Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Judy Nation"'
Autor:
Neha Kaul, Judy Nation, Joshua Laing, John‐Paul Nicolo, Adam M. Deane, Andrew A. Udy, Patrick Kwan, Terence J. O'Brien
Publikováno v:
JPEN. Journal of parenteral and enteral nutritionREFERENCES. 46(8)
Induction of ketosis by manipulation of nutrition intake has been proposed as an adjunctive treatment for super-refractory status epilepticus (SRSE). However, the classical 4:1 ketogenic ratio may not meet the nutrition needs, specifically protein fo
Publikováno v:
Neurol Clin Pract
Purpose of ReviewKetogenic diet therapy can be used as an adjuvant treatment of super-refractory status epilepticus (SRSE). However, the drug and metabolic interactions with concomitant treatments present a challenge for clinicians. In this review, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::946803d3aec0b24ef10d5a9a162caf11
https://europepmc.org/articles/PMC8610547/
https://europepmc.org/articles/PMC8610547/
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
Autor:
Kellie Draffin, Karen G. Stewart, Fergus J. Cameron, Jillian Bicknell-Royle, Jock Lawrie, Judy Nation, Ingrid E. Scheffer, Peter J Simm, Mark T Mackay
Publikováno v:
Epilepsy research. 136
The ketogenic diet (KD) is a medically supervised, high fat, low carbohydrate and restricted protein diet which has been used successfully in patients with refractory epilepsy. Only one published report has explored its effect on the skeleton. We pos
Publikováno v:
Evans, M, Andresen, B S, Nation, J & Boneh, A 2016, ' VLCAD deficiency : Follow-up and outcome of patients diagnosed through newborn screening in Victoria ', Molecular Genetics and Metabolism, vol. 118, no. 4, pp. 282-287 . https://doi.org/10.1016/j.ymgme.2016.05.012
Very long chain acyl-CoA dehydrogenase (VLCAD) deficiency is an inherited metabolic disorder of fatty acid oxidation. Treatment practices of the disorder have changed over the past 10-15years since this disorder was included in newborn screening prog
Autor:
Jillian Bicknell-Royle, Judy Nation, Sasipa Thammongkol, Ingrid E. Scheffer, Danya F. Vears, Kellie Draffin, Karen G. Stewart, Mark T Mackay
Publikováno v:
Epilepsia. 53:e55-e59
We report the efficacy of the ketogenic diet in refractory epilepsies focusing on outcomes with regard to epilepsy syndromes and etiology in children and adults with refractory epilepsy. Sixty-four consecutive children and four adults were prospectiv
Autor:
Leslie Anne Morrison, Jeffrey Buchhalter, Gregory K. Yim, Roberto Caraballo, Judy Nation, Shlomo Shinnar, David A. Griesemer, Juergen Schreck, Carmela Tardo, Eric H. Kossoff, Agustin Legido, Y.M. Christiana Liu, Russell Snyder, Roger Larson, Anne E. Anderson, J. Helen Cross, Jong M. Rho, Bruce A. Cohen, James W. Wheless, Per Åmark, Heidi H. Pfeifer, Edward Kovnar, Pierangelo Veggiotti, Leon Dure, Colette Parker, Douglas R. Nordli, Elaine C. Wirrell, Robyn Blackford, Eileen P.G. Vining, J. Ben Renfroe, G. Dean Timmons, Elizabeth A. Thiele, Brian Grabert, Mary Currey, Carl E. Stafstrom, A. G. Christina Bergqvist, Beth Zupec-Kania, Heung Dong Kim, Michael Goldstein, Joerg Klepper, Diane Donley, Bhuwan P. Garg, Maria Dahlin, Rana S. Jehle, Zahava Turner, Elizabeth J. Donner, Karen Ballaban-Gil
Publikováno v:
Epilepsia. 50:304-317
The ketogenic diet (KD) is an established, effective nonpharmacologic treatment for intractable childhood epilepsy. The KD is provided differently throughout the world, with occasionally significant variations in its administration. There exists a ne
Autor:
Sasipa, Thammongkol, Danya F, Vears, Jillian, Bicknell-Royle, Judy, Nation, Kellie, Draffin, Karen G, Stewart, Ingrid E, Scheffer, Mark T, Mackay
Publikováno v:
Epilepsia. 53(3)
We report the efficacy of the ketogenic diet in refractory epilepsies focusing on outcomes with regard to epilepsy syndromes and etiology in children and adults with refractory epilepsy. Sixty-four consecutive children and four adults were prospectiv
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