Proposal for an individualized dietary strategy in patients with very long‐chain acyl‐CoA dehydrogenase deficiency-Reference-Cited by-同舟云学术

Proposal for an individualized dietary strategy in patients with very long‐chain acyl‐CoA dehydrogenase deficiency

Published:2019-01 Issue:1 Volume:42 Page:159-168
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:Jrnl of Inher Metab Disea

Author:

Bleeker Jeannette C.¹²³,Kok Irene L.¹⁴,Ferdinandusse Sacha²,de Vries Maaike⁵,Derks Terry G.J.⁶,Mulder Margot F.⁷,Williams Monique⁸,Gozalbo Estela Rubio⁹,Bosch Annet M.³,van den Hurk Dorine T.⁴,de Sain‐van der Velden Monique G.M.¹⁰,Waterham Hans R.²,Wijburg Frits A.³,Visser Gepke¹³

Affiliation:

1. Department of Metabolic Diseases, Dutch Fatty Acid Oxidation Expertise CenterWilhelmina Children’s Hospital (UMCU), University Medical Center Utrecht, Internal Mail KE 04.306.0, PO Box 85090 3508 AB Utrecht Netherlands

2. Laboratory Genetic Metabolic DiseasesAcademic Medical Center Amsterdam Netherlands

3. Department of Pediatrics, Academic Medical CenterUniversity of Amsterdam Amsterdam Netherlands

4. Department of Internal Medicine and Dermatology, DieteticsUniversity Medical Center Utrecht Utrecht Netherlands

5. Department of PediatricsRadboud University Medical Center Nijmegen Netherlands

6. Department of Metabolic DiseasesBeatrix Children’s Hospital, University Medical Center Groningen Groningen Netherlands

7. Department of PediatricsVU University Medical Center Amsterdam Amsterdam Netherlands

8. Department of PediatricsErasmus MC‐Sophia Rotterdam Netherlands

9. Department of Pediatrics and Laboratory Genetic Metabolic DiseasesMaastricht University Medical Center Maastricht Netherlands

10. Department of Medical Genetics, Section Metabolic DiagnosticsWilhelmina Children’s Hospital, University Medical Center Utrecht Utrecht Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jimd.12037

Reference30 articles.

1. Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency

2. Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients

3. Arrhythmias and Conduction Defects as Presenting Symptoms of Fatty Acid Oxidation Disorders in Children

4. Recognition and management of fatty acid oxidation defects: A series of 107 patients

5. Current issues regarding treatment of mitochondrial fatty acid oxidation disorders

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4. Functional meat products: experience of introducing dietary fiber into chopped semi-finished products;Proceedings of the Voronezh State University of Engineering Technologies;2022-01-17

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