166 related articles for article (PubMed ID: 16450046)
1. Cavernous malformation within a schwannoma: review of the literature and hypothesis of a common genetic etiology.
Feiz-Erfan I; Zabramski JM; Herrmann LL; Coons SW
Acta Neurochir (Wien); 2006 Jun; 148(6):647-52; discussion 652. PubMed ID: 16450046
[TBL] [Abstract][Full Text] [Related]
2. Cavernous malformation of the internal auditory canal.
Di Rocco F; Paterno V; Safavi-Abbasi S; El-Shawarby A; Samii A; Samii M
Acta Neurochir (Wien); 2006 Jun; 148(6):695-7. PubMed ID: 16572279
[TBL] [Abstract][Full Text] [Related]
3. Cavernous malformation of the trigeminal nerve manifesting with trigeminal neuralgia: case report.
Deshmukh VR; Hott JS; Tabrizi P; Nakaji P; Feiz-Erfan I; Spetzler RF
Neurosurgery; 2005 Mar; 56(3):E623; discussion E623. PubMed ID: 15730590
[TBL] [Abstract][Full Text] [Related]
4. Extra-axial cavernomas of the cerebellopontine angle involving the seventh-eighth nerve complex.
Beskonakli E; Kaptanoglu E; Okutan O; Solaroglu I; Taskin Y
Neurosurg Rev; 2002 Aug; 25(4):222-4. PubMed ID: 12172728
[TBL] [Abstract][Full Text] [Related]
5. Novel CCM1 mutation in a patient with paraparesis and thoracic cord cavernous malformation.
Waters MF; Shields DC; Martin NA; Baloh RW; Jen JC
Neurology; 2005 Sep; 65(6):966-7. PubMed ID: 16186553
[No Abstract] [Full Text] [Related]
6. Nerve of origin, tumor size, hearing preservation, and facial nerve outcomes in 359 vestibular schwannoma resections at a tertiary care academic center.
Jacob A; Robinson LL; Bortman JS; Yu L; Dodson EE; Welling DB
Laryngoscope; 2007 Dec; 117(12):2087-92. PubMed ID: 17921903
[TBL] [Abstract][Full Text] [Related]
7. Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation.
Battistini S; Rocchi R; Cerase A; Citterio A; Tassi L; Lando G; Patrosso MC; Galli R; Brunori P; Sgrò DL; Pitillo G; Lo Russo G; Marocchi A; Penco S
Arch Neurol; 2007 Jun; 64(6):843-8. PubMed ID: 17562932
[TBL] [Abstract][Full Text] [Related]
8. CCM3 mutations are uncommon in cerebral cavernous malformations.
Verlaan DJ; Roussel J; Laurent SB; Elger CE; Siegel AM; Rouleau GA
Neurology; 2005 Dec; 65(12):1982-3. PubMed ID: 16380626
[TBL] [Abstract][Full Text] [Related]
9. Identification of an Arg35X mutation in the PDCD10 gene in a patient with cerebral and multiple spinal cavernous malformations.
Lee ST; Choi KW; Yeo HT; Kim JW; Ki CS; Cho YD
J Neurol Sci; 2008 Apr; 267(1-2):177-81. PubMed ID: 18035376
[TBL] [Abstract][Full Text] [Related]
10. [Cerebral cavernous malformation--its genetic and biological background].
Fujimura M; Tominaga T
Brain Nerve; 2008 Nov; 60(11):1271-4. PubMed ID: 19069160
[TBL] [Abstract][Full Text] [Related]
11. Cavernous malformation after radiation therapy for astrocytoma in adult patients: report of 2 cases.
Furuse M; Miyatake SI; Kuroiwa T
Acta Neurochir (Wien); 2005 Oct; 147(10):1097-101; discussion 1101. PubMed ID: 16021386
[TBL] [Abstract][Full Text] [Related]
12. Bleeding of a familial cerebral cavernous malformation after prophylactic anticoagulation therapy. Case report.
Pozzati E; Zucchelli M; Marliani AF; Riccioli LA
Neurosurg Focus; 2006 Jul; 21(1):e15. PubMed ID: 16859253
[TBL] [Abstract][Full Text] [Related]
13. Recent insights into cerebral cavernous malformations.
Faurobert E
FEBS J; 2010 Mar; 277(5):1069. PubMed ID: 20096039
[No Abstract] [Full Text] [Related]
14. Spectrum of genotype and clinical manifestations in cerebral cavernous malformations.
Gault J; Sain S; Hu LJ; Awad IA
Neurosurgery; 2006 Dec; 59(6):1278-84; discussion 1284-5. PubMed ID: 17277691
[TBL] [Abstract][Full Text] [Related]
15. [Genetics of cerebral cavernous malformations (CCM)].
Felbor U
Dtsch Med Wochenschr; 2007 Sep; 132(38):1967-70. PubMed ID: 17853352
[No Abstract] [Full Text] [Related]
16. A splice-site mutation in CCM1/KRIT1 is associated with retinal and cerebral cavernous hemangioma.
Kitzmann AS; Pulido JS; Ferber MJ; Highsmith WE; Babovic-Vuksanovic D
Ophthalmic Genet; 2006 Dec; 27(4):157-9. PubMed ID: 17148043
[TBL] [Abstract][Full Text] [Related]
17. Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Limaye N; Revencu N; Van Regemorter N; Garzon M; Bonduelle M; Chung W; Daras MD; Fahey MC; Garrett C; Gillerot Y; Gillessen-Kaesbach G; Giménez-Arnau A; Guzzetta F; Battaglia D; Heimda K; Lissens W; Taub E; Van Maldergem L; Van Paesschen W; Wieczorek D; Wood NW; Boon L; Vikkula M
Hum Genet; 2007 Dec; 122(5):549. PubMed ID: 18380023
[No Abstract] [Full Text] [Related]
18. Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Limaye N; Revencu N; Van Regemorter N; Garzon M; Bonduelle M; Chung W; Daras MD; Fahey MC; Garrett C; Gillerot Y; Gillessen-Kaesbach G; Giménez-Arnau A; Guzzetta F; Battaglia D; Heimda K; Lissens W; Taub E; Van Maldergem L; Van Paesschen W; Wieczorek D; Wood NW; Boon L; Vikkula M
Hum Genet; 2007 Dec; 122(5):549-50. PubMed ID: 18383587
[No Abstract] [Full Text] [Related]
19. Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Limaye N; Revencu N; Van Regemorter N; Garzon M; Bonduelle M; Chung W; Daras MD; Fahey MC; Garrett C; Gillerot Y; Gillessen-Kaesbach G; Giménez-Arnau A; Guzzetta F; Battaglia D; Heimdal K; Lissens W; Taub E; Van Maldergem L; Van Paesschen W; Wieczorek D; Wood NW; Boon L; Vikkula M
Hum Genet; 2007 Dec; 122(5):551. PubMed ID: 18383595
[No Abstract] [Full Text] [Related]
20. A novel KRIT1 gene mutation in a patient with cerebral and multiple spinal cavernous malformations.
Lee YW; Lee ST; Cha JG; Park JH; Jeon BR; Lee YK; Kim JW; Ki CS
Ann Clin Lab Sci; 2010; 40(3):290-4. PubMed ID: 20689144
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]