Zobrazeno 1 - 10
of 51
pro vyhledávání: '"intracerebral calcification"'
Publikováno v:
Frontiers in Human Neuroscience, Vol 18 (2024)
Fahr’s disease (FD), otherwise known as primary familial brain calcification, is a rare neurodegenerative condition that involves intracerebral calcification at the level of the basal ganglia and other brain regions. It is an inherited neurologic d
Externí odkaz:
https://doaj.org/article/2130bb2308b4486a9979514f2ede192d
Delayed awakening from general anesthesia revealing Fahr syndrome: Case report and literature review
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 3336-3338 (2020)
Abstract Fahr syndrome (FS) is defined by the presence of bilateral and symmetrical intracerebral nonarteriosclerotic calcifications, localized in the central gray nuclei. We report the case of a patient who presented a postoperative delay in awakeni
Externí odkaz:
https://doaj.org/article/4f112f899b6d407fb671453f18715bc0
Akademický článek
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Autor:
Fatima El Boukhrissi, Ghizlane Zoulati, Issam En-nafaa, Hassan Ouleghzal, Sara Derrou, Soumaya Safi, Youssef Bamou, Lhoussine Balouch
Publikováno v:
The Pan African Medical Journal, Vol 26, Iss 2 (2017)
Le syndrome de Fahr est une entité anatomoclinique rare dont la principale étiologie est l'hypoparathyroïdie primitive ou postopératoire. Il est caractérisé par des calcifications intracérébrales bilatérales et symétriques, localisées dans
Externí odkaz:
https://doaj.org/article/81f385c196da48f989a757ad48ed5ef7
Delayed awakening from general anesthesia revealing Fahr syndrome: Case report and literature review
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 8, Iss 12, Pp 3336-3338 (2020)
Clinical Case Reports, Vol 8, Iss 12, Pp 3336-3338 (2020)
Fahr syndrome (FS) is defined by the presence of bilateral and symmetrical intracerebral nonarteriosclerotic calcifications, localized in the central gray nuclei. We report the case of a patient who presented a postoperative delay in awakening and wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::addcf421ccea6eda6dd397f5d94799ef
https://doi.org/10.1002/ccr3.3183
https://doi.org/10.1002/ccr3.3183
Publikováno v:
Journal of Epilepsy Research
Toxoplasmosis is a rare disease caused by intracellular protozoan parasite, Toxoplasma gondii. Though most patients with toxoplasmosis are asymptomatic, congenital toxoplasmosis in the fetus can cause ocular involvement such as chorioretinitis and ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73a1aeb6660938303bec74beba6ad4f7
https://doi.org/10.14581/jer.15007
https://doi.org/10.14581/jer.15007
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
S. Derrou, Youssef Bamou, L. Balouch, Soumaya Safi, Ghizlane Zoulati, Fatima El Boukhrissi, I. En-Nafaa, H. Ouleghzal
Publikováno v:
The Pan African Medical Journal, Vol 26, Iss 2 (2017)
Le syndrome de Fahr est une entité anatomoclinique rare dont la principale étiologie est l'hypoparathyroïdie primitive ou postopératoire. Il est caractérisé par des calcifications intracérébrales bilatérales et symétriques, localisées dans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9c54aad2fcea65a1a47de7e74d9d9d6
https://doi.org/10.11604/pamj.2017.26.2.10689
https://doi.org/10.11604/pamj.2017.26.2.10689
Autor:
Moushumi, Lodh, Rajarshi, Mukhopadhyay
Publikováno v:
EJIFCC
Absent or inappropriately low intact parathyroid hormone along with hypocalcemia is the diagnostic criterion of hypoparathyroidism. Clinically, hypoparathyroidism manifests predominantly as neuromuscular dysfunction caused by hypocalcemia. We present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85060ad08bdec60da67ef1fd31f41456
http://europepmc.org/articles/PMC4975295
http://europepmc.org/articles/PMC4975295
Autor:
Fatima, El Boukhrissi, Ghizlane, Zoulati, Issam, En-Nafaa, Hassan, Ouleghzal, Sara, Derrou, Soumaya, Safi, Youssef, Bamou, Lhoussine, Balouch
Publikováno v:
The Pan African Medical Journal
Le syndrome de Fahr est une entité anatomoclinique rare dont la principale étiologie est l'hypoparathyroïdie primitive ou postopératoire. Il est caractérisé par des calcifications intracérébrales bilatérales et symétriques, localisées dans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ab0c9244332b968645577cf135267c69
https://pubmed.ncbi.nlm.nih.gov/28450981
https://pubmed.ncbi.nlm.nih.gov/28450981