Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rula Hajj Ali"'
Autor:
Parul H, Kothari, Grant R, Kolar, Joanna C, Jen, Rula, Hajj-Ali, Paula, Bertram, Robert E, Schmidt, John P, Atkinson
Publikováno v:
Brain pathology (Zurich, Switzerland)
Background: Mutations in the three-prime repair exonuclease 1 (TREX1) gene have been associated with neurological diseases, including Retinal Vasculopathy with Cerebral Leukoencephalopathy (RVCL). However, the endogenous expression of TREX1 in human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d544e68b334d44a32980b5343a2f6123
https://pubmed.ncbi.nlm.nih.gov/30062819
https://pubmed.ncbi.nlm.nih.gov/30062819
Autor:
Aaron M. Gruver, E. Rene Rodriguez, Lynn Schoenfield, Rula Hajj-Ali, Carmela D. Tan, Joshua F. Coleman
Publikováno v:
Journal of Neuro-Ophthalmology. 31:20-24
Autosomal dominant retinocerebral vasculopathy with cerebral leukodystrophy (RVCL) is a rare neurovascular syndrome causing retinal and central nervous system vasculopathy often recognized as contrast-enhancing white matter changes or pseudotumors on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d91663cb02d0e20cafd73dc3d5917f1
https://doi.org/10.1097/wno.0b013e3181f45dba
https://doi.org/10.1097/wno.0b013e3181f45dba
Publikováno v:
Rheumatology International. 32:737-742
To present three rare mimics of primary angiitis of the central nervous system (PACNS). We describe 3 patients with rare diseases that can mimic PACNS at clinical presentation and neuroimaging. We describe the clinical course of these patients and al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72444884084db5e2dff9bd7be5ae8c68
https://doi.org/10.1007/s00296-010-1679-8
https://doi.org/10.1007/s00296-010-1679-8
Autor:
Seby John, Belinda Willard, Leonard Calabrese, Tariq Hammad, Ken Uchino, Stewart Tepper, Mark Stillman, Rula Hajj-Ali
Publikováno v:
Stroke. 45
Background: The pathophysiology and molecular mechanisms of Reversible Cerebral Vasoconstriction Syndrome (RCVS) are unknown. Objective of the study was to identify putative biomarker proteins for RCVS. Methods: Patients were recruited from our insti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::422b5b5a52e85f4a7d34fb3d84e529c2
https://doi.org/10.1161/str.45.suppl_1.tp172
https://doi.org/10.1161/str.45.suppl_1.tp172