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Journal Abstract Search

253 related items for PubMed ID: 31065320

  • 1. [Sporadic cerebral cavernous malformation revealed by seizure: case study].
    Amadou D, Youssouf K, Oumou M, Abdoulaye K, Bréhima D, Adama D, Mamahadou D.
    Pan Afr Med J; 2018; 31():162. PubMed ID: 31065320
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  • 3. Lingual Seizures Due to Familial Cerebral Cavernous Malformations.
    Rao CK, Sheth RD.
    Pediatr Neurol; 2021 May; 118():46-47. PubMed ID: 33773290
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  • 6. Multiple cerebral cavernous malformations: Clinical course of confirmed, assumed and non-familial disease.
    Santos AN, Rauschenbach L, Saban D, Chen B, Darkwah Oppong M, Herten A, Gull HH, Rieß C, Deuschl C, Schmidt B, Jabbarli R, Wrede KH, Zhu Y, Frank B, Sure U, Dammann P.
    Eur J Neurol; 2022 May; 29(5):1427-1434. PubMed ID: 35060255
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  • 9. Value of gradient-echo magnetic resonance imaging in the diagnosis of familial cerebral cavernous malformation.
    Lehnhardt FG, von Smekal U, Rückriem B, Stenzel W, Neveling M, Heiss WD, Jacobs AH.
    Arch Neurol; 2005 Apr; 62(4):653-8. PubMed ID: 15824268
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  • 12. Prognostic factors for post-operative seizure outcomes after cavernous malformation treatment.
    Kim W, Stramotas S, Choy W, Dye J, Nagasawa D, Yang I.
    J Clin Neurosci; 2011 Jul; 18(7):877-80. PubMed ID: 21561775
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  • 13. Hereditary cerebral cavernous angiomas: presentation as idiopathic familial epilepsy.
    Coghlan D, Lynch B, Allcutt D.
    Ir Med J; 2002 Feb; 95(2):56-8. PubMed ID: 11989951
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  • 15. Ascending Spinal Cord Infarction Secondary to Recurrent Spinal Cord Cavernous Malformation Hemorrhage.
    Huntley GD, Ruff MW, Hicks SB, Yost MD, Fulgham JR.
    J Stroke Cerebrovasc Dis; 2017 Apr; 26(4):e72-e73. PubMed ID: 28236596
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  • 16. Familial Cerebral Cavernous Malformations Are Associated with Adrenal Calcifications on CT Scans: An Imaging Biomarker for a Hereditary Cerebrovascular Condition.
    Strickland CD, Eberhardt SC, Bartlett MR, Nelson J, Kim H, Morrison LA, Hart BL.
    Radiology; 2017 Aug; 284(2):443-450. PubMed ID: 28318403
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  • 20. Cerebral cavernous malformation type 1 with retinal blood vessel tortuosity and KRIT1 gene mutation.
    Kalmár T, Maróti Z, Vadvári Á, Halmosi Á, Kálovits F, Kálmán B.
    Ideggyogy Sz; 2019 Jul 30; 72(7-8):273-277. PubMed ID: 31517460
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