Results 241 to 250 of about 74,884 (346)

Comparison between intratympanic injection of dexamethasone and methylprednisolone in idiopathic sudden sensorineural hearing loss: A randomized clinical trial. [PDF]

open access: yesLaryngoscope Investig Otolaryngol
Eftekharian K   +7 more
europepmc   +1 more source

IDIOPATHIC BILATERAL SENSORINEURAL HEARING LOSS

open access: bronze, 1993
Masatoshi Hirayama   +4 more
openalex   +2 more sources

Provider‐Led Interventions to Reduce Congenital Cytomegalovirus

open access: yesJournal of Midwifery &Women's Health, EarlyView.
Introduction Cytomegalovirus (CMV) infection immediately before or during pregnancy can infect a fetus transplacentally, causing congenital CMV (cCMV). cCMV can cause miscarriage, stillbirth, growth restriction, neurodevelopmental delay, hearing, and vision impairment.
Erin Trisko   +3 more
wiley   +1 more source

Exploring the Potential of Stem Cells: A Systematic Review on Cellular Therapy for Sensorineural Hearing Loss. [PDF]

open access: yesCureus
Henao Rincón MA   +7 more
europepmc   +1 more source

An anatomical investigation of alkaptonuria: Novel insights into ochronosis of cartilage and bone

open access: yesJournal of Anatomy, EarlyView.
Examination of an alkaptonuria body highlights the susceptibility of all cartilage types and associated perichondrium to ochronotic pigmentation and the heterogeneity of ochronotic pigment distribution both within and between tissues. In joints, calcified cartilage pigments before non‐calcified cartilage.
Juliette H. Hughes   +8 more
wiley   +1 more source

Assessing the Recognition of Social Interactions Through Body Motion in the Routine Care of Patients with Post-Lingual Sensorineural Hearing Loss. [PDF]

open access: yesJ Clin Med
Fauvet C   +10 more
europepmc   +1 more source

X‐Linked Hypophosphataemia and Burosumab: A Systemic Disease With a New Treatment

open access: yesJournal of Paediatrics and Child Health, EarlyView.
ABSTRACT X linked hypophosphataemia (XLH) is a systemic, chronic condition that significantly impairs quality of life. In XLH, a phosphate regulating endopeptidase homologue X‐linked (PHEX) gene mutation leads to excess fibroblast growth factor 23 (FGF23), causing hypophosphataemia and subsequent rickets, lower limb deformity, pain and other sequelae ...
Jessica L. Sandy   +5 more
wiley   +1 more source

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