Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Aleksander Krasnow"'
Autor:
Miroslava Bosheva, Istvan Tokodi, Aleksander Krasnow, Helle Krogh Pedersen, Oksana Lukjancenko, Aron C. Eklund, Dominik Grathwohl, Norbert Sprenger, Bernard Berger, Colin I. Cercamondi, HMO Study Investigator Consortium, Viktor Bauer, Malgorzata Arciszewska, Maria Tarneva, Irina Popova, Svilen Dosev, Sirma Dimitrova, Olga Nikolova, Marzena Nowak, Magdalena Szuflinska-Sidorowicz, Bartosz Korczowski, Rositsa Karcheva-Beloeva, Stefan Banov, Boguslawa Cimoszko, Wieslaw Olechowski, Robert Simko, Zsuzsanna Tengelyi, Piotr Korbal, Marta Zolnowska, Anton Bilev, Georgios Vasilopoulos, Sylwia Korzynska, István Laki, Margarita Koleva-Syarova, Toni Grigorov, Steliyana Kraeva, Éva Kovács, Rada Markova, Grazyna Jasieniak-Pinis, Katalin Fister, Tatyana Stoeva
Publikováno v:
Frontiers in Nutrition, Vol 9 (2022)
BackgroundHuman milk oligosaccharides (HMOs) have important biological functions for a healthy development in early life.ObjectiveThis study aimed to investigate gut maturation effects of an infant formula containing five HMOs (2′-fucosyllactose, 2
Externí odkaz:
https://doaj.org/article/b764f824794a45aaa6aed13c8af2214a
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:
Urszula, Daniluk, Maciej, Kaczmarski, Jolanta, Wasilewska, Elibieta, Matuszewska, Janusz, Semeniuk, Katarzyna, Sidor, Aleksander, Krasnow
Publikováno v:
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 16(94)
The authors present the case of 4-month-old girl, who was admitted to our hospital with hypokalemia, metabolic alkalosis, hyperaldosteronism, hyperreninism with normal blood pressure and high urine concentration of PGE2. All the clinical and biochemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aea2b67b0eaedf8f93d2bd0d62aee298
https://pubmed.ncbi.nlm.nih.gov/15517937
https://pubmed.ncbi.nlm.nih.gov/15517937
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