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162 related items for 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 [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 [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 [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 [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 27; 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 27; 117(12):2087-92. PubMed ID: 17921903 [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 27; 64(6):843-8. PubMed ID: 17562932 [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 15; 267(1-2):177-81. PubMed ID: 18035376 [Abstract] [Full Text] [Related]
10. [Cerebral cavernous malformation--its genetic and biological background]. Fujimura M, Tominaga T. Brain Nerve; 2008 Nov 15; 60(11):1271-4. PubMed ID: 19069160 [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 15; 147(10):1097-101; discussion 1101. PubMed ID: 16021386 [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 15; 21(1):e15. PubMed ID: 16859253 [Abstract] [Full Text] [Related]
13. Recent insights into cerebral cavernous malformations. Faurobert E. FEBS J; 2010 Mar 15; 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 15; 59(6):1278-84; discussion 1284-5. PubMed ID: 17277691 [Abstract] [Full Text] [Related]
15. [Genetics of cerebral cavernous malformations (CCM)]. Felbor U. Dtsch Med Wochenschr; 2007 Sep 15; 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 15; 27(4):157-9. PubMed ID: 17148043 [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 15; 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 15; 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 15; 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 Dec 15; 40(3):290-4. PubMed ID: 20689144 [Abstract] [Full Text] [Related] Page: [Next] [New Search]