Bone mineral density in children and adolescents with Prader-Willi syndrome: a longitudinal study during puberty and 9 years of growth hormone treatment.

Autor: Bakker NE; Dutch Growth Research Foundation (N.E.B., R.J.K., E.P.C.S., R.F.A.T.d. L.v.W., D.A.M.F., A.C.S.H.-K), 3000 CA Rotterdam, The Netherlands; Children's Hospital Erasmus MC-Sophia (N.E.B., R.J.K., E.P.C.S., G.C.B.B.d.H., A.C.S.H.-K.), 3000 CA Rotterdam, The Netherlands; University of Groningen (G.B.), University Medical Center Groningen/Beatrix Children's Hospital, Department of Pediatrics, 9713 GZ Groningen, The Netherlands; Diaconessen Hospital (D.A.J.P.), 2334 CK Leiden, The Netherlands; St. Antonius Hospital (J.J.G.H.-N., H.V.W.), 3430 EM Nieuwegein, The Netherlands; Haga Hospitals/Juliana Children's Hospital (E.C.A.M.H.), 2566 MJ The Hague, The Netherlands; Department of Pediatrics (P.E.J.), Jeroen Bosch Hospital, 5200 ME's-Hertogenbosch, The Netherlands; Gelre Hospitals (L.L.), 7300 SD Apeldoorn, The Netherlands; St. Catharina Hospital (R.J.O.), 5623 EJ Eindhoven, The Netherlands; Department of Pediatrics (W.O.), Leiden University Medical Center, 2333 ZA Leiden, The Netherlands; VU University Medical Center (J.R.), 1081 HV Amsterdam, The Netherlands; Radboud University Nijmegen Medical Center (A.A.E.M.V.A.); 6500 HB Nijmegen, The Netherlands; St. Jansdal Hospital (M.V.L.), 3844 DG Harderwijk, The Netherlands; Medical Center Twente (M.E.J.W.B.), 7511 JX Enschede, The Netherlands; Academic Medical Center (N.Z.-S.), University of Amsterdam, 1105 AZ Amsterdam, The Netherlands., Kuppens RJ, Siemensma EP, Tummers-de Lind van Wijngaarden RF, Festen DA, Bindels-de Heus GC, Bocca G, Haring DA, Hoorweg-Nijman JJ, Houdijk EC, Jira PE, Lunshof L, Odink RJ, Oostdijk W, Rotteveel J, Van Alfen AA, Van Leeuwen M, Van Wieringen H, Wegdam-den Boer ME, Zwaveling-Soonawala N, Hokken-Koelega AC

Publikováno v: The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2015 Apr; Vol. 100 (4), pp. 1609-18. Date of Electronic Publication: 2015 Feb 10.

Mitochondrial trifunctional protein deficiency: a severe fatty acid oxidation disorder with cardiac and neurologic involvement.

Autor: den Boer ME; Department of Pediatrics, Academic Medical Center, University of Amsterdam, The Netherlands. M.E.denBoer@amc.uva.nl, Dionisi-Vici C, Chakrapani A, van Thuijl AO, Wanders RJ, Wijburg FA

Publikováno v: The Journal of pediatrics [J Pediatr] 2003 Jun; Vol. 142 (6), pp. 684-9.

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients.

Autor: den Boer ME; Department of Pediatrics Academic Medical Center, University of Amsterdam, the Netherlands., Wanders RJ, Morris AA, IJlst L, Heymans HS, Wijburg FA

Publikováno v: Pediatrics [Pediatrics] 2002 Jan; Vol. 109 (1), pp. 99-104.

Disorders of mitochondrial fatty acyl-CoA beta-oxidation.

Autor: Wanders RJ; Academic Medical Center, University of Amsterdam, The Netherlands. wanders@amc.uva.nl, Vreken P, den Boer ME, Wijburg FA, van Gennip AH, IJlst L

Publikováno v: Journal of inherited metabolic disease [J Inherit Metab Dis] 1999 Jun; Vol. 22 (4), pp. 442-87.