Results 51 to 60 of about 2,882,247 (326)

Clinical Use of S53P4 Bioactive Glass in the Treatment of Bone Defects and Infected Bone: A Systematic Review of the Quality of Clinical Outcomes and A Grade Assessment

open access: yesAdvanced Healthcare Materials, EarlyView.
Bioactive glass (BAG) S53P4 is a synthetic bone substitute. Clinically it has been used in the treatment of benign bone tumor surgery, in spine surgery, in trauma surgery, in frontal sinus surgery, in diabetic foot osteomyelitis surgery, in mastoid surgery, in oral and maxillofacial surgery in more than 4000 patients, with excellent clinical long‐term ...
Lindfors CES, Arts JJC, Lindfors NC
wiley   +1 more source

De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil   +8 more
wiley   +1 more source

Hubungan Tonsilitis Kronis dan Otitis Media Efusi di Bagian THT RSUD Ulin Banjarmasin Tahun 2014

open access: yesBerkala Kedokteran, 2016
: Chronic tonsillitis is an inflammation of the tonsil was settled as a result of recurrent of acute or subclinical infection which is marked by the widening of the tonsil crypts and size can be enlarged (hypertrophy) or shrink (atrophy).
Farisa Shauma Fachir   +2 more
doaj   +1 more source

Prevalence of Otitis Media in Okada Community, Edo State, Nigeria [PDF]

open access: yes, 2010
Aim. To determine the prevalence of otitis media in Okada, a rural community in Nigeria, and the effect of age and gender on its prevalence as well as susceptibility profile of the bacterial agents in the community.Material and Methods.
Egbe, Christopher   +3 more
core   +1 more source

Recurrent Acute Otitis Media: What Are the Options for Treatment and Prevention?

open access: yesCurrent Otorhinolaryngology Reports, 2017
Purpose of ReviewTo survey current strategies for treatment and prevention of recurrent acute otitis media (rAOM).Recent FindingsTreatment with systemic antibiotics is required in recurrent episodes of acute otitis media.
A. Granath
semanticscholar   +1 more source

GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10‐year‐old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA).
Lauren N. Meiss   +8 more
wiley   +1 more source

RISK FACTORS FOR ACUTE OTITIS MEDIA DEVELOPMENT IN INFANTS AND CHILDREN DURING THE FIRST MONTHS OF LIFE

open access: yesМедицинский совет, 2018
Diagnosis of acute otitis media in infants is complicated due to few symptoms of clinical and laboratory manifestations dictating the need to find possible predictors of the disease.Material and methods.
K. N. Ustinovich   +2 more
doaj   +1 more source

New horizons: otitis media research in Australia [PDF]

open access: yes, 2009
Otitis media affects nearly all children worldwide. Despite an enormous amount of research, our understanding of this common condition continues to be challenged. New pathogens involved in otitis media are still being identified.
Coates, Harvey L. C.   +5 more
core  

Streptococcus pneumoniae Otitis Media Pathogenesis and How It Informs Our Understanding of Vaccine Strategies

open access: yesCurrent Otorhinolaryngology Reports, 2017
Purpose of ReviewThis study aimed to review the literature regarding the mechanisms of transition from asymptomatic colonization to induction of otitis media and how the insight into the pathogenesis of otitis media has the potential to help design ...
C. Bergenfelz, A. Hakansson
semanticscholar   +1 more source

Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat   +4 more
wiley   +1 more source

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