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Impact of music therapy before first‐trimester instrumental termination of pregnancy: a randomised controlled trial

BJOG : an international journal of obstetrics and gynaecology, 2020-05, Vol.127 (6), p.738-745

2020

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Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective study

Journal of neurology, 2022-12, Vol.269 (12), p.6354-6365

2022

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Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients

Journal of medical genetics, 2009-03, Vol.46 (3), p.183-191

2009

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Surfactant-polymer interactions: molecular architecture does matter

Soft matter, 2015-01, Vol.11 (12), p.2504-2511

2015

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Deciphering the natural history of SCA7 in children

European journal of neurology, 2020-11, Vol.27 (11), p.2267-2276

2020

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Pre-symptomatic diagnosis in ALS

Revue neurologique, 2020-03, Vol.176 (3), p.166-169

2020

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Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work

Journal of neurology, 2017-06, Vol.264 (6), p.1118-1126

2017

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ABORD DE LA SANTE AFFECTIVE ET SEXUELLE DES ADOLESCENTS PAR LES CONSEILLERES CONJUGALES ET FAMILIALES

EXERCER, 2021-11, Vol.32 (177), p.395-401

2021

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Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia

Journal of medical genetics, 2007-04, Vol.44 (4), p.281-284

2007

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Motor neuron disease of very long disease duration or Charcot–Marie–Tooth disease? A novel phenotype related to the SOD1 p.E22G variant

Revue neurologique, 2017-12, Vol.173 (10), p.671-673

2017

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Mélanome sur naevus spilus : 5 observations

Annales de dermatologie et de vénéréologie, 2006-04, Vol.133 (4), p.323-328

2006

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Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

Human mutation, 2000-08, Vol.16 (2), p.143-156

2000

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Methodology to study polymers interaction by surface plasmon resonance imaging

MethodsX, 2015-01, Vol.2 (C), p.14-18

2015

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Low disease risk in relatives of north african lrrk2 Parkinson disease patients

Neurology, 2010-09, Vol.75 (12), p.1118-1119

2010

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Intrafamilial segregation analysis of the p.E148Q MEFV allele in familial Mediterranean fever

Annals of the rheumatic diseases, 2006-09, Vol.65 (9), p.1154-1157

2006

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Autosomal dominant cerebellar ataxias

Revue neurologique, 2011-05, Vol.167 (5), p.385-400

2011

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Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia

Brain (London, England : 1878), 2009-07, Vol.132 (7), p.1753-1763

2009

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Comprehensive Cystic Fibrosis Mutation Epidemiology and Haplotype Characterization in a Southern Italian Population

Annals of human genetics, 2005-01, Vol.69 (1), p.15-24

2005

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Screening practices for mutations in the CFTR gene ABCC7

Human mutation, 2000-02, Vol.15 (2), p.135-149

2000

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Clinical versus genetic diagnosis of familial Mediterranean fever

QJM : An International Journal of Medicine, 2000-04, Vol.93 (4), p.223-229

2000

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ALPK3 gene in cardiomyopathies: Which phenotypes? Which mode of inheritance?

Archives of cardiovascular diseases supplements, 2023-01, Vol.15 (1), p.38

2023

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Subcellular localisation of marenostrin/pyrin isoforms carrying the most common mutations involved in familial Mediterranean fever in the presence or absence of its binding partner ASC

Journal of medical genetics, 2004-03, Vol.41 (3), p.e24-24

2004

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Melanoma within naevus spilus: 5 cases

Annales de dermatologie et de vénéréologie, 2006-04, Vol.133 (4), p.323-328

2006

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Bioinspired Self-Assembled 3D Patterned Polymer Textures as Skin Coatings Models: Tribology and Tactile Behavior

Biotribology (Oxford), 2020-12, Vol.24, p.100151, Article 100151

2020

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Impact of music therapy before first‐trimester instrumental termination of pregnancy: a randomised controlled trial

Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective study

Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients

SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

Surfactant-polymer interactions: molecular architecture does matter

Deciphering the natural history of SCA7 in children

Pre-symptomatic diagnosis in ALS

Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work

ABORD DE LA SANTE AFFECTIVE ET SEXUELLE DES ADOLESCENTS PAR LES CONSEILLERES CONJUGALES ET FAMILIALES

Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia

Motor neuron disease of very long disease duration or Charcot–Marie–Tooth disease? A novel phenotype related to the SOD1 p.E22G variant

Mélanome sur naevus spilus : 5 observations

Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

Methodology to study polymers interaction by surface plasmon resonance imaging

Low disease risk in relatives of north african lrrk2 Parkinson disease patients

Intrafamilial segregation analysis of the p.E148Q MEFV allele in familial Mediterranean fever

Autosomal dominant cerebellar ataxias

Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia

Comprehensive Cystic Fibrosis Mutation Epidemiology and Haplotype Characterization in a Southern Italian Population

Screening practices for mutations in the CFTR gene ABCC7

Clinical versus genetic diagnosis of familial Mediterranean fever

ALPK3 gene in cardiomyopathies: Which phenotypes? Which mode of inheritance?

Subcellular localisation of marenostrin/pyrin isoforms carrying the most common mutations involved in familial Mediterranean fever in the presence or absence of its binding partner ASC

Melanoma within naevus spilus: 5 cases

Bioinspired Self-Assembled 3D Patterned Polymer Textures as Skin Coatings Models: Tribology and Tactile Behavior

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