Hyperthyroidism in adolescents

by Marek Niedziela
Published 2021-10-01

Czynniki prozapalne u dzieci z młodzieńczym idiopatycznym zapaleniem stawów

by Dominika Kaminiarczyk, Karolina Adamczak, Marek Niedziela
Published 2010-02-01

Diagnostic significance of serum concentrations of soluble Fas ligand (sFasL) in children with autoimmune thyroid disease

by Hanna Mikos, Marcin Mikos, Marek Niedziela
Published 2017-04-01

Ultrasound features of multinodular goiter in DICER1 syndrome

by Marek Niedziela, Karl Muchantef, William D. Foulkes
Published 2022-09-01

Syndrome of Congenital Insulin Resistance Caused by a Novel INSR Gene Mutation

by Aleksandra Rojek, Beata Wikiera, Anna Noczynska, Marek Niedziela
Published 2023-09-01

Autoimmune polyglandular syndrome type 2 in the form of Carpenter syndrome in a 16.5-year-old girl

by Hanna Nowak, Dominika Szwacka, Marek Niedziela, Witold Stankiewicz, Monika Obara-Moszyńska
Published 2024-02-01

Limited Mandibular Movements as a Consequence of Unilateral or Asymmetrical Temporomandibular Joint Involvement in Juvenile Idiopathic Arthritis Patients

by Tamara Pawlaczyk-Kamieńska, Tomasz Kulczyk, Elżbieta Pawlaczyk-Wróblewska, Maria Borysewicz-Lewicka, Marek Niedziela
Published 2020-08-01

Uterine Development During Induced Puberty in Girls with Turner Syndrome

by Monika Obara-Moszynska, Lukasz Dzialach, Barbara Rabska-Pietrzak, Marek Niedziela, Karina Kapczuk, Karina Kapczuk
Published 2021-07-01

Mental health and adjustment to juvenile idiopathic arthritis: Level of agreement between parent and adolescent reports according to Strengths and Difficulties Questionnaire and Ad...

by Ewa Misterska, Dominika Kaminiarczyk-Pyzałka, Karolina Adamczak, Katarzyna A Adamczyk, Marek Niedziela, Maciej Głowacki, Jakub Głowacki
Published 2017-01-01

X-Linked Adrenal Hypoplasia Congenita in a Boy due to a Novel Deletion of the Entire NR0B1 (DAX1) and MAGEB1–4 Genes

by Aleksandra Rojek, Maciej R. Krawczynski, Aleksander Jamsheer, Anna Sowinska-Seidler, Barbara Iwaniszewska, Ewa Malunowicz, Marek Niedziela
Published 2016-01-01

Case report: The cardio-facio-cutaneous syndrome due to a novel germline mutation in MAP2K1: A multifaceted disease with immunodeficiency and short stature

by Aleksandra Szczawińska-Popłonyk, Natalia Popłonyk, Marek Niedziela, Anna Sowińska-Seidler, Paweł Sztromwasser, Paweł Sztromwasser, Aleksander Jamsheer, Monika Obara-Moszyńska
Published 2022-10-01

Thyroid diseases in children and adolescents requiring surgical treatment—indications, techniques, results, and complications based on 10 years of the single center’s own experienc...

by Patrycja Sosnowska-Sienkiewicz, Dajana Danielewicz, Danuta Januszkiewicz-Lewandowska, Paulina Rusak, Iwona Anderko, Maciej Rzepecki, Marek Niedziela, Jerzy Harasymczuk, Przemysław Mańkowski
Published 2024-01-01

NKX2-5 Variant in Two Siblings with Thyroid Hemiagenesis

by Ewelina Szczepanek-Parulska, Bartłomiej Budny, Martyna Borowczyk, Igor Zhukov, Kosma Szutkowski, Katarzyna Zawadzka, Raiha Tahir, Andrzej Minczykowski, Marek Niedziela, Marek Ruchała
Published 2022-03-01

Integrating clinical and genetic approaches in the diagnosis of 46,XY disorders of sex development

by Zofia Kolesinska, James Acierno, S Faisal Ahmed, Cheng Xu, Karina Kapczuk, Anna Skorczyk-Werner, Hanna Mikos, Aleksandra Rojek, Andreas Massouras, Maciej R Krawczynski, Nelly Pitteloud, Marek Niedziela
Published 2018-12-01

The Usefulness of Magnetic Resonance Imaging of the Cardiovascular System in the Diagnostic Work-Up of Patients With Turner Syndrome

by Monika Obara-Moszynska, Justyna Rajewska-Tabor, Szymon Rozmiarek, Katarzyna Karmelita-Katulska, Anna Kociemba, Barbara Rabska-Pietrzak, Magdalena Janus, Andrzej Siniawski, Bartlomiej Mrozinski, Agnieszka Graczyk-Szuster, Marek Niedziela, Malgorzata Pyda
Published 2018-10-01

SEMA3A and IGSF10 Are Novel Contributors to Combined Pituitary Hormone Deficiency (CPHD)

by Bartlomiej Budny, Tomasz Zemojtel, Tomasz Zemojtel, Malgorzata Kaluzna, Pawel Gut, Marek Niedziela, Monika Obara-Moszynska, Barbara Rabska-Pietrzak, Katarzyna Karmelita-Katulska, Marek Stajgis, Urszula Ambroziak, Tomasz Bednarczuk, Elzbieta Wrotkowska, Ewelina Bukowska-Olech, Aleksander Jamsheer, Marek Ruchala, Katarzyna Ziemnicka
Published 2020-06-01

Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex developmentResearch in context

by Chrysanthi Kouri, Grit Sommer, Idoia Martinez de Lapiscina, Rawda Naamneh Elzenaty, Lloyd J.W. Tack, Martine Cools, S. Faisal Ahmed, Christa E. Flück, Saygin Abali, Zehra Yavas Abali, Leyla Akin, Maricruz Almaraz, Laura Audí, Murat Aydin, Antonio Balsamo, Federico Baronio, Jillian Bryce, Kanetee Busiah, Maria Caimari, Núria Camats-Tarruella, Ariadna Campos-Martorell, Luis Castaño, Anna Casteràs, Semra Çetinkaya, Yee-Ming Chan, Hedi L. Claahsen-van der Grinten, Ines Costa, Fatma Feyza Darendeliler, Justin H. Davies, Isabel Esteva, Helena Fabbri-Scallet, Courtney A. Finlayson, Emilio Garcia, Beatriz Garcia Cuartero, Alina German, Evgenia Globa, Gil Guerra-Junior, Julio Guerrero, Tulay Guran, Sabine E. Hannema, Olaf Hiort, Josephine Hirsch, Leuan Hughes, Marco Janner, Zofia Kolesinska, Katherine Lachlan, Anna Lauber-Biason, Jana Krenek Malikova, Dagmar l'Allemand, Nina Lenhnerr-Taube, Angela Lucas-Herald, Jamala Mammadova, Kenneth MсElreavey, Veronica Mericq, Isabel Mönig, Francisca Moreno, Julia Mührer, Marek Niedziela, Anna Nordenstrom, Burçe Orman, Sukran Poyrazoglu, Jose M. Rial, Meilan M. Rutter, Amaia Rodríguez, Tara Schafer-Kalkhoff, Kay-Sara Sauter, Sumudu Nimali Seneviratne, Maria Sredkova-Ruskova, Rieko Tadokoro-Cuccaro, Ajay Thankamony, Mónica Tomé, Amaia Vela, Malgorzata Wasniewska, David Zangen, Nataliya Zelinska
Published 2024-01-01