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Browsing by Author "Claahsen-van der Grinten, H.L."
Now showing items 1-50 of 82
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Karyotype - Phenotype Associations in Patients with Turner Syndrome ; Velden, J.A.; ; Pienkowski, C.; Kohler, B.; ; Reisch, N.; Richter-Unruh, A.; Arlt, W.; Nordenstrom, A.; et al.2019, Article / Letter to editor (Pediatric Endocrinology Reviews, vol. 16, iss. 4, (2019), pp. 431-440)
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Gonadal function in adult male patients with congenital adrenal hyperplasia ; Gehrmann, K.; Falhammar, H.; Webb, E.A.; Nordenstrom, A.; ; ; ; ; ; et al.2018, Article / Letter to editor (European Journal of Endocrinology, vol. 178, iss. 3, (2018), pp. 285-294)
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A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency Jansen, S; ; Coe, B.P.; Carvill, G.L.; Esch, H. Van; Bosch, D.G.M.; ; ; ; ; et al.2018, Article / Letter to editor (European Journal of Human Genetics, vol. 26, iss. 1, (2018), pp. 54-63)
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Management and consequences of postoperative fluctuations in plasma sodium concentration after pediatric brain tumor surgery in the sellar region: a national cohort analysis Kruis, R.W.J.; Schouten-van Meeteren, A.Y.N.; Finken, M.J.; Oostdijk, W.; Trotsenburg, A.S. van; Boot, A.M.; ; ; Han, K.S.; Hoving, E.W.; et al.2018, Article / Letter to editor (Pituitary, vol. 21, iss. 4, (2018), pp. 384-392)
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GATA transcription factors in testicular adrenal rest tumours ; ; Mitchell, R.T.; ; Marijnissen-van Zanten, M.A.; ; ; ; ; Smith, L.B.; et al.2017, Article / Letter to editor (Endocrine Connections, vol. 6, iss. 8, (2017), pp. 866-875)
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Bilateral Testicular Tumors Resulting in Recurrent Cushing Disease After Bilateral Adrenalectomy Puar, T.; ; ; ; ; Kamphuis-van Ulzen, K.; Chortis, V.; Arlt, W.; ; ; et al.2017, Article / Letter to editor (Journal of Clinical Endocrinology and Metabolism, vol. 102, iss. 2, (2017), pp. 339-344)
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Birth Weight in Different Etiologies of Disorders of Sex Development Poyrazoglu, S.; Darendeliler, F.; Ahmed, S.F.; Hughes, I.; Bryce, J.; Jiang, J.; Rodie, M.; Hiort, O.; Hannema, S.E.; Bertelloni, S.; et al.2017, Article / Letter to editor (Journal of Clinical Endocrinology and Metabolism, vol. 102, iss. 3, (2017), pp. 1044-1050)
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Prevalence and Risk Factors of Early Endocrine Disorders in Childhood Brain Tumor Survivors: A Nationwide, Multicenter Study Clement, S.C.; Schouten-van Meeteren, A.Y.; Boot, A.M.; ; Granzen, B.; Han, K.; Janssens, G.O.; Michiels, E.M.; Trotsenburg, A.S. van; Vandertop, W.P.; et al.2016, Article / Letter to editor (Journal of Clinical Oncology, vol. 34, iss. 36, (2016), pp. 4362-4370)
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Clinical outcome of cloacal exstrophy, current status, and a change in surgical management Vliet, R.; ; Rassouli, R.; ; ; ; ; ; ; ; et al.2015, Article / Letter to editor (European Journal of Pediatric Surgery, vol. 25, iss. 1, (2015), pp. 87-93)
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Copy number variants in patients with short stature Duyvenvoorde, H.A. van; Lui, J.C.; Kant, S.G.; Oostdijk, W.; ; Hoffer, M.J.V.; Karperien, M.; Walenkamp, M.J.; ; Voorhoeve, P.G.; et al.2014, Article / Letter to editor (European Journal of Human Genetics, vol. 22, iss. 5, (2014), pp. 602-609)
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Genetic analysis of short children with apparent growth hormone insensitivity. Wit, J.M.; Duyvenvoorde, H.A. van; Scheltinga, S.A.; Bruin, S. de; Hafkenscheid, L.; Kant, S.G.; Ruivenkamp, C.A.; ; Doorn, J. van; Feigerlova, E.; et al.2012, Article / Letter to editor (Hormone Research in Paediatrics, vol. 77, iss. 5, (2012), pp. 320-333)
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Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family ; Kuhnisch, J.; Drijvers, J.M.; ; ; Setten, P. van; Branten, A.J.W.; Stumpp, S.; Jong, A. de; ; et al.2011, Article / Letter to editor (Journal of Clinical Endocrinology and Metabolism, vol. 96, iss. 1, (2011), pp. E189-98)
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Now showing items 1-50 of 82
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