About: Anthony Behin

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Behin, Anthony (1970-....) Behin, Anthony (1970-....) Behin, Anthony (1970-....) Behin, Anthony (1970-....)
Life Event	http://www.idref.fr/069104972/birth
preferred label	Behin, Anthony (1970-....)
name	Anthony Behin
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000121261988
Given name	Anthony
familyName	Behin
has biographical i...tion (Deprecated)	Auteur d'une thèse d'exercice en médecine soutenue à l'Université Pierre et Marie Curie en 2003 Praticien hospitalier chez AP-HP. Clinicien de centre expert, investigateur principal d'essai clinique à l'Institut de Myologie (Hôpital Pitié-Salpêtrière) en 2018
gender	male
ORCID iD	0000-0001-7179-5152
is sameAs of	Behin, Anthony (1970-....) Behin, Anthony (1970-....) Behin, Anthony (1970-....) Behin, Anthony (1970-....)
is Author of	http://www.sudoc.fr/148850804/id http://www.sudoc.fr/076478009/id Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies High risk of cancer in autoimmune necrotizing myopathies: usefulness of myositis specific antibody A multicenter cross-sectional French study of the impact of COVID-19 on neuromuscular diseases Bezafibrate for an Inborn Mitochondrial Beta-Oxidation Defect Late-onset cervicoscapular muscle atrophy and weakness after radiotherapy for Hodgkin's disease: a case series Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA A diagnostic flow chart for POLG-related diseases based on signs sensitivity and specificity. https://hal.archives-ouvertes.fr/ensl-00960910#id Quickly progressive amyotrophy of the thigh: An unusual cause of rapid chondrolysis of the knee Sirolimus for treatment of patients with inclusion body myositis: a randomised, double-blind, placebo-controlled, proof-of-concept, phase 2b trial Risk factors associated with myasthenia gravis in thymoma patients: The potential role of thymic germinal centers Natural History of Cardiac and Respiratory Involvement, Prognosis and Predictive Factors for Long-Term Survival in Adult Patients with Limb Girdle Muscular Dystrophies Type 2C and 2D The spinal and cerebral profile of adult spinal-muscular atrophy: A multimodal imaging study Causes and Consequences of miR-150-5p Dysregulation in Myasthenia Gravis A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies A new case of SMA phenotype without epilepsy due to biallelic variants in ASAH1 Genetic Characterization of a French Cohort of GNE-mutation negative inclusion body myopathy patients with exome sequencing The motor unit number index (MUNIX) profile of patients with adult spinal muscular atrophy Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study Development of new outcome measures for adult SMA type III and IV: a multimodal longitudinal study Efficient Bypass of Mutations in Dysferlin Deficient Patient Cells by Antisense-Induced Exon Skipping Improved cardiac outcomes by early treatment with angiotensin-converting enzyme inhibitors in Becker muscular dystrophy Regulatory B cells in myasthenia gravis are differentially affected by therapies FSHD1 and FSHD2 form a disease continuum Deep phenotyping of an international series of patients with late‐onset dysferlinopathy Non Random Distribution of DMD Deletion Breakpoints and Implication of Double Strand Breaks Repair and Replication Error Repair Mechanisms Efficacy and safety of mexiletine in non-dystrophic myotonias: A randomised, double-blind, placebo-controlled, cross-over study Myofibrillar Myopathies: New Perspectives from Animal Models to Potential Therapeutic Approaches Cardiac Outcomes in Adults With Mitochondrial Diseases https://serval.unil.ch/notice/serval:BIB_DC240AF4B1D3#id The diagnostic value of hyperammonaemia induced by the non-ischaemic forearm exercise test https://orbi.uliege.be/handle/2268/256207#id http://hub.abes.fr/edp/periodical/medsci/2015/volume_31/issue_2015/medsci2015313sp20/w Endplate denervation correlates with Nogo-A muscle expression in amyotrophic lateral sclerosis patients
is primary topic of	http://www.idref.fr/069104972
is Editor of	http://www.sudoc.fr/06910414X/id
is Opponent of	http://www.sudoc.fr/253409918/id http://www.sudoc.fr/231450486/id

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