Search Results - "Labella, B."

Author Correction: SARS-CoV-2 antibody dynamics and transmission from community-wide serological testing in the Italian municipality of Vo'.

Authors: Dorigatti I Lavezzo E Manuto L et al.

Source: Nature communications [Nat Commun] 2021 Aug 12; Vol. 12 (1), pp. 5020. Date of Electronic Publication: 2021 Aug 12.

Publication Type: Published Erratum

Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE; PubMed not MEDLINE

Unveiling MYH2-related myopathy: Histological-genetic insights from a case series and systematic review.

Authors: Labella B Brochier G Beuvin M et al.

Source: Journal of neuromuscular diseases [J Neuromuscul Dis] 2026 May; Vol. 13 (3), pp. 388-404. Date of Electronic Publication: 2025 Nov 18.

Publication Type: Journal Article; Systematic Review

Journal Info: Publisher: IOS Press Country of Publication: United States NLM ID: 101649948 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2214-3602 (Electronic) Linking ISSN: 22143599 NLM ISO Abbreviation: J Neuromuscul Dis Subsets: MEDLINE

Survival in a Contemporary, Real-World Cohort of Patients with Mixed-Phenotype Transthyretin Amyloid Cardiomyopathy Treated with Tafamidis: An Analysis from THAOS.

Authors: Wixner, Jonas Dispenzieri, Angela Amass, Leslie et al.

Source: Cardiology & Therapy. Dec2025, Vol. 14 Issue 4, p583-599. 17p.

Hereditary Transthyretin Amyloidosis in Austria: Clinical, Genetic, and Demographic Insights from a Nationwide Cohort.

Authors: Ermolaev, Nikita Löscher, Wolfgang N. Verheyen, Nicolas et al.

Source: Journal of Clinical Medicine. Mar2026, Vol. 15 Issue 5, p1958. 14p.

Author Correction: Suppression of a SARS-CoV-2 outbreak in the Italian municipality of Vo'.

Authors: Lavezzo E Franchin E Ciavarella C et al.

Corporate Authors: Lavezzo E Franchin E Ciavarella C et al.

Source: Nature [Nature] 2021 Feb; Vol. 590 (7844), pp. E11.

Publication Type: Published Erratum

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print Cited Medium: Internet ISSN: 1476-4687 (Electronic) Linking ISSN: 00280836 NLM ISO Abbreviation: Nature Subsets: MEDLINE; PubMed not MEDLINE

Transthyretin amyloid deposition in the ligamentum flavum of an Italian cohort of patients with lumbar spinal stenosis.

Authors: Vitali, Francesca Fenu, Silvia Izzo, Alessandro et al.

Source: Neurological Sciences. Jul2025, Vol. 46 Issue 7, p3295-3298. 4p.

Subjects: Spinal stenosis, Amyloid plaque, Spinal canal, DNA analysis, Amyloid

Contemporary Description of Clinical Characteristics and Outcomes in Patients with Hereditary ATTR Amyloidosis: Results from the Multicountry OverTTuRe Study.

Authors: Alexander, Kevin M. Kohsaka, Shun Poulsen, Steen Hvitfeldt et al.

Source: Cardiology & Therapy. Jun2026, Vol. 15 Issue 2, p201-229. 29p.

Wearables for Telemonitoring in ATTR-Amyloidosis: Current Perspectives.

Authors: Kind, Andreas Pernice, Helena Barzen, Gina et al.

Source: Sensors (14248220). May2026, Vol. 26 Issue 10, p3035. 21p.

A novel transthyretin variant p.Val114Glu (Val94Glu) in an Italian patient with mixed phenotype hereditary transthyretin amyloidosis.

Authors: Vitali, Francesca Nuvolone, Mario Romano, Angela et al.

Source: Amyloid. Sep2025, Vol. 32 Issue 3, p292-296. 5p.

Extensive digital health technology assessment detects subtle motor impairment in mild and asymptomatic Pompe disease.

Authors: Pilotto, Andrea Labella, Beatrice Rizzardi, Andrea et al.

Source: Scientific Reports. 8/14/2025, Vol. 15 Issue 1, p1-7. 7p.

The Vagal Link: Autonomic Nervous System Dysfunction in Cardiac Amyloidosis.

Authors: Barocelli, Federico Canu, Eleonora Pasini, Nicolò et al.

Source: Journal of Clinical Medicine. Dec2025, Vol. 14 Issue 24, p8963. 27p.

Degenerative Cervical Myelopathy Diagnosis and Its Differentiation from Neurological Mimics, MS and ALS: A Literature Review.

Authors: Klumb, Sydney Haley, Lauren Hathaway, Chase et al.

Source: Journal of Clinical Medicine. Dec2025, Vol. 14 Issue 24, p8711. 15p.

Multimodal Biomarker Characterization of the ALS/FTD Spectrum: A Real-World Clinical Dataset Analysis.

Authors: Mukhija, Sasha Hering, Lisa Schreiner, Simon J. et al.

Source: International Journal of Molecular Sciences. Dec2025, Vol. 26 Issue 23, p11496. 15p.

The European reference network for metabolic diseases (MetabERN) clinical pathway recommendations for Pompe disease (acid maltase deficiency, glycogen storage disease type II).

Authors: Parenti, Giancarlo Fecarotta, Simona Alagia, Marianna et al.

Source: Orphanet Journal of Rare Diseases. 11/1/2024, Vol. 19 Issue 1, p1-23. 23p.

A Comprehensive Update on Pompe Disease: From Existing Therapies to Emerging Curative Strategies.

Authors: Estevez Barcia, Rebeca Colón, Cristóbal Hermida-Ameijeiras, Álvaro et al.

Source: International Journal of Molecular Sciences. Jul2026, Vol. 27 Issue 13, p5726. 25p.

Cell Death in Skeletal Muscle Diseases: Diverse Roles and Pathological Processes.

Authors: Yang, Ya-Lan Guo, Liang

Source: Cells (2073-4409). May2026, Vol. 15 Issue 9, p744. 38p.

Hereditary transthyretin amyloidosis: a comprehensive review with a focus on peripheral neuropathy.

Authors: Poli L Labella B Cotti Piccinelli S et al.

Source: Frontiers in neurology [Front Neurol] 2023 Oct 05; Vol. 14, pp. 1242815. Date of Electronic Publication: 2023 Oct 05 (Print Publication: 2023).

Publication Type: Journal Article; Review

Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101546899 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2295 (Print) Linking ISSN: 16642295 NLM ISO Abbreviation: Front Neurol Subsets: PubMed not MEDLINE

Effectiveness and Utility of Genetic Testing in Establishing a Diagnosis of Hereditary Transthyretin Amyloidosis †.

Authors: Singh, Akash Wyatt, John Théaudin, Marie et al.

Source: Journal of Clinical Medicine. Oct2025, Vol. 14 Issue 19, p6821. 13p.

Atypical Presentation of Hereditary ATTR Amyloidosis with Gastrointestinal and Hepatic Manifestations in an 88-Year-Old Woman: A Case Report.

Authors: Singh, Anaiya Panchal, Viraj Gaddam, Shiva Jashwanth et al.

Source: American Journal of Case Reports. 8/17/2025, Vol. 26, p1-6. 6p.

SELENON-related myopathy as a cause of acute respiratory failure in middle age: a case report.

Authors: Risi B Caria F Damioli S et al.

Source: Journal of medical case reports [J Med Case Rep] 2025 Feb 20; Vol. 19 (1), pp. 64. Date of Electronic Publication: 2025 Feb 20.

Publication Type: Journal Article; Case Reports

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101293382 Publication Model: Electronic Cited Medium: Internet ISSN: 1752-1947 (Electronic) Linking ISSN: 17521947 NLM ISO Abbreviation: J Med Case Rep Subsets: MEDLINE