Results 71 to 80 of about 528,981 (304)

Mutant NPM1 in Acute Myeloid Leukemia Initiation and Maintenance

open access: yesAging and Cancer, EarlyView.
NPM1 mutations drive acute myeloid leukemia by acting as neomorphic transcriptional regulators that cooperate with Menin–MLL and XPO1 to sustain HOX/MEIS1 expression and block differentiation. Targeting these mutant‐specific transcriptional dependencies provides a rational therapeutic strategy for NPM1‐mutated AML.
Yanan Jiang   +3 more
wiley   +1 more source

PERBANDINGAN PARAMETER FUNGSI PARU ATLET PUTRA CABANG OLAHRAGA BOLA VOLI DENGAN SEPAK TAKRAW DI PUSAT PENDIDIKAN DAN LATIHAN PELAJAR JAWA TENGAH

open access: yesJurnal Kedokteran Diponegoro, 2016
Latar belakang : Beberapa cabang olahraga prestasi yang dilatih secara intensif di PPLP untuk ditingkatkan prestasinya diantaranya adalah cabang olahraga Bola Voli dan Sepak Takraw.
Aulia Izzati   +2 more
doaj   +1 more source

Vital capacity and COPD: the Swedish CArdioPulmonary bioImage Study (SCAPIS)

open access: yes, 2016
Kjell Torén,1 Anna-Carin Olin,1 Anne Lindberg,2 Jenny Vikgren,3 Linus Schiöler,1 John Brandberg,3 Åse Johnsson,3 Gunnar Engström,4 H Lennart Persson,5 Magnus Sköld,6 Jan Hedner,7 Eva Lindberg,8 Andrei Malinovschi,8 Eeva ...
Torén K   +18 more
core  

Factors Associated with Vital Lung Capacity on Road Sweeper Workers

open access: yes, 2022
The decrease level of vital capacity can be restriction, obstruction or both of them. Some factors, like non jobs and environment can lead the decrease level of vital capacity.
Novziransyah, Nanda   +3 more
core  

Validity of a Wearable Digital Insole for Assessing Gait ON and OFF in Parkinson's Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Gait impairment is a distinctive symptom of Parkinson's disease that negatively impact mobility. We assessed the validity of wearable digital insoles against a validated reference gait analysis system for measuring select gait characteristics in patients with Parkinson's disease. Methods A comparative analysis between digital insoles
Deborah A. Hall   +16 more
wiley   +1 more source

Clinical Validation of Plasma p‐217tau in Neurological Diseases

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Plasma p‐217tau is a minimally invasive but specific biomarker for diagnosing Alzheimer's disease (AD). However, its disease specificity remains to be clinically evaluated. We validated the reliability of the p‐217tau biomarker in 12 other neurological diseases.
Takeshi Kawarabayashi   +13 more
wiley   +1 more source

TÜRKİYE’DEKİ MİNİK FUTBOLCULARDA REAKSİYON ZAMANI, VİTAL KAPASİTE DEĞERLERİ VE LATERİZASYON DAĞILIMINDA SOLAKLIK SORUNU

open access: yesSpormetre Beden Eğitimi ve Spor Bilimleri Dergisi, 2007
Bu çalışmada amaç, Türkiye’deki minik futbolcularda reaksiyon zamanı ve vital kapasite değerlerinin belirlenmesi ve Türkiye’de sol kulvarda oynayabilecek futbolculardaki yetersizlik sorununun kaynağını tespit etmektir.
Osman İmamoğlu, Ertan Kılcıgil
doaj   +1 more source

Weight corrected vital capacity.

open access: yes, 2015
A. Group weight corrected vital capacity (VC/kg) (mean ± standard deviation) for 9 participants, recorded at 9 weekly assessment sessions. A black line represents stimulated, and a blue line unstimulated, breaths.
Henrik Gollee (290596)   +4 more
core   +1 more source

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach   +23 more
wiley   +1 more source

Brazilian consensus on Duchenne muscular dystrophy. Part 2: rehabilitation and systemic care

open access: yesArquivos de Neuro-Psiquiatria
Significant advances in the understanding and management of Duchenne muscular dystrophy (DMD) have occurred since the publication of international guidelines for DMD care in 2010.
Alexandra P. Q. C. Araujo   +10 more
doaj   +1 more source

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