A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome [PDF]
, 2014 Otitis media (OM), the inflammation of the middle ear, is the most common disease and cause for surgery in infants worldwide. Chronic Otitis media with effusion (OME) often leads to conductive hearing loss and is a common feature of a number of ...
Fuchs, JC +3 more
core
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT ADNP‐related Helsmoortel–Van der Aa syndrome (ADNP‐related HVDAS) is a single gene form of autism spectrum disorder (ASD) caused by pathogenic sequence variants in the activity‐dependent neuroprotective protein (ADNP) gene. In addition to ASD, ADNP‐related HVDAS is associated with a wide range of cognitive, behavioral, and physical health ...
Jarrett Fastman +11 more
wiley +1 more source
Otitis Media Efusi Facts! [PDF]
, 2022 Poster Otitis Media Efusi Facts! adalah poster yang dibuat dengan tujuan memberikan informasi kepada masyarakat luas seputar penyakit otitis media efusi.
Fransiska, Fransiska +3 more
core +1 more source
Occurrence and identification of yeasts in dogs external ear canal with and without otitis [PDF]
Revista Mvz Cordoba, 2012 Objective. To analyze the presence of yeast in the external ear canal of 116 dogs with and without a diagnosis of otitis from veterinary clinic in the Chapecó city, Santa Catarina, Brazil, and to examine the secretion of the proteinase in isolates ...
Elidiana de Bona +2 more
doaj
Brazilian Journal of Otorhinolaryngology, 2009 Este estudo tem como objetivo descrever uma técnica cirúrgica alternativa à inserção do tubo de ventilação na membrana timpânica: a miringotomia por radiofrequência isolada e associada à mitomicina C.
Vanessa Chisté Guimarães Faccini +1 more
doaj +1 more source
Association of Single Nucleotide Polymorphisms in Surfactant Protein A and D with Otitis Media. [PDF]
, 2007 Otitis Media is one of the most common childhood diseases. Recurrent acute otitis media RAOM is characterized by repeated episodes of inflammation of the middle ear in conjunction with middle ear fluid, and often with an inflamed or bulging eardrum ...
Barnett, Catherine Margaret Eleanor
core
Systematic Review of Females With Intellectual Disability and MECP2 Duplication
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT MECP2 Duplication Syndrome (MDS) is a rare, X‐linked neurodevelopmental disorder typically affecting males. Females with MDS have been reported and are compiled here. We conducted a systematic review (PROSPERO CRD420250652426) of PubMed, EMBASE, and Google Scholar extracting individual participant data.
Paul Malik +10 more
wiley +1 more source
MANIFESTACIONES OTORRINOLARINGOLÓGICAS DE LA DISQUINESIA CILIAR PRIMARIA
Neumología Pediátrica, 2019 La Disquinesia Ciliar Primaria (DCP) es una enfermedad genética heterogénea rara que puede estar presente en hasta un 5% de los pacientes que presentan infecciones respiratorias a repetición.
Álvaro Pacheco Tejerina
doaj +1 more source
Clinical and Surgical Survey on most common skin affections in police guard and explosive dogs [PDF]
Veterinary Medical Journal - Giza, 2010 Medicinal and surgical skin affections are common health problems in police guard and explosive dogs used for protection of organizations of high economic importance and tourism in Egypt.
KELANY M, HAITHEM M, FARGHALI M
doaj +1 more source
Protective effect of antibiotics against serious complications of common respiratory tract infections: retrospective cohort study with the UK General Practice research database [PDF]
, 2007 Objective: To determine the extent to which antibiotics reduce the risk of serious complications after common respiratory tract infections. Design: Retrospective cohort study.
Johnson, A. M. +9 more
core +1 more source