Results 21 to 30 of about 24,602 (271)

The Functional Severity Assessment of Coronary Stenosis Using Coronary Computed Tomography Angiography-Based Myocardial Mass at Risk and Minimal Lumen Diameter

Cardiovascular Therapeutics, 2020
Background. We investigated whether or not the addition of myocardial mass at risk (MMAR) to quantitative coronary angiography was useful for diagnosing functionally significant coronary stenosis in the daily practice. Methods.
Kenji Sadamatsu, Kazuhiro Nagaoka, Yasuaki Koga, Kotaro Kagiyama, Kohei Muramatsu, Kiyoshi Hironaga, Hideki Tashiro, Takafumi Ueno, Yoshihiro Fukumoto   +8 more
doaj   +1 more source

An international study of caregiver-reported burden and quality of life in metachromatic leukodystrophy

Orphanet Journal of Rare Diseases, 2022
Background Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal disorder caused by mutations in the arylsulfatase A gene. Until now, there has been little information on the burden of MLD on patients and their caregivers.
Caroline Sevin, Magalie Barth, Alexandra Wilds, Abena Afriyie, Markus Walz, Annamarie Dillon, Kenneth Howie, Francis Pang   +7 more
doaj   +1 more source

An in silico approach to identify early damage biomarker candidates in metachromatic leukodystrophy

Molecular Genetics and Metabolism Reports, 2023
Metachromatic leukodystrophy (MLD) is a rare, autosomal recessive lysosomal storage disease. Deficient activity of arylsulfatase A causes sulfatides to accumulate in cells of different tissues, including those in the central and peripheral nervous ...
Jessica Gómez, Laura Artigas, Raquel Valls, Javier Gervas-Arruga   +3 more
doaj   +1 more source

E. MLD Mapping EMPTY Sheet

, 2021
Empty spreadsheet with MLD field headings for students to use to code mediveal London ...
Kowaleski, Maryanne
core   +1 more source

Insights into the natural history of metachromatic leukodystrophy from interviews with caregivers

Orphanet Journal of Rare Diseases, 2019
Background and methods Metachromatic leukodystrophy (MLD) is a rare, autosomal recessive lysosomal storage disease caused by deficient activity of arylsulfatase A.
Magdalena Harrington, Diane Whalley, James Twiss, Rebecca Rushton, Susan Martin, Lynn Huynh, Hongbo Yang   +6 more
doaj   +1 more source

Difficultés spécifiques d'élèves avec MLD sur les fractions

International audienceL'apprentissage des fractions pose des difficultés à de nombreux élèves, notamment ceux avec des troubles d'apprentissage en mathématiques (MLD).
Florence, Peteers, Fabienne, Barroca-Paccard, Gregorio, Francesca, Deruaz, Michel, Gardes, Marie-Line, Lemrich, Chloé, Ouvrier-Buffet, Cécile, Robotti, Elisabetta   +7 more
core   +5 more sources

Tubular Discectomy Versus Conventional Microdiscectomy for the Treatment of Lumbar Disc Herniation: A Comparative Study [PDF]

Journal of Minimally Invasive Spine Surgery and Technique, 2020
Objective The study aims to compare the outcomes of micro-lumbar discectomy (MLD) with tubular micro-endoscopic discectomy (MED). Methods A retrospective analysis of 414 patients who underwent single-level lumbar discectomy either by tubular MED or MLD ...
Sanjeev Asati, Sanyam Jain, Vishal G Kundnani   +2 more
doaj   +1 more source

Learner-generated drawings by students with mathematical learning difficulties in finishing open number sentences

Jurnal Elemen, 2022
Although MLD students do not have good mathematical performance in completing addition and subtraction operations of integers, MLD students have suggestive ideas in the form of drawings produced in solving open number sentences questions. This study aims
Mohammad Faizal Amir
doaj   +1 more source

Masker bandwidth and the MLD [PDF]

The Journal of the Acoustical Society of America, 1983
Thresholds for binaurally in-phase (SO) and out-of-phase (Sπ) tones masked by diotic noise were measured as a function of noise bandwidth at 250 and 4000 Hz. Results show that the familiar dependence of the MLD for a tone in wideband noise on the frequency of the tone derives primarily from the dependence of critical bandwidth on frequency and only ...
P. M. Zurek, N. I. Durlach, H. S. Colburn, K. J. Gabriel   +3 more
openaire   +1 more source

The burden of disease in metachromatic leukodystrophy: results of a caregiver survey in the UK and Republic of Ireland

Orphanet Journal of Rare Diseases
Background Metachromatic Leukodystrophy (MLD) is a rare, autosomal recessive lysosomal storage disease characterised by the progressive loss of motor function and severe decline in cognitive function.
Sophie Thomas, Alexandra Morrison, Georgina Morton, Pat Roberts, Vivienne Clark, Jackie Imrie   +5 more
doaj   +1 more source