Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Călin Popoiu"'
Autor:
Maria-Corina Stănciulescu, Marius-Călin Popoiu, Anca Maria Cîmpean, Vlad-Laurentiu David, Rodica Heredea, Simona Cerbu, Eugen-Sorin Boia
Publikováno v:
Journal of International Medical Research, Vol 49 (2021)
Objective Controversial, heterogeneous, and inconsistent responses to beta-blockers have been reported in some cases of infantile proliferative hemangiomas. On the basis of these clinical observations, we aimed to examine the β1 adrenergic receptor
Externí odkaz:
https://doaj.org/article/26d4fffe6746499ca65f2ae9f53a3638
Autor:
Timea E. Brandibur, Aniko Maria Manea, Abhinav Sharma, Nilima Rajpal Kundnani, Marius Călin Popoiu, Bilal Ahmad, Diala S. Dahdal, Daniela Cioboata, Nicoleta Lungu, Florina Marinela Doandes, Eugen Radu Boia, Marioara D. Boia
Publikováno v:
Medical science monitor : international medical journal of experimental and clinical research. 28
BACKGROUND Congenital gastrointestinal (GI) malformations are developmental disorders that can result in secondary intestinal failure. Nutrient intakes must be adapted according to the newborn's nutritional requirements based on frequent anthropometr
Autor:
Ada Claudia Silvana Gruescu, Calin Popoiu, Mihaela Codrina Levai, Paula Irina Barata, Caius Glad Streian
Publikováno v:
Pediatric Reports, Vol 16, Iss 3, Pp 657-668 (2024)
Pediatric seizure disorders profoundly impact family dynamics, often escalating stress and impairing coping mechanisms. This study aimed to longitudinally assess the impact of pediatric seizures on family stress and coping, evaluating the efficacy of
Externí odkaz:
https://doaj.org/article/1601667e5ba84c55bb14b1bf52fe6886
Autor:
Maria-Corina Stănciulescu, Florica Ramona Dorobantu, Eugen Sorin Boia, Marius-Călin Popoiu, Simona Cerbu, Rodica Heredea, Emil Radu Iacob, Anca Maria Cimpean, Borislav Dusan Caplar, Anca Voichita Popoiu
Publikováno v:
Children. 9:1970
A rare, uncommon disorder called PHACE(S) (P-posterior fossa anomalies, H-hemangioma, A-arterial anomalies, C-cardiac anomalies, E-eye anomalies, and S-sternal cleft) of unknown etiology was rarely reported. Children are susceptible to developing PHA
Autor:
Amăricăi, Elena, Suciu, Oana, Onofrei, Roxana, Iacob, Emil, Iacob, Daniela, Călin Popoiu, Negru, Marius, Belei, Oana, Luminița Bădițoiu, Boia, Eugen
Additional file 2. Raw data.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3318b28b45998649f4ad8476b7cc6d70
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 55(4)
Solid pseudopapillary tumor of the pancreas or Gruber-Frantz tumor is a rare pathological entity. Its incidence is even lower in children. This neoplasm has low malignant potential and with adequate surgical treatment has a very good prognosis. We pr
Autor:
Adela Chirita Emandi, Andreea Iulia Dobrescu, Gabriela Doros, Capucine Hyon, Diana Miclea, Calin Popoiu, Maria Puiu, Smaranda Arghirescu
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
3q29 deletion syndrome is a rare disorder, causing a complex phenotype. Clinical features are variable and relatively non-specific. Our report aims to present an atypical, de novo deletion in chromosome band 3q29 in a preschool boy, first child of he
Externí odkaz:
https://doaj.org/article/4f9ab447177e4dc9bf32755f87f4dc03
Publikováno v:
Procedia - Social and Behavioral Sciences. :2262-2266
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