MovDisordV3, PascalFrancis, Corpus, bibRecord, 001663

Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy

Identifieur interne : 001663 ( PascalFrancis/Corpus ); précédent : 001662; suivant : 001664

Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy

Auteurs : Bart P. C. Van De Warrenburg ; Carla Cordivari ; Peter Brown ; Kailash P. Bhatia

Source :

Movement disorders [ 0885-3185 ] ; 2007.

RBID : Pascal:07-0314960

Descripteurs français

Pascal (Inist)
- Système nerveux pathologie, Encéphalopathie, Trismus, Autoimmunité, Myoclonie, Idiopathique, Réflexe, Muscle masticateur, Hyperekplexie.

English descriptors

KwdEn :
- Autoimmunity, Encephalopathy, Hyperekplexia, Idiopathic, Masticatory muscle, Myoclonus, Nervous system diseases, Reflex, Trismus.

Abstract

Symptomatic hyperekplexia is a relatively rare entity, but has been documented in various, mostly brainstem diseases. We report the clinical and neurophysiologic vignette of a patient with a self-limiting, possibly inflammatory brainstem encephalopathy. Trismus was the presenting feature, but she later developed hyperekplexia. Although most brainstem features resolved spontaneously, the hyperekplexia has persisted.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A03		`1`		`@0 Mov. disord.`
A05				`@2 22`
A06				`@2 7`
A08	`01`	`1`	`ENG`	`@1 Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy`
A11	`01`	`1`		`@1 VAN DE WARRENBURG (Bart P. C.)`
A11	`02`	`1`		`@1 CORDIVARI (Carla)`
A11	`03`	`1`		`@1 BROWN (Peter)`
A11	`04`	`1`		`@1 BHATIA (Kailash P.)`
A14	`01`			`@1 Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology @2 London @3 GBR @Z 1 aut. @Z 3 aut. @Z 4 aut.`
A14	`02`			`@1 Department of Neurology, Radboud University Nijmegen Medical Centre @2 Nijmegen @3 NLD @Z 1 aut.`
A14	`03`			`@1 Department of Neurophysiology, National Hospital of Neurology and Neurosurgery @2 London @3 GBR @Z 2 aut.`
A20				`@1 1017-1020`
A21				`@1 2007`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000149881420180`
A44				`@0 0000 @1 © 2007 INIST-CNRS. All rights reserved.`
A45				`@0 9 ref.`
A47	`01`	`1`		`@0 07-0314960`
A60				`@1 P`
A61				`@0 A`
A64	`01`	`1`		`@0 Movement disorders`
A66	`01`			`@0 USA`
C01	`01`		`ENG`	`@0 Symptomatic hyperekplexia is a relatively rare entity, but has been documented in various, mostly brainstem diseases. We report the clinical and neurophysiologic vignette of a patient with a self-limiting, possibly inflammatory brainstem encephalopathy. Trismus was the presenting feature, but she later developed hyperekplexia. Although most brainstem features resolved spontaneously, the hyperekplexia has persisted.`
C02	`01`	`X`		`@0 002B17`
C02	`02`	`X`		`@0 002B05C02A`
C02	`03`	`X`		`@0 002A26D05`
C03	`01`	`X`	`FRE`	`@0 Système nerveux pathologie @5 01`
C03	`01`	`X`	`ENG`	`@0 Nervous system diseases @5 01`
C03	`01`	`X`	`SPA`	`@0 Sistema nervioso patología @5 01`
C03	`02`	`X`	`FRE`	`@0 Encéphalopathie @5 02`
C03	`02`	`X`	`ENG`	`@0 Encephalopathy @5 02`
C03	`02`	`X`	`SPA`	`@0 Encefalopatía @5 02`
C03	`03`	`X`	`FRE`	`@0 Trismus @5 03`
C03	`03`	`X`	`ENG`	`@0 Trismus @5 03`
C03	`03`	`X`	`SPA`	`@0 Trismo @5 03`
C03	`04`	`X`	`FRE`	`@0 Autoimmunité @5 04`
C03	`04`	`X`	`ENG`	`@0 Autoimmunity @5 04`
C03	`04`	`X`	`SPA`	`@0 Autoinmunidad @5 04`
C03	`05`	`X`	`FRE`	`@0 Myoclonie @5 05`
C03	`05`	`X`	`ENG`	`@0 Myoclonus @5 05`
C03	`05`	`X`	`SPA`	`@0 Mioclonia @5 05`
C03	`06`	`X`	`FRE`	`@0 Idiopathique @5 09`
C03	`06`	`X`	`ENG`	`@0 Idiopathic @5 09`
C03	`06`	`X`	`SPA`	`@0 Idiopático @5 09`
C03	`07`	`X`	`FRE`	`@0 Réflexe @5 10`
C03	`07`	`X`	`ENG`	`@0 Reflex @5 10`
C03	`07`	`X`	`SPA`	`@0 Reflejo @5 10`
C03	`08`	`X`	`FRE`	`@0 Muscle masticateur @5 78`
C03	`08`	`X`	`ENG`	`@0 Masticatory muscle @5 78`
C03	`08`	`X`	`SPA`	`@0 Músculo masticatorio @5 78`
C03	`09`	`X`	`FRE`	`@0 Hyperekplexie @4 CD @5 96`
C03	`09`	`X`	`ENG`	`@0 Hyperekplexia @4 CD @5 96`
C07	`01`	`X`	`FRE`	`@0 Muscle strié pathologie @5 37`
C07	`01`	`X`	`ENG`	`@0 Striated muscle disease @5 37`
C07	`01`	`X`	`SPA`	`@0 Músculo estriado patología @5 37`
C07	`02`	`X`	`FRE`	`@0 Encéphale pathologie @5 38`
C07	`02`	`X`	`ENG`	`@0 Cerebral disorder @5 38`
C07	`02`	`X`	`SPA`	`@0 Encéfalo patología @5 38`
C07	`03`	`X`	`FRE`	`@0 Système nerveux central pathologie @5 39`
C07	`03`	`X`	`ENG`	`@0 Central nervous system disease @5 39`
C07	`03`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 39`
C07	`04`	`X`	`FRE`	`@0 Mouvement involontaire @5 40`
C07	`04`	`X`	`ENG`	`@0 Involuntary movement @5 40`
C07	`04`	`X`	`SPA`	`@0 Movimiento involuntario @5 40`
C07	`05`	`X`	`FRE`	`@0 Trouble neurologique @5 41`
C07	`05`	`X`	`ENG`	`@0 Neurological disorder @5 41`
C07	`05`	`X`	`SPA`	`@0 Trastorno neurológico @5 41`
N21				`@1 204`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

Format Inist (serveur)

NO :	PASCAL 07-0314960 INIST
ET :	Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy
AU :	VAN DE WARRENBURG (Bart P. C.); CORDIVARI (Carla); BROWN (Peter); BHATIA (Kailash P.)
AF :	Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology/London/Royaume-Uni (1 aut., 3 aut., 4 aut.); Department of Neurology, Radboud University Nijmegen Medical Centre/Nijmegen/Pays-Bas (1 aut.); Department of Neurophysiology, National Hospital of Neurology and Neurosurgery/London/Royaume-Uni (2 aut.)
DT :	Publication en série; Niveau analytique
SO :	Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2007; Vol. 22; No. 7; Pp. 1017-1020; Bibl. 9 ref.
LA :	Anglais
EA :	Symptomatic hyperekplexia is a relatively rare entity, but has been documented in various, mostly brainstem diseases. We report the clinical and neurophysiologic vignette of a patient with a self-limiting, possibly inflammatory brainstem encephalopathy. Trismus was the presenting feature, but she later developed hyperekplexia. Although most brainstem features resolved spontaneously, the hyperekplexia has persisted.
CC :	002B17; 002B05C02A; 002A26D05
FD :	Système nerveux pathologie; Encéphalopathie; Trismus; Autoimmunité; Myoclonie; Idiopathique; Réflexe; Muscle masticateur; Hyperekplexie
FG :	Muscle strié pathologie; Encéphale pathologie; Système nerveux central pathologie; Mouvement involontaire; Trouble neurologique
ED :	Nervous system diseases; Encephalopathy; Trismus; Autoimmunity; Myoclonus; Idiopathic; Reflex; Masticatory muscle; Hyperekplexia
EG :	Striated muscle disease; Cerebral disorder; Central nervous system disease; Involuntary movement; Neurological disorder
SD :	Sistema nervioso patología; Encefalopatía; Trismo; Autoinmunidad; Mioclonia; Idiopático; Reflejo; Músculo masticatorio
LO :	INIST-20953.354000149881420180
ID :	07-0314960

Links to Exploration step

Pascal:07-0314960

Le document en format XML

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<front><div type="abstract" xml:lang="en">Symptomatic hyperekplexia is a relatively rare entity, but has been documented in various, mostly brainstem diseases. We report the clinical and neurophysiologic vignette of a patient with a self-limiting, possibly inflammatory brainstem encephalopathy. Trismus was the presenting feature, but she later developed hyperekplexia. Although most brainstem features resolved spontaneously, the hyperekplexia has persisted.</div>
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<fC01 i1="01" l="ENG"><s0>Symptomatic hyperekplexia is a relatively rare entity, but has been documented in various, mostly brainstem diseases. We report the clinical and neurophysiologic vignette of a patient with a self-limiting, possibly inflammatory brainstem encephalopathy. Trismus was the presenting feature, but she later developed hyperekplexia. Although most brainstem features resolved spontaneously, the hyperekplexia has persisted.</s0>
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<fC03 i1="03" i2="X" l="SPA"><s0>Trismo</s0>
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<s5>05</s5>
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<s5>96</s5>
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<fC03 i1="09" i2="X" l="ENG"><s0>Hyperekplexia</s0>
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<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Mouvement involontaire</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Involuntary movement</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Movimiento involuntario</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Trouble neurologique</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Neurological disorder</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Trastorno neurológico</s0>
<s5>41</s5>
</fC07>
<fN21><s1>204</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
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<server><NO>PASCAL 07-0314960 INIST</NO>
<ET>Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy</ET>
<AU>VAN DE WARRENBURG (Bart P. C.); CORDIVARI (Carla); BROWN (Peter); BHATIA (Kailash P.)</AU>
<AF>Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology/London/Royaume-Uni (1 aut., 3 aut., 4 aut.); Department of Neurology, Radboud University Nijmegen Medical Centre/Nijmegen/Pays-Bas (1 aut.); Department of Neurophysiology, National Hospital of Neurology and Neurosurgery/London/Royaume-Uni (2 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2007; Vol. 22; No. 7; Pp. 1017-1020; Bibl. 9 ref.</SO>
<LA>Anglais</LA>
<EA>Symptomatic hyperekplexia is a relatively rare entity, but has been documented in various, mostly brainstem diseases. We report the clinical and neurophysiologic vignette of a patient with a self-limiting, possibly inflammatory brainstem encephalopathy. Trismus was the presenting feature, but she later developed hyperekplexia. Although most brainstem features resolved spontaneously, the hyperekplexia has persisted.</EA>
<CC>002B17; 002B05C02A; 002A26D05</CC>
<FD>Système nerveux pathologie; Encéphalopathie; Trismus; Autoimmunité; Myoclonie; Idiopathique; Réflexe; Muscle masticateur; Hyperekplexie</FD>
<FG>Muscle strié pathologie; Encéphale pathologie; Système nerveux central pathologie; Mouvement involontaire; Trouble neurologique</FG>
<ED>Nervous system diseases; Encephalopathy; Trismus; Autoimmunity; Myoclonus; Idiopathic; Reflex; Masticatory muscle; Hyperekplexia</ED>
<EG>Striated muscle disease; Cerebral disorder; Central nervous system disease; Involuntary movement; Neurological disorder</EG>
<SD>Sistema nervioso patología; Encefalopatía; Trismo; Autoinmunidad; Mioclonia; Idiopático; Reflejo; Músculo masticatorio</SD>
<LO>INIST-20953.354000149881420180</LO>
<ID>07-0314960</ID>
</server>
</inist>
</record>

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	Movement Disorders (revue)
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Movement Disorders (revue)

Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy

Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy

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