Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mirela, Crisan"'
Autor:
Cecilia Lazea, Simona Bucerzan, Camelia Al-Khzouz, Victoria Cret, Mirela Crisan, Diana Miclea, Paula Grigorescu-Sido
Publikováno v:
Romanian Journal of Cardiology. 31:847-854
Turner syndrome is characterized by growth failure, pubertal delay and different skeletal, cardiovascular and renal malformations. In this study we investigated the prevalence of cardiac abnormalities and the correlation with the karyotype in girls w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e810093dc5f28889773552f5b45a3ef
https://doi.org/10.47803/rjc.2020.31.4.847
https://doi.org/10.47803/rjc.2020.31.4.847
Autor:
Cecilia, Lazea, Simona, Bucerzan, Mirela, Crisan, Camelia, Al-Khzouz, Diana, Miclea, Crina, Şufană, Gabriel, Cismaru, Paula, Grigorescu-Sido
Publikováno v:
Med Pharm Rep
Marfan syndrome (MFS) is an autosomal dominant inherited disease of the connective tissue with multiorgan involvement (skeleton, cardiovascular, eyes, skin, lungs). Cardiovascular involvement is variable and represents the major cause of morbidity an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2912a4e0d3ea1ccdf11260247b32c4d0
https://pubmed.ncbi.nlm.nih.gov/34527904
https://pubmed.ncbi.nlm.nih.gov/34527904
Autor:
Simona, Bucerzan, Camelia, Alkhzouz, Mirela, Crisan, Diana, Miclea, Carmen, Asavoaie, Roxana, Ilies, Paula, Grigorescu-Sido
Publikováno v:
Med Pharm Rep
INTRODUCTION: Achondroplasia is a common form of chondrodysplasia. It is transmitted by autosomal dominant trait. The disease is determined by mutations in receptor-3 gene of the fibroblast growth factor. The most frequent mutations are c.1138G>A and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::863420507f646f76f3104911776e1fa7
https://pubmed.ncbi.nlm.nih.gov/34527903
https://pubmed.ncbi.nlm.nih.gov/34527903