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Publications by Ute Hehr

Identification of Variants in MBNL1 in Patients With a Myotonic Dystrophy-Like Phenotype

European Journal of Human Genetics
Genetics
2016English

Related publications

Identification of Variants in the 4q35 GeneFAT1in Patients With a Facioscapulohumeral Dystrophy-Like Phenotype

Human Mutation
Genetics
2015English

Hypothalamo-Pituitary Dopaminergic System in Patients With Myotonic Dystrophy.

Tohoku Journal of Experimental Medicine
BiochemistryMedicineGeneticsMolecular Biology
1988English

Laboratory Abnormalities in Ambulatory Patients With Myotonic Dystrophy Type 1

Archives of Neurology
2006English

Cancer Risk Among Patients With Myotonic Muscular Dystrophy

JAMA - Journal of the American Medical Association
Medicine
2011English

Electrodiagnostic Findings in Myotonic Dystrophy: A Study on 12 Patients

Neurology International
Neurology
2019English

Lymphocyte Capping in Myotonic Dystrophy

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
1983English

Ocular Changes in Myotonic Dystrophy

American Journal of Ophthalmology
Ophthalmology
1967English

Glucocorticoid Hypofunction in Myotonic Dystrophy

Anales del Sistema Sanitario de Navarra
Medicine
2008English

Normalization of Frequency-Domain Parameters of Heart Rate Variability in Patients With Myotonic Dystrophy

Annals of Noninvasive Electrocardiology
MedicineCardiovascular MedicinePhysiologyCardiology
2018English

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