Results 61 to 70 of about 34,352 (291)
Probable first report of a motor deafferentation syndrome in the Paraguayan War
The Paraguayan War ended 150 years ago. Back then, there were outbreaks of combatants’ limb weakness and tingling related to "palustrian cachexia", not clearly funded at the time on nutritional deficiency, the use of native flora to feed troops, and ...
Marleide da Mota GOMES+1 more
doaj +1 more source
Wernicke Encephalopathy Presenting in a Patient with Severe Acute Pancreatitis [PDF]
Context Acute pancreatitis can lead to prolonged fasting and malnutrition. Many metabolic changes, including thiamine deficiency, may lead to the well know pancreatic encephalopathy.
Arana-Guajardo, Ana Cecilia+5 more
core +2 more sources
Two Key Ferredoxins for Nitrogen Fixation Have Different Specificities and Biophysical Properties
Two ferredoxins, FdC and FdN, are collectively essential for the process of nitrogen fixation by the iron nitrogenase in R. capsulatus. We explore the biophysical factors, through spectroscopic and structural characterizations, which determine ferredoxin functionality and pathway specificity. The structure of FdC (PDB: 9I2A) and model of FdN (AF‐D5ARY6)
Holly Addison+5 more
wiley +1 more source
Wernicke Encephalopathy Mimicking MELAS
Objectives: a stroke-like lesion, the morphological equivalent of a stroke-like episode and the hallmark of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome, have not been reported as manifestations of thiamine ...
Josef Finsterer
doaj +1 more source
ABSTRACT Cells have an intrinsic ability to rapidly respond to environmental change to regulate cell cycle progression and membrane organisation, thereby affecting cell growth and division. The actin cytoskeleton is a highly dynamic complex of proteins that can rapidly reorganise to change the growth pattern of a cell.
Holly R. Brooker+7 more
wiley +1 more source
Inherited metabolic epilepsies–established diseases, new approaches
Abstract Inherited metabolic epilepsies (IMEs) represent the inherited metabolic disorders (IMDs) in which epilepsy is a prevailing component, often determining other neurodevelopmental outcomes associated with the disorder. The different metabolic pathways affected by individual IMEs are the basis of their rarity and heterogeneity.
Itay Tokatly Latzer, Phillip L. Pearl
wiley +1 more source
Shoshin Beriberi in a Child With Intestinal Failure: A Case Report
Background:. Acute illness states with increased metabolic demand can precipitate severe thiamine deficiency if physiologic needs exceed endogenous stores and supplementation.
Madeleine Böhrer, MD, FRCPC+4 more
doaj +1 more source
Wernicke-Korsakoff Syndrome in a Hunger Striker Despite Oral Thiamine Supplementation
Phillip Wagner,1,2 Thuy Bui1 1Department of Internal Medicine, University of Pittsburgh Medical Center, Pittsburgh, PA, USA; 2Department of Internal Medicine, Johns Hopkins Hospital, Baltimore, MD, USACorrespondence: Phillip Wagner, Email Pwagner6@jh ...
Wagner P, Bui T
doaj
Seeing double: the low-carb diet [PDF]
No abstract ...
Drummond, Russell S.+4 more
core +1 more source
ERYTHROCYTOSIS IN THIAMINE DEFICIENT RATS
A thiamine (T) deficient state in rats was produced by feeding the rats a T deficient diet (TDD). At the stage of 13 days (TDD13 group), the number of red blood cells (RBC) and white blood cells (WBC), hematocrit (Ht) and hemoglobin (Hb) values decreased.
Hajime Yasuhara, Reiko Hobara
openaire +3 more sources