Results 281 to 290 of about 1,223,402 (387)

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

Applied 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, Andrew Katumba, Joyce Nakatumba‐Nabende, Sudi Murindanyi, Jonathan Serugunda, Cosmas Mwikirize, Samuel Bugeza, Anthony Oriekot, Juliet Bosa, Eva Nabawanuka   +9 more
wiley   +1 more source

Multidisciplinary Management of a Permanent Central Incisor Fused with a Supernumerary Tooth: A Case Report. [PDF]

Front Dent
Isaabadi M, Yaghobee S, Bolhari B, Malekpour F.   +3 more
europepmc   +1 more source

TBX3‐ Related Disorder

American 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

Bilateral Symmetrical Fusion of Permanent Mandibular Lateral Incisors and Canines: A Rare Clinical Case. [PDF]

Clin Case Rep
Veerabhadrappa SK, Vadivel JK, Huqh MZU, Selvaraj S, Marya A, Yadav S.   +5 more
europepmc   +1 more source

Prevalence and distribution of dental anomalies in Hail Province of Saudi Arabia

Abdulrahman K. Alshammari, Muteb Algharbi, Freah Alshammary, Nabeel Almotairy, Hatem Alshammari, Maha M. Rashdi, Sukinah H. Alrahin, Fatimah H. Alsalem, Ahmed A. Madfa   +8 more
openalex   +1 more source

The HRAS Variant c.175G>A (p.Ala59Thr) Causes a Predominantly Ectodermal Phenotype Lacking Classic Costello Syndrome Features

American Journal of Medical Genetics Part A, Volume 200, Issue 2, Page 407-418, February 2026.
ABSTRACT Costello syndrome (CS) is a rare dominant HRAS RASopathy characterized by curly hair, cardiac abnormalities, craniofacial anomalies, and developmental delay. HRAS codon 58, 59, and 60 variants are associated with milder phenotypes. We describe a three‐generation family with a previously unreported heterozygous HRAS variant c.175G>A (p.Ala59Thr)
Nikole Rautiainen, Eveliina Brandt, Kaisa Kettunen, Outi Elomaa, Sirpa Kivirikko, Leila Jeskanen, Katriina Lappalainen, Nelli Sjöblom, Juha Kere, Katariina Hannula‐Jouppi, Liisa Harjama   +10 more
wiley   +1 more source

Clinical and Radiographic Evaluation of Molar Root-Incisor Malformation (MRIM): A Case Series. [PDF]

Case Rep Dent
Karahan A, Mısır M, Koruyucu M.
europepmc   +1 more source

Identification and characterization of predisposing genetic factors in patients with oral cleft and/or dental anomalies

, 2013
Mickaël Quentric
openalex   +1 more source

De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder

American Journal of Medical Genetics Part A, Volume 200, Issue 2, Page 521-530, February 2026.
ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil, Allison Daley, Emily R. Sites, Shayne M. Plourde, Jesse M. Hunter, Dennis W. Bartholomew, April N. Lehman, Daniel C. Koboldt, Rolf W. Stottmann   +8 more
wiley   +1 more source

Incidental Detection of Unilateral Mandibular Bone Thinning Without Clinical Asymmetry in an Adult Female: A Rare Radiographic Finding. [PDF]

Cureus
Srivastava SK, Sikdar C, Rana A, Srivastava S, Choudhury SA.   +4 more
europepmc   +1 more source