Results 251 to 260 of about 40,267 (360)

Mechanism of UV-C-Induced Oxygen Vacancies Altering the Colour of Dental Zirconia. [PDF]

Materials (Basel)
Xu M, Bai X, Yang S, Wen W, Cho K, Lee YH, Jin S, Tsoi JKH.   +7 more
europepmc   +1 more source

Influence of curing light irradiance and ceramic thickness on color stability and translucency of cemented ceramic laminate veneers [PDF]

Hui-Fen Qian, Yi‐Chun Chen, Xingxing Li, Jin Chen, Zhemin Li, Wanni Fu, Yunhong Lin   +6 more
openalex   +1 more source

Evolving Features of RASopathies Among Pregnancies With Abnormal Fetal Fluid Collections

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective We aimed to characterize the fetal features across gestation and describe genotype‐phenotype correlations for pregnancies with fetal RASopathies that were more severely affected as they presented with at least one abnormal fluid collection.
Natalie B. Gulrajani, John Boscardin, Billie R. Lianoglou, Katie Tick, Carmen M. A. Santoli, Kristen A. Miller, Angie C. Jelin, Lorraine Dugoff, Rose Giardine, Cori Feist, Rachel Pilliod, Stephanie Dukhovny, Kelly Gilmore, Neeta L. Vora, Aisling Murphy, Peter N. Robinson, Mary E. Norton, Teresa N. Sparks   +17 more
wiley   +1 more source

Comparative Evaluation of the Translucency of Polyetheretherketone (PEEK) Veneered With Two Different Materials: An In Vitro Study. [PDF]

Cureus
Chinmayi MP, Shetty G, Kedar SM, Kanchan LB, Kundu RS, Kumar U K, Jenifer M.   +6 more
europepmc   +1 more source

Regenerator Placement Strategies for Translucent OBS Networks

, 2011
Oscar Pedrola, Davide Careglio, Mirosław Klinkowski, Josep Solé‐Pareta   +3 more
openalex   +2 more sources

Clinical Utility of Nuchal Translucency Measurement in First‐Trimester Ultrasound Screening in a Setting With First‐Tier NIPT for Aneuploidy Screening

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To investigate the additional clinical value of nuchal translucency (NT) measurement at the first‐trimester anomaly scan (FTAS) in a setting with first‐tier non‐invasive prenatal testing (NIPT). Method This nationwide prospective cohort study, part of the IMITAS study on FTAS implementation, included all pregnancies with increased NT
Eline E. R. Lust, Kim Bronsgeest, Lidewij Henneman, Neeltje M. T. H. Crombag, Caterina M. Bilardo, Robert‐Jan H. Galjaard, Esther Sikkel, Audrey B. C. Coumans, Ayten Elvan‐Taşpınar, Sander Galjaard, Attie T. J. I. Go, Gwendolyn T. R. Manten, Eva Pajkrt, Elisabeth van Leeuwen, Monique C. Haak, Mireille N. Bekker   +15 more
wiley   +1 more source

Erosive Resistance of High-Translucency Resin Composites: New Insights for Esthetic Dentistry. [PDF]

J Clin Exp Dent
Tozo-Burgos JG, Escalante-Otárola W, Sánchez-Tito M.   +2 more
europepmc   +1 more source

A Framework for Bioinformatic Reporting in Prenatal Sequencing: Insights From a Systematic Review

Prenatal Diagnosis, EarlyView.
ABSTRACT Genomic sequencing has become a key tool in the investigation of foetal anomalies, with a growing shift from targeted panels to exome and genome sequencing. These broader approaches generate significantly more data, underscoring the need for robust bioinformatics pipelines. However, practices vary widely between laboratories.
Ashley J. Pritchard, Karen Mei Xian Lim, Graeme Smith, Elizabeth Scotchman, Alexander Gibbs, Patrick Lombard, Natalie J. Chandler   +6 more
wiley   +1 more source

Influence of Sintering Parameters on the Mechanical Behaviour of Lithium Disilicate Glass Ceramics: An In-Vitro Study. [PDF]

J Funct Biomater
Soliman M, Alotaibi R, Almutairi A, Alzahrani A, Abunyan R, Rozi A, Alamri D, Almakenzi S, Eldwakhly E, Aldegheishem A.   +9 more
europepmc   +1 more source

NONO‐Related Syndromic X‐Linked Developmental Disability 34: Further Clinical and Molecular Delineation in a Prenatal Cohort

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To characterize the prenatal sonographic features across different trimesters and genomic spectrum of NONO‐related X‐linked intellectual developmental disorder. Method We analyzed two fetuses presenting with corpus callosum agenesis and rare cardiac anomalies using genome sequencing and exome sequencing.
Yilin Zhao, Gang Zou, Mengmeng Shi, Kwok Ming Law, So Ling Lau, Meng Meng, Yuen Ha Ting, Chiu Yee Liona Poon, Zirui Dong, Matthew Hoi Kin Chau, Tak Yeung Leung, Kwong Wai Choy, Xinwen Zhang, Ye Cao   +13 more
wiley   +1 more source