Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Elzbieta Moszczynska"'
Autor:
Elzbieta Moszczynska, Arnika Wydra, Klaudia Zasada, Marta Baszynska-wilk, Dorota Majak, Anna Sliwinska, Wieslawa Grajkowska
Publikováno v:
JCRPE, Vol 16, Iss 1, Pp 106-110 (2024)
Insulinoma is one of the pancreatic neuroendocrine tumors (PanNET) and is exceptionally rare in children. The tumor leads to severe hypoglycemia caused by excessive insulin release. We report a pediatric patient with malignant insulinoma who underwen
Externí odkaz:
https://doaj.org/article/d9172455f5724d2bba91990d5874d1c9
Autor:
Elzbieta Moszczynska, Arnika Wydra, Klaudia Zasada, Marta Bazsynka-wilk, Dorota Majak, Anna Sliwinska, Wieslawa Grajkowska
Publikováno v:
Journal of clinical research in pediatric endocrinology.
Insulinoma belongs to pancreatic neuroendocrine tumors and is immensely rare in children. The tumor leads to severe consequences of hypoglycemia caused by excessive insulin release. We report a pediatric patient with malignant insulinoma linked with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cefea02a42d3b11febf1f33c2e665793
https://pubmed.ncbi.nlm.nih.gov/36047503
https://pubmed.ncbi.nlm.nih.gov/36047503
Autor:
Monika Prokop-Piotrkowska, Kamila Marszałek-Dziuba, Elżbieta Moszczyńska, Mieczysław Szalecki, Elżbieta Jurkiewicz
Publikováno v:
JCRPE, Vol 13, Iss 3, Pp 251-262 (2021)
Bone age is one of biological indicators of maturity used in clinical practice and it is a very important parameter of a child’s assessment, especially in paediatric endocrinology. The most widely used method of bone age assessment is by performing
Externí odkaz:
https://doaj.org/article/1896c1728b7044e0881ff18a2dbd8d95
Autor:
Elżbieta Moszczyńska, Karolina Kunecka, Marta Baszyńska-Wilk, Marta Perek-Polnik, Dorota Majak, `Wiesława Grajkowska
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundPituitary stalk thickening (PST) is a rare abnormality in the pediatric population. Its etiology is heterogeneous. The aim of the study was to identify important clinical, radiological and endocrinological manifestations of patients with PS
Externí odkaz:
https://doaj.org/article/cbfb247fd0744183a369d76b3e923800
Autor:
Elzbieta Moszczyńska, Elzbieta Marczak, Mieczysław Szalecki, Krzysztof Kądziołka, Marcin Roszkowski, Patrycja Zagata-Lesnicka
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundThis study aims to analyze the diagnostic accuracy of bilateral inferior petrosal sinus sampling (BIPSS), the gold standard test for the differential diagnosis of ACTH-dependent Cushing’s syndrome (CS) in a group of pediatric patients wit
Externí odkaz:
https://doaj.org/article/ea9cb45107f34ebab9930a5fc8f4c27f
Autor:
Joanna Trubicka, Tomasz Żemojtel, Jochen Hecht, Katarzyna Falana, Dorota Piekutowska- Abramczuk, Rafał Płoski, Marta Perek-Polnik, Monika Drogosiewicz, Wiesława Grajkowska, Elżbieta Ciara, Elżbieta Moszczyńska, Bożenna Dembowska-Bagińska, Danuta Perek, Krystyna H. Chrzanowska, Małgorzata Krajewska-Walasek, Maria Łastowska
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-11 (2017)
Abstract Background The defects in DNA repair genes are potentially linked to development and response to therapy in medulloblastoma. Therefore the purpose of this study was to establish the spectrum and frequency of germline variants in selected DNA
Externí odkaz:
https://doaj.org/article/a96162f4796c4a65bf39ef853fbba71b
Autor:
Katarzyna Pasternak-Pietrzak, Elżbieta Moszczyńska, Marcin Roszkowski, Karolina Kot, Elżbieta Marczak, Wiesława Grajkowska, Maciej Pronicki, Mieczysław Szalecki
Publikováno v:
PLoS ONE, Vol 14, Iss 12, p e0226033 (2019)
INTRODUCTION:Cushing's disease (CD) is a rare cause of hypercortisolemia presenting a major diagnostic and therapeutic challenge. Data on pituitary function in long-term follow-up after CD treatment in childhood is limited. AIM:Long-term assessment o
Externí odkaz:
https://doaj.org/article/d10da6bbd2fd49dd83f0abc86613e47d
Autor:
Mieczyslaw Szalecki, Pawel Daszkiewicz, Monika Prokop-Piotrkowska, Agnieszka Bogusz-Wójcik, Marcin Roszkowski, Elzbieta Moszczynska
Publikováno v:
Publons
Background: Rathke cleft cysts (RCC) are benign, epithelium-lined intrasellar and/or suprasellar cysts believed to originate from the remnants of the Rathke pouch. The aim of this study was to analyse the symptoms and surgical outcome of patients wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4014a730eadc940ecdd0a6643b7b4a7d
https://publons.com/publon/42305356/
https://publons.com/publon/42305356/
