Results 211 to 220 of about 54,480 (306)
Understanding the Role of Genetic Testing in Diagnosing a Complex Pediatric Case
Visualization of ZPR1 protein variants. ABSTRACT We report the case of a 13‐month‐old female with multiple congenital anomalies including microcephaly, generalized hypotonia, sensorineural hearing loss, visual impairment, alopecia, and hypoplastic kidneys with chronic kidney disease, and dysmorphic craniofacial features.
Giavanna Verdi +6 more
wiley +1 more source
Serum sCD163 indicates disease severity and prognosis in sudden sensorineural hearing loss. [PDF]
Xu T, Miao H, Xie B.
europepmc +1 more source
Traditionally, clinical outcomes measuring how a patient feels, functions, or survives are preferred endpoints in clinical trials; however, some may take a long time to manifest in slowly developing diseases. Biomarkers, if properly validated, can serve as surrogate endpoints, acting as substitutes for clinical outcomes.
Renske Johanna Grupstra +4 more
wiley +1 more source
ABSTRACT Background Hearing loss affects 1.5 billion people globally, with sensorineural hearing loss (SNHL) linked to hypertension. Hypertension affects 1.39 billion people worldwide and its prevalence is rising sharply in Sub‐Saharan Africa. While 12% of Tanzanian population has cardiovascular diseases, including hypertension and recent studies ...
Johnson Shayo +3 more
wiley +1 more source
Efficacy of sound therapy on tinnitus in idiopathic sudden sensorineural hearing loss: a systematic review and meta-analysis protocol. [PDF]
Ren Q +6 more
europepmc +1 more source
Sudden sensorineural hearing loss
Newsted, Daniel +2 more
openaire +2 more sources
Increased incidence of sudden sensorineural hearing loss in patients with rheumatoid arthritis: a nationwide propensity-matched cohort study. [PDF]
Chen MJ +7 more
europepmc +1 more source

