Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alice Nicoleta Azoicai"'
Autor:
Ileana Katerina Ioniuc, Monica Mihaela Alexoae, Iuliana Magdalena Starcea, Adriana Mocanu, Elena Hanganu, Luiza Pohaci Antonesei, Catalin Pohaci, Irina Tarnita, Stefana Nangiu, Tatiana Chisnoiu, Ionela Daniela Morariu, Alice Nicoleta Azoicai
Publikováno v:
Romanian Journal of Oral Rehabilitation, Vol 15, Iss 4, Pp 266-271 (2023)
Exercise-induced bronchoconstriction (EIB) is a dysfunction of the respiratory tract consisting of transient airflow obstruction that occurs during or immediately after physical exercise, being the preferred term to define what was known for years as
Externí odkaz:
https://doaj.org/article/38e5158769704ee4bcd0b184e1cc1cc7
Autor:
Iuliana Magdalena Starcea, Ileana Katerina Ioniuc, Alice Nicoleta Azoicai, Roxana Alexandra Bogos, Tudor Ilie Lazaruc, Madalina Andreea Beldie, Ana-Maria Daniela Nistor, Diana Maria Cira, Anca Ivanov, Mirabela Alecsa, Tatiana Chisnoiu, Ionela Daniela Morariu, Adriana Mocanu
Publikováno v:
Romanian Journal of Oral Rehabilitation, Vol 15, Iss 4, Pp 372-379 (2023)
Vasculitis are disorders characterized by the presence of an inflammatory process in the blood vessel wall, resulting in damage or necroses of certain tissues or organs. Numerous clinical symptoms, ranging from acute localized hypersensitivity reacti
Externí odkaz:
https://doaj.org/article/d928e17fbe0348df8a17e386afcfaa8d
Autor:
Alice Nicoleta Azoicai, Ancuta Lupu, Laura Mihaela Trandafir, Monica Mihaela Alexoae, Mirabela Alecsa, Iuliana Magdalena Starcea, Magdalena Cuciureanu, Anton Knieling, Delia Lidia Salaru, Elena Hanganu, Adriana Mocanu, Vasile Valeriu Lupu, Ileana Ioniuc
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations of the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR). In 1949, it's been identified as a monogenic disease and was thought to primarily affect i
Externí odkaz:
https://doaj.org/article/b7f474b2c6f746eeb160816c6a0e8708
Autor:
Dana-Teodora Anton-Păduraru, Alice Nicoleta Azoicăi, Felicia Trofin, Dana Elena Mîndru, Alina Mariela Murgu, Ana Simona Bocec, Codruța Olimpiada Iliescu Halițchi, Carmen Iulia Ciongradi, Ioan Sȃrbu, Maria Liliana Iliescu
Publikováno v:
Diagnostics, Vol 14, Iss 7, p 763 (2024)
Cystic fibrosis (CF) is a chronic and potentially life-threatening condition, wherein timely diagnosis assumes paramount significance for the prompt initiation of therapeutic interventions, thereby ameliorating pulmonary function, addressing nutritio
Externí odkaz:
https://doaj.org/article/2297fe6263bf4ac3abd7ed2c91c1ddda
Autor:
Dana-Teodora Anton-Păduraru, Alice Nicoleta Azoicăi, Felicia Trofin, Alina Mariela Murgu, Dana Elena Mîndru, Ana Simona Bocec, Codruța Olimpiada Iliescu Halițchi, Gabriela Rusu Zota, Diana Păduraru, Eduard Vasile Nastase
Publikováno v:
Diagnostics, Vol 14, Iss 5, p 538 (2024)
Cystic fibrosis (CF) is a multifaceted disorder predominantly investigated for its pulmonary manifestations, yet patients with CF also exhibit a spectrum of extrapulmonary manifestations, notably those involving the hepatobiliary system. The latter c
Externí odkaz:
https://doaj.org/article/1d7a566614c64c1a9276388f4ae4fc26
Autor:
Dana-Teodora Anton-Păduraru, Alina Mariela Murgu, Laura Iulia Bozomitu, Dana Elena Mîndru, Codruța Olimpiada Iliescu Halițchi, Felicia Trofin, Carmen Iulia Ciongradi, Ioan Sârbu, Irina Mihaela Eṣanu, Alice Nicoleta Azoicăi
Publikováno v:
Diagnostics, Vol 14, Iss 2, p 228 (2024)
Cystic fibrosis (CF) is primarily known for its pulmonary consequences, which are extensively explored in the existing literature. However, it is noteworthy that individuals with CF commonly display gastrointestinal (G-I) manifestations due to the su
Externí odkaz:
https://doaj.org/article/99ab52d4b32f44d98d5e91922b9c36e8
Autor:
Dana-Teodora Anton-Păduraru, Alina Mariela Murgu, Mădălina Andreea Donos, Felicia Trofin, Alice Nicoleta Azoicăi, Paula Popovici, Aurelian Bogdan Stana, Ionela Gheorghiescu, Laura Mihaela Trandafir
Publikováno v:
Children, Vol 10, Iss 12, p 1879 (2023)
This paper delineates several aspects of cystic fibrosis-related diabetes (CFRD)—a common complication of cystic fibrosis (CF). CFRD exhibits a predilection for older individuals with CF, yet it also extends its influence on children and adolescent
Externí odkaz:
https://doaj.org/article/4fe78d7a905b4a0e935af7f1837fd5cf
Autor:
Dana Elena Mîndru, Gabriela Păduraru, Carmen Daniela Rusu, Elena Țarcă, Alice Nicoleta Azoicăi, Solange Tamara Roșu, Alexandrina-Ștefania Curpăn, Irina Mihaela Ciomaga Jitaru, Ioana Alexandra Pădureț, Alina Costina Luca
Publikováno v:
Medicina, Vol 59, Iss 6, p 1113 (2023)
Foreign body aspiration (FBA) is a frequent diagnosis in children. In the absence of other lung conditions, such as asthma or chronic pulmonary infections, this manifests as a sudden onset of cough, dyspnea, and wheezing. The differential diagnosis i
Externí odkaz:
https://doaj.org/article/73afcccb9ba9451e808679e38abf373a