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Lista de obras de Hakan Cetin

A homozygous AP3D1 missense variant in patients with sensorineural hearing loss as the leading manifestation

scientific article published in 2022

Associations between co-medications and survival in ALS-a cohort study from Austria

artículo científico publicado en 2015

Characterization of an anti-fetal AChR monoclonal antibody isolated from a myasthenia gravis patient.

artículo científico publicado en 2017

Epidemiology of Amyotrophic Lateral Sclerosis and Effect of Riluzole on Disease Course

scholarly article by Hakan Cetin et al published 2015 in Neuroepidemiology

Epidemiology of Multiple Sclerosis in Austria.

artículo científico

Epidemiology of myasthenia gravis in Austria: rising prevalence in an ageing society

artículo científico publicado en 2012

Genotype–phenotype correlations in valosin-containing protein disease: a retrospective muticentre study

scientific article published in 2022

Increased risk of death associated with the use of proton pump inhibitors in dementia patients and controls - a pharmacoepidemiological claims data analysis

artículo científico publicado en 2020

Iodinated contrast agents in patients with myasthenia gravis: a retrospective cohort study

artículo científico publicado en 2017

Multiple roles of integrin-α3 at the neuromuscular junction

artículo científico publicado en 2017

Muscle acetylcholine receptor conversion into chloride conductance at positive potentials by a single mutation

scientific article published on 30 September 2019

Myasthenia gravis AChR antibodies inhibit function of rapsyn-clustered AChRs

scientific article published on 12 March 2020

P03-013 - Symptomatic neuromuscular sarcoidosis.

artículo científico publicado en 2013

Rapsyn facilitates recovery from desensitization in fetal and adult acetylcholine receptors expressed in a muscle cell line

scientific article published on 17 June 2019

Serological and experimental studies in different forms of myasthenia gravis

artículo científico publicado en 2018

The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNA.

artículo científico publicado en 2016

The effect of early prednisolone treatment on the generalization rate in ocular myasthenia gravis.

artículo científico publicado en 2012