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Issue Date	Title	Author(s)
2011	GATA6 haploinsufficiency causes pancreatic agenesis in humans.	Allen, H.L.; Flanagan, S.E.; Shaw-Smith, C.; Franco, E. De; Akerman, I.; Caswell, R.; Ferrer, J.; Hattersley, A.T.; Ellard, S.; Aanstoot, H.J.; Aberg, E.; Adolfsson, P.; Anthony, M.; Batlle, M.; Bruining, J.; Bühr, P.; Cummings, E.; Edge, J.; Garcia-Hurtado, J.; Hathout, E.; Ho, J.; Jeffries, C.; Temple, I.K.; Kaufman, E.; Kotori, V.M.; Krijger, R. de; Kummer, M.; Mackay, D.; Mace, J.; Noordam, C.; O'Brien, F.; Rubio-Cabezas, O.; Shield, J.; Skidmore, D.; White, S.; Zanier, U.
2011	Exercise training improves physical fitness and vascular function in children with type 1 diabetes	Seeger, J.P.H.; Thijssen, D.H.J.; Noordam, K.; Cranen, M.E.; Hopman, M.T.E.; Nijhuis-Van der Sanden, M.W.G.
2011	[Congenital hyperinsulinism in the north-east Netherlands. Clinical features and DNA diagnostics in 22 children]	Verheul, J.C.; Ris-Stalpers, C.; Bikker, H.; Bakker-van Waarde, W.M.; Noordam, C.
2011	The severe short stature in two siblings with a heterozygous IGF1 mutation is not caused by a dominant negative effect of the putative truncated protein	Duyvenvoorde, H.A. van; Doorn, J. van; Koenig, J.; Gauguin, L.; Oostdijk, W.; Wade, J.D.; Karperien, M.; Ruivenkamp, C.A.; Losekoot, M.; Setten, P.A. van; Walenkamp, M.J.; Noordam, C.; Meyts, P. De; Wit, J.M.
2011	Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation	Jongmans, M.C.J.; Burgt, I. van der; Hoogerbrugge, P.M.; Noordam, K.; Yntema, H.G.; Nillesen, W.M.; Kuiper, R.P.; Ligtenberg, M.J.L.; Geurts van Kessel, A.H.M.; Krieken, J.H. van; Kiemeney, L.A.L.M.; Hoogerbrugge, N.
2011	Mitochondrial dysfunction and organic aciduria in five patients carrying mutations in the Ras-MAPK pathway	Kleefstra, T.; Wortmann, S.B.; Rodenburg, R.J.T.; Bongers, M.H.F.; Hadzsiev, K.; Noordam, C.; Heuvel, L.P.W.J. van den; Nillesen, W.M.; Hollody, K.; Gillessen-Kaesbach, G.; Lammens, M.M.Y.; Smeitink, J.A.M.; Burgt, C.J.A.M. van der; Morava, E.
2010	Short stature associated with a novel heterozygous mutation in the insulin-like growth factor 1 gene.	Duyvenvoorde, H.A. van; Setten, P.A. van; Walenkamp, M.J.; Doorn, J. van; Koenig, J.; Gauguin, L.; Oostdijk, W.; Ruivenkamp, C.A.; Losekoot, M.; Wade, J.D.; Meyts, P. De; Karperien, M.; Noordam, C.; Wit, J.M.
2010	Noonan syndrome, the SOS1 gene and embryonal rhabdomyosarcoma.	Jongmans, M.C.J.; Hoogerbrugge, P.M.; Hilkens, L.; Flucke, U.E.; Burgt, C.J.A.M. van der; Noordam, C.; Ruiterkamp-Versteeg, M.; Yntema, H.G.; Nillesen, W.M.; Ligtenberg, M.J.L.; Geurts van Kessel, A.H.M.; Kuiper, R.P.; Hoogerbrugge, N.
2010	Successful treatment of severe subcutaneous insulin resistance with inhaled insulin therapy.	Alfen-van der Velden, J. van; Noordam, C.; Galan, B.E. de; Hoorweg-Nijman, J.J.G.; Voorhoeve, P.G.; Westerlaken, C.
2010	Biosimilars: controversies as illustrated by rhGH.	Declerck, P.J.; Darendeliler, F.; Goth, M.; Kolouskova, S.; Micle, I.; Noordam, C.; Peterkova, V.; Volevodz, N.N.; Zapletalova, J.; Ranke, M.B.
2009	Solitaire schildkliernoduli bij kinderen	Bech, A.; Claahsen-van der Grinten, H.L.; Noordam, C.
2009	Growth in Noonan syndrome	Otten, B.J.; Noordam, C.
2009	Klinisch denken en beslissen in de praktijk Een jongen met vermoeidheidsklachten en buikpijn	Os, E. van; Noordam, C.; Hart, W.; Draaisma, J.M.T.
2009	Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births.	Slingerland, A.S.; Shields, B.M.; Flanagan, S.E.; Bruining, G.J.; Noordam, K.; Gach, A.; Mlynarski, W.; Malecki, M.T.; Hattersley, A.T.; Ellard, S.
2009	Inactivating PAPSS2 mutations in a patient with premature pubarche.	Noordam, C.; Dhir, V.; McNelis, J.C.; Schlereth, F.; Hanley, N.A.; Krone, N.; Smeitink, J.A.M.; Smeets, R.; Sweep, C.G.J.; Claahsen-van der Grinten, H.L.; Arlt, W.
2009	Growth hormone and the heart in Noonan syndrome	Noordam, C.
2009	Decreased bone density and treatment in patients with autosomal recessive cutis laxa.	Noordam, C.; Funke, S.; Slobbe-Knoers, V.V.A.M.; Jira, P.E.; Wevers, R.A.; Urban, Z.; Morava, E.
2009	Reduced levels of GH during GnRH analogue treatment in pubertal short girls born small for gestational age (SGA).	Kaay, D.C.M. van der; Rose, S.R.; Dijk, M.; Noordam, C.; Rheenen, E. van; Hokken-Koelega, A.C.
2008	Spinal stenosis with paraparesis in albright hereditary osteodystrophy. Case report and review of the literature.	Lindert, E.J. van; Bartels, R.H.M.A.; Noordam, K.
2008	Denys-Drash syndrome and congenital diaphragmatic hernia: another case with the 1097G > A(Arg366His) mutation.	Antonius, T.A.J.; Bon, B. van; Eggink, A.; Burgt, I. van der; Noordam, K.; Heijst, A.
2008	Impaired Sertoli cell function in males diagnosed with Noonan syndrome.	Marcus, K.A.; Sweep, C.G.J.; Burgt, I van der; Noordam, C.
2008	Response to growth hormone treatment and final height in Noonan syndrome in a large cohort of patients in the KIGS database.	Raaijmakers, R.; Noordam, C.; Karagiannis, G.; Gregory, J.W.; Hertel, N.T.; Sipila, I.; Otten, B.J.
2008	Sulphonylurea therapy improves cognition in a patient with the V59M KCNJ11 mutation.	Slingerland, A.S.; Hurkx, W.; Noordam, K.; Flanagan, S.E.; Jukema, J.W.; Meiners, L.C.; Bruining, G.J.; Hattersley, A.T.; Hadders-Algra, M.
2008	Are ECG abnormalities in Noonan syndrome characteristic for the syndrome?	Raaijmakers, R.; Noordam, C.; Noonan, J.A.; Croonen, E.A.; Burgt, C.J. van der; Draaisma, J.M.T.
2008	Homozygous and heterozygous expression of a novel mutation of the acid-labile subunit.	Duyvenvoorde, H.A. van; Kempers, M.J.E.; Twickler, T.B.; Doorn, J. van; Gerver, W.J.; Noordam, C.; Losekoot, M.; Karperien, M.; Wit, J.M.; Hermus, A.R.
2008	Long-term GH treatment improves adult height in children with Noonan syndrome with and without mutations in protein tyrosine phosphatase, non-receptor-type 11.	Noordam, C.; Peer, P.G.M.; Francois, I.; Schepper, J. de; Burgt, I. van der; Otten, B.J.
2007	Klinefelter's syndrome and Prader-Willi syndrome: a rare combination	Verhoeven, W.M.A.; Vries, B.B. van; Duffels, S.J.H.; Egger, J.I.M.; Noordam, C.; Tuinier, S.
2007	Klinefelter's syndrome and Prader-Willi syndrome: a rare combination.	Verhoeven, W.M.A.; Vries, B.B. van; Duffels, S.J.H.; Egger, J.I.M.; Noordam, C.; Tuinier, S.
2007	[Persistent neonatal hypoglycaemia caused by arterial positioning of the umbilical venous catheter]	Peters, P.A.; Brus, F.; Noordam, C.; Smorenburg, M.K.; Setten, P.A. van
2006	Klinefelter syndrome and Prader-Willi syndrome: a rare combination	Verhoeven, W.M.A.; Tuinier, S.; Duffels, S.J.H.; Egger, J.I.M.; Vries, L.B.A. de; Noordam, C.; Ravenswaaij-Arts, C.M.A. van
2006	[Central congenital hypothyroidism due to Graves' disease in the mother]	Liebrand, C.A.; Mol, A.C. de; Kempers, M.J.E.; Noordam, C.
2006	Treatment of tall stature in boys with somatostatin analogue 201-995: effect on final height.	Noordam, C.; Daalen, S. van; Otten, B.J.
2006	Absence of increased height velocity in the first year of life in untreated children with simple virilizing congenital adrenal hyperplasia.	Claahsen-van der Grinten, H.L.; Noordam, K.; Borm, G.F.; Otten, B.J.
2006	High serum levels of growth hormone (GH) and insulin-like growth factor-I (IGF-I) during high-dose GH treatment in short children born small for gestational age.	Dijk, M. van; Mulder, P.; Houdijk, M.; Mulder, J.; Noordam, K.; Odink, R.J.; Rongen-Westerlaken, C.; Voorhoeve, P.; Waelkens, J.; Stokvis-Brantsma, J.; Hokken-Koelega, A.C.
2005	Genotypic and phenotypic characterization of Noonan syndrome: new data and review of the literature.	Jongmans, M.; Sistermans, E.A.; Rikken, A.; Nillesen, W.M.; Tamminga, R.; Patton, M.A.; Maier, E.M.; Tartaglia, M.; Noordam, K.; Burgt, C.J.A. van der
2005	[A genetic childhood disease with consequences in adult life: the Denys-Drash syndrome]	Lowik, M.; Berk-Mortel, F. van den; Noordam, C.; Hamersvelt, H.W. van; Heuvel, L.P.W.J. van den; Levtchenko, E.N.
2005	Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.	Vallette-Kasic, S.; Brue, T.; Pulichino, A.M.; Gueydan, M.; Barlier, A.; David, M.; Nicolino, M.; Malpuech, G.; Dechelotte, P.; Deal, C.; Vliet, G. van; Vroede, M.A. de; Riepe, F.G.; Partsch, C.J.; Sippell, W.G.; Berberoglu, M.; Atasay, B.; Zegher, F. de; Beckers, D.; Kyllo, J.; Donohoue, P.; Fassnacht, M.; Hahner, S.; Allolio, B.; Noordam, C.; Dunkel, L.; Hero, M.; Pigeon, B.; Weill, J.; Yigit, S.; Brauner, R.; Heinrich, J.J.; Cummings, E.; Riddell, C.; Enjalbert, A.; Drouin, J.
2004	Congenital isolated ACTH deficiency, an underestimated cause of neonatal death, explained by TPIT mutations	Vallette-Kasic, S.; Brue, T.; Pulichino, A.M.; Gueydan, M.; Barlier, A.; David, M.; Nicolino, M.; Malpuech, G.; Dechelotte, P.; Deal, C.; Vliet, G. van; Vroede, M.A. de; Riepe, F.G.; Partsch, C.J.; Sippell, W.G.; Berberoglu, M.; Atasay, B.; Zegher, F. de; Beckers, D.; Kyllo, J.; Donohoue, P.; Fassnacht, M.; Hahner, S.; Allolio, B.; Noordam, C.; Dunkel, L.; Hero, M.; Pigeon, B.; Weill, J.; Yigit, S.; Brauner, R.; Heinrich, J.J.; Cummings, E.; Riddell, C.; Enjalbert, A.; Drouin, J.
2004	Genetics and variation in phenotype in Noonan syndrome	Jongmans, M.J.; Otten, B.J.; Noordam, K.; Burgt, C.J.A. van der
2004	[Congenital hyperinsulinism in 15 infants, 1981-1999; experiences and new insights]	Kuijpers, S.C.; Noordam, C.; Boelen, C.; Wijnen, R.M.H.
2004	From bone biology to bone analysis.	Schoenau, E.; Saggese, G.; Peter, F.; Baroncelli, G.I.; Shaw, N.J.; Crabtree, N.J.; Zadik, Z.; Neu, C.M.; Noordam, C.; Radetti, G.; Hochberg, Z.
1997	Growth before and during growth hormone treatment in children operated for craniopharyngioma	Hogeveen, M.; Noordam, C.; Otten, B.J.; Wit, J.M.; Massa, G.G.