Results 191 to 200 of about 76,904 (360)

Birth prevalence, clinical sequelae, and management of congenital cytomegalovirus infections in Australia, 1999–2023: a national prospective study

Medical Journal of Australia, EarlyView.
Abstract Objectives To investigate the birth prevalence, clinical manifestations, and management of congenital cytomegalovirus (CMV) infections in Australia, 1999–2023. Study design Longitudinal observational study; analysis of prospectively collected Australian Paediatric Surveillance Unit (APSU) data. Setting, participants Australia, 1 January 1999 –
Ece Egilmezer, Suzy M Teutsch, Carlos Nunez, Stuart T Hamilton, Adam W Bartlett, Pamela Palasanthiran, Elizabeth J Elliott, William D Rawlinson   +7 more
wiley   +1 more source

Sudden sensorineural hearing loss. [PDF]

CMAJ
Newsted D, Bajin MD, You P.
europepmc   +1 more source

Adverse Effects of Steroid Therapy in Sudden Sensorineural Hearing Loss: A Scoping Review. [PDF]

Clin Otolaryngol
ABSTRACT Objective Sudden sensorineural hearing loss (SSNHL) is an otologic emergency and is treated with steroid therapy. Despite adverse events (AEs) associated with long‐term steroid use being well evidenced, there is sparsity of literature regarding the AEs of short‐course prescriptions in the SSNHL cohort, which limits the quality of patient ...
Achanta M, Kasetti P, Fortune-Ely M, Ross T, Magos T, Manjaly JG.   +5 more
europepmc   +2 more sources

Lupus Anticoagulant Induced Sudden Profound Sensorineural Hearing Loss.

, 1991
Kazutaka Hisashi, S. Komune, Toshiaki Taira, Seizo Sadoshima   +3 more
openalex   +2 more sources

Survivorship of Individuals With Double Heterozygosity for Achondroplasia and Type 2 Collagenopathy

American Journal of Medical Genetics Part A, Volume 197, Issue 10, October 2025.
ABSTRACT Historically, double heterozygosity, or a diagnosis of two separate, dominant genetic conditions, was often thought to be lethal in individuals with autosomal dominant skeletal dysplasias. In previously published studies of individuals with dual dysplasia diagnoses of achondroplasia and type 2 collagenopathy, infants died of respiratory ...
Valerie R. Schwartz, Andrea Schelhaas, Angela L. Duker, Ricki S. Carroll   +3 more
wiley   +1 more source

Evaluation of Acute Low Tone Sensorineural Hearing Loss utilizing Evoked Otoacoustic Emissions.

, 1994
Taku Hattori, Niang Dan Qiu, Masayuki Sawaki, Hiromi Ueda, Noriyuki Yanagita, Hideto Niwa   +5 more
openalex   +2 more sources

A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350) [PDF]

, 2000
Kirsten Heathcote
openalex   +1 more source

Chromosome 3q22.2‐q26.2 Interstitial Deletion in a Patient With Wisconsin Syndrome, Blepharophimosis‐Ptosis‐Epicanthus Inversus Syndrome, Dandy‐Walker Malformation, Pierre Robin Sequence, and Recurrent Infections

American Journal of Medical Genetics Part A, Volume 197, Issue 10, October 2025.
ABSTRACT Wisconsin syndrome is a very rare genetic condition characterized by coarse facies, prominent nasal tip, bushy high arched/upsweeping eyebrows, and a full/everted lower lip. Deletion of chromosome 3q24q25 region is considered critical for its manifestation.
Pankaj Prasun, Sonja Henry, Vivek Balasubramaniam   +2 more
wiley   +1 more source

Audiogram Shape: Does It Have a Significant Prognostic Role in Idiopathic Sudden Sensorineural Hearing Loss Outcome? [PDF]

J Pers Med
Cadoni G, Rizzuti A, Sollazzo M, Picciotti PM, Galli J.   +4 more
europepmc   +1 more source

The Long Term Follow Up by Questionnaire for Acute Low-tone Sensorineural Hearing Loss

, 1992
Shiro Iwabuchi, Kazuo Matsui, Michihiko Nozue   +2 more
openalex   +2 more sources