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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2004 3
2005 1
2006 4
2007 2
2008 4
2009 1
2010 3
2011 6
2012 2
2013 8
2014 9
2015 3
2016 7
2017 10
2018 5
2019 2
2020 7
2021 12
2022 7
2023 4
2024 2

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93 results

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Page 1
Hyperthyroidism in adolescents.
Niedziela M. Niedziela M. Endocr Connect. 2021 Oct 25;10(11):R279-R292. doi: 10.1530/EC-21-0191. Endocr Connect. 2021. PMID: 34596580 Free PMC article. Review.
Thyroid nodules.
Niedziela M. Niedziela M. Best Pract Res Clin Endocrinol Metab. 2014 Mar;28(2):245-77. doi: 10.1016/j.beem.2013.08.007. Epub 2013 Aug 30. Best Pract Res Clin Endocrinol Metab. 2014. PMID: 24629865 Review.
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.
Miraoui H, Dwyer AA, Sykiotis GP, Plummer L, Chung W, Feng B, Beenken A, Clarke J, Pers TH, Dworzynski P, Keefe K, Niedziela M, Raivio T, Crowley WF Jr, Seminara SB, Quinton R, Hughes VA, Kumanov P, Young J, Yialamas MA, Hall JE, Van Vliet G, Chanoine JP, Rubenstein J, Mohammadi M, Tsai PS, Sidis Y, Lage K, Pitteloud N. Miraoui H, et al. Among authors: niedziela m. Am J Hum Genet. 2013 May 2;92(5):725-43. doi: 10.1016/j.ajhg.2013.04.008. Am J Hum Genet. 2013. PMID: 23643382 Free PMC article.
[Y chromosome in Turner syndrome].
Rojek A, Kwasiuk K, Obara-Moszyńska M, Kolesińska Z, Niedziela M. Rojek A, et al. Among authors: niedziela m. Pediatr Endocrinol Diabetes Metab. 2017;23(1):37-41. doi: 10.18544/PEDM-23.01.0072. Pediatr Endocrinol Diabetes Metab. 2017. PMID: 29073306 Free article. Review. Polish.
Central Diabetes Insipidus in Children as a Diagnostic Challenge.
Dyrka K, Dzialach L, Niedziela M, Jonczyk-Potoczna K, Derwich K, Obara-Moszynska M. Dyrka K, et al. Among authors: niedziela m. Clin Pediatr (Phila). 2023 Oct 5:99228231202607. doi: 10.1177/00099228231202607. Online ahead of print. Clin Pediatr (Phila). 2023. PMID: 37798950
PAPP-A2 a new key regulator of growth.
Banaszak-Ziemska M, Niedziela M. Banaszak-Ziemska M, et al. Among authors: niedziela m. Endokrynol Pol. 2017;68(6):682-691. doi: 10.5603/EP.a2017.0060. Endokrynol Pol. 2017. PMID: 29238946 Free article. Review.
NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile mice.
Chachlaki K, Messina A, Delli V, Leysen V, Maurnyi C, Huber C, Ternier G, Skrapits K, Papadakis G, Shruti S, Kapanidou M, Cheng X, Acierno J, Rademaker J, Rasika S, Quinton R, Niedziela M, L'Allemand D, Pignatelli D, Dirlewander M, Lang-Muritano M, Kempf P, Catteau-Jonard S, Niederländer NJ, Ciofi P, Tena-Sempere M, Garthwaite J, Storme L, Avan P, Hrabovszky E, Carleton A, Santoni F, Giacobini P, Pitteloud N, Prevot V. Chachlaki K, et al. Among authors: niedziela m. Sci Transl Med. 2022 Oct 5;14(665):eabh2369. doi: 10.1126/scitranslmed.abh2369. Epub 2022 Oct 5. Sci Transl Med. 2022. PMID: 36197968 Free PMC article.
NKX2-5 Variant in Two Siblings with Thyroid Hemiagenesis.
Szczepanek-Parulska E, Budny B, Borowczyk M, Zhukov I, Szutkowski K, Zawadzka K, Tahir R, Minczykowski A, Niedziela M, Ruchała M. Szczepanek-Parulska E, et al. Among authors: niedziela m. Int J Mol Sci. 2022 Mar 21;23(6):3414. doi: 10.3390/ijms23063414. Int J Mol Sci. 2022. PMID: 35328834 Free PMC article.
93 results