Silver-Russell syndrome and Turner syndrome in a girl with short stature treated with growth hormone – case report

por Wikiera, Beata, Nocoń-Bohusz, Julita, Noczyńska, Anna
Publicado 2022

Soluble Klotho Is Decreased in Children With Type 1 Diabetes and Correlated With Metabolic Control

por Zubkiewicz-Kucharska, Agnieszka, Wikiera, Beata, Noczyńska, Anna
Publicado 2021

Weight gain in type 1 diabetes during the SARS-CoV-2 pandemic. Does lockdown affect the metabolic control of pediatric patients?

por Zubkiewicz-Kucharska, Agnieszka, Wikiera, Beata, Noczyńska, Anna
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

To increase body height and muscle strength – one medicine for two diseases? Case report of a boy with Silver-Russell syndrome and Duchenne muscular dystrophy

por Chrzanowska, Joanna A., Bubula, Lidia, Noczyńska, Anna, Zubkiewicz-Kucharska, Agnieszka
Publicado 2021

Complex glycerol kinase deficiency – long-term follow-up of two patients

por Wikiera, Beata, Jakubiak, Aleksandra, Łaczmanska, Izabela, Noczyńska, Anna, Śmigiel, Robert
Publicado 2021

Clinical evaluation of 31 children with pituitary insufficiency in the course of the pituitary stalk interruption syndrome. The unexpected growth without growth hormone in 2 childr...

por Chrzanowska, Joanna A., Zubkiewicz-Kucharska, Agnieszka, Seifert, Monika, Całkosiński, Aleksander, Noczyńska, Anna
Publicado 2021

Itch in Children with Type 1 Diabetes: A Cross-Sectional Study

por Stefaniak, Aleksandra A., Zubkiewicz-Kucharska, Agnieszka, Matusiak, Łukasz, Noczyńska, Anna, Szepietowski, Jacek C.
Publicado 2020

Prevalence of haplotype DQ2/DQ8 and celiac disease in children with type 1 diabetes

por Zubkiewicz-Kucharska, Agnieszka, Jamer, Tatiana, Chrzanowska, Joanna, Akutko, Katarzyna, Pytrus, Tomasz, Stawarski, Andrzej, Noczyńska, Anna
Publicado 2022

Polymorphism of the FTO Gene Influences Body Weight in Children with Type 1 Diabetes without Severe Obesity

por Łuczyński, Włodzimierz, Fendler, Wojciech, Ramatowska, Anna, Szypowska, Agnieszka, Szadkowska, Agnieszka, Młynarski, Wojciech, Chumiecki, Miron, Jarosz-Chobot, Przemysława, Chrzanowska, Joanna, Noczyńska, Anna, Brandt, Agnieszka, Myśliwiec, Małgorzata, Głowińska-Olszewska, Barbara, Bernatowicz, Paweł, Kowalczuk, Oksana, Bossowski, Artur
Publicado 2014

Correlation of Genotype and Perinatal Period, Time of Diagnosis and Anthropometric Data before Commencement of Recombinant Human Growth Hormone Treatment in Polish Patients with Pr...

por Lecka-Ambroziak, Agnieszka, Wysocka-Mincewicz, Marta, Doleżal-Ołtarzewska, Katarzyna, Zygmunt-Górska, Agata, Żak, Teresa, Noczyńska, Anna, Birkholz-Walerzak, Dorota, Stawerska, Renata, Hilczer, Maciej, Obara-Moszyńska, Monika, Rabska-Pietrzak, Barbara, Gołębiowska, Elżbieta, Dudek, Adam, Petriczko, Elżbieta, Szalecki, Mieczysław
Publicado 2021

Effects of Recombinant Human Growth Hormone Treatment, Depending on the Therapy Start in Different Nutritional Phases in Paediatric Patients with Prader–Willi Syndrome: A Polish Mu...

por Lecka-Ambroziak, Agnieszka, Wysocka-Mincewicz, Marta, Doleżal-Ołtarzewska, Katarzyna, Zygmunt-Górska, Agata, Wędrychowicz, Anna, Żak, Teresa, Noczyńska, Anna, Birkholz-Walerzak, Dorota, Stawerska, Renata, Hilczer, Maciej, Obara-Moszyńska, Monika, Rabska-Pietrzak, Barbara, Gołębiowska, Elżbieta, Dudek, Adam, Petriczko, Elżbieta, Szalecki, Mieczysław
Publicado 2021

The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency: a case series

por Sun, Min, Mueller, Jonathan W, Gilligan, Lorna C, Taylor, Angela E, Shaheen, Fozia, Noczyńska, Anna, T’Sjoen, Guy, Denvir, Louise, Shenoy, Savitha, Fulton, Piers, Cheetham, Timothy D, Gleeson, Helena, Rahman, Mushtaqur, Krone, Nils P, Taylor, Norman F, Shackleton, Cedric H L, Arlt, Wiebke, Idkowiak, Jan
Publicado 2021