Annick Labarre‐Vila

Management Guidelines for Children with Thyroid Nodules and Differentiated Thyroid Cancer

Genetics of normal and pathological sleep in humans

Neurocognitive Consequences of Sleep Deprivation

Bruxism physiology and pathology: an overview for clinicians*

Estimation of the global prevalence and burden of obstructive sleep apnoea: a literature-based analysis

The primary periodic paralyses: diagnosis, pathogenesis and treatment

Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1

Acromegaly: An Endocrine Society Clinical Practice Guideline

Genes for normal sleep and sleep disorders

Occurrence of myofascial pain in patients with possible carpal tunnel syndrome – A single‐blinded study

International Consensus on Diagnostic Criteria and Clinical Considerations of Myofascial Trigger Points: A Delphi Study

Obstructive sleep apnoea syndrome

Endocrine Aspects of Obstructive Sleep Apnea

Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis

About Sleep's Role in Memory

Hypermorphic mutation of the voltage-gated sodium channel encoding gene Scn10a causes a dramatic stimulus-dependent neurobehavioral phenotype

Absence of β-tropomyosin is a new cause of Escobar syndrome associated with nemaline myopathy

Exercise test in muscle channelopathies and other muscle disorders

Pathophysiology inferred from electrodiagnostic nerve tests and classification of polyneuropathies. Suggested guidelines

Charcot-Marie-Tooth disease and sleep apnoea syndrome: a family study