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Papillary thyroid carcinoma in a boy with familial tuberous sclerosis complex attributable to a TSC2 deletion-a case report.
Curr Oncol. 2017 Oct;24(5):e423-e428. doi: 10.3747/co.24.3555. Epub 2017 Oct 25.
Curr Oncol. 2017.
PMID: 29089812
Free PMC article.
Is growth without IGF1 possible? A case report.
Flader M, Zalas D, Niedziela M.
Flader M, et al.
Pediatr Endocrinol Diabetes Metab. 2017;23(4):215-220. doi: 10.18544/PEDM-23.04.0096.
Pediatr Endocrinol Diabetes Metab. 2017.
PMID: 29574475
Free article.
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A novel mutation in the NR0B1 (DAX1) gene in a large family with two boys affected by congenital adrenal hypoplasia.
Rojek A, Flader M, Malecka E, Niedziela M.
Rojek A, et al. Among authors: flader m.
Hormones (Athens). 2014 Jul-Sep;13(3):413-9. doi: 10.14310/horm.2002.1495.
Hormones (Athens). 2014.
PMID: 25079468
Free article.
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Multiples of Median-Transformed, Normalized Reference Ranges of Steroid Profiling Data Independent of Age, Sex, and Units.
Zalas D, Reinehr T, Niedziela M, Borzikowsky C, Flader M, Simic-Schleicher G, Akkurt HI, Heger S, Hornig N, Holterhus PM, Kulle AE.
Zalas D, et al. Among authors: flader m.
Horm Res Paediatr. 2018;89(4):255-264. doi: 10.1159/000488028. Epub 2018 Apr 25.
Horm Res Paediatr. 2018.
PMID: 29694956
Clinical Trial.
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