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Highlighting the value of polymyography in childhood onset movement disorders.

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Title: Highlighting the value of polymyography in childhood onset movement disorders.
Authors: Moretti R; Department of Clinical Neurophysiology, Armand Trousseau Hospital, AP-HP-Sorbonne Université, Paris, France., Ravelli C; Department of Paediatric Neurology, Armand Trousseau Hospital, Referral Centre for Neurogenetic Rare Disease, APHP-Sorbonne Université, Paris, France., Ahmar Y; Department of Clinical Neurophysiology, Saint-Antoine Hospital and Pitié-Salpêtrière Hospital, APHP-Sorbonne Université, Paris, France., Dorison N; Unité Dyspa, Neurochirurgie Pédiatrique, Hôpital Fondation Rothschild, Paris, France., De Salins M; Department of Clinical Neurophysiology, Armand Trousseau Hospital, AP-HP-Sorbonne Université, Paris, France., Rodriguez D; Department of Paediatric Neurology, Armand Trousseau Hospital, Referral Centre for Neurogenetic Rare Disease, APHP-Sorbonne Université, Paris, France.; Sorbonne University, Paris, France., Deiva K; Sorbonne University, Paris, France.; Department of Paediatric Neurology, Armand Trousseau Hospital, AP-HP Sorbonne University Hospital, Paris, France., Vermersch AI; Department of Clinical Neurophysiology, Armand Trousseau Hospital, AP-HP-Sorbonne Université, Paris, France., Triboulet MH; Department of Clinical Neurophysiology, Armand Trousseau Hospital, AP-HP-Sorbonne Université, Paris, France.; Department of Paediatric Neurology, Armand Trousseau Hospital, AP-HP Sorbonne University Hospital, Paris, France., Valence S; Service de Neurologie Pédiatrique, Hôpital Armand Trousseau, AP-HP Sorbonne Université, Paris, France.; Centre de Référence Maladies Rares 'Déficience Intellectuelle de Cause Rare et Polyhandicap', Paris, France., Harion M; Service de Neurologie Pédiatrique, Hôpital Armand Trousseau, AP-HP Sorbonne Université, Paris, France.; Centre de Référence Maladies Rares 'Déficience Intellectuelle de Cause Rare et Polyhandicap', Paris, France., Burglen L; Sorbonne University, Paris, France.; Centre de Référence des Malformations et Maladies Congénitales du Cervelet et Laboratoire de Neurogénétique Pédiatrique, Département de génétique, Hôpital Armand Trousseau, Paris, France., Apartis E; Department of Clinical Neurophysiology, Saint-Antoine Hospital and Pitié-Salpêtrière Hospital, APHP-Sorbonne Université, Paris, France.; Paris Brain Institute, ICM, Inserm, CNRS, Sorbonne Université, Paris, France., Doummar D; Department of Paediatric Neurology, Armand Trousseau Hospital, Referral Centre for Neurogenetic Rare Disease, APHP-Sorbonne Université, Paris, France.
Source: Frontiers in neurology [Front Neurol] 2026 May 28; Vol. 17, pp. 1771878. Date of Electronic Publication: 2026 May 28 (Print Publication: 2026).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101546899 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2295 (Print) Linking ISSN: 16642295 NLM ISO Abbreviation: Front Neurol Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: <searchLink fieldCode="AU" term="%22Moretti+R%22">Moretti R</searchLink>; Department of Clinical Neurophysiology, Armand Trousseau Hospital, AP-HP-Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Ravelli+C%22">Ravelli C</searchLink>; Department of Paediatric Neurology, Armand Trousseau Hospital, Referral Centre for Neurogenetic Rare Disease, APHP-Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Ahmar+Y%22">Ahmar Y</searchLink>; Department of Clinical Neurophysiology, Saint-Antoine Hospital and Pitié-Salpêtrière Hospital, APHP-Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Dorison+N%22">Dorison N</searchLink>; Unité Dyspa, Neurochirurgie Pédiatrique, Hôpital Fondation Rothschild, Paris, France.<br /><searchLink fieldCode="AU" term="%22De+Salins+M%22">De Salins M</searchLink>; Department of Clinical Neurophysiology, Armand Trousseau Hospital, AP-HP-Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Rodriguez+D%22">Rodriguez D</searchLink>; Department of Paediatric Neurology, Armand Trousseau Hospital, Referral Centre for Neurogenetic Rare Disease, APHP-Sorbonne Université, Paris, France.; Sorbonne University, Paris, France.<br /><searchLink fieldCode="AU" term="%22Deiva+K%22">Deiva K</searchLink>; Sorbonne University, Paris, France.; Department of Paediatric Neurology, Armand Trousseau Hospital, AP-HP Sorbonne University Hospital, Paris, France.<br /><searchLink fieldCode="AU" term="%22Vermersch+AI%22">Vermersch AI</searchLink>; Department of Clinical Neurophysiology, Armand Trousseau Hospital, AP-HP-Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Triboulet+MH%22">Triboulet MH</searchLink>; Department of Clinical Neurophysiology, Armand Trousseau Hospital, AP-HP-Sorbonne Université, Paris, France.; Department of Paediatric Neurology, Armand Trousseau Hospital, AP-HP Sorbonne University Hospital, Paris, France.<br /><searchLink fieldCode="AU" term="%22Valence+S%22">Valence S</searchLink>; Service de Neurologie Pédiatrique, Hôpital Armand Trousseau, AP-HP Sorbonne Université, Paris, France.; Centre de Référence Maladies Rares 'Déficience Intellectuelle de Cause Rare et Polyhandicap', Paris, France.<br /><searchLink fieldCode="AU" term="%22Harion+M%22">Harion M</searchLink>; Service de Neurologie Pédiatrique, Hôpital Armand Trousseau, AP-HP Sorbonne Université, Paris, France.; Centre de Référence Maladies Rares 'Déficience Intellectuelle de Cause Rare et Polyhandicap', Paris, France.<br /><searchLink fieldCode="AU" term="%22Burglen+L%22">Burglen L</searchLink>; Sorbonne University, Paris, France.; Centre de Référence des Malformations et Maladies Congénitales du Cervelet et Laboratoire de Neurogénétique Pédiatrique, Département de génétique, Hôpital Armand Trousseau, Paris, France.<br /><searchLink fieldCode="AU" term="%22Apartis+E%22">Apartis E</searchLink>; Department of Clinical Neurophysiology, Saint-Antoine Hospital and Pitié-Salpêtrière Hospital, APHP-Sorbonne Université, Paris, France.; Paris Brain Institute, ICM, Inserm, CNRS, Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Doummar+D%22">Doummar D</searchLink>; Department of Paediatric Neurology, Armand Trousseau Hospital, Referral Centre for Neurogenetic Rare Disease, APHP-Sorbonne Université, Paris, France.
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