Search Results - "Lazea, C"

Novel insights on acute myocarditis in pediatric patients by Popa, A, Lazea, C, Agoston-Coldea, L

“…Acute myocarditis (AM) is an inflammatory affliction of the heart muscle characterized by recent onset with a broad spectrum of clinical manifestations that…”
Get more information

Paget-Schroetter syndrome in a teenager after throwing firecrackers - A case report by Lazea, C, Asavoaie, C

“…Paget-Schroetter syndrome (PSS), or effort thrombosis, refers to axillary and/or subclavian vein thrombosis associated with repetitive effort of the superior…”
Get full text

PFAPA Syndrome: Clinical, Laboratory and Therapeutic Features in a Single-Centre Cohort by Lazea, Cecilia, Damian, Laura, Vulturar, Romana, Lazar, Calin

“…Objective: The aim of this study is to describe a group of Romanian children with periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis…”
Get full text

ROHHAD (Rapid-onset Obesity with Hypoventilation, Hypothalamic Dysfunction, Autonomic Dysregulation) Syndrome-What Every Pediatrician Should Know About the Etiopathogenesis, Diagnosis and Treatment: A Review by Lazea, Cecilia, Sur, Lucia, Florea, Mira

“…Rapid-onset obesity with hypoventilation, hypothalamic dysfunction, autonomic dysregulation (ROHHAD) syndrome is a rare disease with unknown and debated…”
Get full text

Different response to vitamin D supplementation of PVCs from RVOT and non-outflow tract RV regions by Cismaru, G, Tomoaia, R, Minciuna, I, Lazea, C, Cainap, S.S, Fringu, F, Gurzau, D, Rosu, R, Gusetu, G, Puiu, M, Caloian, B, Comsa, D.H, Pop, D, Zdrenghea, D

“…Abstract Background Recent publications have shown that premature ventricular contractions (PVCs)_ from the right ventricular outflow tract (RVOT) have a good…”
Get full text

Diagnosis and Management of Genetic Causes of Middle Aortic Syndrome in Children: A Comprehensive Literature Review by Lazea, Cecilia, Al-Khzouz, Camelia, Sufana, Crina, Miclea, Diana, Asavoaie, Carmen, Filimon, Ioana, Fufezan, Otilia

“…Middle aortic syndrome (MAS) is a rare vascular disease representing an important cause of severe hypertension in children. MAS is characterized by segmental…”
Get full text

Lights and Shadows of the Perception of the Use of Telemedicine by Romanian Family Doctors During the COVID-19 Pandemic by Florea, Mira, Lazea, Cecilia, Gaga, Remus, Sur, Genel, Lotrean, Lucia, Puia, Aida, Stanescu, Ana Maria Alexandra, Lupsor-Platon, Monica, Florea, Horatiu, Sur, Maria Lucia

“…Telemedicine has emerged as a critical technology to mitigate SARS-CoV-2 infection. We aim in this work to explore how general practitioners (GPs) perceived…”
Get full text

Rare complications of neurofibromatosis 1 diagnosed incidentally in two children by Lazea, Cecilia, Asavoaie, Carmen, Al-Khzouz, Camelia, Popa, Lenuta

“…Neurofibromatosis 1 (NF1) is an autosomal-dominant disorder with various clinical expressivity and complications. Arterial hypertension may be present in…”
Get full text

Unusual Presentation Of Kawasaki Disease With Gastrointestinal And Renal Manifestations by Lazea, Cecilia, Man, Oana, Sur, Lucia Maria, Serban, Radu, Lazar, Calin

“…Diagnosis of Kawasaki disease (KD) is based on well-established clinical criteria. In incomplete or atypical KD, the diagnosis is challenging, because of the…”
Get full text

Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study) by Bucerzan, Simona, Miclea, Diana, Popp, Radu, Alkhzouz, Camelia, Lazea, Cecilia, Pop, Ioan Victor, Grigorescu-Sido, Paula

“…Recent years have seen a shift in perspective on Turner syndrome, as it is no longer considered a significant disability due to therapeutic advances. The delay…”
Get full text

Skeletal Abnormalities and VDR1 Gene Polymorphisms in Mucopolysaccharidosis Patients by Alkhzouz, Camelia, Cabau, Georgiana, Lazea, Cecilia, Asavoaie, Carmen, Bucerzan, Simona, Mirea, Andreea Manuela, Farcas, Marius, Miclaus Jnr, Maria, Popp, Radu, Miclea, Diana

“…Articular and bone damage, which is so disabling in Mucopolysaccharidosis (MPS), requires attention as to the explanatory bias of the pathogenetic mechanisms…”
Get full text

Diagnostic Usefulness of MLPA Techniques for Recurrent Copy Number Variants Detection in Global Developmental Delay/Intellectual Disability by Miclea, Diana, Szucs, Adriana, Mirea, Andreea, Stefan, Delia-Maria, Nazarie, Florina, Bucerzan, Simona, Lazea, Cecilia, Grama, Alina, Pop, Tudor Lucian, Farcas, Marius, Zaharie, Gabriela, Matyas, Melinda, Mager, Monica, Vintan, Mihaela, Popp, Radu, Alkhzouz, Camelia

“…Genetic testing has become a standardized practice in the diagnosis of patients with global developmental delay/intellectual disability (GDD/ID). The aim of…”
Get full text

Paget-Schroetter syndrome in a teenager after throwing firecrackers - A case report by Lazea, C, Asavoaie, C

Get full text

MRI findings and genotype analysis in patients with childhood onset growth hormone deficiency--correlation with severity of hypopituitarism by Zimmermann, Anca, Schenk, Jens-Peter, Grigorescu Sido, Paula, Pfaffle, Roland, Lazea, Cecilia, Zimmermann, Tim, Heinrich, Udo, Weber, Matthias M, Bettendorf, Markus

“…To evaluate the relationship between pituitary size, PIT1 and PROP1 genotype, and the severity of childhood onset growth hormone deficiency (coGHD). Forty-four…”
Get more information