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4 in total

1. Childhood chronic disease and family functioning: a study of phenylketonuria.

Authors: A E Kazak; M Reber; L Snitzer
Journal: Pediatrics Date: 1988-02 Impact factor: 7.124

2. [Experience of the mothers of phenylketonuric children].

Authors: C Vidailhet; M Vidailhet; A M Guine; C Gonot; P Tridon; J M Guine
Journal: Neuropsychiatr Enfance Adolesc Date: 1982 Apr-May

3. Neonatal screening in Italy for congenital hypothyroidism and metabolic disorders: hyperphenylalaninemia, maple syrup urine disease and homocystinuria.

Authors: I Antonozzi; R Dominici; M Andreoli; F Monaco
Journal: J Endocrinol Invest Date: 1980 Oct-Dec Impact factor: 4.256

4. [Psychological consequences, on the child and its family, of continuous management of phenylketonuric and hypothyroid children].

Authors: A F Thieffry; M F Lebecq; J P Farriaux; P Parquet
Journal: Ann Pediatr (Paris) Date: 1985-10

4 in total

2 in total

1. Dietary protein counting as an alternative way of maintaining metabolic control in phenylketonuria.

Authors: A L Sweeney; R M Roberts; J M Fletcher
Journal: JIMD Rep Date: 2011-09-16

2. Parenting a Child with Phenylketonuria (PKU): an Interpretative Phenomenological Analysis (IPA) of the Experience of Parents.

Authors: Katie Carpenter; Anja Wittkowski; Dougal J Hare; Emma Medford; Stewart Rust; Simon A Jones; Debbie M Smith
Journal: J Genet Couns Date: 2018-02-21 Impact factor: 2.537

2 in total