Search Results - "Kurt,Can Ebru"
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Functional exercise capacity evaluated by timed walk tests in myasthenia gravis
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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2
Cellular infiltrates in skin and sural nerve of patients with polyneuropathies
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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3
Identifying A Cut-Off Point for Timed Up and Go Test in Neuromuscular Diseases
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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4
Giant cell myositis associated with myasthenia gravis and thymoma
Published in Neurological sciences and neurophysiology (01-12-2019)Get full text
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5
Recent therapeutic developments in spinal muscular atrophy
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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6
Dysferlinopathy: A Case Report and Literature Update
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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7
Cutaneous activation of rage in nonsystemic vasculitic and diabetic neuropathy
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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8
Organelle Positioning in Neurons and Skeletal Muscle Cells
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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9
Psychosocial Adjustment and Adherence to Medication in Patients with Myasthenia Gravis
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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10
ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree
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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11
Two sisters with anti-MuSK-positive myasthenia gravis
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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12
The Activation of RAGE and NF-ΚB in Nerve Biopsies of Patients with Axonal and Vasculitic Neuropathy
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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13
Trigeminal sensory-motor neuropathy in a patient with mixed connective tissue disease and review of the literature
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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14
A Rare Cause of Dystonia: Spinal Meningioma
Published in Türk nöroloji dergisi (01-06-2021)Get full text
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15
Comprehensive clinical, biochemical, radiological and genetic analysis of 28 Turkish cases with suspected metachromatic leukodystrophy and their relatives
Published in Molecular genetics and metabolism reports (01-12-2020)“…Metachromatic leukodystrophy (MLD) is a glycosphingolipid storage disease caused by deficiency of the lysosomal enzyme arylsulfatase A (ASA) or its activator…”
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16
Reliability and Validity of Turkish Myasthenia Gravis-Activities of Daily Living Scale
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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17
Evaluation of Inflammatory and Glial Cell-related Biomarkers in Adults with Spinal Muscular Atrophy Under Nusinersen Treatment (P2-11.003)
Published in Neurology (09-04-2024)“…Abstract only…”
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Clinical and Laboratory Remission with Rituximab Treatment in anti-MuSK-positive Myasthenia Gravis Patients (P6-13.007)
Published in Neurology (03-05-2022)“…Abstract only…”
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Real-World Data of Nusinersen in Adults with Spinal Muscular Atrophy: A Single Center Experience (P5-13.009)
Published in Neurology (03-05-2022)“…Abstract only…”
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Nusinersen for adults with spinal muscular atrophy
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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