Results 171 to 180 of about 13,290 (279)

High-Resolution MIMO Millimeter-Wave Radar Imaging Method for Non-Cooperative Targets. [PDF]

Sensors (Basel)
Guan J, An J, Liao G.
europepmc   +1 more source

Diagnostic Delay in Pediatric Nasopharyngeal Burkitt Lymphoma Presenting With Chronic Otalgia and Multiple Cranial Nerve Palsies: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Persistent unilateral otalgia, especially when refractory to treatment and associated with cranial nerve signs, should prompt early imaging and nasopharyngeal evaluation to avoid delayed diagnosis of aggressive malignancies such as Burkitt lymphoma.
Sultaneh Haddad, Abdulwahhab Al‐Shaikhli, Fehmat Hallak, Halima Hamdan, Ahmed Farag, Ranim Nakhal, Sameh Alramdani, Mohammad Obada Alsadi, Rawad Hamza, Othman Hamdan   +9 more
wiley   +1 more source

Awareness and perceptions of child eye health services among parents and community stakeholders in rural Uttar Pradesh, India. [PDF]

Indian J Ophthalmol
Sethu S, Sharma B, Sabherwal S, Shroff K, Saini S, Tyagi P, Ganesh S, Borah R.   +7 more
europepmc   +1 more source

Bardet–Biedl Syndrome Presenting With Acute Kidney Injury Revealing Previously Undiagnosed Advanced Chronic Kidney Disease in a Young Adult: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Bardet–Biedl syndrome (BBS) is an autosomal recessive disorder characterized by obesity, rod‐cone dystrophy, polydactyly, developmental delay, renal dysfunction, and genitourinary abnormalities. We report the case of a 27‐year‐old female with previously undiagnosed BBS who presented with acute kidney injury precipitated by acute ...
Aqeel Abbas, Nouman Amjad, Amna Faheem Mufti, Muhammad Waqas, Minahil Iqbal, Hamza Ali, Amir Habib, Yahya Samadi, Muhammad Usman Haider   +8 more
wiley   +1 more source

Management of a large limbal dermoid with excision and ipsilateral limbal epithelial translocation. [PDF]

Indian J Ophthalmol
Chaurasia S, Ramappa M.
europepmc   +1 more source

A Novel De Novo Heterozygous Missense Variant in CTNNB1 (c.2215A>C, p.Met739Leu) Underlying Neurodevelopmental Disorder With Spastic Diplegia and Visual Defects (NEDSDV): A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT We report a 7‐year‐old male with microcephaly, spasticity, strabismus, dysmorphism, autistic behaviors, and moderate ID due to a novel de novo likely pathogenic CTNNB1 variant (c.2215A>C, p.Met739Leu). This case underscores Whole Exome Sequencing's diagnostic utility for early detection of rare monogenic neurodevelopmental disorders.
Omar Jamal Ibrahim, Ali Rajabi, Mortaza Bonyadi, Mohammad Barzegar   +3 more
wiley   +1 more source

The inwardly pointing knee angle: A novel computed tomography‐based measurement technique and validation study

Journal of Experimental Orthopaedics, Volume 13, Issue 4, October 2026.
Abstract Purpose Inwardly pointing knee (IPK) is a clinically recognized manifestation of torsional malalignment in patients with patellofemoral pain and instability. However, current imaging protocols primarily quantify isolated components of malalignment, such as femoral anteversion or tibial torsion, without also capturing the net orientation of the
Ricardo David Manilov, Angel Sebastián Maldonado, Adrián Bórbore, Estefanía Ivana Vrancovich, Raúl Oscar Cáceres Orellano, Daniela Bravo, Felix Ferner, Matthieu Ollivier   +7 more
wiley   +1 more source

Polar questions in Dutch Sign Language (NGT): A production experiment. [PDF]

PLoS One
Oomen M, Esselink L, Roelofsen F.
europepmc   +1 more source

Using Interpretative Phenomenological Analysis to Explore the Experiences of Mothers Who Have a Child With the Rare Genetic Disorder, HNRNPU‐Related Neurodevelopmental Disorder: “Some Days, I Wear a Cape and I'm Super Mom and Some Days, I Have to Hide Under My Cape and I Can't Get Out for a Few Days”

Journal of Genetic Counseling, Volume 35, Issue 5, October 2026.
ABSTRACT HNRNPU‐related neurodevelopmental disorder is an ultra‐rare genetic condition characterised by developmental delay, intellectual disability, seizures and a range of complex health needs. Yet, little is known about how families experience and navigate life with this diagnosis.
I. Overton, F. Docherty, M. Balasubramanian   +2 more
wiley   +1 more source

Ocean of the In-Between. [PDF]

Anesthesiology
Brown NJ.
europepmc   +1 more source