📇 Rhumatologue · BRON CEDEX · (69) · Salarié
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3 raisons identifiées
Plateau technique de référence
Hospices Civils de Lyon (HCL) — équipements et expertise pointus pour les cas complexes
Auteur de référence en rhumatologie
26 articles scientifiques publiés — un praticien à la pointe de la recherche
Délais de RDV courts dans la région
144.6 rhumatos / 100 000 hab. — département bien doté
✨ Génération du profil synthétique IA en cours…
Articles déposés en accès libre sur l'archive ouverte des universités françaises (HAL) — gage d'activité de recherche en France.
Données ANS publiques (Licence Ouverte 2.0) · Enrichissements MonRhumato 100 % opt-in · Toute personne référencée peut demander la suppression ou la rectification.
Source : HAL — archive ouverte CCSD/CNRS (couvre articles, chapitres EMC, communications congrès, thèses).
HOPITAL PIERRE WERTHEIMER - HCL
59 BD PINEL, 69677 BRON CEDEX
Secteur de conventionnement non disponible (médecin hospitalier ou non présent dans l'Annuaire santé CNAM des libéraux conventionnés).
Lien Doctolib = recherche Google site:doctolib.fr (le 1er résultat est presque toujours le profil correct s'il existe).
Orphanet journal of rare diseases · 2020
AbstractBackgroundKennedy’s disease (KD), also known as spinal and bulbar muscular atrophy (SBMA), is a rare, adult-onset, X-linked recessive neuromuscular disease caused by CAG expansions in exon 1 of the androgen receptor gene (AR). The objective of the French national diagnostic and management protocol is to provide evidence-based best practice recommendations and outline an optimised care pathway for patients with KD, based on a systematic literature review and consensus multidisciplinary observations.ResultsThe initial evaluation, confirmation of the diagnosis, and management should ideally take place in a tertiary referral centre for motor neuron diseases, and involve an experienced multidisciplinary team of neurologists, endocrinologists, cardiologists and allied healthcare professionals. The diagnosis should be suspected in an adult male presenting with slowly progressive lower motor neuron symptoms, typically affecting the lower limbs at onset. Bulbar involvement (dysarthria and dysphagia) is often a later manifestation of the disease. Gynecomastia is not a constant feature, but is suggestive of a suspected diagnosis, which is further supported by electromyography showing diffuse motor neuron involvement often with asymptomatic sensory changes. A suspected diagnosis is confirmed by genetic testing. The multidisciplinary assessment should ascertain extra-neurological involvement such as cardiac repolarisation abnormalities (Brugada syndrome), signs of androgen resistance, genitourinary abnormalities, endocrine and metabolic changes (glucose intolerance, hyperlipidemia). In the absence of effective disease modifying therapies, the mainstay of management is symptomatic support using rehabilitation strategies (physiotherapy and speech therapy). Nutritional evaluation by an expert dietician is essential, and enteral nutrition (gastrostomy) may be required. Respiratory management centres on the detection and treatment of bronchial obstructions, as well as screening for aspiration pneumonia (chest physiotherapy, drainage, positioning, breath stacking, mechanical insufflation-exsufflation, cough assist machnie, antibiotics). Non-invasive mechanical ventilation is seldom needed. Symptomatic pharmaceutical therapy includes pain management, endocrine and metabolic interventions. There is no evidence for androgen substitution therapy.ConclusionThe French national Kennedy’s disease protocol provides management recommendations for patients with KD. In a low-incidence condition, sharing and integrating regional expertise, multidisciplinary experience and defining consensus best-practice recommendations is particularly important. Well-coordinated collaborative efforts will ultimately pave the way to the development of evidence-based international guidelines.
Journal of neurology · 2019
Journal of the neurological sciences · 2018
Source PubMed · Recherche par auteur (homonymes possibles, vérifier l'affiliation).
Brain : a journal of neurology · 2026 · Journal Article
Yogeshwar SM, Bartels F, Grüter T, Muñiz-Castrillo S, et al.
Neurology(R) neuroimmunology & neuroinflammation · 2025 · Journal Article
Farina A, Villagrán-García M, Abichou-Klich A, Benaiteau M, et al.
Journal of neurology · 2025 · Journal Article
Farina A, Villagrán-García M, Abichou-Klich A, Benaiteau M, et al.
Annals of clinical and translational neurology · 2025 · Journal Article
Delorme C, Pégat A, Theuriet J, Brandel JP, et al.
The Journal of surgical research · 2025 · Journal Article
Sathe SV, Sparkman B, Bernard E, Smith ER, et al.
Neurology(R) neuroimmunology & neuroinflammation · 2023 · Journal Article
Cluse F, Hermier M, Demarquay G, Rogemond V, et al.
Neurology(R) neuroimmunology & neuroinflammation · 2023 · Case Reports
Svahn J, Coudert L, Streichenberger N, Kraut A, et al.
Annals of neurology · 2022 · Letter
Pegat A, Vogrig A, Khouri C, Masmoudi K, et al.
Genetics in medicine : official journal of the American College of Medical Genetics · 2021 · Journal Article
Benkirane M, Marelli C, Guissart C, Roubertie A, et al.
Frontiers in neuroscience · 2020 · Journal Article
Esselin F, Mouzat K, Polge A, Juntas-Morales R, et al.
Journal of neurology · 2019 · Journal Article
Vogrig A, Joubert B, Maureille A, Thomas L, et al.
Medecine et maladies infectieuses · 2015 · Journal Article
Roger PM, Tabutin J, Blanc V, Léotard S, et al.
Communications medicine · 2025 · Journal Article
Gobert F, Merida I, Maby E, Seguin P, et al.
Neurology(R) neuroimmunology & neuroinflammation · 2025 · Journal Article
Cluse F, Do LD, Bernard E, Rogemond V, et al.
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2023 · Case Reports
Tankéré P, Le Cam P, Folliet L, Bernard E, et al.
Neurology(R) neuroimmunology & neuroinflammation · 2022 · Case Reports
European journal of human genetics : EJHG · 2024 · Journal Article
Theuriet J, Fernandez-Eulate G, Latour P, Stojkovic T, et al.
European journal of neurology · 2023 · Journal Article
Pons N, Fernández-Eulate G, Pegat A, Théaudin M, et al.
Journal of neurology, neurosurgery, and psychiatry · 2021 · Journal Article
Muratet F, Teyssou E, Chiot A, Boillée S, et al.
Lancet (London, England) · 2025 · Journal Article
Bensimon G, Leigh PN, Tree T, Malaspina A, et al.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2017 · Journal Article
Courjon J, Demonchy E, Cua E, Bernard E, et al.
Muscle & nerve · 2025 · Journal Article
Theuriet J, Bernard E, Guy N, Taithe F, et al.
Journal of the neurological sciences · 2018 · Case Reports
Bourgeois-Vionnet J, Joubert B, Bernard E, Sia MA, et al.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2017 · Journal Article
Courjon J, Demonchy E, Cua E, Bernard E, et al.
Lancet (London, England) · 2025 · Journal Article
Bensimon G, Leigh PN, Tree T, Malaspina A, et al.
European journal of neurology · 2025 · Case Reports
Pegat A, Svahn J, Gerfaud-Valentin M, Durel CA, et al.
Orphanet journal of rare diseases · 2020 · Journal Article
Pradat PF, Bernard E, Corcia P, Couratier P, et al.
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2023 · Case Reports
Tankéré P, Le Cam P, Folliet L, Bernard E, et al.
The French national protocol for Kennedy’s disease (SBMA): consensus diagnostic and management recommendations
Abstract Background Kennedy’s disease (KD), also known as spinal and bulbar muscular atrophy (SBMA), is a rare, adult-onset, X-linked recessive neuromuscular disease caused by CAG expansions in exon 1 of the androgen rec
Mapping total suspended matter from geostationary satellites: a feasibility study with SEVIRI in the Southern North Sea
Geostationary ocean colour sensors have not yet been launched into space, but are under consideration by a number of space agencies. This study provides a proof of concept for mapping of Total Suspended Matter (TSM) in t
Immunoglobulin light-chain amyloidosis mimicking bulbar amyotrophic lateral sclerosis
Immunoglobulin light-chain amyloidosis mimicking bulbar amyotrophic lateral sclerosis
Mapping total suspended matter from geostationary satellites: a feasibility study with SEVIRI in the Southern North Sea
Geostationary ocean colour sensors have not yet been launched into space, but are under consideration by a number of space agencies. This study provides a proof of concept for mapping of Total Suspended Matter (TSM) in t
The French national protocol for Kennedy’s disease (SBMA): consensus diagnostic and management recommendations
Abstract Background Kennedy’s disease (KD), also known as spinal and bulbar muscular atrophy (SBMA), is a rare, adult-onset, X-linked recessive neuromuscular disease caused by CAG expansions in exon 1 of the androgen rec
Immunoglobulin light-chain amyloidosis mimicking bulbar amyotrophic lateral sclerosis
Immunoglobulin light-chain amyloidosis mimicking bulbar amyotrophic lateral sclerosis
Source : DataCite — DOIs pour datasets, logiciels, protocoles, registres patient. Hors articles (déjà couverts).
Pegat A, Delmont E, Svahn J, Bernard E, et al.
Journal of the neurological sciences · 2018 · Case Reports
Bourgeois-Vionnet J, Joubert B, Bernard E, Sia MA, et al.
Journal of neurology, neurosurgery, and psychiatry · 2021 · Journal Article
Corcia P, Camu W, Brulard C, Marouillat S, et al.