Found: 23
Select item for more details and to access through your institution.
Undetected Neuromuscular Disease in Patients after Heart Transplantation.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 14, p. 7819, doi. 10.3390/ijms25147819
- By:
- Publication type:
- Article
Caveolin-3 and Caveolin-1 Interaction Decreases Channel Dysfunction Due to Caveolin-3 Mutations.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 2, p. 980, doi. 10.3390/ijms25020980
- By:
- Publication type:
- Article
Targeting gut dysbiosis against inflammation and impaired autophagy in Duchenne muscular dystrophy.
- Published in:
- EMBO Molecular Medicine, 2023, v. 15, n. 3, p. 1, doi. 10.15252/emmm.202216225
- By:
- Publication type:
- Article
"suMus," a novel digital system for arm movement metrics and muscle energy expenditure.
- Published in:
- Frontiers in Physiology, 2023, v. 14, p. 1, doi. 10.3389/fphys.2023.1057592
- By:
- Publication type:
- Article
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular Dystrophy.
- Published in:
- Pharmaceuticals (14248247), 2022, v. 15, n. 1, p. 89, doi. 10.3390/ph15010089
- By:
- Publication type:
- Article
Diagnostik und Therapie von statinassoziierten Muskelsymptomen.
- Published in:
- Der Internist, 2021, v. 62, n. 8, p. 827, doi. 10.1007/s00108-021-01059-0
- By:
- Publication type:
- Article
eATP/P2X7R Axis: An Orchestrated Pathway Triggering Inflammasome Activation in Muscle Diseases.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 17, p. 5963, doi. 10.3390/ijms21175963
- By:
- Publication type:
- Article
Effects of non-euphoric plant cannabinoids on muscle quality and performance of dystrophic mdx mice.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Genetic and pharmacological regulation of the endocannabinoid CB1 receptor in Duchenne muscular dystrophy.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06267-1
- By:
- Publication type:
- Article
Zidovudine ameliorates pathology in the mouse model of Duchenne muscular dystrophy via P2RX7 purinoceptor antagonism.
- Published in:
- Acta Neuropathologica Communications, 2018, v. 6, n. 1, p. N.PAG, doi. 10.1186/s40478-018-0530-4
- By:
- Publication type:
- Article
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy.
- Published in:
- Annals of Neurology, 2014, v. 76, n. 2, p. 206, doi. 10.1002/ana.24170
- By:
- Publication type:
- Article
Neuromuscular Disorders of Glycogen Metabolism.
- Published in:
- Current Neurology & Neuroscience Reports, 2013, v. 13, n. 3, p. 1, doi. 10.1007/s11910-012-0333-0
- By:
- Publication type:
- Article
Hyccin, the Molecule Mutated in the Leukodystrophy Hypomyelination and Congenital Cataract (HCC), Is a Neuronal Protein.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0032180
- By:
- Publication type:
- Article
The spectrum of GNE mutations: allelic heterogeneity for a common phenotype.
- Published in:
- Neurological Sciences, 2010, v. 31, n. 3, p. 377, doi. 10.1007/s10072-010-0248-y
- By:
- Publication type:
- Article
Caveolinopathies: from the biology of caveolin-3 to human diseases.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 2, p. 137, doi. 10.1038/ejhg.2009.103
- By:
- Publication type:
- Article
Caveolinopathies: from the biology of caveolin-3 to human diseases.
- Published in:
- 2009
- By:
- Publication type:
- Correction notice
Phenotypic characterization of hypomyelination and congenital cataract.
- Published in:
- Annals of Neurology, 2007, v. 62, n. 2, p. 121, doi. 10.1002/ana.21175
- By:
- Publication type:
- Article
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1111, doi. 10.1038/ng1870
- By:
- Publication type:
- Article
Role of the Ram Domain and Ankyrin Repeats on Notch Signaling and Activity in Cells of Osteoblastic Lineage.
- Published in:
- Journal of Bone & Mineral Research, 2006, v. 21, n. 8, p. 1317, doi. 10.1359/jbmr.060505
- By:
- Publication type:
- Article
Bone morphogenetic proteins and their antagonists.
- Published in:
- Reviews in Endocrine & Metabolic Disorders, 2006, v. 7, n. 1/2, p. 51, doi. 10.1007/s11154-006-9000-6
- By:
- Publication type:
- Article
Genetic Analyses of the HRPT2 Gene in Primary Hyperparathyroidism: Germline and Somatic Mutations in Familial and Sporadic Parathyroid Tumors.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 11, p. 5583, doi. 10.1210/jc.2004-0294
- By:
- Publication type:
- Article
A reappraisal of the Rb1 gene abnormalities in the diagnosis of parathyroid cancer.
- Published in:
- Clinical Endocrinology, 2004, v. 60, n. 1, p. 99, doi. 10.1111/j.1365-2265.2004.01954.x
- By:
- Publication type:
- Article
Relationship between Cognitive Function, Growth Hormone and Insulin-Like Growth Factor I Plasma Levels in Aged Subjects.
- Published in:
- Neuropsychobiology, 1998, v. 38, n. 2, p. 73, doi. 10.1159/000026520
- By:
- Publication type:
- Article