Results 211 to 220 of about 161,394 (344)
Optimal antimicrobial duration for common bacterial infections [PDF]
Daveson, Kathryn +2 more
core +1 more source
ABSTRACT A 75‐year‐old man presented with an esophageal subepithelial lesion (SEL) measuring 2.5 cm, first identified over a decade ago. The patient was followed up regularly with computed tomography and endoscopy and remained asymptomatic since then. However, over the past year, the patient developed dysphagia, and endoscopic evaluation revealed that ...
Mai Fukuda +10 more
wiley +1 more source
THE ASSOCIATION OF SUPPURATIVE DISEASE OF THE NASAL ACCESSORY SINUSES AND ACUTE OTITIS MEDIA IN ADULTS [PDF]
CORNELIUS G. COAKLEV
openalex +1 more source
Ototoxicity in Cancer Therapies
Oral Diseases, EarlyView.
Sady Selaimen da Costa +2 more
wiley +1 more source
The Expanding Clinical and Genetic Spectrum of Muscle Glycogen Storage Disease 0, (GSD0B)
ABSTRACT Glycogen storage disorders are a group of genetic disorders affecting glucose homeostasis in the body. Muscular glycogen stores are essential for liberating glucose for energy supply during bursts of activity and sustained muscle work. Muscle glycogen storage disease 0 (GSD0B) is associated with biallelic variants in GYS1 causing muscular ...
Sarah Donoghue +16 more
wiley +1 more source
Unmasking Rarity: An Atypical Presentation of Lemierre's Syndrome. [PDF]
Abdela HA +6 more
europepmc +1 more source
THE SYMPTOMS AND TREATMENT OF THE INTRACRANIAL COMPLICATIONS OF OTITIS MEDIA; WITH CASES.*1 [PDF]
Gregory Heaton
openalex +1 more source
ABSTRACT Natural History Studies can help inform clinician and caregiver expectations, form the basis of management guidelines, and provide a comparator for therapeutic intervention. In rare conditions, where collection of prospective longitudinal data is untimely and impractical, quasi‐natural history data—from multiple individuals of different ages ...
E. Woods +16 more
wiley +1 more source
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero +17 more
wiley +1 more source

