Highlighting the value of polymyography in childhood onset movement disorders.
Saved in:
| 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 |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 1664-2295 |
|---|---|
| DOI: | 10.3389/fneur.2026.1771878 |
