Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Mihaela, Zăvăleanu"'
Autor:
Alina Chiracu, Germina-Alina Cosma, Amalia Raluca Stepan, Marian Alexandru Cosma, Ionuț Corlaci, Eleonora Daniela Ciupeanu Călugăru, Florin Voinea, Mihaela Zăvăleanu, Horia Alin Burileanu, Taina Avramescu
Publikováno v:
Frontiers in Psychology, Vol 14 (2023)
IntroductionCaused by an error in cell division that produces an additional chromosome 21, Down syndrome (DS) is one of the most common developmental disorders in the world. This study aims to analyze the relationship between psychological capital, q
Externí odkaz:
https://doaj.org/article/bc34145d977a4850bc3ab1dd5bb62e32
Autor:
Germina, Cosma1, Mihaela, Zăvăleanu1, Alin, Burileanu1, Costin, Nanu Marian1, Alexandru, Cosma1
Publikováno v:
International Multidisciplinary Scientific Conference on Social Sciences & Arts SGEM. 2019, Vol. 6, p561-567. 7p.
Autor:
Ilona, Ilinca1, Mihaela, Zăvăleanu1, Eugenia, Roşulescu1, Mircea, Dănoiu1, Ștefan, Zăvăleanu2
Publikováno v:
International Multidisciplinary Scientific Conference on Social Sciences & Arts SGEM. 2016, p1111-1117. 7p.
Autor:
Mihaela, Zăvăleanu1, Eugenia, Roşulescu1, Mircea, Dănoiu1, Ilona, Ilinca1, Ștefan, Zăvăleanu2
Publikováno v:
International Multidisciplinary Scientific Conference on Social Sciences & Arts SGEM. 2015, p431-438. 8p.
Autor:
MIHAELA, ZĂVĂLEANU, ALINA, COSMA GERMINA, LUMINIŢA, BRĂBIESCU-CĂLINESCU, ALEXANDRU, COSMA, ELIANA, LICĂ
Publikováno v:
Ovidius University Annals, Series Physical Education & Sport/Science, Movement & Health; 2018 Supplement, Vol. 18, p442-446, 5p
Autor:
Eugenia, Roşulescu, Cosmina, Stănoiu, Elena, Buteică, B, Stănoiu, F, Burada, Mihaela, Zăvăleanu
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 50(2)
Hereditary spastic paraplegia (HSP) or Strümpell-Lorrain syndrome is a heterogeneous group of inherited disorders, with prevalence ranged from 4.3 to 9.6 cases per 100,000 population. A common feature of these disorders is the slowly progressive and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::44777bbcbbc279ee8f7e5a2dd65a60b4
https://pubmed.ncbi.nlm.nih.gov/19434327
https://pubmed.ncbi.nlm.nih.gov/19434327
Publikováno v:
Citius Altius Fortius, Vol 22, Iss 1 (2009)
Objective: To evaluate the growth, physical development and nutrition status for a sample of cerebral palsied children with spastic, dyskinetic and ataxic type.Material and methods: A total of 81 children with CP, who were rehabilitated in the pediat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::4672395d05d0b62fb06cf301a791b1ea
http://efsupit.ro/images/stories/imgs/JPES/2009/9_Rosculescu.pdf
http://efsupit.ro/images/stories/imgs/JPES/2009/9_Rosculescu.pdf
Publikováno v:
Citius Altius Fortius, Vol 22, Iss 1 (2009)
Aim – this study consists in the constructing of a tridimensional musculoskeletal model for the attack hit and the quantification of mechanical stress, in order to prevent traumatism in the knee joint.Goal: Minimizing the risk of patellar tendoniti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::37732b016d379ec650ab939727d84566
http://efsupit.ro/images/stories/imgs/JPES/2009/8_ilona.pdf
http://efsupit.ro/images/stories/imgs/JPES/2009/8_ilona.pdf
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 49(2)
Merosin-deficient congenital muscular dystrophy type 1A (MDC1A) is the most common form of congenital muscular dystrophy. MDC1A is caused by mutation of the laminin alpha-2 gene (LAMA2), localized to chromosome 6q22-23. The diagnosis of merosin-defic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::36f3f0e31140537ed3b71a6caf247b12
https://pubmed.ncbi.nlm.nih.gov/18516331
https://pubmed.ncbi.nlm.nih.gov/18516331
Publikováno v:
Sports Medicine Journal / Medicina Sportiva; 2014, Vol. 10 Issue 1, p2292-2298, 7p