Results 31 to 40 of about 2,739,321 (263)

Tashmim al-Ikhtibar li Maharah al-Kalam al-‘Arabi wafqhan li al-Ithar al-al-Marja’i al-Urubi al-Musytarak li al-Lughat li al-Thullab al-Jami’ah fi Indunisiya

open access: yesArabiyatuna: Jurnal Bahasa Arab, 2023
This study aimed to develop a speaking-skill test at the B1 of CEFR, to determine the levels of validity, reliability, and difficulty of each item, and to organize the distinguishing power of each item on the prepared test. This research was motivated by the need of Arabic Language Test as an evaluation activity that required for various purposes ...
Agus Yasin, Hidia Tarauni
openaire   +2 more sources

ALS IMPLICATED PROTEIN TDP-43 SUSTAINS LEVELS OF STMN2 A MEDIATOR OF MOTOR NEURON GROWTH AND REPAIR

open access: yesNature Neuroscience, 2019
The findings that amyotrophic lateral sclerosis (ALS) patients almost universally display pathological mislocalization of the RNA-binding protein TDP-43 and that mutations in its gene cause familial ALS have nominated altered RNA metabolism as a disease ...
Joseph R. Klim   +15 more
semanticscholar   +1 more source

A proposal for new diagnostic criteria for ALS.

open access: yesClinical Neurophysiology, 2020
https://doi.org/10.1016/j.clinph.2020.04.005 1388-2457/ 2020 The Authors. Published by Elsevier B.V. on behalf of International Federation of Clinical Neurophysiology.
J. Shefner   +22 more
semanticscholar   +1 more source

Knowledge of the in-hospital resuscitation algorithm among medical staff of selected hospital departments

open access: yesCritical Care Innovations, 2019
INTRODUCTION: The hospitalized patient has a potentially greater chance of surviving sudden cardiac arrest compared to pre-hospital conditions. This, however, requires proper preparation of medical personnel who should recognize and treat reversible ...
Tomasz Klejne , Akila Randika Jayamaha
doaj   +1 more source

ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?

open access: yesFrontiers in Neuroscience, 2019
The scientific landscape surrounding amyotrophic lateral sclerosis (ALS) continues to shift as the number of genes associated with the disease risk and pathogenesis, and the cellular processes involved, continues to grow.
R. Mejzini   +10 more
semanticscholar   +1 more source

Atsār Al-Azmah Al-Khalījiyyah ‘alā Al-Āmal Al-Insāniy Al-Qathariy [PDF]

open access: yesInsaniyat: Journal of Islam and Humanities, 2018
The Gulf crisis, which broke out on June 5, 2017 between Qatar and the four countries (Saudi Arabia, the UAE, Egypt and Bahrain), surprised the world. The four countries initiated punitive action against Qatar and justified it in seeking to stop Qatar from supporting terrorism.
openaire   +2 more sources

Amyotrophic lateral sclerosis - frontotemporal spectrum disorder (ALS-FTSD): Revised diagnostic criteria

open access: yesAmyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 2017
This article presents the revised consensus criteria for the diagnosis of frontotemporal dysfunction in amyotrophic lateral sclerosis (ALS) based on an international research workshop on frontotemporal dementia (FTD) and ALS held in London, Canada in ...
M. Strong   +13 more
semanticscholar   +1 more source

Archaeological Ground Point Filtering of Airborne Laser Scan Derived Point-Clouds in a Difficult Mediterranean Environment

open access: yesJournal of Computer Applications in Archaeology, 2020
Digital terrain models (DTM) based on airborne laser scanning (ALS) are an important source for identifying and monitoring archaeological sites and landscapes. However, a DTM is only one of many representations of a given surface.
Michael Doneus   +2 more
doaj   +1 more source

ALS Genetics: Gains, Losses, and Implications for Future Therapies

open access: yesNeuron, 2020
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder caused by loss of motor neurons from the brain and spinal cord. The ALS community has made remarkable strides over three decades by identifying novel familial mutations, generating
Garam Kim   +4 more
semanticscholar   +1 more source

ATXN2 polyQ intermediate repeats are a modifier of ALS survival [PDF]

open access: yes, 2015
To analyze the frequency and clinical characteristics of patients with amyotrophic lateral sclerosis (ALS) with intermediate-length (CAG) expansion (encoding 27-33 glutamines, polyQ) in the ATXN2 gene, in a population-based cohort of Italian patients ...
Conte, Amelia   +11 more
core   +1 more source

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