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Neurology|November 24, 2004
Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson diseaseH Hochstrasser, P Bauer, U Walter, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|January 31, 2012
Hypericin for visualization of high grade gliomas: first clinical experienceR Ritz, R Daniels, S Noell, et al.
Muscle & Nerve|July 9, 1998
Alternative dystrophin gene transcripts in golden retriever muscular dystrophyS J Schatzberg, L V Anderson, S D Wilton, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 30, 2005
Long-term MRI and clinical follow-up of symptomatic and presymptomatic carriers of dysferlin gene mutationsD Brummer, M C Walter, M Palmbach, et al.
Cureus|January 20, 2023
Safety and Efficacy of Mesenchymal Stem Cells for the Treatment of Evolving and Established Bronchopulmonary Dysplasia: A Systematic Literature ReviewSheiniz Giva, Ahmed Abdelrahim, Blessing T Ojinna, et al.
Human Molecular Genetics|July 1, 1997
Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophyL Metzinger, D J Blake, M V Squier, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain diseaseM Auranen, J Rapola, H Pihko, et al.
The American Journal of Pathology|October 20, 1998
Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2AL V Anderson, K Davison, J A Moss, et al.
Neuroreport|March 10, 2001
Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutationE Vafiadaki, A Reis, S Keers, et al.
The Journal of Biological Chemistry|September 20, 1996
Dystroglycan is a dual receptor for agrin and laminin-2 in Schwann cell membraneH Yamada, A J Denzer, H Hori, et al.
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