Results 51 to 60 of about 5,207 (210)

Wernicke encephalopathy [PDF]

Canadian Medical Association Journal, 2020
Tatsuya, Fujikawa, Yuka, Sogabe
openaire   +3 more sources

Wernicke–Korsakoff syndrome

Неврология, нейропсихиатрия, психосоматика, 2014
Wernicke’s encephalopathy and Korsakoff’s psychosis are the acute and chronic phases of Wernicke–Korsakov syndrome, a neurodegenerative process that is caused by thiamine deficiency and predominantly develops in persons with severe alcohol problems.
Yu. P. Sivolap, I. V. Damulin
doaj   +1 more source

Beriberi 10 years after gastric bypass surgery - case report [PDF]

, 2016
Efst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á ...
Linda Ó. Árnadóttir, Svanur Sigurbjörnsson, Tómas Guðbjartsson   +2 more
core   +1 more source

Update on Non‐Biological and RNA‐Based Therapeutics in Chronic Inflammatory Diseases: Precision Medicine Through Small Molecules: An EAACI Position Paper

Allergy, EarlyView.
ABSTRACT In the last decades, critical advancements in research technology and knowledge on disease mechanisms steered therapeutic approaches for chronic inflammatory diseases towards unprecedented target specificity. For allergic and chronic lung diseases, biologic drugs pioneered this goal, acquiring on the way—through the clinical use of monoclonal ...
F. Roth‐Walter, I. M. Adcock, C. Benito‐Villalvilla, R. Bianchini, L. Bjermer, G. Caramori, L. Cari, K. F. Chung, Z. Diamant, I. Eguiluz‐Gracia, E. F. Knol, M. Jesenak, F. Levi‐Schaffer, G. Nocentini, L. O'Mahony, O. Palomares, F. Redegeld, M. Sokolowska, B. Van Esch, M. Zurlo, C. Stellato   +20 more
wiley   +1 more source

Brain MRI: A safe and a specific tool in the diagnosis of Gayet Wernicke's encephalopathy in pregnant women: Case report

Radiology Case Reports
Gayet-Wernicke encephalopathy (GWE) is a neuropsychiatric syndrome due to Vitamin B1 (thiamine) deficiency, fatal in 30% of cases and preventable if treatment is initiated early, characterized by the classic triad of encephalopathy, ocular involvement ...
Hicham Ziani, Samia Boussaaden, Nora El Idrissi Jallal, Zakariae Slaihi, Sophia Lahbabi, Nezha El Oudghiri, Rajae Tachinante   +6 more
doaj   +1 more source

Encefalopatía de Wernicke : descripción de 26 casos [PDF]

, 2012
La encefalopatía de Wernicke es una enfermedad por déficit de tiamina. Su causa más frecuente es el enolismo. La clínica típica es la tríada de trastornos de la motilidad ocular, ataxia y confusión mental.
Gargallo Rico, Eduardo, Universitat Autònoma de Barcelona. Departament de Medicina, Universitat Autònoma de Barcelona. Facultat de Medicina, Álvarez Sabin, José   +3 more
core  

Time course of evoked-potential changes in different forms of anomia in aphasia [PDF]

, 2009
No abstract ...
Laganaro, Marina, Morand, Stéphanie, Schnider, Armin   +2 more
core   +2 more sources

Dose‐dependent impairment of brain functional and microstructural connectivity during leukaemia chemotherapy

British Journal of Haematology, EarlyView.
Prospective functional MRI brain and neurocognitive assessments were performed serially during intensive chemotherapy for a cohort of adults with newly diagnosed acute myeloid leukaemia to elucidate ‘chemobrain’ language phenomena. At completion of consolidation, significant reductions in functional and microstructural connectivity were observed ...
Ashleigh P. Scott, Ada Lo, Ying Xia, Kate Thompson, Harriet Bodimeade, Amir Fazlollahi, Nicholas Weber, Cameron Curley, Stewart Hunt, Kirk Morris, Caroline McNamara, Nilu Perera, Elango Subramoniapillai, Steven W. Lane, Glen A. Kennedy, Olivier Salvado, Javier Urriola, Katie L. McMahon   +17 more
wiley   +1 more source

Fundus Findings in Wernicke Encephalopathy

Case Reports in Ophthalmology, 2017
Wernicke encephalopathy (WE) is an acute neuropsychiatric syndrome resulting from thiamine (vitamin B1) deficiency, classically characterized by the triad of ophthalmoplegia, confusion, and ataxia.
Tal Serlin, Elad Moisseiev
doaj   +1 more source

Ataxias esporádicas de início no adulto: um desafio diagnóstico [PDF]

, 2014
Patients with adult onset non-familial progressive ataxia are classified in sporadic ataxia group. There are several disease categories that may manifest with sporadic ataxia: toxic causes, immune-mediated ataxias, vitamin deficiency, infectious diseases,
Albuquerque, Marcus Vinicius Cristino De, Barsottini, Orlando Graziani Povoas, Braga Neto, Pedro, Pedroso, José Luiz   +3 more
core   +3 more sources