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Oncology Reports|October 18, 2001
Predictive value of altered p27Kip1 and p21WAF/Cip1 protein expression for the clinical prognosis of patients with localized prostate cancerM A Kuczyk, C Bokemeyer, J Hartmann, et al.
JAMA|June 30, 2001
Development and validation of a prognostic index for 1-year mortality in older adults after hospitalizationL C Walter, R J Brand, S R Counsell, et al.
Journal of the American Geriatrics Society|August 19, 2007
The relationship between self-rated health and mortality in older black and white AmericansSei J Lee, Sandra Y Moody-Ayers, C Seth Landefeld, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|August 10, 2004
Respiratory insufficiency as a presenting symptom of LGMD2D in adulthoodM C Walter, G Dekomien, B Schlotter-Weigel, et al.
Biorxiv : the Preprint Server for Biology|December 9, 2024
TTF2 promotes replisome eviction from stalled forks in mitosisGeylani Can, Maksym Shyian, Archana Krishnamoorthy, et al.
Virus Genes|October 9, 2020
Whole genome sequencing and phylogenetic classification of Tunisian SARS-CoV-2 strains from patients of the Military Hospital in TunisSusann Handrick, Malena Bestehorn-Willmann, Simone Eckstein, et al.
Journal of Neuromuscular Diseases|June 27, 2022
Slowly Progressive Limb-Girdle Weakness and HyperCKemia - Limb Girdle Muscular Dystrophy or Anti-3-Hydroxy-3-Methylglutaryl-CoA-Reductase-Myopathy?Miriam Hiebeler, Raimo Franke, Maria Ingenerf, et al.
European Journal of Neurology|March 22, 2008
No muscle involvement in myoclonus-dystonia caused by epsilon-sarcoglycan gene mutationsL E Hjermind, J Vissing, F Asmus, et al.
Neuromuscular Disorders : NMD|October 16, 2009
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblastsJouni Vesa, Hailing Su, Giles D Watts, et al.
Human Molecular Genetics|August 4, 2009
Evaluation of the therapeutic potential of carbonic anhydrase inhibitors in two animal models of dystrophin deficient muscular dystrophyJean Giacomotto, Cordula Pertl, Caroline Borrel, et al.
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