kocoglu, Cemile, Çevik, Betül, Bekircan-Kurt, Can Ebru, Tan, Ersin, Başak, A Nazlı

    Published in European journal of human genetics : EJHG (01-05-2018)
    “…Amyotrophic lateral sclerosis (ALS) is a late-onset motor neuron disease with mostly dominant inheritance and a life expectancy of 2-5 years; however, a quite…”
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    Journal Article
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    Two sisters with anti-MuSK-positive myasthenia gravis by Kurt, Erdal, Bekircan-Kurt, Can Ebru, Konuşkan, Bahadır, Erkent, İrem, Tan, Ersin, Anlar, Banu

    Published in Clinical neurology and neurosurgery (01-07-2019)
    “…•Familial myasthenia gravis (MG) is very rare in anti-MuSK positive patients.•Here, two sisters with anti-MuSK positive MG were reported.•HLA DQB1*05 and…”
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    The Activation of RAGE and NF-ΚB in Nerve Biopsies of Patients with Axonal and Vasculitic Neuropathy by Bekircan-Kurt, Can Ebru, Tan, Ersin, Ozdamar, Sevim Erdem

    Published in Noro-Psikiyatri Arsivi (01-09-2015)
    “…Introduction: The receptor for advanced glycation end products (RAGE) is a pattern recognition receptor expressed in tissues and cells, which plays a role in…”
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    Trigeminal sensory-motor neuropathy in a patient with mixed connective tissue disease and review of the literature by Bekircan-Kurt, Can, Temuçin, Çağrı, Bilgen, Şule, Erdem-Ozdamar, Sevim

    Published in Neurological sciences and neurophysiology (01-07-2020)
    “…Trigeminal neuropathy is an infrequent condition, usually limited to the sensorial component of the nerve, and it is one of the most common neurologic…”
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    Reliability and Validity of Turkish Myasthenia Gravis-Activities of Daily Living Scale by Karanfil, Ecem, Salcı, Yeliz, Fil-Balkan, Ayla, Bekircan-Kurt, Can Ebru, Erdem Özdamar, Sevim, Armutlu, Kadriye

    Published in OTJR (Thorofare, N.J.) (01-04-2021)
    “…Linguistic, reliable, and valid secondary efficacy measures are important in clinical settings and studies. The aim of the study is to report test–retest…”
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    Nusinersen for adults with spinal muscular atrophy by Arslan, Doruk, Inan, Berin, Kilinc, Muhammed, Bekircan-Kurt, Can Ebru, Erdem-Ozdamar, Sevim, Tan, Ersin

    Published in Neurological sciences (01-07-2023)
    “…Introduction Nusinersen was effective in improving motor function and survival in infantile and childhood-onset spinal muscular atrophy (SMA), and the value of…”
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