Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Andrei Ioan Munteanu"'
Publikováno v:
Life, Vol 13, Iss 10, p 2039 (2023)
Celiac disease (CD) is an immune-mediated enteropathy caused by exposure to gluten and related prolamins in genetically susceptible individuals. It is a complex genetic disorder with multiple contributing genes. Linkage studies have identified severa
Externí odkaz:
https://doaj.org/article/a8bda0a5b2f34fbebdcee382a889a801
Autor:
Meda-Ada Bugi, Iulius Jugănaru, Raluca Isac, Iulia-Elena Simina, Andrei-Ioan Munteanu, Niculina Mang, Georgiana-Flavia Brad, Delia-Maria Nicoară, Daniela Cîrnatu, Otilia Mărginean
Publikováno v:
Nutrients, Vol 16, Iss 6, p 768 (2024)
Food neophobia (FN), the fear of sampling new foods, can have a significant impact on children’s eating habits. Children with phenylketonuria (PKU), a hereditary condition that inhibits the body’s capacity to metabolize phenylalanine, should take
Externí odkaz:
https://doaj.org/article/208999a907cf40a0acfbbb4bc50fe1b1
Autor:
Delia-Maria Nicoară, Andrei-Ioan Munteanu, Alexandra-Cristina Scutca, Giorgiana-Flavia Brad, Iulius Jugănaru, Meda-Ada Bugi, Raluca Asproniu, Otilia Mărginean
Publikováno v:
Cells, Vol 13, Iss 5, p 442 (2024)
Juvenile Idiopathic Arthritis (JIA), the leading childhood rheumatic condition, has a chronic course in which persistent disease activity leads to long-term consequences. In the era of biologic therapy and tailored treatment, precise disease activity
Externí odkaz:
https://doaj.org/article/146a90bfffbb4886a6b96be1c8da2d24
Autor:
Delia-Maria Nicoară, Andrei-Ioan Munteanu, Alexandra-Cristina Scutca, Giorgiana-Flavia Brad, Raluca Asproniu, Iulius Jugănaru, Otilia Mărginean
Publikováno v:
Biomedicines, Vol 12, Iss 1, p 65 (2023)
In pediatric care, the range of potential diagnoses for arthritis can be relatively extensive, primarily involving infectious and inflammatory causes and, to a lesser extent, oncological conditions. Specifically, when addressing inflammatory causes,
Externí odkaz:
https://doaj.org/article/39a9308ddd224784b6788a786c611550
Autor:
Delia-Maria Nicoară, Alexandra-Cristina Scutca, Niculina Mang, Iulius Juganaru, Andrei-Ioan Munteanu, Luiza Vitan, Otilia Mărginean
Publikováno v:
Frontiers in Endocrinology. 14
Prader-Willi syndrome (PWS, OMIM176270) is a rare genetic disorder with recognizable dysmorphic features and multisystemic consequences such as endocrine, neurocognitive and metabolic ones. Although most patients with Prader-Willi syndrome exhibit hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6a23a59f49e46a356a9fd2a6a05ce75
https://doi.org/10.3389/fendo.2023.1150323
https://doi.org/10.3389/fendo.2023.1150323
Autor:
Delia-Maria Nicoară, Andrei-Ioan Munteanu, Alexandra-Cristina Scutca, Niculina Mang, Iulius Juganaru, Giorgiana-Flavia Brad, Otilia Mărginean
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 9; Pages: 8414
Childhood obesity represents a worldwide concern as many countries have reported an increase in its incidence, with possible cardiovascular long-term implications. The mechanism that links cardiovascular disease to obesity is related to low-grade inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a7fffb613bea309d43a9424ebb952f1
Autor:
Smaranda Arghirescu, D. Savescu, Mihaela Lelik, Nicoleta Anamaria Pascalau, Margit Serban, Andreas Tiede, Cristian Jinca, Andrei Ioan Munteanu, Oana Belei, Emilia Ursu
Publikováno v:
Romanian Journal of Laboratory Medicine, Vol 29, Iss 3, Pp 287-298 (2021)
Introduction: Lupus anticoagulant (LAC) belongs to a heterogeneous group of antibodies directed against negatively charged phospholipid-binding proteins, inhibiting phospholipid-dependent reactions. We assessed the frequency, etiological background,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0d71709cc8383f1fc42402ffeae1298
https://doaj.org/article/3ab870820404476a946a902038256bbb
https://doaj.org/article/3ab870820404476a946a902038256bbb
Autor:
Victor Babes, Aniko Manea, Childcare, Romania Pharmacy Timișoara, Marioara Boia, Cristian Jinca, Andrei Ioan Munteanu
Publikováno v:
Jurnalul Pediatrului. :51-60
ntroduction: Thrombocytopenia is one of the most common haematological disorders detected in the newborn period, especially in neonates admitted to intensive care units and usually indicates an underlying pathological process. Objectives: To determin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78a3fcd3227a032996404bab5185ba5e
https://doi.org/10.37224/jp.2020.9192.09
https://doi.org/10.37224/jp.2020.9192.09
Primary autoimmune neutropenia of infancy and childhood in a cohort of patients from western Romania
Publikováno v:
Exp Ther Med
Neutropenia is commonly diagnosed in pediatric clinics. Due to the special vulnerability of neutropenic patients, the assessment of the etiopathogenic background of neutropenia is mandatory. In this retrospective cross-sectional cohort study, we aime
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc07fd05c987a60ab510a0cd7f105ec6
https://doi.org/10.3892/etm.2021.9711
https://doi.org/10.3892/etm.2021.9711
Publikováno v:
Exp Ther Med
Perinatal hypoxic-ischemic encephalopathy (HIE) represents a major cause of neonatal death or long-term disability. Inflammation plays an important role in mediating brain damage induced by neonatal hypoxic-ischemic encephalopathy. The mechanisms und
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b9aca34fde040b612978dddcd7b8ff0
https://doi.org/10.3892/etm.2021.9690
https://doi.org/10.3892/etm.2021.9690