[HTML][HTML] International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people

…, J Oh, RD Perrone, MD Sinha, A Titieni… - Nature Reviews …, 2019 - nature.com
These recommendations were systematically developed on behalf of the Network for Early
Onset Cystic Kidney Disease (NEOCYST) by an international group of experts in autosomal …

European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia

…, D Snijders, T Tonia, A Titieni… - European …, 2017 - Eur Respiratory Soc
The diagnosis of primary ciliary dyskinesia is often confirmed with standard, albeit complex
and expensive, tests. In many cases, however, the diagnosis remains difficult despite the …

Phenotypic spectrum of children with nephronophthisis and related ciliopathies

…, S König, KP Schlingmann, A Titieni… - Clinical Journal of the …, 2017 - journals.lww.com
Results In total, 51% of the children presented with isolated nephronophthisis, whereas the
other 49% exhibited related ciliopathies. Monogenetic defects were identified in 97 of 152 …

Imaging of kidney cysts and cystic kidney diseases in children: an international working group consensus statement

…, MC Liebau, D Mekahli, ACM Ong, L Pape, A Titieni… - Radiology, 2019 - pubs.rsna.org
Kidney cysts can manifest as focal disease (simple and complex kidney cysts), affect a whole
kidney (eg, multicystic dysplastic kidney or cystic dysplasia), or manifest as bilateral cystic …

Risk factors for early dialysis dependency in autosomal recessive polycystic kidney disease

…, S Schmidt, C Huppertz-Kessler, B Kranz, A Titieni… - The Journal of …, 2018 - Elsevier
Objective To identify prenatal, perinatal, and postnatal risk factors for dialysis within the first
year of life in children with autosomal recessive polycystic kidney disease (ARPKD) as a …

Perinatal diagnosis, management, and follow-up of cystic renal diseases: a clinical practice recommendation with systematic literature reviews

…, MC Liebau, L Pape, G Rellensmann, A Titieni… - JAMA …, 2018 - jamanetwork.com
Importance Prenatal and neonatal cystic kidney diseases are a group of rare disorders
manifesting as single, multiple unilateral, or bilateral cysts or with increased echogenicity of the …

[HTML][HTML] Network for early Onset cystic Kidney Diseases—A comprehensive Multidisciplinary Approach to Hereditary cystic Kidney Diseases in childhood

JC König, A Titieni, M Konrad… - Frontiers in …, 2018 - frontiersin.org
Hereditary cystic kidney diseases comprise a complex group of genetic disorders representing
one of the most common causes of end-stage renal failure in childhood. The main …

Systematic evaluation of olfaction in patients with hereditary cystic kidney diseases/renal ciliopathies

…, S Kollmann, C Schleithoff, A Titieni… - Journal of Medical …, 2021 - jmg.bmj.com
Background Hereditary cystic kidney diseases such as nephronophthisis, polycystic kidney
disease and Bardet-Biedl syndrome (BBS) are caused by a dysfunction of primary cilia. Cilia …

Use Of Virtual Reality For Artistic Education

A Nanu, A Titieni, M Nedelcu, F Nedelcu… - ICERI2013 …, 2013 - library.iated.org
The aims: The mission of teachers in today’s classroom is to create the proper conditions to
determine the shift from the static transmission of knowledge to the student-centered learning…

The Romanian Folk Costume as a Component of the Country Brand. Use of Modern Methods of Education Based on Virtual Reality

A Nanu, A Titieni, M Nedelcu, F Nedelcu… - EDULEARN14 …, 2014 - library.iated.org
The cultural globalization led to a uniform human image: everywhere, at work we wear classic
suit or costume, leisure time jeans and jacket. A natural question arises: we are citizens of …