Hyperthyroidism in adolescents

por Niedziela, Marek
Publicado 2021

Precise jet measurements and search for Supersymmetry particles

por Niedziela, Marek Adam
Publicado 2018

Adrenal function and MC1R gene analysis in a prepubertal girl with generalized hyperpigmentation: case report

por Rojek, Aleksandra, Niedziela, Marek
Publicado 2013

Ultrasound features of multinodular goiter in DICER1 syndrome

por Niedziela, Marek, Muchantef, Karl, Foulkes, William D.
Publicado 2022

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

por Rojek, Aleksandra, Wikiera, Beata, Noczynska, Anna, Niedziela, Marek
Publicado 2023

Amiodarone-induced thyrotoxicosis with paroxysmal supraventricular (ectopic atrial) tachycardia: case report and review of the literature

por Kolesińska, Zofia, Siuda, Katarzyna, Bobkowski, Waldemar, Niedziela, Marek
Publicado 2013

Moderate congenital adrenal hyperplasia in two girls diagnosed by newborn screening

por Banaszak-Ziemska, Magdalena, Małecka, Elżbieta, Łacna, Katarzyna, Ginalska-Malinowska, Maria, Niedziela, Marek
Publicado 2021

Uterine Development During Induced Puberty in Girls with Turner Syndrome

por Obara-Moszynska, Monika, Dzialach, Lukasz, Rabska-Pietrzak, Barbara, Niedziela, Marek, Kapczuk, Karina
Publicado 2021

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

por Pawlaczyk-Kamieńska, Tamara, Kulczyk, Tomasz, Pawlaczyk-Wróblewska, Elżbieta, Borysewicz-Lewicka, Maria, Niedziela, Marek
Publicado 2020

A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treat...

por Obara-Moszynska, Monika, Maceluch, Jaroslaw, Bobkowski, Waldemar, Baszko, Artur, Jaremba, Oskar, Krawczynski, Maciej R, Niedziela, Marek
Publicado 2013

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

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

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

por Misterska, Ewa, Kaminiarczyk-Pyzałka, Dominika, Adamczak, Karolina, Adamczyk, Katarzyna A., Niedziela, Marek, Głowacki, Maciej, Głowacki, Jakub
Publicado 2017

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

por Szczawińska-Popłonyk, Aleksandra, Popłonyk, Natalia, Niedziela, Marek, Sowińska-Seidler, Anna, Sztromwasser, Paweł, Jamsheer, Aleksander, Obara-Moszyńska, Monika
Publicado 2022

CDON gene contributes to pituitary stalk interruption syndrome associated with unilateral facial and abducens nerve palsy

por Obara-Moszyńska, Monika, Budny, Bartłomiej, Kałużna, Małgorzata, Zawadzka, Katarzyna, Jamsheer, Aleksander, Rohde, Anna, Ruchała, Marek, Ziemnicka, Katarzyna, Niedziela, Marek
Publicado 2021

NKX2-5 Variant in Two Siblings with Thyroid Hemiagenesis

por Szczepanek-Parulska, Ewelina, Budny, Bartłomiej, Borowczyk, Martyna, Zhukov, Igor, Szutkowski, Kosma, Zawadzka, Katarzyna, Tahir, Raiha, Minczykowski, Andrzej, Niedziela, Marek, Ruchała, Marek
Publicado 2022

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

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

Evidence of a significant vitamin D deficiency among 9–13-year-old Polish children: results of a multicentre study

por Chlebna-Sokół, Danuta, Konstantynowicz, Jerzy, Abramowicz, Paweł, Kulik-Rechberger, Beata, Niedziela, Marek, Obuchowicz, Anna, Ziora, Katarzyna, Karalus-Gach, Jolanta, Golec, Joanna, Michałus, Izabela, Karczmarewicz, Elżbieta, Halaba, Zenon Piotr
Publicado 2018

Mutations in proteasome-related genes are associated with thyroid hemiagenesis

por Budny, Bartlomiej, Szczepanek-Parulska, Ewelina, Zemojtel, Tomasz, Szaflarski, Witold, Rydzanicz, Malgorzata, Wesoly, Joanna, Handschuh, Luiza, Wolinski, Kosma, Piatek, Katarzyna, Niedziela, Marek, Ziemnicka, Katarzyna, Figlerowicz, Marek, Zabel, Maciej, Ruchala, Marek
Publicado 2017

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

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

Pituitary Microsomal Autoantibodies in Patients with Childhood-Onset Combined Pituitary Hormone Deficiency: an Antigen Identification Attempt

por Ziemnicka, Katarzyna, Gut, Paweł, Gołąb, Monika, Dworacki, Grzegorz, Wrotkowska, Elżbieta, Stajgis, Marek, Katulska, Katarzyna, Rabska-Pietrzak, Barbara, Obara-Moszyńska, Monika, Niedziela, Marek, Budny, Bartłomiej, Kałużna, Małgorzata, Waśko, Ryszard, Ruchała, Marek
Publicado 2016