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D Kemlink

Showing results (11-20 of 17) with videos related to

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European Journal of Neurology|June 17, 2010
Sleep disorders in Wilson's diseaseS Nevsimalova, J Buskova, R Bruha, et al.
Prague Medical Report|June 25, 2009
Advanced oxidation protein products in obstructive sleep apneaK Sonka, L Fialová, J Volná, et al.
Sleep Medicine|May 22, 2012
Restless legs syndrome in Czech patients with multiple sclerosis: an epidemiological and genetic studyJ Vávrová, D Kemlink, K Sonka, et al.
Sleep Medicine|May 14, 2020
Comparative study of the substantia nigra echogenicity and <sup>123</sup>I-Ioflupane SPECT in patients with synucleinopathies with and without REM sleep behavior disorderJ Mašková, D Školoudík, P Štofaniková, et al.
Clinical Genetics|September 2, 2017
Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's diseaseB Schormair, D Kemlink, B Mollenhauer, et al.
Journal of Medical Genetics|March 13, 2009
Replication of restless legs syndrome loci in three European populationsD Kemlink, O Polo, B Frauscher, et al.
Resuscitation|July 19, 2024
EEG for good outcome prediction after cardiac arrest: A multicentre cohort studyS Turella, J Dankiewicz, N Ben-Hamouda, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
European Journal of Neurology|June 17, 2010
Sleep disorders in Wilson's diseaseS Nevsimalova, J Buskova, R Bruha, et al.
Prague Medical Report|June 25, 2009
Advanced oxidation protein products in obstructive sleep apneaK Sonka, L Fialová, J Volná, et al.
Sleep Medicine|May 22, 2012
Restless legs syndrome in Czech patients with multiple sclerosis: an epidemiological and genetic studyJ Vávrová, D Kemlink, K Sonka, et al.
Sleep Medicine|May 14, 2020
Comparative study of the substantia nigra echogenicity and <sup>123</sup>I-Ioflupane SPECT in patients with synucleinopathies with and without REM sleep behavior disorderJ Mašková, D Školoudík, P Štofaniková, et al.
Clinical Genetics|September 2, 2017
Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's diseaseB Schormair, D Kemlink, B Mollenhauer, et al.
Journal of Medical Genetics|March 13, 2009
Replication of restless legs syndrome loci in three European populationsD Kemlink, O Polo, B Frauscher, et al.
Resuscitation|July 19, 2024
EEG for good outcome prediction after cardiac arrest: A multicentre cohort studyS Turella, J Dankiewicz, N Ben-Hamouda, et al.
Pageof 2