Výsledky vyhledávání - "Monia Milani"

Abnormalities of Gq-mediated cell signaling in Bartter and Gitelman syndromes1*1See Editorial by Warnock, p. 1197

Autor: Andrea Semplicini, Lambertus P. van den Heuvel, Lorenzo A. Calò, Elisa Pagnin, Monia Milani, Giulio Ceolotto, Paul A. Davis, Michelangelo Sartori, Rodolfo Costa

Publikováno v: Kidney International. 60(3):882-889

Abnormalities of Gq-mediated cell signaling in Bartter and Gitelman syndromes.BackgroundThe constitutive endothelial isoform of nitric oxide synthase (ecNOS) and nitric oxide (NO) production are increased in patients with Bartter syndrome (BS) and Gi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea6f886788ff5083fa36c639b3a1288a

Zobrazit plný text záznamu

Constitutive Endothelial Nitric Oxide Synthase (ecNOS) Gene Expression in Human Monocytes

Autor: A. Antonello, Umberto Fagiolo, Monia Milani, Lorenzo Calo, Paul A. Davis, Salvatore Cantaro, Angela D'Angelo

Publikováno v: Angiology. 49:419-422

This study evaluates using a polymerase chain reaction (PCR)-based molecular biological approach to study the gene expression of the constitutive endothelial isoform of nitric oxide synthase (ecNOS) in human monocytes. When PCR was carried out with s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9c4413efb6aa2c2bb8f668a4c116fc8
https://doi.org/10.1177/000331979804900601

Zobrazit plný text záznamu

Genetic testing for adult-type hypolactasia in Italian families

Autor: Francesca Belpinati, Roberta Chierici, Monia Milani, Pier Franco Pignatti, Caterina Borgna-Pignatti, Elena Petrelli, Monica Mottes, Marisa Calacoci, Daniela Saccomandi

Publikováno v: Clinical chemistry and laboratory medicine. 46(7)

Background: Adult-type hypolactasia is characterized by the inability to digest lactose during adulthood, due to lactase (LCT) deficiency. It is usually diagnosed by the measurement of breath hydrogen increase after a lactose load (breath hydrogen te

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d689f3919c2dc2ffbc76551f2b950a3
https://pubmed.ncbi.nlm.nih.gov/18605960

Zobrazit plný text záznamu

Celiac disease in children with migraine

Autor: Marisa Calacoci, Stefano Soriani, Elisa Fiumana, Caterina Borgna-Pignatti, Monia Milani

To the Editor. In an interesting article, Zelnik et al1 recently investigated the presence of neurologic disorders in patients with celiac disease (CD). They found those disorders to be more common in children with CD (51.4%) than in controls (19.9%)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6953abe4e2e078d3dd815538dcbebe6b
http://hdl.handle.net/11392/1690698

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání