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Letter by Aimo et al Regarding Article, "Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies"
Aimo A, Barison A, Emdin M
Circulation, 2019, 140, 23
Letter by Barriales-Villa et al Regarding Article, "Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies"
Barriales-Villa R, Larranaga-Moreira JM, Ochoa JP
Circulation, 2019, 140, 23
Response by Wahbi and Stalens to Letter Regarding Article, "Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies"
Wahbi K, Stalens C
Circulation, 2019, 140, 23
ERK1/2 Phosphorylation of FHOD Connects Signaling and Nuclear Positioning Alternations in Cardiac Laminopathy
Antoku S, Wu W, Joseph LC, et al.
Developmental cell, 2019, 51, 5, p 602
Lamin A/C Cardiomyopathy: Implications for Treatment
Chen SN, Sbaizero O, Taylor MRG, et al.
Current Cardiology Reports, 2019, 21, 12, p 160
Emery-Dreifuss muscular dystrophy: focal point nuclear envelope
Muchir A, Worman HJ
Current opinion in neurology, 2019, 32, 5, p 728
Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies
Wahbi K, Ben Yaou R, Gandjbakhch E, et al.
Circulation, 2019
L’imagerie musculaire corps entier s’avère très utile dans le diagnostic différentiel du syndrome de la colonne raide
Urtizberea JA
2018
Lamin and the heart
Captur G, Arbustini E, Bonne G, et al.
Heart (British Cardiac Society), 2018, 104, 6, p 468
Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy
Azibani F, Brull A, Arandel L, et al.
Molecular therapy. Nucleic acids, 2018, 10, p 376
Low-symptomatic skeletal muscle disease in patients with a cardiac disease - Diagnostic approach in skeletal muscle laminopathies
Madej-Pilarczyk A, Marchel M, Ochman K, et al.
Neurologia i neurochirurgia polska, 2018, 52, 2, p 174
Clinical aspects of Emery-Dreifuss muscular dystrophy
Madej-Pilarczyk A
Nucleus (Austin, Tex.), 2018, 9, 1, p 268
SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells
Janin A, Bauer D, Ratti F, et al.
Scientific Reports, 2018, 8, 1
Nuclear Lamins: Thin Filaments with Major Functions
de Leeuw R, Gruenbaum Y, Medalia O
Trends in cell biology, 2018, 28, 1, p 34
Congenital muscular dystrophies in the UK population: Clinical and molecular spectrum of a large cohort diagnosed over a 12-year period
Sframeli M, Sarkozy A, Bertoli M, et al.
Neuromuscular disorders : NMD, 2017, 27, 9, p 793
Congenital Muscular Dystrophies and Myopathies: An Overview and Update
Schorling DC, Kirschner J, Bonnemann CG
Neuropediatrics, 2017, 48, 4, p 247
A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus
Barateau A, Vadrot N, Vicart P, et al.
PLoS ONE, 2017, 12, 1
Un diabète particulièrement compliqué
Ambonville C, Bouldouyre MA, Laforêt P, et al.
La Revue de medecine interne, 2017, 38, 10, p 695
Adult-onset spinal muscular atrophy: An update
Juntas Morales R, Pageot N, Taïeb G, et al.
Revue neurologique, 2017, 173, 5, p 308
Lamins and nesprin-1 mediate inside-out mechanical coupling in muscle cell precursors through FHOD1
Schwartz C, Fischer M, Mamchaoui K, et al.
Scientific Reports, 2017, 7, 1
Myology 2016 : 5th International Congress of Myology ; Symposium - Laminopathies
Gomes E, Bonne G, Lévy N
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 17
Myology 2016 : 5th International Congress of Myology ; Posters n° 66 to 75 - Congenital muscular dystrophies / Dystrophinopathies
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 55-59
Skeletal Muscle Laminopathies: A Review of Clinical and Molecular Features
Maggi L, Carboni N, Bernasconi P
Cells, 2016, 5, 3
Distal acroosteolysis, poikiloderma and joint stiffness: a novel laminopathy?
Sewairi W, Assiri A, Patel N, et al.
European journal of human genetics : EJHG, 2016, 24, 8, p 1220
