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Publications by Clemens R Müller
Identification of Variants in MBNL1 in Patients With a Myotonic Dystrophy-Like Phenotype
European Journal of Human Genetics
Genetics
RYR1 Mutation Screening 1992 – 2014: A Genetic Report on 22 Years From the Würzburg MH Unit
BMC Anesthesiology
Anesthesiology
Pain Medicine
Related publications
Identification of Variants in the 4q35 GeneFAT1in Patients With a Facioscapulohumeral Dystrophy-Like Phenotype
Human Mutation
Genetics
Hypothalamo-Pituitary Dopaminergic System in Patients With Myotonic Dystrophy.
Tohoku Journal of Experimental Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
Laboratory Abnormalities in Ambulatory Patients With Myotonic Dystrophy Type 1
Archives of Neurology
Cancer Risk Among Patients With Myotonic Muscular Dystrophy
JAMA - Journal of the American Medical Association
Medicine
Electrodiagnostic Findings in Myotonic Dystrophy: A Study on 12 Patients
Neurology International
Neurology
Lymphocyte Capping in Myotonic Dystrophy
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Ocular Changes in Myotonic Dystrophy
American Journal of Ophthalmology
Ophthalmology
Glucocorticoid Hypofunction in Myotonic Dystrophy
Anales del Sistema Sanitario de Navarra
Medicine
Normalization of Frequency-Domain Parameters of Heart Rate Variability in Patients With Myotonic Dystrophy
Annals of Noninvasive Electrocardiology
Medicine
Cardiovascular Medicine
Physiology
Cardiology