Results 231 to 240 of about 163,596 (354)

Global incidence of lip, oral cavity, and pharyngeal cancers by subsite in 2022

open access: yesCA: A Cancer Journal for Clinicians, Volume 76, Issue 1, January/February 2026.
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]

open access: yesSurg Neurol Int
Uwabe K   +6 more
europepmc   +1 more source

Myasthenia Gravis in a Child With Schimke Immuno‐Osseous Dysplasia: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
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

Concomitant Rhinosinusitis is a Risk Factor for Refractory Acute Otitis Media in Children

open access: diamond, 2014
Noboru Yamanaka   +9 more
openalex   +1 more source

Myiasis of the Mastoid Cavity: Case Report

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
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

Rottweilers under primary veterinary care in the UK: demography, mortality and disorders [PDF]

open access: yes, 2017
A Agresti   +82 more
core   +2 more sources

Novel Nonsense Mutation in SMARCD2 Gene Results in Dysplasia of All Myeloid Cell Lines

open access: yeseJHaem, Volume 6, Issue 6, December 2025.
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

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