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Late gadolinium enhancement role in arrhythmic risk stratification of patients with LMNA cardiomyopathy: results from a long-term follow-up multicentre study.
- Published in:
- 2020
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- Publication type:
- journal article
Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants.
- Published in:
- 2019
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- Publication type:
- journal article
Assessing and enhancing migration of human myogenic progenitors using directed iPS cell differentiation and advanced tissue modelling.
- Published in:
- EMBO Molecular Medicine, 2022, v. 14, n. 10, p. 1, doi. 10.15252/emmm.202114526
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- Publication type:
- Article
Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next‐generation human artificial chromosomes for Duchenne muscular dystrophy.
- Published in:
- EMBO Molecular Medicine, 2018, v. 10, n. 2, p. 254, doi. 10.15252/emmm.201607284
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- Publication type:
- Article
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy.
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- EMBO Molecular Medicine, 2016, v. 8, n. 12, p. 1470, doi. 10.15252/emmm.201607129
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- Publication type:
- Article
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy.
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- EMBO Molecular Medicine, 2015, v. 7, n. 12, p. 1513, doi. 10.15252/emmm.201505636
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- Publication type:
- Article
In vivo generation of a mature and functional artificial skeletal muscle.
- Published in:
- EMBO Molecular Medicine, 2015, v. 7, n. 4, p. 411, doi. 10.15252/emmm.201404062
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- Publication type:
- Article
The empowerment of translational research: lessons from laminopathies.
- Published in:
- 2012
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- Publication type:
- Letter
The empowerment of translational research: lessons from laminopathies.
- Published in:
- Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 37, doi. 10.1186/1750-1172-7-37
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- Publication type:
- Article
Gene therapy of experimental brain tumors using neural progenitor cells.
- Published in:
- Nature Medicine, 2000, v. 6, n. 4, p. 447, doi. 10.1038/74710
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- Publication type:
- Article
Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 11, p. 9548, doi. 10.3390/ijms24119548
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- Publication type:
- Article
Molecular Genetics of GLUT1DS Italian Pediatric Cohort: 10 Novel Disease-Related Variants and Structural Analysis.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 21, p. 13560, doi. 10.3390/ijms232113560
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- Publication type:
- Article
Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 9, p. 4700, doi. 10.3390/ijms22094700
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- Publication type:
- Article
Novel SCN5A p.V1429M Variant Segregation in a Family with Brugada Syndrome.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 16, p. 5902, doi. 10.3390/ijms21165902
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- Publication type:
- Article
Novel SCN5A p.W697X Nonsense Mutation Segregation in a Family with Brugada Syndrome.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 19, p. 4920, doi. 10.3390/ijms20194920
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- Publication type:
- Article
Efficacy and Safety of Ceftazidime–Avibactam Alone versus Ceftazidime–Avibactam Plus Fosfomycin for the Treatment of Hospital-Acquired Pneumonia and Ventilator-Associated Pneumonia: A Multicentric Retrospective Study from the SUSANA Cohort.
- Published in:
- Antibiotics (2079-6382), 2024, v. 13, n. 7, p. 616, doi. 10.3390/antibiotics13070616
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- Publication type:
- Article
Pre and Post-Monoclonal Infusion Neutralizing Activity in a Subgroup of Patients Treated in the Presence of two SARS-CoV-2 Dominant Variant of Concern (VOCs) and an Ongoing Vaccination. Overall Clinical Efficacy of Two Monoclonal Antibodies Association in Umbria
- Published in:
- Mediterranean Journal of Hematology & Infectious Diseases, 2022, v. 14, n. 1, p. 1, doi. 10.4084/MJHID.2022.050
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- Publication type:
- Article
Bictegravir/Tenofovir Alafenamide/Emtricitabine: A Real-Life Experience in People Living with HIV (PLWH).
- Published in:
- Infectious Disease Reports, 2023, v. 15, n. 6, p. 766, doi. 10.3390/idr15060069
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- Publication type:
- Article
Brugada syndrome genetics is associated with phenotype severity.
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- European Heart Journal, 2021, v. 42, n. 11, p. 1082, doi. 10.1093/eurheartj/ehaa942
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- Publication type:
- Article
Expanding the central nervous system disease spectrum associated with FLNC mutation.
- Published in:
- 2019
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- Publication type:
- journal article
Separazione coniugale e relazioni genitori-figli in età adulta.
- Published in:
- Terapia Familiare, 2002, n. 70, p. 5
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- Publication type:
- Article
Cognitive Impairment Affects Physical Recovery of Patients with Heart Failure Undergoing Intensive Cardiac Rehabilitation.
- Published in:
- Rehabilitation Research & Practice, 2012, p. 1, doi. 10.1155/2012/218928
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- Publication type:
- Article
Genetics can contribute to the prognosis of Brugada syndrome: a pilot model for risk stratification.
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- European Journal of Human Genetics, 2013, v. 21, n. 9, p. 911, doi. 10.1038/ejhg.2012.289
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- Publication type:
- Article
A Brugada syndrome mutation (p.S216L) and its modulation by p.H558R polymorphism: standard and dynamic characterization.
- Published in:
- Cardiovascular Research, 2011, v. 91, n. 4, p. 606, doi. 10.1093/cvr/cvr142
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- Publication type:
- Article
Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer.
- Published in:
- BMC Genomics, 2008, v. 9, p. 1, doi. 10.1186/1471-2164-9-464
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- Publication type:
- Article
Novel SCN5A Frameshift Mutation in Brugada Syndrome Associated With Complex Arrhythmic Phenotype.
- Published in:
- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00547
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- Publication type:
- Article
Immunosuppressive therapy in childhood‐onset arrhythmogenic inflammatory cardiomyopathy.
- Published in:
- Pacing & Clinical Electrophysiology, 2021, v. 44, n. 3, p. 552, doi. 10.1111/pace.14153
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- Publication type:
- Article
Repair or replace? Exploiting novel gene and cell therapy strategies for muscular dystrophies.
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- FEBS Journal, 2013, v. 280, n. 17, p. 4263, doi. 10.1111/febs.12178
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- Publication type:
- Article
PW1/Peg3 expression regulates key properties that determine mesoangioblast stem cell competence.
- Published in:
- Nature Communications, 2015, v. 6, n. 3, p. 6364, doi. 10.1038/ncomms7364
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- Publication type:
- Article
Neutrophil unsaturated fatty acid release by GM-CSF is impaired in cystic fibrosis.
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- Lipids in Health & Disease, 2010, v. 9, p. 129, doi. 10.1186/1476-511X-9-129
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- Publication type:
- Article
A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation.
- Published in:
- 2015
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- Publication type:
- Letter
Hypnosis-induced modulation of corticospinal excitability during motor imagery.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-74020-0
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- Publication type:
- Article
Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation.
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- Human Molecular Genetics, 2020, v. 29, n. 2, p. 177, doi. 10.1093/hmg/ddz211
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- Publication type:
- Article
High-throughput genetic characterization of a cohort of Brugada syndrome patients.
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- Human Molecular Genetics, 2015, v. 24, n. 20, p. 5828, doi. 10.1093/hmg/ddv302
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- Publication type:
- Article
Transplantation of Genetically Corrected Human iPSC-Derived Progenitors in Mice with Limb-Girdle Muscular Dystrophy.
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- Science Translational Medicine, 2012, v. 4, n. 140, p. 1, doi. 10.1126/scitranslmed.3003541
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- Publication type:
- Article
Stem Cell-Mediated Transfer of a Human Artificial Chromosome Ameliorates Muscular Dystrophy.
- Published in:
- Science Translational Medicine, 2011, v. 3, n. 96, p. 1, doi. 10.1126/scitranslmed.3002342
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- Publication type:
- Article
Mesoangioblasts at 20: From the embryonic aorta to the patient bed.
- Published in:
- Frontiers in Genetics, 2023, v. 13, p. 1, doi. 10.3389/fgene.2022.1056114
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- Publication type:
- Article
Genotype/Phenotype Relationship in a Consanguineal Family With Brugada Syndrome Harboring the R1632C Missense Variant in the SCN5A Gene.
- Published in:
- Frontiers in Physiology, 2019, p. N.PAG, doi. 10.3389/fphys.2019.00666
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- Publication type:
- Article
Vascular growth factors play critical roles in kidney glomeruli.
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- Clinical Science, 2015, v. 129, n. 12, p. 1225, doi. 10.1042/CS20150403
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- Publication type:
- Article
Comparison of biochemical analysis of fetal serum and fetal urine in the prediction of postnatal renal outcome in lower urinary tract obstruction.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Concealed Substrates in Brugada Syndrome: Isolated Channelopathy or Associated Cardiomyopathy?
- Published in:
- Genes, 2022, v. 13, n. 10, p. N.PAG, doi. 10.3390/genes13101755
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- Publication type:
- Article
Corrigendum: Efficient derivation and inducible differentiation of expandable skeletal myogenic cells from human ES and patient-specific iPS cells.
- Published in:
- Nature Protocols, 2015, v. 10, n. 9, p. 1457, doi. 10.1038/nprot0915-1457d
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- Publication type:
- Article
Efficient derivation and inducible differentiation of expandable skeletal myogenic cells from human ES and patient-specific iPS cells.
- Published in:
- Nature Protocols, 2015, v. 10, n. 7, p. 941, doi. 10.1038/nprot.2015.057
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- Publication type:
- Article
When Paying Attention Pays Back: Missense Mutation c.1006G>A p. (Val336Ile) in PRKAG2 Gene Causing Left Ventricular Hypertrophy and Conduction Abnormalities in a Caucasian Patient: Case Report and Literature Review.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 17, p. 9171, doi. 10.3390/ijms25179171
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- Publication type:
- Article