Results 211 to 220 of about 3,539,647 (271)

Engineering Human 3D Cardiac Tissues for Predictive Functional Drug Screening. [PDF]

Pharmaceutics
Baruch ES, Rosner D, Riska E, Yadid M, Shapira A, Dvir T.   +5 more
europepmc   +1 more source

Diagnostic Value of Exome Sequencing in Isolated Polyhydramnios

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To evaluate the diagnostic yield of exome sequencing (ES) in isolated polyhydramnios. Methods This retrospective study included 40 cases of isolated polyhydramnios. All patients underwent screening for gestational diabetes mellitus (GDM) and chromosomal microarray analysis (CMA).
Vered Offen Glassner, Adi Botvinik, Adi Mory, Adi Reches, Karina Krajden Haratz, Britannia Morgan Fleming, Hagit Baris Feldman, Lena Sagi‐Dain, Mordechai Shohat, Rayna Joy Goldstein, Yuval Yaron, Michal Levy   +11 more
wiley   +1 more source

Clinical Parameters Associated with Achieving Negative Fluid Balance in Critically Ill Patients: A Retrospective Cohort Study. [PDF]

J Clin Med
Stavi D, Gal Oz A, Adi N, Dayan RR, Angel Y, Nevo A, Khoury N, Moshkovits I, Lichter Y, Wald R, Goder N.   +10 more
europepmc   +1 more source

The “Dynamic Tongue Contraction Technique” for Diagnosis of Soft Palate Cleft in Cases of Cleft Lip and Palate Sequence

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To present and evaluate the dynamic tongue contraction technique as a novel prenatal sonographic method for detecting soft palate clefts in fetuses with a cleft lip and palate (CLP) sequence. Methods This prospective cross‐sectional study was conducted at a tertiary care center between September 2023 and September 2024. Seven fetuses
Ettie Piura, Yoav Alpert, Or Touval, Offra Engel, Biader Samih Bilal, Yaniv Ebner, Ofer Markovitch   +6 more
wiley   +1 more source

Developments in TEL: Pushing the Boundaries of Open Education

Journal of Learning for Development
Santosh Panda
doaj   +1 more source

Monogenic and syndromic obesity in children: Clinical recognition, genetics, and precision management

Pediatric Investigation, EarlyView.
Monogenic and syndromic obesity in children often arises from defects in the leptin–melanocortin pathway. Understanding these rare genetic causes not only clarifies mechanisms of appetite regulation but also enables precision therapies, offering hope beyond lifestyle interventions.
Hadel Khalil, Eugene Feigin, Hussein Zaitoon   +2 more
wiley   +1 more source

Thyroid-stimulating immunoglobulins as a reliable predictive blood test for thyroid eye disease. [PDF]

Indian J Ophthalmol
Madgar S, Simon GB, Priel A, Sagiv O, Landau-Prat D, Cukierman-Yaffe T, Agmon-Levin N, Shavit R, Smadar L, Zloto O.   +9 more
europepmc   +1 more source