Background This is an updated version of the original Cochrane review, published in 2009, Issue 2. Kleine-Levin syndrome (KLS) is a rare disorder that mainly affects adolescent men. It is characterised by recurrent episodes of hypersomnia, usually accompanied by hyperphagia, cognitive and mood disturbances, abnormal behaviour, such as hypersexuality, and signs of dysautonomia. In 1990, the diagnostic criteria for Kleine-Levin syndrome were modified in the International Classification of Sleep Disorders, where KLS was defined as a syndrome comprised of recurring episodes of undue sleepiness lasting some days, which may or may not be associated with hyperphagia and abnormal behaviour. According to the International Classification of Sleepines...
INTRODUCTION: Autism, like other neurodevelopmental disorders (NDDs), has a strong association with ...
Background: Friedreich ataxia is a rare inherited autosomal recessive neurological disorder, charact...
Commentary by David McGillivray, Peter Dayan and Martin Pusic The treatment of an acute convulsion c...
BackgroundThis is an updated version of the original Cochrane review, published in Issue 2, 2009.Kle...
AIM: The aim of the study is to present the aetiology, pathogenesis, symptoms, diagnosis and treatme...
Kleine-Levin syndrome (KLS) is a rare disorder with symptoms that include periodic hypersomnia, cogn...
ABSTRACT- We report the first episode of Kleine-Levin (KLS) syndrome in a 17-year-old male. The illn...
BACKGROUND: There is uncertainty about the most appropriate ways to manage non-respiratory sleep dis...
Kleine-Levin syndrome (KLS) is a rare disease of unknown etiology, the diagnosis of which can be cha...
Kleine-Levin syndrome (KLS) is a rare sleep disorder mainly affecting teenage boys in which the main...
Background: Antipsychotic medication can cause tardive dyskinesia (TD) – late-onset, involuntary, re...
Kleine-Levin Syndrome (KLS) is a rare and frequently misdiagnosed disorder with typical onset at ado...
BACKGROUND: Severe myoclonic epilepsy in infants (SMEI), also known as Dravet syndrome, is a rare, r...
Lennox-Gastaut syndrome (LGS) is a severe epileptic and developmental encephalopathy that is associa...
Introduction: Lewy body disease (LBD) is the second most common neurodegenerative disorder in patien...
INTRODUCTION: Autism, like other neurodevelopmental disorders (NDDs), has a strong association with ...
Background: Friedreich ataxia is a rare inherited autosomal recessive neurological disorder, charact...
Commentary by David McGillivray, Peter Dayan and Martin Pusic The treatment of an acute convulsion c...
BackgroundThis is an updated version of the original Cochrane review, published in Issue 2, 2009.Kle...
AIM: The aim of the study is to present the aetiology, pathogenesis, symptoms, diagnosis and treatme...
Kleine-Levin syndrome (KLS) is a rare disorder with symptoms that include periodic hypersomnia, cogn...
ABSTRACT- We report the first episode of Kleine-Levin (KLS) syndrome in a 17-year-old male. The illn...
BACKGROUND: There is uncertainty about the most appropriate ways to manage non-respiratory sleep dis...
Kleine-Levin syndrome (KLS) is a rare disease of unknown etiology, the diagnosis of which can be cha...
Kleine-Levin syndrome (KLS) is a rare sleep disorder mainly affecting teenage boys in which the main...
Background: Antipsychotic medication can cause tardive dyskinesia (TD) – late-onset, involuntary, re...
Kleine-Levin Syndrome (KLS) is a rare and frequently misdiagnosed disorder with typical onset at ado...
BACKGROUND: Severe myoclonic epilepsy in infants (SMEI), also known as Dravet syndrome, is a rare, r...
Lennox-Gastaut syndrome (LGS) is a severe epileptic and developmental encephalopathy that is associa...
Introduction: Lewy body disease (LBD) is the second most common neurodegenerative disorder in patien...
INTRODUCTION: Autism, like other neurodevelopmental disorders (NDDs), has a strong association with ...
Background: Friedreich ataxia is a rare inherited autosomal recessive neurological disorder, charact...
Commentary by David McGillivray, Peter Dayan and Martin Pusic The treatment of an acute convulsion c...