Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText.
Kick-your-searchterm to multiple Engines kick-your-query now !>
A dictionary by aggregated review articles of nephrology, medicine and the life sciences
Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

suck abstract from ncbi


10.1016/j.ajo.2018.01.029

http://scihub22266oqcxt.onion/10.1016/j.ajo.2018.01.029
suck pdf from google scholar
29421294!5873517!29421294
unlimited free pdf from europmc29421294    free
PDF from PMC    free
html from PMC    free

Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=29421294&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215

suck abstract from ncbi

pmid29421294      Am+J+Ophthalmol 2018 ; 188 (?): 123-130
Nephropedia Template TP

gab.com Text

Twit Text FOAVip

Twit Text #

English Wikipedia


  • Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients With Cone-Rod Dystrophy and Amelogenesis Imperfecta #MMPMID29421294
  • Hirji N; Bradley PD; Li S; Vincent A; Pennesi ME; Thomas AS; Heon E; Bhan A; Mahroo OA; Robson A; Inglehearn CF; Moore AT; Michaelides M
  • Am J Ophthalmol 2018[Apr]; 188 (?): 123-130 PMID29421294show ga
  • PURPOSE: To characterize a series of 7 patients with cone-rod dystrophy (CORD) and amelogenesis imperfecta (AI) owing to confirmed mutations in CNNM4, first described as "Jalili Syndrome." DESIGN: Retrospective observational case series. METHODS: Seven patients from 6 families with Jalili Syndrome were identified at 3 tertiary referral centers. We systematically reviewed their available medical records, spectral-domain optical coherence tomography (SD-OCT), fundus autofluorescence imaging (FAF), color fundus photography, and electrophysiological assessments. RESULTS: The mean age at presentation was 6.7 years (range 3-16 years), with 6 male and 1 female patient. CNNM4 mutations were identified in all patients. The mean Snellen best-corrected visual acuity (BCVA) at presentation was 20/246 (range 20/98 to 20/399) in the right eye and 20/252 (range 20/98 to 20/480) in the left. Nystagmus was observed in all 7 patients, and photophobia was present in 6. Funduscopic findings at presentation were variable, ranging from only mild disc pallor to retinal vascular attenuation and macular atrophy. Multimodal imaging demonstrated disease progression in all 7 patients over time. Electroretinography uniformly revealed progressive cone-rod dysfunction. CONCLUSIONS: Jalili Syndrome is a rare CORD associated with AI. We have further characterized its ocular phenotype, including describing SD-OCT, FAF, and electrophysiological features; and report several novel disease-causing sequence variants. Moreover, this study presents novel longitudinal data demonstrating structural and functional progression over time, allowing better informed advice on prognosis.
  • |Adolescent[MESH]
  • |Amelogenesis Imperfecta/*diagnosis/genetics[MESH]
  • |Cation Transport Proteins/genetics[MESH]
  • |Child[MESH]
  • |Child, Preschool[MESH]
  • |Cone-Rod Dystrophies/*diagnosis/genetics[MESH]
  • |Cross-Sectional Studies[MESH]
  • |Electroretinography[MESH]
  • |Female[MESH]
  • |Fluorescein Angiography[MESH]
  • |Humans[MESH]
  • |Longitudinal Studies[MESH]
  • |Male[MESH]
  • |Multimodal Imaging[MESH]
  • |Mutation[MESH]
  • |Retrospective Studies[MESH]
  • |Tomography, Optical Coherence[MESH]


  • DeepDyve
  • Pubget Overpricing
  • suck abstract from ncbi

    Linkout box