Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Ingrith-Crenguta Miron"'
Autor:
Stefana Maria Moisa, Elena-Lia Spoiala, Laura Mihaela Trandafir, Lacramioara Ionela Butnariu, Ingrith-Crenguta Miron, Antonela Ciobanu, Adriana Mocanu, Anca Ivanov, Carmen Iulia Ciongradi, Ioan Sarbu, Anamaria Ciubara, Carmen Daniela Rusu, Alina Costina Luca, Alexandru Burlacu
Publikováno v:
Medicina, Vol 59, Iss 2, p 362 (2023)
Diamond–Blackfan anemia is a rare (6–7 million live births), inherited condition manifesting as severe anemia due to the impaired bone marrow production of red blood cells. We present the unusual case of a six month old infant with a de novo muta
Externí odkaz:
https://doaj.org/article/a46cf09496f74c4c89a4e59eab18eb32
Autor:
Stefana Maria Moisa, Ingrith Crenguta Miron, Elena Tarca, Laura Trandafir, Vasile Valeriu Lupu, Ancuta Lupu, Tania Elena Rusu
Publikováno v:
Children, Vol 9, Iss 3, p 335 (2022)
Background: Pediatricians and pediatric surgeons often face children with cardiomegaly and dilatative or hypertrophic cardiomyopathies presenting with or without symptoms. Some of these patients have already been diagnosed and received medication, an
Externí odkaz:
https://doaj.org/article/5c1e85814dc94dd98aa9acc17df28dce
Autor:
Tudor Ilie Lazaruc, Lavinia Bodescu Amancei Ionescu, Vasile Valeriu Lupu, Carmen Muntean (Duicu), Roxana Alexandra Bogos, Anca Ivanov, Georgiana Scurtu, Iuliana Magdalena Starcea, Ingrith Crenguta Miron, Maria Adriana Mocanu
Publikováno v:
Diagnostics; Volume 12; Issue 12; Pages: 2931
Venous thromboembolism (VTE) in children is a rare condition. An increased incidence has been observed in the last few years due to several factors, such as increased survival in chronic conditions, especially chronic kidney disease (CKD), use of cat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::559431e555146dcd8bf697a25a43782f
https://pubmed.ncbi.nlm.nih.gov/36552938
https://pubmed.ncbi.nlm.nih.gov/36552938
Autor:
Ancuta, Lupu, Ingrith Crenguta, Miron, Anca Lavinia, Cianga, Andrei Tudor, Cernomaz, Vasile Valeriu, Lupu, Cristina, Gavrilovici, Iuliana Magdalena, Stârcea, Elena, Tarca, Dragos Catalin, Ghica, Silvia, Fotea
Publikováno v:
Children (Basel, Switzerland). 9(10)
(1) Background: The relationship between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b11aa212d261e11296d98e7023a7085b
https://pubmed.ncbi.nlm.nih.gov/36291434
https://pubmed.ncbi.nlm.nih.gov/36291434
Autor:
Stefana Maria Moisa, Laura Mihaela Trandafir, Crischentian Brinza, Ingrith Crenguta Miron, Elena Tarca, Lacramioara Ionela Butnariu, Alexandru Burlacu
Publikováno v:
Children (Basel, Switzerland). 9(7)
(1) Background: The incidence of thromboembolic events is relatively low in the general population, but it increases in hospitalized children and those who underwent thrombogenic procedures. Although the evidence regarding direct oral anticoagulants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cce8b1a2d69af2dd71ff9b84212aafe8
https://pubmed.ncbi.nlm.nih.gov/35884077
https://pubmed.ncbi.nlm.nih.gov/35884077
Autor:
Vasile Eduard Rosu, Solange Tamara Roșu, Anca Viorica Ivanov, Iuliana Magdalena Starcea, Violeta Streanga, Ingrith Crenguta Miron, Adriana Mocanu, Ancuta Lupu, Vasile Valeriu Lupu, Cristina Gavrilovici
Publikováno v:
Children; Volume 10; Issue 6; Pages: 911
(1) Background: Immune thrombocytopenia (ITP) is an acute autoimmune blood disorder that is the main cause of thrombocytopenia in children. It is characterized by a decrease in platelets below 100 × 109/L, and limited evolution with severe complicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd95332519236ebf2673bcb25398e82a
https://doi.org/10.3390/children10060911
https://doi.org/10.3390/children10060911
Autor:
Adriana Mocanu, Roxana Alexandra Bogos, Tudor Ilie Lazaruc, Anca Lavinia Cianga, Vasile Valeriu Lupu, Ileana Ioniuc, Mirabela Alecsa, Ancuta Lupu, Anca Viorica Ivanov, Ingrith Crenguta Miron, Iuliana Magdalena Starcea
Publikováno v:
Diagnostics. 13:1228
Thrombotic microangiopathy can present itself in the form of several clinical entities, representing a real challenge for diagnosis and treatment in pediatric practice. Our article aims to explore the evolution of two rare cases of pediatric thrombot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca4780cf32fd59bf3e650c697d48c9f
https://doi.org/10.3390/diagnostics13071228
https://doi.org/10.3390/diagnostics13071228
Autor:
Iuliana Magdalena Starcea, Roxana Alexandra Bogos, Georgiana Scurtu, Mihaela Munteanu, Radu Russu, Vasile Valeriu Lupu, Ancuta Lupu, Laura Trandafir, Ingrith Crenguta Miron, Maria Adriana Mocanu
Publikováno v:
International Journal of General Medicine.
Iuliana Magdalena Starcea,1,2 Roxana Alexandra Bogos,1 Georgiana Scurtu,1 Mihaela Munteanu,2 Radu Russu,2 Vasile Valeriu Lupu,1 Ancuta Lupu,1 Laura Trandafir,1 Ingrith Crenguta Miron,1 Maria Adriana Mocanu1,2 1Pediatrics Department, âGrigore T.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bd49dde4d7ea1a185ef46058f21e9a5
https://www.dovepress.com/pathological-and-evolutive-correlations-in-steroid-resistant-nephrotic-peer-reviewed-fulltext-article-IJGM
https://www.dovepress.com/pathological-and-evolutive-correlations-in-steroid-resistant-nephrotic-peer-reviewed-fulltext-article-IJGM
Autor:
Anca Viorica Ivanov, Mirabela Smaranda Alecsa, Roxana Popescu, Magdalena Iuliana Starcea, Adriana Maria Mocanu, Cristina Rusu, Ingrith Crenguta Miron
Publikováno v:
International Journal of Molecular Sciences. 24:4661
Over the past 40 years, the 5-years-overall survival rate of pediatric cancer reached 75–80%, and for acute lymphoblastic leukemia (ALL), exceeded 90%. Leukemia continues to be a major cause of mortality and morbidity for specific patient populatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60ef6c6219399d8873b27b95fbc0953c
https://doi.org/10.3390/ijms24054661
https://doi.org/10.3390/ijms24054661
Autor:
Iuliana Magdalena Starcea, Lavinia Bodescu Amancei Ionescu, Tudor Ilie Lazaruc, Vasile Valeriu Lupu, Roxana Alexandra Bogos, Ileana Ioniuc, Felicia Dragan, Ancuta Lupu, Laura Stefana Galatanu, Ingrith Crenguta Miron, Adriana Mocanu
Publikováno v:
Genes. 14:516
Fabry disease is an X-linked lysosomal storage disease, second in prevalence after Gaucher disease. The onset of symptoms occurs in childhood or adolescence with palmo-plantar burning pains, hypo hidrosis, angiokeratomas, and corneal deposits. In the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c2c9e92f806278b73cab4dbc9376c47
https://doi.org/10.3390/genes14020516
https://doi.org/10.3390/genes14020516