Results 121 to 130 of about 130,419 (249)
MICRO-INVASIVE AESTHETIC TREATMENT OF NON-CAVITATED WHITE-SPOT LESIONS
Aim: Micro-invasive treatment of white-spot lesions through resin infiltration technique was performed. Materials and method: Icon smooth surface (DMG, Hamburg, Germany) was applied to 21 non-cavitated carious lesions, located on the buccal surfaces ...
Albertine Leon +4 more
doaj
Benign and malignant neoplasms of the temporomandibular joint are uncommon. Their presence poses a diagnostic and therapeutic challenge for clinicians.
Jordan Gigliotti, DMD +3 more
doaj +1 more source
A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice Immunological evidence [PDF]
F. Pons +9 more
openalex +1 more source
Second-generation compound for the modulation of utrophin in the therapy of DMD
Duchenne muscular dystrophy (DMD) is a lethal, X-linked muscle-wasting disease caused by lack of the cytoskeletal protein dystrophin. There is currently no cure for DMD although various promising approaches are progressing through human clinical trials ...
S. Guiraud +13 more
semanticscholar +1 more source
INTRODUCTION. Currently, manufacturers of adeno-associated virus (AAV)-based gene therapy products are facing a number of systemic problems stemming from the difficulties in assessing the quality of medicinal products due to insufficient scientific data,
D. S. Kopein +2 more
doaj +1 more source
Increased Sensitivity of DMD Lymphoblastoid Cell To Low Doses of X-Irradiation [PDF]
Loredana Melchiorri +4 more
openalex +1 more source
A team at Columbia University has found a new target for muscular dystrophy—a leaky RyR1 channel. Stopping the leak of calcium from the channel could help protect skeletal muscle.
openaire +2 more sources
Identification of point mutations in Turkish DMD/BMD families using multiplex-single stranded conformation analysis (SSCA) [PDF]
Serpil Eraslan +3 more
openalex +1 more source
Screening of Dystrophin Gene Deletions in Egyptian Patients with DMD/BMD Muscular Dystrophies [PDF]
Laila K. Effat +5 more
openalex +1 more source
Severe cognitive impairment in DMD: obvious clinical evidence for Dp71 isoform point mutations screening [PDF]
Marie‐Pierre Moizard +7 more
openalex +1 more source

