Results 181 to 190 of about 105,746 (338)

Clinical Presentation of the Longest Reported Living Individual With Bent Bone Dysplasia—FGFR2‐Related

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 728-732, March 2026.
ABSTRACT The FGFR2 gene, encoding the FGFR2 protein, plays a crucial role in embryonic cell development, particularly in bone tissue. Bent Bone Dysplasia (BBD), FGFR2‐related (MIM# 614592), is a rare severe skeletal dysplasia characterized by craniofacial differences, reduced bone mineral density, and bowed long bones.
Cheyenne Bates   +6 more
wiley   +1 more source

Report on the general design of commercial aircraft [PDF]

open access: yes
Given here are evaluations of six different European aircraft from the point of view of a passenger. The aircraft discussed are the DH 34, the Handley-Page W8B, the Farman Goliath, the Potez IX, the Spad 33 (Berline), and the Fokker F.III.
Warner, Edward P
core   +1 more source

[The effect of operation success on middle ear ventilation in patients with nasal septal deviation].

open access: yesKulak burun bogaz ihtisas dergisi : KBB = Journal of ear, nose, and throat, 2013
H. Eyigör   +4 more
semanticscholar   +1 more source

Shifting the paradigm from person‐centered to Indigenous‐centered: A qualitative study to inform a framework for culturally appropriate approaches to dementia care in Alberta, Canada

open access: yesAlzheimer's &Dementia: Behavior &Socioeconomics of Aging, Volume 2, Issue 1, March 2026.
Abstract INTRODUCTION Dementia prevalence in Indigenous populations worldwide is increasing at disproportionately higher rates compared to non‐Indigenous populations, and current care systems are insufficient. This project developed a foundational understanding of Indigenous‐centered approaches to dementia care provision in Alberta, Canada.
Meagan Ody   +10 more
wiley   +1 more source

Postoperative Otorrhea as a Predictor of Early Ventilation Tube Extrusion in Children. [PDF]

open access: yesTurk Arch Otorhinolaryngol
Uzunoğlu E   +3 more
europepmc   +1 more source

Saul Wilson Syndrome: A Case Report With New Features in Saudi Arabia

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Saul Wilson syndrome is an extremely rare genetic disorder caused by heterozygous de novo mutations in the COG4 gene. We report the first case from Saudi Arabia with previously unreported facial dysmorphic features, expanding the known phenotypic spectrum and emphasizing the importance of recognizing phenotypic variability in rare disorders.
Saad A. Bin Owaimer   +4 more
wiley   +1 more source

Otitis Media With Effusion in Patients With Cleft Palate. [PDF]

open access: yesClin Pediatr (Phila)
McGlone M   +5 more
europepmc   +1 more source

A Novel Long-Term Tympanostomy Tube: The U-Tube. [PDF]

open access: yesBioengineering (Basel)
Chen I, Sichel JY, Shaul C, Perez R.
europepmc   +1 more source

Cleavage and Polyadenylation Specificity Factor Subunit 5 Regulates Pulmonary Artery Smooth Muscle Expansion and Hypoxic Response

open access: yesMedComm, Volume 7, Issue 2, February 2026.
Increased miR‐3163 targets NUDT21, reducing CPSF5 levels and driving APA dysregulation. This results in 3′UTR shortening of CBFB, which stabilizes RUNX1 and promotes smooth muscle proliferation. PTGER3, is also shortened amplifying hypoxia‐induced RVSP. Together, these pathways contribute to vascular remodeling in PH. Image Created in https://BioRender.
Scott D. Collum   +17 more
wiley   +1 more source

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