Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Elzbieta, Matuszewska"'
Autor:
Beata Cudowska, Janusz Semeniuk, Elzbieta Matuszewska, Jolanta Wasilewska, Mark Klukowski, Maciej Kaczmarski
Publikováno v:
Advances in medical sciences. 58(1)
Purpose: The rate of cow’s milk allergy diminishes with age. There is not enough information concerning geographical trends in persistent cow’s milk allergy in children. The objective of the study was to evaluate the prevalence of persistent cow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::688d78397b005add1477075ad685319e
https://pubmed.ncbi.nlm.nih.gov/23612699
https://pubmed.ncbi.nlm.nih.gov/23612699
Autor:
Maria, Gołebiowska-Wawrzyniak, Katarzyna, Markiewicz, Agata, Kozar, Marta, Pojawa, Jolanta, Wacławek, Krystyna, Jastrzebska-Janas, Iwona, Czerwińska-Kartowicz, Krzysztof, Rytwiński, Piotr, Derentowicz, Elzbieta, Matuszewska, Anna, Stasiak-Barmuta, Jolanta, Wasilewska, Urszula, Daniluk, Zbigniew M, Wawrzyniak
Publikováno v:
Medycyna wieku rozwojowego. 11(1)
Food allergy is an abnormal response of the immunological system, especially of mucosal immunological system on antigens supplied per os. There are very complicated and still unexplained immunological mechanisms, which lead to hypersensitivity reacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f9927f5e79da4b956aa3f6c0ac4f485c
https://pubmed.ncbi.nlm.nih.gov/17965461
https://pubmed.ncbi.nlm.nih.gov/17965461
Autor:
Elzbieta, Matuszewska, Barbara, Miks, Jacek, Grygalewicz, Joanna, Załtska-Ponganis, Maria, Mordasewicz-Goliszewska, Bozenna, Bełzecka
Publikováno v:
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 19(110)
The aim of this preliminary study was (1) to evaluate the usefulness of the Limulus amebocyte lysate (LAL) test as a diagnostic tool in pediatric clinic, and (2) to examine the serum ET levels in hospitalized patients.Bacterial blood endotoxin (ET) w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2de45ea67dd76fd3d18984a4b08ada14
https://pubmed.ncbi.nlm.nih.gov/16245427
https://pubmed.ncbi.nlm.nih.gov/16245427
Autor:
Janusz, Semeniuk, Maciej, Kaczmarski, Katarzyna, Sidor, Aleksander, Krasnow, Urszula, Daniluk, Elzbieta, Matuszewska
Publikováno v:
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 16(95)
Gastroesophageal reflux (GER) plays an important role in pathogenesis of recurrent/chronic disorders of the respiratory tract. Atypical symptoms of GER can be suggested to be cause of the otorhinolaryngological problems. For these last manifestations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8595b36208471541ff5d9356adf6d929
https://pubmed.ncbi.nlm.nih.gov/15518427
https://pubmed.ncbi.nlm.nih.gov/15518427
Autor:
Urszula, Daniluk, Maciej, Kaczmarski, Jolanta, Wasilewska, Elzbieta, Matuszewska, Janusz, Semeniuk, Katarzyna, Sidor, Aleksander, Krasnow
Publikováno v:
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 16(95)
Bartter syndrome is an uncommon tubular disorder inherited as an autosomal recessive entity. It is associated with hypokalemic metabolic alkalosis with high renin and aldosterone plasma concentration with low or normal blood pressure. Recent studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1ed4b42036e77b13cc4bdce17cc12179
https://pubmed.ncbi.nlm.nih.gov/15518434
https://pubmed.ncbi.nlm.nih.gov/15518434
Autor:
Janusz, Semeniuk, Maciej, Kaczmarski, Aleksander, Krasnow, Katarzyna, Sidor, Elzbieta, Matuszewska, Urszula, Daniluk
Publikováno v:
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 14(83)
The aim of the current study was to analyse selected parameters of pH monitoring in the proximal and distal parts of esophagus. One hundred and twelve infants aged 1.25 to 18 months (mean = 5.6) with symptoms and signs suggesting gastroesophageal ref
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0298d667441bbf49d7d1ad7bb839c1d3
https://pubmed.ncbi.nlm.nih.gov/12939813
https://pubmed.ncbi.nlm.nih.gov/12939813
Autor:
Elzbieta, Matuszewska, Maciej, Kaczmarski, Jolanta, Wasilewska, Urszula, Daniluk, Aleksander, Krasnow, Bozena, Mikołuć
Publikováno v:
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 14(83)
Alkaptonuria is a rare metabolic condition caused by congenital homogentisate oxidase deficiency of recessive inheritance. Homogentisate polymers are accumulated and cause urine darkening, brown pigmentation of connective tissue, articular cartilage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6ebb0f047399f71ef865df5205a41bbe
https://pubmed.ncbi.nlm.nih.gov/12939823
https://pubmed.ncbi.nlm.nih.gov/12939823