Publications by authors named "Remi Bellance"

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Overall and by subtype epidemiology of idiopathic inflammatory myopathies among African descent patients with free access to high standard healthcare.
Aurore Abel, Rachel Robert, Arthur Felix, Illitch Coco-Viloin, Florence Moinet, Remi Bellance

Semin Arthritis Rheum· December 2025

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Huntington's Disease and Huntington's Disease-like 2 (HDL2) in Martinique.
Ignacio Antolin-Sanfeliz, Anna-Gaelle Giguet-Valard, Sophie Duclos, Cécile Cazeneuve, Chloé Angelini, Rémi Bellance

Mov Disord Clin Pract· October 2025

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A Late-Onset and Mild Phenotype of Mitochondrial Complex I Deficiency Due to a Novel Reported Variant Within the Gene.
Anna Gaelle Giguet-Valard, Samira Ait-El-Mkadem Saadi, Sophie Duclos, Didier Lacombe, Rémi Bellance, Nadège Bellance

Int J Mol Sci· July 2025

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Prevalence of Fabry disease in patients with chronic pain: Lessons from the DOUFAB and DOUFABIS studies.
Chloé Angelini, Claire Bar, Marie Pierre Baudier, Patricia Fergelot, Gwenaëlle Lancelot, Rémi Bellance

Eur J Pain· January 2025

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Multidisciplinary team meetings in treatment of spinal muscular atrophy adult patients: a real-life observatory for innovative treatments.
Emmanuelle Salort-Campana, Guilhem Solé, Armelle Magot, Céline Tard, Jean-Baptiste Noury, Rémi Bellance

Orphanet J Rare Dis· January 2024

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Autosomal Dominant MPAN: Mosaicism Expands the Clinical Spectrum to Atypical Late-Onset Phenotypes.
Chloé Angelini, Christelle Marie Durand, Patricia Fergelot, Julie Deforges, Anne Vital, Rémi Bellance

Mov Disord· November 2023

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[Not Available].
Rémi Bellance, Ignacio Antolín Sanféliz, Sophie Duclos, Anna-Gäelle Guiget-Valard, Jocelyn Inamo

Med Sci (Paris)· November 2023

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Juvenile Dermatomyositis in Afro-Caribbean children: a cohort study in the French West Indies.
Arthur Felix, Frederique Delion, Fabienne Louis-Sidney, Lindsay Osei, Aurélie Armougon, Remi Bellance

Pediatr Rheumatol Online J· October 2023

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SOD1-related ALS with anticipation in a large family from Martinique.
Anna-Gaelle Giguet-Valard, Rémi Bellance, Séverine Jeannin, Sophie Duclos, Pascale Olive

Amyotroph Lateral Scler Frontotemporal Degener· November 2021

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Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) Myopathy Misdiagnosed as Polymyositis.
Andrea Barp, Rémi Bellance, Edoardo Malfatti, Odile Rigal, Cécile Acquaviva-Bourdain

J Clin Rheumatol· August 2020

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Single-fiber studies for assigning pathogenicity of eight mitochondrial DNA variants associated with mitochondrial diseases.
Elamine Zereg, Annabelle Chaussenot, Godelieve Morel, Sylvie Bannwarth, Sabrina Sacconi, Rémi Bellance

Hum Mutat· August 2020

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Deciphering the complexity of the 4q and 10q subtelomeres by molecular combing in healthy individuals and patients with facioscapulohumeral dystrophy.
Karine Nguyen, Natacha Broucqsault, Charlene Chaix, Stephane Roche, Jérôme D Robin, Remi Bellance

J Med Genet· September 2019

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X-linked myotubular myopathy: A prospective international natural history study.
Mélanie Annoussamy, Charlotte Lilien, Teresa Gidaro, Elena Gargaun, Virginie Chê, Rémi Bellance

Neurology· April 2019

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A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management.
Emmanuelle Lagrue, Céline Dogan, Marie De Antonio, Frédérique Audic, Nathalie Bach, Rémi Bellance

Neurology· February 2019

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[An overview of Duchenne muscular dystrophy in Martinique].
Elisabeth Sarrazin, Anna-Gaëlle Valard-Giguet, France Leturcq, Rémi Bellance

Med Sci (Paris)· November 2018

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Phenotypic and genotypic studies of ALS cases in ALS-SMA families.
Philippe Corcia, Patrick Vourc'h, Helene Blasco, Philippe Couratier, Audrey Dangoumau, Remi Bellance

Amyotroph Lateral Scler Frontotemporal Degener· August 2018

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[Episodes of recurrent pneumothorax in a patient with collagen VI-related congenital muscular dystrophy].
Rémi Bellance, Rudy Valentino, Bruno Sanchez, Octavio Labrada-Blanco, Linda Manere

Med Sci (Paris)· November 2017

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Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study.
Celine Dogan, Marie De Antonio, Dalil Hamroun, Hugo Varet, Marianne Fabbro, Remi Bellance

PLoS One· July 2016

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Cylindrical spirals associated with severe congenital muscle weakness and epileptic encephalopathy.
Edoardo Malfatti, Marcelo Chaves, Remi Bellance, Mai Thao Viou, Elisabeth Sarrazin

Muscle Nerve· November 2015

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[The Caribbean Reference Centre for rare neuromuscular and neurological disorders].
Rémi Bellance

Med Sci (Paris)· November 2015

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Anti-HMGCR autoantibodies in European patients with autoimmune necrotizing myopathies: inconstant exposure to statin.
Yves Allenbach, Laurent Drouot, Aude Rigolet, Jean Luc Charuel, Fabienne Jouen, Remi Bellance

Medicine (Baltimore)· May 2014

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Muscle histopathology in nebulin-related nemaline myopathy: ultrastrastructural findings correlated to disease severity and genotype.
Edoardo Malfatti, Vilma-Lotta Lehtokari, Johann Böhm, Josine M De Winter, Ursula Schäffer, Remi Bellance

Acta Neuropathol Commun· April 2014

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Antisignal recognition particle antibodies-related cardiomyopathy.
Mathilde Thiébaut, Benjamin Terrier, Samia Menacer, Alice Berezne, Guillaume Bussone, Rémi Bellance

Circulation· February 2013

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Absence of consistent association between human leukocyte antigen-I and -II alleles and human T-lymphotropic virus type 1 (HTLV-1)-associated myelopathy/tropical spastic paraparesis risk in an HTLV-1 French Afro-Caribbean population.
Romain Deschamps, Odile Béra, Gilda Belrose, Agnès Lezin, Rémi Bellance

Int J Infect Dis· November 2010

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Mutations in TPM3 are a common cause of congenital fiber type disproportion.
Nigel F Clarke, Hanna Kolski, Danielle E Dye, Esther Lim, Robert L L Smith, Rémi Bellance

Ann Neurol· March 2008

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