Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ewa Maria Małunowicz"'
Autor:
Urszula Ambroziak, Alina Kurylowicz, Emilia Pawłowska, Agnieszka Kondracka, Anna Kępczyńska-Nyk, Michal Dadlez, Tomasz Bednarczuk, Aleksandra Wysłouch-Cieszyńska, Ewa Maria Małunowicz, Magdalena Szcześniak, Zbigniew Bartoszewicz, Radosław Jaźwiec
Publikováno v:
Gynecological Endocrinology. 31:296-300
Basal serum 17OHP measurement remains the first screening step for nonclassic congenital adrenal hyperplasia (NCCAH) and the accuracy of the test is of high value. The aim of this study was to compare the accuracy of immunoassays to LC-MS/MS in the a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ca9c7c0a97072f151568cc93247f1ce
https://doi.org/10.3109/09513590.2014.994599
https://doi.org/10.3109/09513590.2014.994599
Autor:
Tomasz Bednarczuk, Ewa Maria Małunowicz, Urszula Ambroziak, Anna Kępczyńska-Nyk, Krystian Jazdzewski, Maja Lenkiewicz-Sidor
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc9f4c2fb0a246664609e353692a599a
https://doi.org/10.1530/endoabs.41.ep20
https://doi.org/10.1530/endoabs.41.ep20
Autor:
Piotr Miśkiewicz, Ewa Maria Małunowicz, Alina Kurylowicz, Urszula Ambroziak, Anna Kępczyńska-Nyk, Anna Wojcicka, Magdalena Macech
Publikováno v:
Clinical endocrinology. 84(1)
OBJECTIVE As nonclassic congenital adrenal hyperplasia (NCCAH) needs to be taken into account in women with hyperandrogenism, we aimed to assess whether the recommended level of poststimulated 17OHP ≥30 nmol/l confirms NCCAH. PATIENTS AND METHODS F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fa5f08a1e7a9b3bc35dc546cee53c87
https://pubmed.ncbi.nlm.nih.gov/26331608
https://pubmed.ncbi.nlm.nih.gov/26331608
Autor:
Michal Kunicki, Anna Kępczyńska-Nyk, Urszula Ambroziak, Tomasz Bednarczuk, Karolina M. Nowak, Emilia Morawska, Ewa Maria Małunowicz
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c3bccd1d07fcc70e432140345763227
https://doi.org/10.1530/endoabs.32.p18
https://doi.org/10.1530/endoabs.32.p18
Autor:
Urszula, Ambroziak, Tomasz, Bednarczuk, Maria, Ginalska-Malinowska, Ewa Maria, Małunowicz, Barbara, Grzechocińska, Paweł, Kamiński, Leszek, Bablok, Jerzy, Przedlacki, Ewa, Bar-Andziak
Publikováno v:
Endokrynologia Polska. 61
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is one of the most common autosomal recessive hereditary diseases. The impairment of cortisol synthesis leads to excessive stimulation of the adrenal glands by adrenocorticotropic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::05b5a147e6f6d8328d290542adf9066b
https://pubmed.ncbi.nlm.nih.gov/22127631
https://pubmed.ncbi.nlm.nih.gov/22127631
Autor:
Urszula, Ambroziak, Tomasz, Bednarczuk, Maria, Ginalska-Malinowska, Ewa Maria, Małunowicz, Barbara, Grzechocińska, Paweł, Kamiński, Leszek, Bablok, Jerzy, Przedlacki, Ewa, Bar-Andziak
Publikováno v:
Endokrynologia Polska. 61(1)
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is one of the most common autosomal recessive hereditary diseases. The impairment of cortisol synthesis leads to excessive stimulation of the adrenal glands by adrenocorticotropic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b38ba0c11c4fda7a413ea481a711f55c
https://pubmed.ncbi.nlm.nih.gov/20205117
https://pubmed.ncbi.nlm.nih.gov/20205117