Results 21 to 30 of about 96,687 (267)

Intra-Subject Variability in Mathematical Learning Difficulties

open access: yesJournal of Cognition, 2022
Objective: Mathematical learning difficulties (MLD) are characterized by difficulties in the understanding and processing of numbers and quantities. While MLD is related mainly to numerical deficits, studies show that this population has several other ...
Sharon Levy, Liat Goldfarb
doaj   +1 more source

Sustenance of phytoplankton in the subpolar North Atlantic during the winter through patchiness [PDF]

open access: yes, 2017
This study investigates the influence of two factors that change the mixed layer depth and can potentially contribute to the phytoplankton sustenance over winter: 1) variability of air-sea fluxes and 2) three-dimensional processes arising from strong ...
Karimpour, Farid   +2 more
core   +2 more sources

Predicting disease severity in metachromatic leukodystrophy using protein activity and a patient phenotype matrix

open access: yesGenome Biology, 2023
Background Metachromatic leukodystrophy (MLD) is a lysosomal storage disorder caused by mutations in the arylsulfatase A gene (ARSA) and categorized into three subtypes according to age of onset. The functional effect of most ARSA mutants remains unknown;
Marena Trinidad   +11 more
doaj   +1 more source

A closer look at ARSA activity in a patient with metachromatic leukodystrophy. [PDF]

open access: yes, 2019
Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal storage disease mainly caused by a deficiency of arylsulfatase A activity. The typical clinical course of patients with the late infantile form includes a regression in motor skills ...
Childers, Anna   +6 more
core   +2 more sources

Program Rozwoju Obszarów Wiejskich na lata 2007–2013 na tle wcześniejszych programów wiejskich, współfinansowanych ze środków unijnych (analiza struktury programu)

open access: yesWieś i Rolnictwo, 2008
„PROW 2007—2013” jest kolejnym programem wspierającym rozwój polskiego rolnictwa i regionów wiejskich unijnymi i krajowymi środkami publicznymi.
Janusz Rowiński
doaj   +1 more source

Long‐term disease course of two patients with multiple sulfatase deficiency differs from metachromatic leukodystrophy in a broad cohort

open access: yesJIMD Reports, 2021
Multiple sulfatase deficiency (MSD) is a lysosomal storage disease caused by a deficiency of formylglycine‐generating enzyme due to SUMF1 defects. MSD may be misdiagnosed as metachromatic leukodystrophy (MLD), as neurological and neuroimaging findings ...
Stefanie Beck‐Wödl   +9 more
doaj   +1 more source

The contributions of domain-general and numerical factors to third-grade arithmetic skills and mathematical learning disability [PDF]

open access: yes, 2014
Explanations of the marked individual differences in elementary school mathematical achievement and mathematical learning disability (MLD or dyscalculia) have involved domain-general factors (working memory, reasoning, processing speed and oral language)
Cowan, Richard, Powell, Daisy
core   +3 more sources

Quality of life and functional outcome following microsurgical fasciocutaneous vs. myocutaneous tissue transfer

open access: yesGMS German Plastic, Reconstructive and Aesthetic Surgery – Burn and Hand Surgery, 2017
Background: Coverage of soft tissue defects at the lower extremity may necessitate microsurgical tissue transfer, such as by fasciocutaneous anterolateral thigh (ALT) or myocutaneous musculus latissimus dorsi (MLD) flaps.
Dlugos, Yvonne Denise   +3 more
doaj   +1 more source

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

open access: yesCardiovascular 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   +8 more
doaj   +1 more source

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

open access: yesOrphanet 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   +7 more
doaj   +1 more source

Home - About - Disclaimer - Privacy