Global incidence of lip, oral cavity, and pharyngeal cancers by subsite in 2022
ABSTRACT Cancers of the lip, oral cavity, and pharynx (LOCP) represent a substantial public health challenge worldwide. Using GLOBOCAN national estimates of incidence, detailed cancer registry data from Cancer Incidence in Five Continents, and population statistics from the United Nations, the authors report the distribution of new cases of LOCP ...
Harriet Rumgay +12 more
wiley +1 more source
Intraosseous meningioma mimicking chronic otitis media. [PDF]
Uwabe K +6 more
europepmc +1 more source
Effect of Vitamin-D Supplementation on Recurrence of Acute Otitis Media in Pre-School Children
Osama Refaat +2 more
openalex +1 more source
Myasthenia Gravis in a Child With Schimke Immuno‐Osseous Dysplasia: A Case Report
ABSTRACT We report a rare association between Schimke immune‐osseous dysplasia and myasthenia gravis. Clinicians should be aware of potential autoimmune neuromuscular complications in SIOD, as early recognition and tailored immunosuppression may improve prognosis.
Mohamed S. Al Riyami +7 more
wiley +1 more source
Global, regional, and national burden of neonatal otitis media attributable to PM2.5 air pollution: findings from the Global Burden of Disease study 2021. [PDF]
Gong X +8 more
europepmc +1 more source
Concomitant Rhinosinusitis is a Risk Factor for Refractory Acute Otitis Media in Children
Noboru Yamanaka +9 more
openalex +1 more source
Myiasis of the Mastoid Cavity: Case Report
Otoendoscopic view of the canal wall down mastoidectomy cavity after partial clearance of debris and larvae. The anatomical structures are indicated for orientation: MC, mastoid cavity; Te, tegmen tympani; Ty, tympanic membrane. ABSTRACT Mastoid cavity myiasis is a rare but important differential diagnosis.
Hannes Hefty +4 more
wiley +1 more source
Type 2 Diabetes Mellitus With Complex Necrotizing Otitis Externa, Skull Base Osteomyelitis, and Cranial Nerve Palsies: A Case Report. [PDF]
Mahadevaswamy Susheela MK +4 more
europepmc +1 more source
Rottweilers under primary veterinary care in the UK: demography, mortality and disorders [PDF]
A Agresti +82 more
core +2 more sources
Novel Nonsense Mutation in SMARCD2 Gene Results in Dysplasia of All Myeloid Cell Lines
ABSTRACT Introduction Specific granule deficiency type II (SGD2) is a rare heterogeneous congenital disease characterized by early‐onset life‐threatening infections. SGD2 is caused by autosomal recessive mutations in the SMARCD2 gene. Methods Prenatal screening in our patient revealed a novel homozygous nonsense mutation in SMARCD2 (c.208C>T, p.Gln70*).
Michelle A. E. Brouwer +6 more
wiley +1 more source

