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Research 451–480 of 938
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Towards the Development of AgoKirs: New Pharmacological Activators to Study Kir2.x Channel and Target Cardiac Disease
- Stimuli-responsive nanoformulations for CRISPR-Cas9 genome editing
- A nanocomposite competent to overcome solubility and permeation issues of capsaicin and thiocolchicoside simultaneously in gout management: Fabrication of nanocubosomes
- Activating the healing process: three-dimensional culture of stem cells in Matrigel for tissue repair
- Efectos adversos asociados al uso de anabolizantes en deportistas: revisión sistemática
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- A Layered Framework for Biological Aesthetics: A Narrative Review of Regenerative Medicine in Cosmetic Science
- Incel Identity Development: A Scoping Review of Biopsychosocial Markers
- E-Poster
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- 307 Phenotypic-genotypic expansion of plectinopathy in a patient with muscular dystrophy and immune-mediated myasthenia gravis
- 494 Epidermolysis bullosa pruriginosa, muscular dystrophy, and immune-mediated myasthenia gravis in a patient with homozygous nonsense PLEC mutation
- Corticosteroids for the treatment of Duchenne muscular dystrophy
- G.P.2.16 Valproate, acetylcarnitine, folic acid and vitamin B12 in spinal muscular atrophy: Preliminary data of an open-label study in children
- Glucocorticoid corticosteroids for Duchenne muscular dystrophy
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Risk of muscular adverse effects with finasteride
- Stem cell-derived motor neurons from spinal and bulbar muscular atrophy patients
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Efficacy and safety of glucocorticoids in the treatment of progressive muscular dystrophy in children: a systematic review and meta-analysis
- Relation of Selenium, Vitamin E and Other Factors to Muscular Dystrophy in the Rabbit
- [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?].
- Efeitos da fotobiomodulação no estresse oxidativo e seu impacto sobre a atrofia muscular por desnervação
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Alterations of gut microbiota composition in post-finasteride patients: a pilot study
- Outbreak of thallium poisoning among Iraqi patients
- Assessment of the Embryological Origin, Anatomical and Histological Structure of the Skin
- Ocular Manifestations in Avitaminosis
- Perspectives of Kennedy's disease