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Clinical/Scientific Notes
April 23, 2007

NARP MITOCHONDRIOPATHY: AN UNUSUAL CAUSE OF PROGRESSIVE MYOCLONIC EPILEPSY

April 24, 2007 issue
68 (17) 1429-1430
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Neurology®
Volume 68Number 17April 24, 2007
Pages: 1429-1430
PubMed: 17452590

Publication History

Published online: April 23, 2007
Published in issue: April 24, 2007

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Affiliations & Disclosures

J. Jung, MD
From Hôpital Neurologique, Service de Neurologie Fonctionnelle et d’Epileptologie, Bron (J.J., F.M., P.R.); Hôpital Debrousse, Laboratoire de Biochimie Pédiatrique, Lyon (P.C.-R., B.M.d.C.); Hôpital de la Croix-Rousse, Unité Fonctionnelle Neuro-Génétique, Lyon (E.O.); CTRS-IDEE Hospices Civils de Lyon (P.R.); INSERM U280, Lyon (J.J., P.R.); and INSERM EMI0342, Lyon (F.M.), France.
F. Mauguière, MD, PhD
From Hôpital Neurologique, Service de Neurologie Fonctionnelle et d’Epileptologie, Bron (J.J., F.M., P.R.); Hôpital Debrousse, Laboratoire de Biochimie Pédiatrique, Lyon (P.C.-R., B.M.d.C.); Hôpital de la Croix-Rousse, Unité Fonctionnelle Neuro-Génétique, Lyon (E.O.); CTRS-IDEE Hospices Civils de Lyon (P.R.); INSERM U280, Lyon (J.J., P.R.); and INSERM EMI0342, Lyon (F.M.), France.
P. Clerc-Renaud, MD
From Hôpital Neurologique, Service de Neurologie Fonctionnelle et d’Epileptologie, Bron (J.J., F.M., P.R.); Hôpital Debrousse, Laboratoire de Biochimie Pédiatrique, Lyon (P.C.-R., B.M.d.C.); Hôpital de la Croix-Rousse, Unité Fonctionnelle Neuro-Génétique, Lyon (E.O.); CTRS-IDEE Hospices Civils de Lyon (P.R.); INSERM U280, Lyon (J.J., P.R.); and INSERM EMI0342, Lyon (F.M.), France.
E. Ollagnon, MD
From Hôpital Neurologique, Service de Neurologie Fonctionnelle et d’Epileptologie, Bron (J.J., F.M., P.R.); Hôpital Debrousse, Laboratoire de Biochimie Pédiatrique, Lyon (P.C.-R., B.M.d.C.); Hôpital de la Croix-Rousse, Unité Fonctionnelle Neuro-Génétique, Lyon (E.O.); CTRS-IDEE Hospices Civils de Lyon (P.R.); INSERM U280, Lyon (J.J., P.R.); and INSERM EMI0342, Lyon (F.M.), France.
B. Mousson de Camaret, MD, PhD
From Hôpital Neurologique, Service de Neurologie Fonctionnelle et d’Epileptologie, Bron (J.J., F.M., P.R.); Hôpital Debrousse, Laboratoire de Biochimie Pédiatrique, Lyon (P.C.-R., B.M.d.C.); Hôpital de la Croix-Rousse, Unité Fonctionnelle Neuro-Génétique, Lyon (E.O.); CTRS-IDEE Hospices Civils de Lyon (P.R.); INSERM U280, Lyon (J.J., P.R.); and INSERM EMI0342, Lyon (F.M.), France.
P. Ryvlin, MD, PhD
From Hôpital Neurologique, Service de Neurologie Fonctionnelle et d’Epileptologie, Bron (J.J., F.M., P.R.); Hôpital Debrousse, Laboratoire de Biochimie Pédiatrique, Lyon (P.C.-R., B.M.d.C.); Hôpital de la Croix-Rousse, Unité Fonctionnelle Neuro-Génétique, Lyon (E.O.); CTRS-IDEE Hospices Civils de Lyon (P.R.); INSERM U280, Lyon (J.J., P.R.); and INSERM EMI0342, Lyon (F.M.), France.

Notes

Address correspondence and reprint requests to Dr. Julien Jung, Hôpital Neurologique, Service de Neurologie Fonctionnelle et d’Epileptologie, 69003 Lyon, France; [email protected]

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  4. Epilepsy in MT ‐ ATP6 ‐ related mils/NARP: correlation of elettroclinical features with heteroplasmy , Annals of Clinical and Translational Neurology, 8, 3, (704-710), (2021).https://doi.org/10.1002/acn3.51259
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  5. Renal Involvement in Neuropathy, Ataxia, Retinitis Pigmentosa (NARP) Syndrome: A Case Report, American Journal of Kidney Diseases, 71, 5, (754-757), (2018).https://doi.org/10.1053/j.ajkd.2017.09.020
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  7. Mitochondrial epilepsy in pediatric and adult patients, Acta Neurologica Scandinavica, 128, 3, (141-152), (2013).https://doi.org/10.1111/ane.12122
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  8. Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: An overview study, Mitochondrial DNA, 24, 3, (163-178), (2013).https://doi.org/10.3109/19401736.2012.748045
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  9. Epilepsy in mitochondrial disorders, Seizure, 21, 5, (316-321), (2012).https://doi.org/10.1016/j.seizure.2012.03.003
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  10. Metabolic and degenerative disorders, Epilepsy, (485-511), (2012).https://doi.org/10.1016/B978-0-444-52899-5.00045-9
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