Identification of human D lactate dehydrogenase deficiency.

Autor: Monroe GR; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., van Eerde AM; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., Tessadori F; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.; Hubrecht Institute-KNAW and University Medical Center Utrecht, Utrecht, 3584, CT, The Netherlands., Duran KJ; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., Savelberg SMC; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., van Alfen JC; Bartiméus, Institute for the Visually Impaired, Doorn, 3940, AB, The Netherlands., Terhal PA; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., van der Crabben SN; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, 3584, EA, The Netherlands., Lichtenbelt KD; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., Fuchs SA; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, 3584, EA, The Netherlands., Gerrits J; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., van Roosmalen MJ; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., van Gassen KL; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., van Aalderen M; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., Koot BG; Department of Pediatric Gastroenterology and Nutrition, Academic Medical Center, Amsterdam, 1105, AZ, The Netherlands., Oostendorp M; Department of Clinical Chemistry and Haematology, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.; Laboratory of Clinical Chemistry, Deventer Hospital, Deventer, 7416, SE, The Netherlands., Duran M; Laboratory Genetic Metabolic Diseases, Academic Medical Center, Amsterdam, 1105, AZ, The Netherlands., Visser G; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, 3584, EA, The Netherlands., de Koning TJ; Section of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center Groningen, Groningen, 9713, GZ, The Netherlands., Calì F; Oasi Research Institute-IRCCS, Troina, 94018, Italy., Bosco P; Oasi Research Institute-IRCCS, Troina, 94018, Italy., Geleijns K; Department of Child Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., de Sain-van der Velden MGM; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., Knoers NV; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., Bakkers J; Hubrecht Institute-KNAW and University Medical Center Utrecht, Utrecht, 3584, CT, The Netherlands.; Department of Medical Physiology, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., Verhoeven-Duif NM; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands., van Haaften G; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands. G.vanHaaften@umcutrecht.nl.; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands. G.vanHaaften@umcutrecht.nl., Jans JJ; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, 3584, CX, The Netherlands.

Publikováno v: Nature communications [Nat Commun] 2019 Apr 01; Vol. 10 (1), pp. 1477. Date of Electronic Publication: 2019 Apr 01.

Prevalence of cardiovascular risk factors in older people with intellectual disability.

Autor: de Winter CF; Bartiméus , Organization for People With Vision Impariment and Intellectual Disability, Doorn, Netherlands., Magilsen KW, van Alfen JC, Penning C, Evenhuis HM

Publikováno v: American journal on intellectual and developmental disabilities [Am J Intellect Dev Disabil] 2009 Nov; Vol. 114 (6), pp. 427-36.