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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1988 2
1989 1
1990 1
1991 1
1993 1
1994 3
1995 4
1996 3
1997 1
1998 1
1999 4
2000 2
2001 1
2002 3
2003 3
2004 2
2005 4
2006 3
2007 1
2009 1
2010 3
2011 3
2012 7
2013 4
2014 6
2015 3
2016 4
2017 3
2018 3
2019 3
2020 6
2021 6
2022 3
2023 4
2024 3

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98 results

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Page 1
Repeated intravenous cardiosphere-derived cell therapy in late-stage Duchenne muscular dystrophy (HOPE-2): a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial.
McDonald CM, Marbán E, Hendrix S, Hogan N, Ruckdeschel Smith R, Eagle M, Finkel RS, Tian C, Janas J, Harmelink MM, Varadhachary AS, Taylor MD, Hor KN, Mayer OH, Henricson EK, Furlong P, Ascheim DD, Rogy S, Williams P, Marbán L; HOPE-2 Study Group. McDonald CM, et al. Lancet. 2022 Mar 12;399(10329):1049-1058. doi: 10.1016/S0140-6736(22)00012-5. Lancet. 2022. PMID: 35279258 Free article. Clinical Trial.
The primary outcome was the change in mid-level elbow Performance of Upper Limb version 1.2 (PUL 1.2) score at 12 months, assessed in the intention-to-treat population. ...Longer-term extension studies are needed to confirm the therapeutic durability and safety of CAP-1002 …
The primary outcome was the change in mid-level elbow Performance of Upper Limb version 1.2 (PUL 1.2) score at 12 months, assessed in …
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies.
Ortiz-Genga MF, Cuenca S, Dal Ferro M, Zorio E, Salgado-Aranda R, Climent V, Padrón-Barthe L, Duro-Aguado I, Jiménez-Jáimez J, Hidalgo-Olivares VM, García-Campo E, Lanzillo C, Suárez-Mier MP, Yonath H, Marcos-Alonso S, Ochoa JP, Santomé JL, García-Giustiniani D, Rodríguez-Garrido JL, Domínguez F, Merlo M, Palomino J, Peña ML, Trujillo JP, Martín-Vila A, Stolfo D, Molina P, Lara-Pezzi E, Calvo-Iglesias FE, Nof E, Calò L, Barriales-Villa R, Gimeno-Blanes JR, Arad M, García-Pavía P, Monserrat L. Ortiz-Genga MF, et al. J Am Coll Cardiol. 2016 Dec 6;68(22):2440-2451. doi: 10.1016/j.jacc.2016.09.927. J Am Coll Cardiol. 2016. PMID: 27908349 Free article.
The phenotype consisted of left ventricular dilation (68%), systolic dysfunction (46%), and myocardial fibrosis (67%); inferolateral negative T waves and low QRS voltages on electrocardiography (33%); ventricular arrhythmias (82%); and frequent sudden cardiac death (40 cases in 2 …
The phenotype consisted of left ventricular dilation (68%), systolic dysfunction (46%), and myocardial fibrosis (67%); inferolateral negativ …
Heart Failure-Induced Skeletal Muscle Wasting.
Philippou A, Xanthis D, Chryssanthopοulos C, Maridaki M, Koutsilieris M. Philippou A, et al. Curr Heart Fail Rep. 2020 Oct;17(5):299-308. doi: 10.1007/s11897-020-00468-w. Curr Heart Fail Rep. 2020. PMID: 32743732 Review.
This review focused on the phenotypic characteristics of HF-induced skeletal myopathy as well as the mechanisms of muscle wasting due to HF and highlighted possible therapeutic strategies for skeletal muscle wasting in HF. ...In particular, abnormal energy metabolis …
This review focused on the phenotypic characteristics of HF-induced skeletal myopathy as well as the mechanisms of muscle wast …
Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy.
Escobar-Lopez L, Ochoa JP, Royuela A, Verdonschot JAJ, Dal Ferro M, Espinosa MA, Sabater-Molina M, Gallego-Delgado M, Larrañaga-Moreira JM, Garcia-Pinilla JM, Basurte-Elorz MT, Rodríguez-Palomares JF, Climent V, Bermudez-Jimenez FJ, Mogollón-Jiménez MV, Lopez J, Peña-Peña ML, Garcia-Alvarez A, López-Abel B, Ripoll-Vera T, Palomino-Doza J, Bayes-Genis A, Brugada R, Idiazabal U, Mirelis JG, Dominguez F, Henkens MTHM, Krapels IPC, Brunner HG, Paldino A, Zaffalon D, Mestroni L, Sinagra G, Heymans SRB, Merlo M, Garcia-Pavia P. Escobar-Lopez L, et al. J Am Coll Cardiol. 2022 Sep 20;80(12):1115-1126. doi: 10.1016/j.jacc.2022.06.040. J Am Coll Cardiol. 2022. PMID: 36109106 Free PMC article.
OBJECTIVES: This study sought to develop and externally validate a score that predicts the probability for a positive genetic test result (G+) in DCM/LVSD. ...A score containing these factors predicted a G+ result, ranging from 3% when all predictor …
OBJECTIVES: This study sought to develop and externally validate a score that predicts the probability for a positive genetic …
Skeletal myopathy in heart failure: effects of aerobic exercise training.
Brum PC, Bacurau AV, Cunha TF, Bechara LR, Moreira JB. Brum PC, et al. Exp Physiol. 2014 Apr;99(4):616-20. doi: 10.1113/expphysiol.2013.076844. Epub 2013 Nov 22. Exp Physiol. 2014. PMID: 24273305 Free article. Review.
Reduced aerobic capacity, as measured by maximal oxygen uptake, is a hallmark in cardiovascular diseases and strongly predicts poor prognosis and higher mortality rates in heart failure patients. ...This fact draws substantial attention to the clinical relevance of targeti …
Reduced aerobic capacity, as measured by maximal oxygen uptake, is a hallmark in cardiovascular diseases and strongly predicts poor p …
Skeletal muscle abnormalities in chronic heart failure.
Georgiadou P, Adamopoulos S. Georgiadou P, et al. Curr Heart Fail Rep. 2012 Jun;9(2):128-32. doi: 10.1007/s11897-012-0090-z. Curr Heart Fail Rep. 2012. PMID: 22430147 Review.
These alterations influence both peripheral and ventilatory muscles, are present at rest, and deteriorate during exercise and their occurrence depends upon the severity and the duration of CHF syndrome. Future studies will be needed to elucidate the origin of skeletal " …
These alterations influence both peripheral and ventilatory muscles, are present at rest, and deteriorate during exercise and their occurren …
Current understanding and recent advances in myositis-specific and -associated autoantibodies detected in patients with dermatomyositis.
Gono T, Kuwana M. Gono T, et al. Expert Rev Clin Immunol. 2020 Jan;16(1):79-89. doi: 10.1080/1744666X.2019.1699059. Epub 2019 Dec 8. Expert Rev Clin Immunol. 2020. PMID: 31779485 Review.
Introduction: Dermatomyositis (DM) is characterized by skin lesions, such as heliotrope rash and Gottron's papules/sign, and skeletal myopathy. Patients with DM often have arthritis, cardiomyopathy, interstitial lung disease (ILD), and concomitant malignancy. Since …
Introduction: Dermatomyositis (DM) is characterized by skin lesions, such as heliotrope rash and Gottron's papules/sign, and skeletal …
Sengers syndrome and AGK-related disorders - Minireview of phenotypic variability and clinical outcomes in molecularly confirmed cases.
Wu CW, Caha M, Smoot L, Harris DJ, Roberts AE, Sacharow S, Bodamer O. Wu CW, et al. Mol Genet Metab. 2023 Jul;139(3):107626. doi: 10.1016/j.ymgme.2023.107626. Epub 2023 Jun 10. Mol Genet Metab. 2023. PMID: 37354892 Review.
The syndrome was originally defined as a "triad" of hypertrophic cardiomyopathy, cataracts, and lactic acidosis, with or without skeletal myopathy. The clinical manifestation of Sengers Syndrome exhibits substantial heterogeneity, with mild and severe/infantile form …
The syndrome was originally defined as a "triad" of hypertrophic cardiomyopathy, cataracts, and lactic acidosis, with or without skeletal …
Oxidants, antioxidants and alcohol: implications for skeletal and cardiac muscle.
Preedy VR, Patel VB, Reilly ME, Richardson PJ, Falkous G, Mantle D. Preedy VR, et al. Front Biosci. 1999 Aug 1;4:e58-66. doi: 10.2741/A480. Front Biosci. 1999. PMID: 10430553 Review.
The chronic form of alcoholic skeletal myopathy is characterized by selective atrophy of Type II fibers and affects up to two thirds of all alcohol misusers. ...Plasma carnosinase is also reduced in myopathic alcoholics, implicating a mechanism related to reduced in …
The chronic form of alcoholic skeletal myopathy is characterized by selective atrophy of Type II fibers and affects up to two …
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy.
Töpf A, Cox D, Zaharieva IT, Di Leo V, Sarparanta J, Jonson PH, Sealy IM, Smolnikov A, White RJ, Vihola A, Savarese M, Merteroglu M, Wali N, Laricchia KM, Venturini C, Vroling B, Stenton SL, Cummings BB, Harris E, Marini-Bettolo C, Diaz-Manera J, Henderson M, Barresi R, Duff J, England EM, Patrick J, Al-Husayni S, Biancalana V, Beggs AH, Bodi I, Bommireddipalli S, Bönnemann CG, Cairns A, Chiew MT, Claeys KG, Cooper ST, Davis MR, Donkervoort S, Erasmus CE, Fassad MR, Genetti CA, Grosmann C, Jungbluth H, Kamsteeg EJ, Lornage X, Löscher WN, Malfatti E, Manzur A, Martí P, Mongini TE, Muelas N, Nishikawa A, O'Donnell-Luria A, Ogonuki N, O'Grady GL, O'Heir E, Paquay S, Phadke R, Pletcher BA, Romero NB, Schouten M, Shah S, Smuts I, Sznajer Y, Tasca G, Taylor RW, Tuite A, Van den Bergh P, VanNoy G, Voermans NC, Wanschitz JV, Wraige E, Yoshimura K, Oates EC, Nakagawa O, Nishino I, Laporte J, Vilchez JJ, MacArthur DG, Sarkozy A, Cordell HJ, Udd B, Busch-Nentwich EM, Muntoni F, Straub V. Töpf A, et al. Nat Genet. 2024 Mar;56(3):395-407. doi: 10.1038/s41588-023-01651-0. Epub 2024 Mar 1. Nat Genet. 2024. PMID: 38429495 Free PMC article.
The co-occurrence of predicted deleterious SRPK3/TTN variants was not seen among 76,702 healthy male individuals, and statistical modeling strongly supported digenic inheritance as the best-fitting model. ...We propose that digenic inheritance of deleterious changes impact …
The co-occurrence of predicted deleterious SRPK3/TTN variants was not seen among 76,702 healthy male individuals, and statistical mod …
98 results