Medicina, 2023 Background and Objectives: Type I dentin dysplasia (DD-I) is a rare genetic disorder with autosomal dominant or recessive inheritance at risk of late or long-misunderstood diagnosis because the teeth, compared to other degenerative dentin diseases, do ...
Alessandra Putrino +4 more
doaj +1 more source
Relationship between thoracic kyphosis and neural axis abnormalities in patients with adolescent idiopathic scoliosis. [PDF]
, 2018 Purpose:Previous studies have suggested an association between increased thoracic kyphosis and neural axis abnormalities in patients with adolescent idiopathic scoliosis (AIS). However, the basis for this finding is unclear, and this association has been
Blanco, J +5 more
core +2 more sources
Effect of screening abdominal ultrasound examination on the decision to pursue advanced diagnostic tests and treatment in dogs with neurologic disease. [PDF]
, 2015 BackgroundAbdominal ultrasound examinations (AUS) are commonly performed before advanced neurodiagnostics to screen for diseases that might affect diagnostic plans and prognosis.ObjectivesDescribe the type and frequency of abnormalities found by AUS in ...
Blair, WH +5 more
core +1 more source
Intubation of underestimated airway in a patient with epiglottis adhesion to the posterior wall of the laryngeal cavity -A case report- [PDF]
Anesthesia and Pain MedicineBackground Epiglottis abnormality is rare condition and can lead embarrassing intubation to anesthesiologists. Here, we reported a case of successful management in a patient with unexpected hidden vocal cords due to epiglottis adhesion to the posterior ...
Gayoung Jin, Sukyoung Lee, Jungchan Park
doaj +1 more source
Visual attention in autism families: ‘unaffected’ sibs share atypical frontal activation [PDF]
, 2009 Background: In addition to their more clinically evident abnormalities of social cognition, people with autism spectrum conditions (ASC) manifest perturbations of attention and sensory perception which may offer insights into the underlying neural ...
Baron-Cohen, S, Belmonte, MK, Gomot, M
core +1 more source
Occasional essay: upper motor neuron syndrome in amyotrophic lateral sclerosis [PDF]
, 2020 The diagnosis of amyotrophic lateral sclerosis (ALS) requires recognition of both lower (LMN) and upper motor neuron (UMN) dysfunction.1 However, classical UMN signs are frequently difficult to identify in ALS.2 LMN involvement is sensitively detected ...
Burke, David +6 more
core +1 more source
Chromosomal aberrations in transitional cell carcinoma that are predictive of disease outcome are independent of polyploidy [PDF]
, 1999 Objective To determine whether aneusomy for chromosomes 7, 9 and 17 (reported to predict recurrence in up to 65% of patients with superficial transitional cell bladder cancer and thus providing the opportunity for early and effective treatment) reflects ...
Adie, L. +4 more
core +1 more source
The prevalence of certain upper body abnormalities and their association with mental health among female students at Payame Noor University [PDF]
Sport Sciences and Health ResearchBackground: The modern increase in mechanical and sedentary lifestyles has led to a rise in musculoskeletal abnormalities within society. These physical irregularities may influence individual mental health.Aim: This study explores the correlation ...
khatoon pourmaveddat +1 more
doaj +1 more source
Boletim do Instituto de Pesca, 2016 Severe deformity such as coalescence of vertebrae, compact vertebrae, loss of vertebral parts, and different levels of deformed vertebral centra and minor deformities such as undulation of the haemal spines of the vertebrae are reported in six specimens
Laith JAWAD +2 more
doaj +1 more source
Case Reports in Pediatrics, 2018 The aim of this article was to present a characteristic clinical image of Melnick–Needles syndrome using an example of an 11.5-year-old female patient treated at the Facial Congenital Disorders Outpatient Clinic as well as to present the actual ...
Dorota Kustrzycka +4 more
doaj +1 more source