Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Marta Sumińska"'
Publikováno v:
Pediatria Polska, Vol 98, Iss 4, Pp 307-319 (2023)
Congenital adrenal hyperplasia (CAH) is defined as a group of congenital, autosomal, and recessive disorders associated with functional limitations or deficiency of one of the key enzymes in the biosynthesis of steroid hormones leading to hypocortiso
Externí odkaz:
https://doaj.org/article/d6c90baaf40b4dc88eb107ae16f54e1d
Autor:
Klaudia Bogusz-Górna, Adriana Polańska, Aleksandra Dańczak-Pazdrowska, Ryszard Żaba, Marta Sumińska, Piotr Fichna, Andrzej Kędzia
Publikováno v:
Cardiovascular Diabetology, Vol 22, Iss 1, Pp 1-12 (2023)
Abstract Aims/Hypothesis The study aimed to assess the usefulness of capillaroscopy and photoplethysmography in the search for early vascular anomalies in children with type 1 diabetes. Methods One hundred sixty children and adolescents aged 6–18,
Externí odkaz:
https://doaj.org/article/a44734031e4e4bbb812ab69d7c8b4163
Autor:
Rafał Podgórski, Marta Sumińska, Marta Rachel, Barbara Pikuła, Piotr Fichna, Martin Bidlingmaier, Marta Fichna
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Cystic fibrosis (CF) is a life-threatening inherited disease related to a mutation in the CFTR gene, that leads to serious health complications such as chronic pulmonary infections, pancreatic insufficiency, dysfunction of the sweat glands and reprod
Externí odkaz:
https://doaj.org/article/fa408c4ad9ce4a678cd55d50efeffb40
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Cystic fibrosis (CF) is an inherited syndrome associated with a mutation in a cystic fibrosis transmembrane conductance regulator gene, composed of exocrine gland dysfunction involving multiple systems that may result in chronic respiratory infection
Externí odkaz:
https://doaj.org/article/492bf235de57485db545976fe6750be4
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Alterations in glucocorticoid metabolism may contribute to the development of obesity and insulin resistance (IR). Obesity in turn affects the androgen balance. The peripheral metabolism of steroids is equally an important determinant of their bioava
Externí odkaz:
https://doaj.org/article/403a84623dac4b3eb080f83ed38d614d
Publikováno v:
Nutrients; Volume 15; Issue 7; Pages: 1734
Obesity in childhood is associated with several steroid changes, which result from excess body mass. The aim of this study was to evaluate steroid metabolism in children with obesity compared with those with normal weight, especially in relation to s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a08243a012ddb3d49d2c7ac3dc0f9476
Autor:
Bartosz Słomiński, Marta Sumińska, Natalia Rozwadowska, Agata Czarnywojtek, Marta Fichna, Marek Ruchała, Piotr Fichna, Magdalena Żurawek, Małgorzata Myśliwiec
Publikováno v:
Endocrine
Purpose Genetically predisposed individuals may develop several autoimmune diseases—autoimmune polyendocrine syndromes (APS). APS types 2–4, are complex disorders, which combine various organ-specific autoimmune conditions. Recent reports support
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f072dd42b443409d0cac4bfb5992a566
https://pubmed.ncbi.nlm.nih.gov/33966174
https://pubmed.ncbi.nlm.nih.gov/33966174
Autor:
Marta Sumińska, Agata Dutkiewicz, Katarzyna Jowik, Marta Tyszkiewicz-Nwafor, Agata Pruciak, Monika Dmitrzak-Weglarz, Natalia Pytlińska, Agnieszka Słopień, Agata Krasińska, Bogda Skowrońska
Publikováno v:
Nutrients, Vol 13, Iss 598, p 598 (2021)
Nutrients
Volume 13
Issue 2
Nutrients
Volume 13
Issue 2
Neuropeptide Y (NPY) and peptide YY (PYY) are involved in metabolic regulation. The purpose of the study was to assess the serum levels of NPY and PYY in adolescents with anorexia nervosa (AN) or obesity (OB), as well as in a healthy control group (C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b74744ff7bf1d3238c0d0e8d01e09d6
https://www.mdpi.com/2072-6643/13/2/598
https://www.mdpi.com/2072-6643/13/2/598
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 4622, p 4622 (2020)
International Journal of Molecular Sciences, Vol 21, Iss 4622, p 4622 (2020)
Congenital adrenal hyperplasia (CAH) is the most common cause of primary adrenal insufficiency in children and adolescents. It comprises several clinical entities associated with mutations in genes, encoding enzymes involved in cortisol biosynthesis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ec022d84a74a08774a4bcd215389646
http://europepmc.org/articles/PMC7369945
http://europepmc.org/articles/PMC7369945