Czasopismo Pediatric Endocrinology Diabetes and Metabolism 2022

Editorial

100 years of therapy with insulin in Lower Silesia, Poland

Renata Wąsik, Aleksander Basiak, Ewa Barg

Pediatr Endocrinol Diabetes Metab 2022; 28 (2): 105–107

DOI: https://doi.org/10.5114/pedm.2022.117417

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Original paper

Statin therapy and lipids-lowering supplements – safe and effective treatment of lipids disturbances in children

Małgorzata Grabarczyk, Kinga Pomianowska, Tymoteusz Zaręba-Głód, Agnieszka Zachurzok, Ewa Małecka-Tendera, Paweł Matusik

Pediatr Endocrinol Diabetes Metab 2022; 28 (2): 108–113

DOI: https://doi.org/10.5114/pedm.2022.116114

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Original paper

Assessment of the function and morphology of the thyroid gland in paediatric patients treated with enzyme replacement therapy due to selected storage diseases – preliminary results of our own research and a review of the literature

Aleksandra Furtak, Anna Wędrychowicz, Dorota Roztoczyńska, Dominika Januś, Karolina Orchel-Szastak, Przemko Kwinta, Jerzy B. Starzyk

Pediatr Endocrinol Diabetes Metab 2022; 28 (2): 114–122

DOI: https://doi.org/10.5114/pedm.2022.112860

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Original paper

Prevalence of arterial hypertension among Ukrainian students: the comparison of European and American guidelines

Victoriya Furdela, Halyna Pavlyshyn, Tetiana Kovalchuk, Nataliya Haliyash, Nataliia Luchyshyn, Kateryna Kozak, Kateryna Hlushko

Pediatr Endocrinol Diabetes Metab 2022; 28 (2): 123–131

DOI: https://doi.org/10.5114/pedm.2022.112859

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Original paper

Juvenile obesity in terms of various evaluation methods

Gabriela Chabowska, Marek Czyżewski, Ewa Barg

Pediatr Endocrinol Diabetes Metab 2022; 28 (2): 132–140

DOI: https://doi.org/10.5114/pedm.2022.116111

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Original paper

The fibroblast growth factor 21 concentration in children with mitochondrial disease does not depend on the disease stage, but rather on the disease genotype

Dorota Wesół-Kucharska, Dariusz Rokicki, Milena Greczan, Magdalena Kaczor, Edyta Czekuć-Kryśkiewicz, Dorota Piekutowska-Abramczuk, Paulina Halat-Wolska, Elżbieta Ciara, Maciej Jaworski, Aleksandra Jezela-Stanek

Pediatr Endocrinol Diabetes Metab 2022; 28 (2): 141–151

DOI: https://doi.org/10.5114/pedm.2022.116116

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Review paper

Familial hypercholesterolemia – treatment update in children, systematic review

Sabina Ziółkowska, Noëlle Kijek, Iga Zendran, Ewa Szuster, Ewa Barg

Pediatr Endocrinol Diabetes Metab 2022; 28 (2): 152–161

DOI: https://doi.org/10.5114/pedm.2022.116112

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Case report

Severe malnutrition as a cause of transient carbohydrate metabolism disorders which evolved into hyperosmolar hyperglycaemic state

Magdalena Sokołowska-Gadoux, Agnieszka Pietrusik, Agata Chobot, Przemysława Jarosz-Chobot

Pediatr Endocrinol Diabetes Metab 2022; 28 (2): 162–167

DOI: https://doi.org/10.5114/pedm.2022.114668

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Case report

The efficiency of cinacalcet treatment in delaying parathyroidectomy in a case with neonatal severe hyperparathyroidism caused by homozygous mutation in the CASR gene

Fatma Özgüç Çömlek, Selma Demir, Hakan Gürkan, Mustafa İnan, Atakan Sezer, Emine Dilek, Filiz Tütüncüler Kökenli

Pediatr Endocrinol Diabetes Metab 2022; 28 (2): 168–174

DOI: https://doi.org/10.5114/pedm.2022.115070

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100 years of therapy with insulin in Lower Silesia, Poland

Statin therapy and lipids-lowering supplements – safe and effective treatment of lipids disturbances in children

Assessment of the function and morphology of the thyroid gland in paediatric patients treated with enzyme replacement therapy due to selected storage diseases – preliminary results of our own research and a review of the literature

Prevalence of arterial hypertension among Ukrainian students: the comparison of European and American guidelines

Juvenile obesity in terms of various evaluation methods

The fibroblast growth factor 21 concentration in children with mitochondrial disease does not depend on the disease stage, but rather on the disease genotype

Familial hypercholesterolemia – treatment update in children, systematic review

Severe malnutrition as a cause of transient carbohydrate metabolism disorders which evolved into hyperosmolar hyperglycaemic state

The efficiency of cinacalcet treatment in delaying parathyroidectomy in a case with neonatal severe hyperparathyroidism caused by homozygous mutation in the CASR gene

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