Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Maureen Humphrey"'
Publikováno v:
Journal of Child Neurology. 29:1496-1501
Ketogenic diet is a structured effective treatment for children with intractable epilepsy. Several reports have indicated poor linear growth in children on the diet but the mechanism of poor growth has not been elucidated. We aimed to explore whether
Publikováno v:
The Journal of family practice. 64(3)
Publikováno v:
Molecular genetics and metabolism. 112(4)
Dietary restrictions required to manage individuals with inborn errors of metabolism (IEM) are essential for metabolic control, however may result in an increased risk to both short and long-term nutritional status. Dietary factors most likely to inf
Publikováno v:
Journal of Pediatrics, 161, 2, pp. 328-32
Journal of Pediatrics, 161, 328-32
Journal of Pediatrics, 161, 328-32
Contains fulltext : 111022.pdf (Publisher’s version ) (Open Access) OBJECTIVES: To characterize dietary habits and eating patterns in patients with a urea cycle disorder (UCD), and to identify dietary habits that may serve as clues to lead to earli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e051b8a479bbd1b3a557ac31610f03f
https://doi.org/10.1016/j.jpeds.2012.02.006
https://doi.org/10.1016/j.jpeds.2012.02.006
Publikováno v:
Molecular genetics and metabolism. 104(1-2)
Background Whilst a reduction in blood phenylalanine (Phe) levels is essential in patients with PKU, a decrease in Phe/Tyrosine (Tyr) ratio and fluctuations in blood Phe levels over time have been recently associated with improved neuropsychological
Autor:
Avihu Boneh, Miriam H. Beauchamp, Maureen Humphrey, Heidi Peters, Jemma Watkins, Joy Yaplito-Lee
Publikováno v:
Molecular genetics and metabolism. 94(3)
Between October 2001 and September 2007, a total number of 391,651 neonates were screened in Victoria using Tandem Mass Spectrometry and 6 newborns were diagnosed as having GA I, giving an incidence of 1:65,275 (CI: 1:29,988=1:177,861). Another patie
Publikováno v:
Journal of paediatrics and child health. 42(9)
AIMS: To determine the prevalence, the types and severity of hyperphenylalaninaemia (including phenylketonuria (PKU)) in Victoria and to report on a new treatment modality of PKU. METHODS: We reviewed the medical records of all patients diagnosed wit
Publikováno v:
Journal of paediatrics and child health. 41(7)
OBJECTIVE To report the efficacy and tolerability of the ketogenic diet (KD) in refractory paediatric epilepsy. METHODS Twenty-six consecutive children were treated with the classical KD from 1996 to 2001. The epilepsy syndromes included symptomatic
Megestrol acetate in pediatric oncology patients may lead to severe, symptomatic adrenal suppression
Autor:
David M. Ashley, Kris M. Jamsen, Susan L. Mitchell, Peter Downie, Margaret Zacharin, Jacqueline M. Robinson, Maureen Humphrey, Natalie A. Grapsas, Jodie D. Bond, Lisa Orme
Publikováno v:
Cancer. 98(2)
BACKGROUND Despite the widespread use of megestrol acetate (MA) among a growing number of pediatric oncology departments, there is only one published study on the use of MA in children with malignant disease. The objectives of the current study were
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6f32650b1a166d1650c16a922f332f39
http://www.scopus.com/inward/record.url?eid=2-s2.0-84924297726&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84924297726&partnerID=MN8TOARS