Results 281 to 290 of about 1,253,731 (353)

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 661-672, March 2026.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim   +9 more
wiley   +1 more source

DREAMER: Rapid and Simultaneous Multiple Contrast Magnetic Resonance Imaging of Solid and Soft Tissue

open access: yesMagnetic Resonance in Medicine, Volume 95, Issue 3, Page 1513-1527, March 2026.
ABSTRACT Purpose Pediatric craniofacial imaging may involve examination of both the skull and brain tissues via CT and MRI, respectively. DREAMER (Dual Repetition and Echo Acquisition with Multi‐contrast Encoding and Reconstruction) simultaneously acquires solid‐ and soft‐tissue images, potentially providing a rapid, high‐resolution, and radiation‐free
Brian‐Tinh Duc Vu   +8 more
wiley   +1 more source

Determination of Dental Lesions in Dairy Cattle and Immunochemical Detection of the Biomarker Decorin in Gingival Crevicular Fluid of Dairy Cattle

open access: yesVeterinary Medicine and Science, Volume 12, Issue 2, March 2026.
This study identified dental and gingival lesions in dairy cattle, revealing the significance of routine periodontal assessment for animal welfare. Decorin levels in GCF samples were compared between healthy and diseased cattle, indicating its potential as a non‐invasive biomarker for dental inflammation.
Nihan AVCI
wiley   +1 more source

Risks in Dental Anomalies

open access: yesActa Scientific Dental Scienecs
Luis Frómeta Díaz   +4 more
openaire   +1 more source

Gastroenterological disorders and hepatic disease in adults with cerebral palsy: A systematic review

open access: yesDevelopmental Medicine &Child Neurology, Volume 68, Issue 3, Page 313-331, March 2026.
Abstract Aim To describe the incidence, prevalence, and prognostic factors for gastroenterological disorders and hepatic disease in adults with cerebral palsy (CP), and to examine the effectiveness of any screening or interventions. Method Six databases were searched for articles published in any language since 1990 meeting eligibility criteria ...
Christina M. Marciniak   +18 more
wiley   +1 more source

A Closed‐Loop‐Capable Neural Interface Platform for Deep Brain Modulation via Integrated Non‐Viral Gene Delivery, NIR Optogenetics, and Electrophysiological Recording

open access: yesAdvanced Science, Volume 13, Issue 7, 3 February 2026.
A multifunctional, 3D porous neural interface combines non‐viral gene delivery and NIR optogenetics to enable minimally invasive, closed‐loop modulation of deep‐brain circuits. Abstract Closed‐loop neuromodulation requires precise, stable, and cell‐specific control of neural circuits with minimal invasiveness.
Chao‐Yi Chu   +14 more
wiley   +1 more source

CBCT Imaging Modality Used to Diagnose Dental Anomalies: Case Reports

open access: diamond, 2012
Akhil Rajput   +3 more
openalex   +1 more source

Automated AI‐Based Lung Disease Classification Using Point‐of‐Care Ultrasound

open access: yesApplied AI Letters, Volume 7, Issue 1, February 2026.
Automated, AI‐based Lung Disease Classification using Point‐of‐Care Ultrasound. ABSTRACT Timely and accurate diagnosis of lung diseases is critical for reducing related morbidity and mortality. Lung ultrasound (LUS) has emerged as a useful point‐of‐care tool for evaluating various lung conditions.
Nixson Okila   +9 more
wiley   +1 more source

TBX3‐ Related Disorder

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 2, Page 291-299, February 2026.
ABSTRACT Heterozygous pathogenic variants in TBX3 cause Ulnar‐Mammary syndrome (UMS). The phenotype is classically characterized by upper limb defects, apocrine/mammary gland hypoplasia, hypogonadism, and various midline defects. However, the clinical spectrum is highly variable, and some individuals may present with a mild or atypical presentation ...
Ziv Halperin, Karin Weiss
wiley   +1 more source

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