Results 131 to 140 of about 208,937 (301)

Value of MRI Outcomes for Preventive and Early‐Stage Trials in Spinocerebellar Ataxias 1 and 3

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To examine the value of MRI outcomes as endpoints for preventive and early‐stage trials of two polyglutamine spinocerebellar ataxias (SCAs). Methods A cohort of 100 participants (23 SCA1, 63 SCA3, median Scale for the Assessment and Rating of Ataxia (SARA) score = 5, 42% preataxic, and 14 gene‐negative controls) was scanned at 3T up ...
Thiago J. R. Rezende   +26 more
wiley   +1 more source

Effect of anoxic transformation processes in municipal wastewater on pH and oxidation reduction potential

open access: yes, 2008
This paper presents findings of an investigation into the relationships between nitrate utilization rate (NUR), pH and oxidation reduction potential (ORP) during anoxic transformation processes in municipal wastewater.
Kohsaka, K., Abdul-Talib, S., Yin, C-Y
core  

The optimum pH for the derivative spectrophotometric determination of co-trimoxazole in binary mixtures

open access: yes, 2002
Background: Although the experimental assessment of co-trimoxazole by use of derivative spectrophotmetry underscores the usefulness of this method due to its relative simplicity with which it can be carried out over the official United States ...
Adome, R.O., Balyejjusa, S.
core   +1 more source

Phosphorus Removal from Water and Waste Water by Chemical Precipitation Using Alum and Calcium Chloride

open access: yesIraqi Journal of Chemical and Petroleum Engineering, 2009
Phosphorus is usually the limiting nutrient for eutrophication in inland receiving waters; therefore, phosphorus concentrations must be controlled.
Sawsan A. M. Mohammed   +1 more
doaj  

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

Added Prognostic Value of EEG Reactivity in Comatose Patients Following Cardiac Arrest

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives To evaluate the added prognostic value of EEG reactivity for favorable outcome compared with background analysis during and after targeted temperature management (TTM). Methods Prospective observational cohort study of comatose post–cardiac arrest patients admitted to a single academic center between 2017 and 2022, all undergoing ...
Sarah Caroyer   +11 more
wiley   +1 more source

Penentuan Konsentrasi Ditizon dan pH Optimum dalam Pembuatan Test Kit Timbal [PDF]

open access: yes, 2018
Timbal merupakan golongan logam berat yang beracun yang mudah terakumulasi oleh tubuh dan dapat menyebabkan penyakit serius bahkan kematian. Beberapa metode telah dilakukan untuk analisis timba baik kualitatif maupun kuantitatif.
Hariawan, Elvanda Tika
core  

Relative activity of Lac51 towards lignin-related phenolic compounds at 38°C and optimum pH.

open access: yes, 2012
Relative activity of Lac51 towards lignin-related phenolic compounds at 38°C and optimum pH.
Wei Fang (116739)   +7 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

Unraveling 4‐Phenylbutyrate's Therapeutic Role in SLC6A1 Disorders: Pharmacochaperoning Over HDAC Inhibition

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw   +5 more
wiley   +1 more source

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