Hemiparkinsonism-hemiatrophy syndrome.
Identifieur interne : 000D43 ( Main/Exploration ); précédent : 000D42; suivant : 000D44Hemiparkinsonism-hemiatrophy syndrome.
Auteurs : Subhashie Wijemanne [États-Unis] ; Joseph Jankovic [États-Unis]Source :
- Neurology ; 2007.
English descriptors
- KwdEn :
- Adolescent, Adult, Atrophy (complications), Atrophy (diagnosis), Atrophy (physiopathology), Birth Injuries (complications), Brain (pathology), Brain (physiopathology), Brain Damage, Chronic (complications), Brain Damage, Chronic (etiology), Brain Damage, Chronic (physiopathology), Dystonia (etiology), Dystonia (physiopathology), Extremities (pathology), Facial Hemiatrophy (complications), Facial Hemiatrophy (diagnosis), Facial Hemiatrophy (physiopathology), Female, Growth Disorders (complications), Growth Disorders (diagnosis), Growth Disorders (physiopathology), Humans, Magnetic Resonance Imaging, Male, Middle Aged, Muscle, Skeletal (physiopathology), Parkinson Disease (complications), Parkinson Disease (diagnosis), Parkinson Disease (physiopathology), Scoliosis (etiology), Scoliosis (physiopathology), Seizures, Febrile (complications), Syndrome.
- MESH :
- complications : Atrophy, Birth Injuries, Brain Damage, Chronic, Facial Hemiatrophy, Growth Disorders, Parkinson Disease, Seizures, Febrile.
- diagnosis : Atrophy, Facial Hemiatrophy, Growth Disorders, Parkinson Disease.
- etiology : Brain Damage, Chronic, Dystonia, Scoliosis.
- pathology : Brain, Extremities.
- physiopathology : Atrophy, Brain, Brain Damage, Chronic, Dystonia, Facial Hemiatrophy, Growth Disorders, Muscle, Skeletal, Parkinson Disease, Scoliosis.
- Adolescent, Adult, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Syndrome.
Abstract
To characterize the clinical and radiologic features of hemiparkinsonism-hemiatrophy syndrome (HPHA).
DOI: 10.1212/01.wnl.0000277699.48155.39
PubMed: 17938368
Affiliations:
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Le document en format XML
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(physiopathology)</term><term>Extremities (pathology)</term><term>Facial Hemiatrophy (complications)</term><term>Facial Hemiatrophy (diagnosis)</term><term>Facial Hemiatrophy (physiopathology)</term><term>Female</term><term>Growth Disorders (complications)</term><term>Growth Disorders (diagnosis)</term><term>Growth Disorders (physiopathology)</term><term>Humans</term><term>Magnetic Resonance Imaging</term><term>Male</term><term>Middle Aged</term><term>Muscle, Skeletal (physiopathology)</term><term>Parkinson Disease (complications)</term><term>Parkinson Disease (diagnosis)</term><term>Parkinson Disease (physiopathology)</term><term>Scoliosis (etiology)</term><term>Scoliosis (physiopathology)</term><term>Seizures, Febrile (complications)</term><term>Syndrome</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Atrophy</term><term>Birth Injuries</term><term>Brain Damage, Chronic</term><term>Facial Hemiatrophy</term><term>Growth Disorders</term><term>Parkinson Disease</term><term>Seizures, Febrile</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Atrophy</term><term>Facial Hemiatrophy</term><term>Growth Disorders</term><term>Parkinson Disease</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Brain Damage, Chronic</term><term>Dystonia</term><term>Scoliosis</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Brain</term><term>Extremities</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Atrophy</term><term>Brain</term><term>Brain Damage, Chronic</term><term>Dystonia</term><term>Facial Hemiatrophy</term><term>Growth Disorders</term><term>Muscle, Skeletal</term><term>Parkinson Disease</term><term>Scoliosis</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adolescent</term><term>Adult</term><term>Female</term><term>Humans</term><term>Magnetic Resonance 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