72
Noonan syndrome. Horm Res. 2004;62 Suppl 3:56–9
•
KNMG, V&VN, KNOV, KNGF, KNMP, NIP, NVZ, NFU, GGZ Nederland, NPCF, “Handreiking
Verantwoordelijkheidsverdeling bij samenwerking in de zorg.” 26-Jan-2010
•
Legemaate, J. (2013). De gevolgen van het opnemen van professionele standaarden in een wettelijk
register voor de juridische betekenis van deze standaarden en voor de juridische positie van
zorgaanbieders., Academisch Medisch Centrum Amsterdam en Universiteit van Amsterdam
•
Malaquias AC, Brasil AS, Pereira AC, Arnhold IJP, Mendonca BB, Bertola DR, Jorge AAL.2012. Growth
standards of patients with Noonan and Noonan-like syndromes with mutations in the RAS/MAPK
pathway. Am J Med Genet Part A 158A:2700–2706
•
Ministerie van Veiligheid en Justitie, Burgerlijk Wetboek Boek 7. De overeenkomst inzake geneeskundige
behandeling.
•
Niihori T, Aoki Y, Ohashi H et al. Functional analysis of PTPN11/SHP-2 mutants identified in
Noonan syndrome and childhood leukemia. J Hum Genet. 2005;50:192–202
•
Noonan JA, Ehmke DA. Associated noncardiacmalformations in children with congenital heart
disease. J Pediatr. 1963;31:150–153
•
Noonan JA. Hypertelorism with Turnerphenotype. Am J Dis Child. 1968;116(4):373–380
•
Noordam, C. Draaisma, J. et al. (2001) Effects of growth hormone treatment on left ventricular
dimensoins in children with Noonan syndrome. Hormone research in pediatrics 56(3-4): 110-113
•
Pandit B, Sarkozy A, Pennacchio LA et al. Gain-of-function RAF1 mutations cause Noonan
and LEOPARD syndromes with hypertrophic cardiomyopathy. Nat Genet. 2007;39:1007–12
•
Raaimakers, R. Noordam, C. et al. (2008) Are ECG abnormalities in Noonan syndrome characteristic for
the syndrome? European Journal of Pediatrics 167(12):1363-1367
•
Roberts et al. (2013) Noonan syndrome. Lancet, 381:333-342
•
Romano, A., Allanson, J. et al, Pediatrics 2010;126;746; originally published online September 27, 2010;
DOI: 10.1542/peds.2009-3207)
•
Royal College of Nursing, (2008) “Transitiezorg voor adolescenten. Richtlijn voor verpleegkundigen,”
Richtlijn
•
Shah, N. Rodriguez et al. (1999) Feeding difficulties and foregut dysmotility in Noonan’s syndrome. Arch
Dis Child 81(1):28-31
•
Smpokou P, Tworog-Dube E, Kucherlapati, RS, Roberts AE. 2012. Medical complications, clinical findings,
and educational outcomes in adults with Noonan syndrome. Am J Med Genet Part A 158A:3106–3111
•
Tartaglia M, Kalidas K, Shaw A et al. (2002) PTPN11 mutations in Noonan syndrome: molecular
spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. Am J Hum Genet 70:1555–63
•
Tartaglia M, Gelb BD, Zenker M et al. Noonan syndrome and clinically related disorders. Best
practice & research clinical endocrinology & metabolism. 2011; 25: 161-179
•
Tussenrapportage Project Zelfmanagement in de Praktijk van Vilans (2013)
•
Verhoeven,W., Wingbermuhle, E., Egger, J., et al. (2008). Noonan syndrome: Psychological and
psychiatric aspects. American Journal of Medical Genetics, 146A,191-196
•
VUMC, “Operatie en verblijf in het ziekenhuis,” 12-Jun-2013. [Online]. Via:
•
Wingbermühle, E., Egger, J., Verhoeven, W. & Van der Burgt, I. (2012): Neuropsychologische kenmerken
van het noonansyndroom. Neuropraxis, 2, 46-52
•
Wingbermühle, E., Kessels, R. & Egger, J. (2014). Het syndroom van Noonan: cognitieve en sociaal
emotionele kenmerken. De Psycholoog, 49, 10-20
•
Wingbermühle, E., Egger, J., Verhoeven, W., et al. (2012). Affective functioning and social cognition in
Noonan syndrome. Psychological Medicine, 42,419-426
•
Wingbermühle, E., Roelofs, R., Van der Burgt, I., et al (2012). Cognitive functioning of adults with Noonan
syndrome: A case control study. Genes, Brain and Behavior, 11, 785-793
•
Wingbermühle, E., Theunissen, H., Verhoeven, W., et al. (2012). The neurocognition of alexithymia:
Evidence from neuropsychological and neuro-imaging studies. Acta Neuropsychiatrica, 24, 67-80
