Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Piarroux J"'
Autor:
Barrois, R., Barnerias, C., Deladrière, E., Leloup-Germa, V., Tervil, B., Audic, F., Boulay, C., Cances, C., Cintas, P., Davion, J.B., Espil-Taris, C., Manel, V., Pereon, Y., Piarroux, J., Quijano Roy, S., Vuillerot, C., Walther-Louvier, U., Desguerre, I., Gitiaux, C.
Publikováno v:
In Neuromuscular Disorders April 2023 33(4):309-314
Autor:
Piarroux J; Department of Pediatric Neurology, Gui de Chauliac University Hospital, Montpellier, France., Dimopoulou E; Department of Pediatric Neurology, Gui de Chauliac University Hospital, Montpellier, France., Taieb G; University of Montpellier, CNRS (IGF), Department of Neurology, Montpellier, University Hospital 34295 Montpellier, France., Souvannanorath S; Reference center for neuromuscular diseases, Henri-Mondor University Hospital, Assistance publique-Hôpitaux de Paris, Créteil, France., Roze E; Department of Neurology, Salpêtrière Hospital, Sorbonne University and Assistance Publique - Hôpitaux de Paris, Paris, France., Lion-François L; Department of Pediatric Neurology, Lyon University Hospital, Bron, France., Spitz MA; Department of Pediatry, Strasbourg University Hospitals, Strasbourg, France., Broussolle E; Research Unit UMR 5229, Marc-Jeannerod Institute of Cognitive Science, French National Center for Scientific Research (CNRS), University of Lyon, Bron, France.; Department of Neurology C, Civil Hospices of Lyon, Pierre-Wertheimer Neurological Hospital, Bron, France.; Faculty of Medicine Lyon-Sud Charles-Mérieux, University of Lyon, Oullins, France., Laurencin C; Department of Neurology C, Civil Hospices of Lyon, Pierre-Wertheimer Neurological Hospital, Bron, France.; Lyon Neuroscience Research Center (CRNL), INSERM U1028, CNRS UMR5292, University Lyon 1, Lyon F-69000, France., Chanson JB; Department of Neurology, Strasbourg University Hospitals, Strasbourg, France and Reference centre for neuromuscular diseases Nord/Est/Ile-de-France, France., Belleville-Goffeney J; Departement of Pediatric Neurology, Jean-Minjoz University Hospital, Besançon, France., François-Heude MC; Department of Pediatric Neurology, Gui de Chauliac University Hospital, Montpellier, France., Meyer P; Department of Pediatric Neurology, Gui de Chauliac University Hospital, Montpellier, France., Khalil M; Clinical Investigation Center, Montpellier University Hospital, France. INSERM, CIC1411, Montpellier, France., Dereure M; Clinical Research and Epidemiology Unit, La Colombière University Hospital, Montpellier, France., Doummar D; Department of Pediatric Neurology and developmental pathologies, Sorbonne University and Trousseau University Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France, APHP. SU, FHU I2D2, F-75012, Paris, France., Chevassus H; Clinical Investigation Center, Montpellier University Hospital, France. INSERM, CIC1411, Montpellier, France., Apartis E; Department of Neurophysiology, Saint-Antoine Hospital, Assistance Publique-Hôpitaux de Paris, INSERM U1127, CNRS UMR7225, UM75, ICM, 75013 Paris, France., Roubertie A; Department of Pediatric Neurology, Gui de Chauliac University Hospital, Montpellier, France.; Institute for Neurosciences of Montpellier, INSERM U 1298, University of Montpellier, Montpellier, France.
Publikováno v:
Tremor and other hyperkinetic movements (New York, N.Y.) [Tremor Other Hyperkinet Mov (N Y)] 2023 Dec 20; Vol. 13, pp. 46. Date of Electronic Publication: 2023 Dec 20 (Print Publication: 2023).
Autor:
Gardin A; Department of Pediatric Metabolism, Reference Center of Inherited Metabolic Disorders, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Castelle M; Paediatric Hematology Immunology Rheumatology Unit, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Pichard S; Department of Pediatric Metabolism, Reference Center of Inherited Metabolic Disorders, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Cano A; Department of Neuropediatrics and Metabolism, Reference Center of Inherited Metabolic Disorders, Hôpital Timone Enfants, Marseille, France., Chabrol B; Department of Neuropediatrics and Metabolism, Reference Center of Inherited Metabolic Disorders, Hôpital Timone Enfants, Marseille, France., Piarroux J; Department of Neuropediatrics, Centre Hospitalier Universitaire de Montpellier, Montpellier, France., Roubertie A; Department of Neuropediatrics, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.; INM, Univ Montpellier, INSERM U1298, Montpellier, France., Nadjar Y; Neuro-Metabolism Unit, Reference Center for Lysosomal Diseases, Hôpital Universitaire Pitié-Salpêtrière, AP-HP, Paris, France., Guemann AS; Department of Pediatric Metabolism, Reference Center of Inherited Metabolic Disorders, Hôpital Jeanne de Flandre, Lille, France., Tardieu M; Department of Pediatrics, Center for Inborn Errors of Metabolism ToTeM, Centre Hospitalier Régional Universitaire de Tours, Tours, France., Lacombe D; Department of Medical Genetics, CHU Bordeaux, Université de Bordeaux, INSERM U1211, Bordeaux, France., Robert MP; Department of Ophthalmology, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France; Borelli Centre, UMR 9010 CNRS - SSA - ENS Paris Saclay - Paris Cité University, Paris, France., Caillaud C; Biochemistry, Metabolomics, and Proteomics Department, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Froissart R; Biochemical and Molecular Biology Department, Lyon University Hospital, Bron, France., Leboeuf V; Department of Pediatric Metabolism, Reference Center of Inherited Metabolic Disorders, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Barbier V; Department of Pediatric Metabolism, Reference Center of Inherited Metabolic Disorders, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Bouchereau J; Department of Pediatric Metabolism, Reference Center of Inherited Metabolic Disorders, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Schiff M; Department of Pediatric Metabolism, Reference Center of Inherited Metabolic Disorders, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Fauroux B; Pediatric Noninvasive Ventilation and Sleep Unit, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, EA 7330 VIFASOM, Paris, France., Thierry B; Department of Pediatric Otolaryngology, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Luscan R; Department of Pediatric Otolaryngology, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., James S; Department of Pediatric Neurosurgery, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., de Saint-Denis T; Department of Pediatric Neurosurgery, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Pannier S; Paediatric Orthopaedic Service, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Gitiaux C; Department of Paediatric Neurophysiology, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Vergnaud E; Department of Anesthesia, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Boddaert N; Paediatric Radiology Department, AP-HP, Hôpital Necker-Enfants Malades, Université Paris Cité, Institut Imagine INSERM U1163 and U1299, F-75015, Paris, France., Lascourreges C; Department of Pain and Palliative Care Unit, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Lemoine M; Department of Physical Medicine and Rehabilitation, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Bonnet D; Department of Congenital and Pediatric Cardiology, M3C-Necker, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Blanche S; Paediatric Hematology Immunology Rheumatology Unit, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Dalle JH; Hematology and Immunology Department, Hôpital Robert Debré, GHU AP-HP Nord Université Paris-Cité, Paris, France., Neven B; Paediatric Hematology Immunology Rheumatology Unit, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France.; Institut Imagine, Paris, France., de Lonlay P; Department of Pediatric Metabolism, Reference Center of Inherited Metabolic Disorders, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France., Brassier A; Department of Pediatric Metabolism, Reference Center of Inherited Metabolic Disorders, Hôpital Necker-Enfants Malades, AP-HP, Université Paris-Cité, Paris, France. anais.brassier@aphp.fr.
Publikováno v:
Bone marrow transplantation [Bone Marrow Transplant] 2023 Mar; Vol. 58 (3), pp. 295-302. Date of Electronic Publication: 2022 Dec 09.
Autor:
Khalouaoui A; Neonatology, Public Assistance Hospitals of Marseille, Marseille, France., Piarroux J; Neonatology, Public Assistance Hospitals of Marseille, Marseille, France., Sorin G; Neonatology, Public Assistance Hospitals of Marseille, Marseille, France., Oger M; Neonatology, Public Assistance Hospitals of Marseille, Marseille, France., Nicaise C; Neonatology, Public Assistance Hospitals of Marseille, Marseille, France., Tosello B; Neonatology, Public Assistance Hospitals of Marseille, Marseille, France barthelemy.tosello@ap-hm.fr.
Publikováno v:
Archives of disease in childhood. Fetal and neonatal edition [Arch Dis Child Fetal Neonatal Ed] 2023 Mar; Vol. 108 (2), pp. 128-129. Date of Electronic Publication: 2021 Jun 29.
Autor:
Noel G, Maghoo A; Pediatric Emergency Department, CHU Nord, APHM., Piarroux J; Pediatric Emergency Department, CHU Nord, APHM., Viudes G; From the Observatoire Régional des Urgences PACA, Hyères., Minodier P; Pediatric Emergency Department, CHU Nord, APHM., Gentile S
Publikováno v:
Pediatric emergency care [Pediatr Emerg Care] 2021 Dec 01; Vol. 37 (12), pp. e1239-e1243.
Autor:
Gueguen N; Department of Biochemistry and Molecular Biology, CHU Angers, 49933 Angers, France; University of Angers, Unité Mixte de Recherche (UMR) MITOVASC, Centre National de la Recherche Scientifique (CNRS) 6015, Institut National de la Santé et de la Recherche Médicale (INSERM) U1083, 49933 Angers, France., Piarroux J; CHU Montpellier, Département de Neuropédiatrie, Montpellier, France., Sarzi E; NeuroMyoGene Institute-UCBL/CNRS UMR5310/INSERM U1217-Lyon, France., Benkirane M; PhyMedExp, CNRS, INSERM, University of Montpellier, Montpellier, France; Laboratoire de Génétique Moléculaire, Institut Universitaire de Recherche Clinique, CHU de Montpellier, France., Manes G; INM, University Montpellier, INSERM, Montpellier, France., Delettre C; INM, University Montpellier, INSERM, Montpellier, France., Amedro P; PhyMedExp, CNRS, INSERM, University of Montpellier, Montpellier, France; Pediatric and Adult Congenital Cardiology Department, M3C Rare Cardiac Disease Reference Center, CHU Montpellier, France., Leboucq N; Département de Neuroradiologie, CHU Montpellier, Montpellier, France., Koenig M; PhyMedExp, CNRS, INSERM, University of Montpellier, Montpellier, France; Laboratoire de Génétique Moléculaire, Institut Universitaire de Recherche Clinique, CHU de Montpellier, France., Meyer P; CHU Montpellier, Département de Neuropédiatrie, Montpellier, France; PhyMedExp, CNRS, INSERM, University of Montpellier, Montpellier, France., Meunier I; National Center in Rare Diseases, Genetics of Sensory Diseases, University Hospital, Montpellier, France., Reynier P; Department of Biochemistry and Molecular Biology, CHU Angers, 49933 Angers, France; University of Angers, Unité Mixte de Recherche (UMR) MITOVASC, Centre National de la Recherche Scientifique (CNRS) 6015, Institut National de la Santé et de la Recherche Médicale (INSERM) U1083, 49933 Angers, France., Lenaers G; University of Angers, Unité Mixte de Recherche (UMR) MITOVASC, Centre National de la Recherche Scientifique (CNRS) 6015, Institut National de la Santé et de la Recherche Médicale (INSERM) U1083, 49933 Angers, France., Roubertie A; CHU Montpellier, Département de Neuropédiatrie, Montpellier, France; INM, University Montpellier, INSERM, Montpellier, France; National Center in Rare Diseases, Genetics of Sensory Diseases, University Hospital, Montpellier, France. Electronic address: a-roubertie@chu-montpellier.fr.
Publikováno v:
Mitochondrion [Mitochondrion] 2021 Jul; Vol. 59, pp. 169-174. Date of Electronic Publication: 2021 May 20.
Autor:
Piarroux J; Département de Neuropédiatrie, CHU Gui de Chauliac, Montpellier, France., Riant F; Service de Génétique Moléculaire Neurovasculaire, Groupe hospitalier Saint-Louis - Lariboisière - Fernand Widal AP-HP, Paris, France., Humbertclaude V; Service de Médecine Psychologique Enfants et Adolescents, CHU Saint Eloi, Montpellier, France., Remerand G; Service de néonatologie, CHU Estaing, Clermont-Ferrand, France., Hadjadj J; Service de Génétique Moléculaire Neurovasculaire, Groupe hospitalier Saint-Louis - Lariboisière - Fernand Widal AP-HP, Paris, France., Rejou F; Département de Neuropédiatrie, CHU Gui de Chauliac, Montpellier, France., Coubes C; Service de Génétique Clinique, Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France., Pinson L; Service de Génétique Clinique, Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France., Meyer P; Département de Neuropédiatrie, CHU Gui de Chauliac, Montpellier, France.; PhyMedExp, U1046 INSERM, UMR9214 CNRS, Montpellier, France., Roubertie A; Département de Neuropédiatrie, CHU Gui de Chauliac, Montpellier, France.; INSERM U 1051, Institut des Neurosciences de Montpellier, Montpellier, France.
Publikováno v:
Annals of clinical and translational neurology [Ann Clin Transl Neurol] 2020 Apr; Vol. 7 (4), pp. 565-572. Date of Electronic Publication: 2020 Mar 12.
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Akademický článek
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Autor:
Ando, Masahiro1 (AUTHOR), Higuchi, Yujiro1 (AUTHOR), Yuan, Junhui1 (AUTHOR), Yoshimura, Akiko1 (AUTHOR), Kojima, Fumikazu1 (AUTHOR), Yamanishi, Yuki2 (AUTHOR), Aso, Yasuhiro3 (AUTHOR), Izumi, Kotaro4 (AUTHOR), Imada, Minako5 (AUTHOR), Maki, Yoshimitsu6 (AUTHOR), Nakagawa, Hiroto7 (AUTHOR), Hobara, Takahiro1 (AUTHOR), Noguchi, Yutaka1 (AUTHOR), Takei, Jun1 (AUTHOR), Hiramatsu, Yu1 (AUTHOR), Nozuma, Satoshi1 (AUTHOR), Sakiyama, Yusuke1 (AUTHOR), Hashiguchi, Akihiro1 (AUTHOR), Matsuura, Eiji1 (AUTHOR), Okamoto, Yuji1,8 (AUTHOR)
Publikováno v:
Annals of Clinical & Translational Neurology. Jan2024, Vol. 11 Issue 1, p96-104. 9p.