A Search Service for Abbreviation / Long Form

■ Related PubMed/MEDLINE Info.

[Related PubMed/MEDLINE]
Total Number of Papers: 19
[Display Entries]
[Entries Per Page]
 per page
Page Control
Page: of
Abbreviation : OA
Long Form : optic atrophy
No. Year Title Co-occurring Abbreviation
2019 Diabetic Optic Neuropathy and Its Risk Factors in Chinese Patients With Diabetic Retinopathy. AION, CFT, D.P, DON, DR, HbA1c, HDL, SBP
2018 A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: a case report. DI, DM, NMO, ON, WFS1, WS
2018 Clinical Characteristics of Wolfram Syndrome in Chinese Population and a Novel Frameshift Mutation in WFS1. DM, WS
2017 Etiology of optic atrophy: a prospective observational study from Saudi Arabia. ---
2017 Ophthalmological findings in 74 patients with mitochondrial disease. EOM
2017 Retinal Nerve Fiber Layer and Peripapillary Choroidal Thicknesses in Non-Glaucomatous Unilateral Optic Atrophy Compared with Unilateral Advanced Pseudoexfoliative Glaucoma. PCT, RNFLT
2016 WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity. adWLS, arNSOA, arWS, logMAR, OCT, RNFL, SD, TD, VA
2014 Congenital central diabetes insipidus and optic atrophy in a Wolfram newborn: is there a role for WFS1 gene in neurodevelopment? CDI, DM, MRI, WS
2013 Characteristics of late negative ERG responses elicited by sawtooth flicker. ERG, LNRon, LNRs, PhNRpulse
10  2013 WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victims. DM, SNHI
11  2012 A new structural rearrangement associated to Wolfram syndrome in a child with a partial phenotype. DI, DM, WS
12  2012 Visual function, ocular motility and ocular characteristics in patients with mitochondrial complex I deficiency. ---
13  2011 Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment. OPA1, SNHL
14  2006 Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene. ADOA, LFSNHL
15  1995 Various clinical aspects of DIDMOAD (Wolfram) syndrome. DI, DM
16  1995 [Wolfram syndrome. Peculiar urologic aspects]. DI, DM
17  1990 Diabetes mellitus, diabetes insipidus, optic atrophy and deafness (DIDMOAD syndrome). DI, DM
18  1985 Association of diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. The Wolfram or DIDMOAD syndrome. DI, DM
19  1979 Diabetes insipidus, diabetes mellitus, optic atrophy and deafness. A clinical and genetic study. DI, DM