Results 141 to 150 of about 96,976 (289)

Bezold’s abscess: A rare complication of acute otitis media [PDF]

open access: yesMalaysian Family Physician, 2017
Otitis media is a common disease encountered in the primary practice. Most cases are successfully treated with antibiotics without any sequelae. Because of these, potential serious complications of otitis media may be overlooked. We report a rare case
Zamzil Amin Asha’ari , Fauziah Nasir
doaj  

Finnish nationwide controlled register study found increased inpatient infections in children with 22q11.2 deletion syndrome

open access: yesActa Paediatrica, EarlyView.
Abstract Aim Studies on treating infections in children with 22q11.2 deletion syndrome (22q11.2DS) have been limited. We characterised inpatient infections and outpatient antibiotic treatment. Methods Children born during 2005–2018 were eligible for this national Finnish retrospective register‐based study.
Sakari Wahrmann   +3 more
wiley   +1 more source

Unveiling injustice: Disrupting child removal policies and upholding breastfeeding: An emancipatory framework

open access: yesBirth, EarlyView.
Research with Aboriginal communities must be culturally safe, de‐colonised, and guided by and benefitting the community. It is important to incorporate an Aboriginal Participatory Action Research framework (a), using community consultation and codesign (b); culturally secure data collection methods (c), whilst paying attention to Indigenous data ...
Amanda Peek   +4 more
wiley   +1 more source

A Multicenter Phase II Trial of Nimustine Hydrochloride Administered via Convection‐Enhanced Delivery in Children With DIPG

open access: yesCancer Science, EarlyView.
The efficacy of the CED of nimustine hydrochloride in pediatric DIPG was evaluated. One‐year survival rate from the start of radiotherapy was 60%. The treatment strategy demonstrated potential efficacy. ABSTRACT Diffuse intrinsic pontine glioma (DIPG) is a very challenging‐to‐treat pediatric malignant tumor, with a median survival time of < 12 months ...
Ryuta Saito   +13 more
wiley   +1 more source

A Cryptic CBFB Deletion–Inversion Expands the Mutational Spectrum of Variants Associated With Cleidocranial Dysplasia

open access: yesClinical Genetics, EarlyView.
Following clinical review of a 100 000 Genomes Project family with genetically‐unsolved CCD, we manually inspected read‐alignments and identified a deletion‐inversion‐deletion that removes the first two exons of CBFB. This cryptic variant comprised deletions of 1310/1935bp, was undetectable by array‐CGH and was likely mediated by palindromic AluSx ...
Alistair T. Pagnamenta   +6 more
wiley   +1 more source

Home - About - Disclaimer - Privacy