Results 121 to 130 of about 17,994 (195)

Changes in Child Behaviour Following a Brief Parenting Intervention (Triple P) for Families of Children with Phenylketonuria (PKU): A Case Series. [PDF]

Behav Modif
Kirby G, Morawska A, Mitchell AE, McGill J, Coman D, Inwood A.   +5 more
europepmc   +1 more source

Breaking Barriers: Stakeholder Insights into Physical Activity, Exercise, and Dietary Behaviours Among Individuals with Phenylketonuria (PKU). [PDF]

Healthcare (Basel)
Skidmore AG, MacDonald A, Herbert AJ, Lewis K, Gough LA.   +4 more
europepmc   +1 more source

Executive Functions and Long-Term Metabolic Control in Adults with Phenylketonuria (PKU). [PDF]

Metabolites
Tomm A, Thiele AG, Rohde C, Schlögl H, Kiess W, Beblo S.   +5 more
europepmc   +1 more source

UK Patient Access to Low-Protein Prescription Foods in Phenylketonuria (PKU): An Uneasy Path. [PDF]

Nutrients
Evans S, Arbuckle C, Ashmore C, Bailey S, Blaauw G, Chaudhry W, Dale C, Daly A, Downey B, Dundas J, Ellerton C, Ford S, Gaff L, Gribben J, Grimsley A, Hill M, Murphy L, Newby C, Oxley N, Pereira R, Pinto A, Skeath R, Sparks A, Tapley S, Terry A, Wood G, Woodall A, Yeung K, MacDonald A.   +28 more
europepmc   +1 more source

Epidemiologic study of Phenylketonuria disease in Lorestan province

, 2016
Background : Phenylketonuria (PKU) is a metabolic disease with autosomal recessive pattern of inheritance caused by a deficiency or absence of the enzyme phenylalanine hydroxylase in the liver. Phenylketonuria incidence is 1 in 10,000 births.
Fateme Khodadadi, Naser Motamedi, Azita Zafar Mohtashami, GHolam reza Lashkarara   +3 more
core  

Patient and carer perceptions of video, telephone and in-person clinics for Phenylketonuria (PKU). [PDF]

Orphanet J Rare Dis
McBride H, Evans S, Pinto A, Daly A, Ashmore C, Ilgaz F, Ford S, Buckley S, MacDonald A.   +8 more
europepmc   +1 more source

Uniformity of Food Protein Interpretation Amongst Dietitians for Patients with Phenylketonuria (PKU): 2020 UK National Consensus Statements. [PDF]

Nutrients, 2020
Evans S, Adam S, Adams S, Allen H, Ashmore C, Bailey S, Banks J, Churchill H, Cochrane B, Cook J, Dale C, Daly A, Dixon M, Dunlop C, Ellerton C, Emm A, Firman S, Ford S, French M, Gribben J, Grimsley A, Herlihy I, Hill M, Judd S, Lang K, Males J, McDonald J, McStravick N, Millington C, Newby C, Noble C, Pereira R, Pinto A, Robertson L, Robotham A, Ross K, Singleton K, Skeath R, Terry A, Van Wyk K, White F, White L, Wildgoose J, Woodall A, MacDonald A.   +44 more
europepmc   +1 more source

Patient journey and disease burden characterization of the population with phenylketonuria (PKU) in Brazil: a retrospective analysis through data reported in the public health system administrative database (DATASUS). [PDF]

Lancet Reg Health Am
Vargas PR, Poubel M, Martins B, Velez P, Vilela D, Mesojedovas D, Sá Pacheco Carneiro Magalhães T, Louie KS, Pessoa A.   +8 more
europepmc   +1 more source

Prospects for Cell-Directed Curative Therapy of Phenylketonuria (PKU). [PDF]

Mol Front J, 2019
Harding CO.
europepmc   +1 more source

Acceptability of dried blood spot collection by primary caregivers of Filipino patients with maple syrup urine disease (MSUD) and phenylketonuria (PKU). [PDF]

J Community Genet
Merencilla RJE, Maceda EBG, Basas JRU, Adducul RTY, Francisco ML, Licudo JV, de Castro-Hamoy LG.   +6 more
europepmc   +1 more source