Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Javed L Khanni"'
Publikováno v:
Cureus
Leber hereditary optic neuropathy (LHON) is a genetic condition that typically presents with unilateral, painless, sub-acute central vision loss followed by contralateral vision loss after a few weeks to months. It is a rare disease that typically af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f734d3872bfdf823c5035d8984c27608
https://doi.org/10.7759/cureus.7745
https://doi.org/10.7759/cureus.7745
Publikováno v:
Cureus
The proverbial "zebras" in neurology are often times missed due to their low prevalence and incidence in the community. The number of misdiagnoses and improper therapeutic interventions that occur are further increased when patients with these rare d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd2324e20d9a059fb6aada1ddcbb7eaa
http://europepmc.org/articles/PMC7243655
http://europepmc.org/articles/PMC7243655
Autor:
Kettia Alusma-Hibbert, Javed L Khanni, Kimberly Herard, Courtland R Samuels, Patricio S Espinosa
Publikováno v:
Cureus
Anti-glutamic acid decarboxylase (GAD) antibodies have been discovered in a variety of neurological syndromes with unique presentations. These syndromes include limbic encephalitis (LE), stiff person syndrome (SPS), opsoclonus-myoclonus-ataxia syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5042baa2b347db6df9a50af2bae6711
https://doi.org/10.7759/cureus.4738
https://doi.org/10.7759/cureus.4738
Publikováno v:
Cureus
Idiopathic basal ganglia calcification (IBGC), commonly referred to as Fahr's disease, is a rare neurological disorder characterized by the abnormal, symmetrical, and bilateral calcification of the basal ganglia and other brain regions. Patients typi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79e6078334acf2fa9f818e5029ca259c
http://europepmc.org/articles/PMC6367120
http://europepmc.org/articles/PMC6367120
Publikováno v:
Blood. 136:13-13
Moyamoya disease, well described in literature, is a chronic cerebrovascular occlusive disorder. It is characterized by progressive stenosis/occlusion of the terminal portions of the internal carotid arteries (ICA) and the proximal portions of the mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6628155acb1975d032230cf1d0da853
https://doi.org/10.1182/blood-2020-134202
https://doi.org/10.1182/blood-2020-134202
Artery of Percheron Infarct: An Acute Diagnostic Challenge with a Spectrum of Clinical Presentations
Autor:
Patricio H Espinosa Del Pozo, Joel Casale, Patricio S Espinosa, Adriana Y Koek, Javed L Khanni
Publikováno v:
Cureus
The artery of Percheron (AOP) is a variant of the paramedian thalamic vasculature that supplies blood to the medial aspect of the thalamus and the rostral midbrain. The presentation of an infarct in this territory varies widely and is often character
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81827d755a4942c90dce53be3624691d
http://europepmc.org/articles/PMC6235647
http://europepmc.org/articles/PMC6235647