Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Carmen, Asavoaie"'
Autor:
Simona Bucerzan, Diana Miclea, Cecilia Lazea, Carmen Asavoaie, Andrea Kulcsar, Paula Grigorescu-Sido
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
We describe the case of a seven-year-old female patient who presented in our service with severe developmental delay, intellectual disability, facial dysmorphism, and femur fracture, observed in the context of very low bone mineral density. Array-bas
Externí odkaz:
https://doaj.org/article/dd3e9da729164cdcb9acf871cf17f677
Autor:
Daniela Pop, Radu Pop, Teodora Blaga, Liliana David, Carmen Asavoaie, Marcel Tantau, Dan Dumitrascu, Dorin Farcau
Publikováno v:
Experimental and Therapeutic Medicine. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5acff4175efe32a490659f40a61e0fb
https://doi.org/10.3892/etm.2023.11800
https://doi.org/10.3892/etm.2023.11800
Autor:
Cecilia Lazea, Camelia Al-Khzouz, Crina Sufana, Diana Miclea, Carmen Asavoaie, Ioana Filimon, Otilia Fufezan
Publikováno v:
Therapeutics and clinical risk management. 18
Middle aortic syndrome (MAS) is a rare vascular disease representing an important cause of severe hypertension in children. MAS is characterized by segmental or diffuse narrowing of the abdominal and/or distal descending aorta with involvement of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bad1ce3ddcbb5f8dd59fc53f5df09ed7
https://pubmed.ncbi.nlm.nih.gov/35330917
https://pubmed.ncbi.nlm.nih.gov/35330917
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
Autor:
Camelia Alkhzouz, Mirela Crișan, Ioana Nașcu, Victoria Creț, Ștefan Cristian Vesa, Cecilia Lazea, Carmen Asavoaie, Anca Zimmermann, Paula Grigorescu-Sido, Diana Miclea, Simona Bucerzan
Publikováno v:
Diagnostics
Diagnostics, Vol 11, Iss 989, p 989 (2021)
Volume 11
Issue 6
Diagnostics, Vol 11, Iss 989, p 989 (2021)
Volume 11
Issue 6
Gaucher disease (GD), one of the most common lysosomal disorders, is characterised by clinical heterogeneity. Cardiac involvement is rare and refers to pulmonary hypertension (PH), valvular abnormalities and myocardial infiltrative damage. The aim of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2312e96a586b621494f346c7e0958a9a
http://europepmc.org/articles/PMC8227770
http://europepmc.org/articles/PMC8227770
Autor:
Simona Bucerzan, Camelia Alkhzouz, Diana Miclea, Marius F. Farcaş, Andreea Manuela Mirea, Maria Miclaus Jnr, Georgiana Cabau, Radu A. Popp, Cecilia Lazea, Carmen Asavoaie
Publikováno v:
Pharmacogenomics and Personalized Medicine
Camelia Alkhzouz,1,2 Georgiana Cabau,2 Cecilia Lazea,2,3 Carmen Asavoaie,3 Simona Bucerzan,1,2 Andreea Manuela Mirea,2 Marius Farcas,2 Maria Miclaus Jnr,2 Radu Popp,2 Diana Miclea1,2 1Department of Medical Genetics, Clinical Emergency Hospital for Ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36db849b9ddfc827d0edb91ba022d32d
https://www.dovepress.com/skeletal-abnormalities-and-vdr1-gene-polymorphisms-in-mucopolysacchari-peer-reviewed-article-PGPM
https://www.dovepress.com/skeletal-abnormalities-and-vdr1-gene-polymorphisms-in-mucopolysacchari-peer-reviewed-article-PGPM
Autor:
Dorin Farcău, Otilia Fufezan, Oana Serban, Sorin Man, Daniela Elena Serban, Dan L. Dumitrascu, Ioana Fodor, Carmen Asavoaie
Publikováno v:
Medical ultrasonography. 23(2)
Aim: To evaluate the value of abdominal ultrasonography (US) in the follow-up of paediatric patients with ulcerative colitis (UC) compared to faecal calprotectin (FC) and colonoscopy. Material and method: In this retrospective study we enrolled 30 pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f84a565063c2d93a1c1b1f86919e5cfb
https://pubmed.ncbi.nlm.nih.gov/33626119
https://pubmed.ncbi.nlm.nih.gov/33626119
Autor:
Ionela Lungu, Carmen Asavoaie, Silaghi Cristina Alina, Camelia Alkhzouz, Georgescu Carmen Emanuela
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a92c88073a87e4a26a5022ad7f8e9a3
https://doi.org/10.1530/endoabs.70.ep549
https://doi.org/10.1530/endoabs.70.ep549
Publikováno v:
Central European Annals of Clinical Research. 2:1
Background and Aims Pituitary stalk interruption syndrome (PSIS) is characterized by the presence of a thin or absent pituitary stalk in association with a hypoplastic or aplastic anterior pituitary or an ectopic neurohypophysis [1,2]. The phenotype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44726f4b7b86c3ba2ad4531e5644a190
https://doi.org/10.35995/ceacr2010018
https://doi.org/10.35995/ceacr2010018
Publikováno v:
Therapeutics and Clinical Risk Management
Cecilia Lazea,1 Carmen Asavoaie,2 Camelia Al-Khzouz,3 Lenuta Popa1 1Department of Pediatrics I, Emergency Clinic Hospital for Children, “Iuliu Hatieganu” University of Medicine and Pharmacy, 2Department of Imaging and Radiology, Emergency Clinic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::130d50cfa34988c4c1d813c98a5a4c2b
https://pubmed.ncbi.nlm.nih.gov/30214218
https://pubmed.ncbi.nlm.nih.gov/30214218