Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sheena Grant"'
Autor:
Louise Victoria Mahon, Michelle Lomax, Sheena Grant, Elaine Cross, Dougal Julian Hare, James Ed Wraith, Simon Jones, Brian Bigger, Kia Langford-Smith, Maria Canal
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e84128 (2014)
Sleep disturbances are prevalent in mucopolysaccharidosis Type III (MPS III), yet there is a lack of objective, ecologically valid evidence detailing sleep quantity, quality or circadian system. Eight children with MPS III and eight age-matched typic
Externí odkaz:
https://doaj.org/article/9ba649d9071741afa52aa864f2774ded
Publikováno v:
Clinical Nursing Research. 32:445-451
The aim of this study was to evaluate the psychometric properties of the Brief Fatigue Inventory (BFI) in hemodialysis patients. During a dialysis day, patients completed both 9-item BFI and 21-item Beck Depression Inventory (BDI)-II questionnaires.
Autor:
Subrata Debnath, Nimmy Thomas, Afaf Saliba, Saket Kottewar, Sheena Grant, Balakuntalam S. Kasinath, Kumar Sharma, Carlos Lorenzo
Publikováno v:
Journal of Nephrology. 36:1083-1085
Autor:
James E. Wraith, Sheena Grant, Elaine Cross, Louise V. Mahon, Simon Jones, Dougal Julian Hare, Brian W. Bigger, Michelle Lomax
Publikováno v:
Journal of Neurodevelopmental Disorders
Background\ud Mucopolysaccharidosis type-III (MPS III) is an autosomal recessive lysosomal storage disorder. It causes progressive physical and cognitive decline and has been linked to increased incidences of behavioural problems.\ud \ud Methods\ud D
Autor:
Sheena Grant, Elaine Cross, Kia J. Langford-Smith, Dougal Julian Hare, Louise V. Mahon, Maria Mercè Canal, Simon Jones, James Ed Wraith, Brian W. Bigger, Michelle Lomax
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e84128 (2014)
PLoS ONE
PLoS ONE
Sleep disturbances are prevalent in mucopolysaccharidosis Type III (MPS III), yet there is a lack of objective, ecologically valid evidence detailing sleep quantity, quality or circadian system. Eight children with MPS III and eight age-matched typic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a716afd0ed7d3574ae23905e0b8aae
Autor:
Simon Jones, Brian W. Bigger, Louise V. Mahon, James E. Wraith, Sheena Grant, Elaine Cross, Michelle Lomax, Dougal Julian Hare
Publikováno v:
Journal of inherited metabolic disease. 36(2)
Mucopolysaccharidosis type III (MPS III, Sanfilippo syndrome) is a lysosomal storage disorder, caused by a deficiency in one of four enzymes involved in the catabolism of the glycosaminoglycan heparan sulphate. It is a degenerative disorder, with a p