Results 71 to 80 of about 177,763 (249)

Cognitive behavioural therapy for myalgic encephalomyelitis/chronic fatigue syndrome is not effective. Re-analysis of a Cochrane review

open access: yesHealth Psychology Open, 2019
Analysis of the 2008 Cochrane review of cognitive behavioural therapy for chronic fatigue syndrome shows that seven patients with mild chronic fatigue syndrome need to be treated for one to report a small, short-lived subjective improvement of fatigue ...
Mark Vink, Alexandra Vink-Niese
doaj   +1 more source

The relationship between chronic fatigue syndrome, burnout, job satisfaction, social support and age among academics at a tertiary institution

open access: yesInternational Journal of Occupational Medicine and Environmental Health, 2019
Objectives Over the last 20 years, tertiary institutions have been subjected to several changes. This has resulted in increased workloads for academics.
Nicoleen Coetzee   +2 more
doaj   +1 more source

Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy   +16 more
wiley   +1 more source

Chronic Fatigue and its Syndromes [PDF]

open access: yesJournal of Neurology, Neurosurgery & Psychiatry, 1999
Chronic Fatigue and its Syndromes . By simon wessely, matthew hotopf, and michael sharpe. (Pp 428, £29.50). Published by Oxford University Press, Oxford, 1998. ISBN 0-19-263046-6. My first sensation is that such a book is long overdue. There is a paucity of books written by clinicians on this subject compared with the many gloom and doom tracts ...
openaire   +2 more sources

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1‐Related Autosomal Recessive Disorder Associated With Usher‐Like Symptoms

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu   +23 more
wiley   +1 more source

JOBCONTEX AS A PREDICTOR OF CHRONIC FATIGUE SYNDROME IN TEACHERS

open access: yesAstra Salvensis, 2019
The article examines the impact of work on the development of chronic fatigue syndrome (CFS). Today, cause of CFS, the mechanisms of formation and development of this syndrome have not been established, since this syndrome is relatively new.
Marina Anatolievna Kruglova   +5 more
doaj  

Multifactor dimensionality reduction analysis of syndrome characteristics of chronic persistent asthma

open access: yesJournal of Traditional Chinese Medical Sciences, 2015
Objective: To analyze the syndrome characteristics in patients with chronic persistent asthma. Methods: 365 patients (121 males, 244 females, 60.8 ± 29.1 years old) with chronic persistent asthma were enrolled in this cross-sectional study.
Yanyan Meng   +6 more
doaj   +1 more source

Immune Modulatory Therapy for Severe Dengue Hemorrhagic Fever in a Patient With Mitochondrial Complex I Deficiency: A Case Report

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Dengue virus (DENV) poses a serious global health challenge, particularly in cases of dengue hemorrhagic fever (DHF). Patients with preexisting mitochondrial disorders may be at increased risk for complications due to the specific impact of DENV on mitochondrial‐dependent cellular processes and immune function.
Audra N. Iness   +11 more
wiley   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young   +6 more
wiley   +1 more source

The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway — A Description of Demographic, Medical, and Neurological Findings

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis Multiplex Congenita (AMC) encompasses several hundred conditions with diverse genetic, pathophysiological, and clinical origins. The overarching EXPLAIN study explores underlying causes and implications of AMC and represents the largest clinical cohort of adults with AMC reported to date.
My Vuong Hermansen   +5 more
wiley   +1 more source

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