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Page 1
[Y chromosome in Turner syndrome].
Rojek A, Kwasiuk K, Obara-Moszyńska M, Kolesińska Z, Niedziela M. Rojek A, et al. Among authors: obara moszynska 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: obara moszynska m. Clin Pediatr (Phila). 2023 Oct 5:99228231202607. doi: 10.1177/00099228231202607. Online ahead of print. Clin Pediatr (Phila). 2023. PMID: 37798950
Uterine Development During Induced Puberty in Girls with Turner Syndrome.
Obara-Moszynska M, Dzialach L, Rabska-Pietrzak B, Niedziela M, Kapczuk K. Obara-Moszynska M, et al. Front Endocrinol (Lausanne). 2021 Jul 6;12:707031. doi: 10.3389/fendo.2021.707031. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34295308 Free PMC article.
SEMA3A and IGSF10 Are Novel Contributors to Combined Pituitary Hormone Deficiency (CPHD).
Budny B, Zemojtel T, Kaluzna M, Gut P, Niedziela M, Obara-Moszynska M, Rabska-Pietrzak B, Karmelita-Katulska K, Stajgis M, Ambroziak U, Bednarczuk T, Wrotkowska E, Bukowska-Olech E, Jamsheer A, Ruchala M, Ziemnicka K. Budny B, et al. Among authors: obara moszynska m. Front Endocrinol (Lausanne). 2020 Jun 16;11:368. doi: 10.3389/fendo.2020.00368. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32612575 Free PMC article.
Case report: The cardio-facio-cutaneous syndrome due to a novel germline mutation in MAP2K1: A multifaceted disease with immunodeficiency and short stature.
Szczawińska-Popłonyk A, Popłonyk N, Niedziela M, Sowińska-Seidler A, Sztromwasser P, Jamsheer A, Obara-Moszyńska M. Szczawińska-Popłonyk A, et al. Among authors: obara moszynska m. Front Pediatr. 2022 Oct 14;10:990111. doi: 10.3389/fped.2022.990111. eCollection 2022. Front Pediatr. 2022. PMID: 36313893 Free PMC article.
26 results