Pendred's syndrome
|
0.050 |
Biomarker
|
disease |
BEFREE |
The shape and function of thyroid were confirmed to be normal by thyroid ultrasound scan and thyroid hormone assays in 19 of the 20 patients with EVA or other inner ear malformation except one who had cystoid change in the right side of thyroid.No Pendred syndrome was diagnosed.
|
19040761 |
2008 |
Pendred's syndrome
|
0.050 |
Biomarker
|
disease |
BEFREE |
Besides clinical and radiological assessments, molecular and functional studies are essential for the correct diagnosis of Pendred syndrome and non-syndromic EVA.
|
22116360 |
2011 |
Pendred's syndrome
|
0.050 |
GeneticVariation
|
disease |
BEFREE |
Loss or reduction in the function of pendrin results in both syndromic (Pendred syndrome) and non-syndromic (non-syndromic enlarged vestibular aqueduct (ns-EVA)) hearing loss.
|
22116359 |
2011 |
Pendred's syndrome
|
0.050 |
Biomarker
|
disease |
BEFREE |
Nineteen patients with PS and 23 patients with nonsyndromic EVA, aged 5-53 years, were included.
|
24224479 |
2014 |
Pendred's syndrome
|
0.050 |
Biomarker
|
disease |
BEFREE |
These mutations may be of value for the diagnosis of Pendred syndrome and NSRD with EVA.
|
16924389 |
2006 |
Sensorineural Hearing Loss (disorder)
|
0.040 |
Biomarker
|
disease |
BEFREE |
We thus present MPZL2 as a novel gene associated with sensorineural hearing loss.
|
29982980 |
2018 |
Sensorineural Hearing Loss (disorder)
|
0.040 |
Biomarker
|
disease |
BEFREE |
<b>Material and Methods:</b> HRCT scanning of the temporal bones of 82 cases with normal inner ear structures and 104 cases with an EVA and bilaterally sensorineural hearing loss (SNHL) was performed.
|
31124731 |
2019 |
Sensorineural Hearing Loss (disorder)
|
0.040 |
GeneticVariation
|
disease |
BEFREE |
SLC26A4 mutations have also been identified in patients exhibiting isolated sensorineural hearing loss without apparent thyroid abnormality (nonsyndromic enlargement of the vestibular aqueduct; nonsyndromic EVA).
|
24224479 |
2014 |
Sensorineural Hearing Loss (disorder)
|
0.040 |
Biomarker
|
disease |
BEFREE |
A total of 271 children with nonsyndromic sensorineural hearing loss and EVA underwent SLC26A4 gene screening.
|
24245694 |
2013 |
Congenital Abnormality
|
0.020 |
GeneticVariation
|
group |
BEFREE |
The most common malformation found in cases with EVA was incomplete partition type II (IP-II; 90.4%).
|
31124731 |
2019 |
Congenital Abnormality
|
0.020 |
Biomarker
|
group |
BEFREE |
1.Three types malformations include EVA, EVA with Mondini and Mondini were found.
|
30762457 |
2019 |
Carotid Stenosis
|
0.020 |
Biomarker
|
disease |
BEFREE |
Follow-up data from 2184 carotid artery stenting and 2261 carotid endarterectomy patients from 4 randomized trials (EVA-3S [Endarterectomy Versus Angioplasty in Patients With Symptomatic Severe Carotid Stenosis], SPACE [Stent-Protected Angioplasty Versus Carotid Endarterectomy], ICSS [International Carotid Stenting Study], and CREST [Carotid Revascularization Endarterectomy Versus Stenting Trial]) were used to validate 23 short-term outcome models to estimate stroke or death risk ≤30 days after the procedure and the original outcome measure for which the model was developed.
|
30012816 |
2018 |
Carotid Stenosis
|
0.020 |
Biomarker
|
disease |
BEFREE |
Methods- We combined individual patient data of 4754 patients with symptomatic carotid stenosis from 4 randomized trials (EVA-3S [Endarterectomy Versus Angioplasty in Patients With Symptomatic Severe Carotid Stenosis], SPACE [Stent-Protected Angioplasty Versus Carotid Endarterectomy], ICSS [International Carotid Stenting Study], and CREST [Carotid Revascularization Endarterectomy Versus Stenting Trial]).
|
30621529 |
2019 |
Paraganglioma
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
The value of a rapid contrast-enhanced angio-MRI protocol in the detection of head and neck paragangliomas in SDHx mutations carriers: a retrospective study on behalf of the PGL.EVA investigators.
|
26427697 |
2016 |
Paraganglioma
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA Investigators.
|
23162105 |
2013 |
Congenital ear anomaly NOS (disorder)
|
0.020 |
Biomarker
|
group |
BEFREE |
Among them, 28 patients with isolated Mondini dysplasia (MD group), 50 patients with enlarged vestibular aqueduct with Mondini dysplasia (EVA with MD group), 50 patients with enlarged vestibular aqueduct without Mondini dysplasia (EVA group), and 16 patients with other types of inner ear malformations (IEM group) were identified.
|
21961810 |
2011 |
Congenital ear anomaly NOS (disorder)
|
0.020 |
Biomarker
|
group |
BEFREE |
Among them, 17 patients with bi-allelic SLC26A4 mutations were all confirmed to have EVA or other inner ear malformation by CT scan.
|
19040761 |
2008 |
Impaired cognition
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Polymorphism of the prion protein is associated with cognitive impairment in the elderly: the EVA study.
|
9748018 |
1998 |
Impaired cognition
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Effect of the angiotensin I-converting enzyme I/D polymorphism on cognitive decline. The EVA Study Group.
|
10794851 |
2000 |
Advanced breast cancer
|
0.020 |
Biomarker
|
disease |
BEFREE |
Correction 2: Everolimus (EVE) and exemestane (EXE) in patients with advanced breast cancer aged ≥ 65 years: new lessons for clinical practice from the EVA study.
|
30613355 |
2018 |
Advanced breast cancer
|
0.020 |
Biomarker
|
disease |
BEFREE |
Everolimus (EVE) and exemestane (EXE) in patients with advanced breast cancer aged ≥ 65 years: new lessons for clinical practice from the EVA study.
|
30159129 |
2018 |
Nonsyndromic Deafness
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
By screening a cohort of phenotype-matched subjects and a cohort of HI subjects in whom WES had been performed previously, we identified two additional families with biallelic truncating variants of MPZL2.
|
29961571 |
2018 |
Nonsyndromic Deafness
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Here, we report a loss-of-function variant (c.72delA) in MPZL2 in three unrelated multiplex families from Turkey and Iran with autosomal recessive nonsyndromic hearing loss.
|
29982980 |
2018 |
Alopecia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.
|
19054061 |
2009 |
Arteriosclerosis
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
To check its possible implication in atherosclerosis, this polymorphism was then genotyped in the AXA Study (ultrasound examinations of carotid and femoral arteries in the context of an employment medical examination, 733 subjects), the EVA Study (ultrasound examinations of carotid arteries in a study of cognitive and vascular ageing, 1092 subjects) and the GENIC Study (on brain infarction (BI), 912 subjects).
|
14694358 |
2004 |