Fedi M - Search Results

1

Spontaneous intracranial hypotension presenting as a reversible dorsal midbrain syndrome.

Fedi M, Cantello R, Shuey NH, Mitchell LA, Comi C, Monaco F, Versino M. Fedi M, et al. J Neuroophthalmol. 2008 Dec;28(4):289-92. doi: 10.1097/WNO.0b013e31818eb48d. J Neuroophthalmol. 2008. PMID: 19145127

2

Cystic meningioangiomatosis in neurofibromatosis type 2: an MRI-pathological study.

Fedi M, Kalnins RM, Shuey N, Fitt GJ, Newton M, Mitchell LA. Fedi M, et al. Br J Radiol. 2009 Jul;82(979):e129-32. doi: 10.1259/bjr/56536580. Br J Radiol. 2009. PMID: 19541939

3

Glioneuronal tumours in neurofibromatosis type 1: MRI-pathological study.

Fedi M, Anne Mitchell L, Kalnins RM, Gutmann DH, Perry A, Newton M, Brodtmann A, Berkovic SF. Fedi M, et al. J Clin Neurosci. 2004 Sep;11(7):745-7. doi: 10.1016/j.jocn.2003.10.017. J Clin Neurosci. 2004. PMID: 15337138

4

A GABAA receptor mutation causing generalized epilepsy reduces benzodiazepine receptor binding.

Fedi M, Berkovic SF, Marini C, Mulligan R, Tochon-Danguy H, Reutens DC. Fedi M, et al. Neuroimage. 2006 Sep;32(3):995-1000. doi: 10.1016/j.neuroimage.2006.05.059. Epub 2006 Jul 27. Neuroimage. 2006. PMID: 16875845

5

Association of a nicotinic receptor mutation with reduced height and blunted physostigmine-stimulated growth hormone release.

Fedi M, Bach LA, Berkovic SF, Willoughby JO, Scheffer IE, Reutens DC. Fedi M, et al. J Clin Endocrinol Metab. 2008 Feb;93(2):634-7. doi: 10.1210/jc.2007-1611. Epub 2007 Nov 27. J Clin Endocrinol Metab. 2008. PMID: 18042647

6

Intracortical hyperexcitability in humans with a GABAA receptor mutation.

Fedi M, Berkovic SF, Macdonell RA, Curatolo JM, Marini C, Reutens DC. Fedi M, et al. Cereb Cortex. 2008 Mar;18(3):664-9. doi: 10.1093/cercor/bhm100. Epub 2007 Jul 5. Cereb Cortex. 2008. PMID: 17615250

7

Exercise-induced temporal lobe epilepsy.

Sturm JW, Fedi M, Berkovic SF, Reutens DC. Sturm JW, et al. Among authors: fedi m. Neurology. 2002 Oct 22;59(8):1246-8. doi: 10.1212/wnl.59.8.1246. Neurology. 2002. PMID: 12391356

8

alpha-[11C]-Methyl-L-tryptophan PET identifies the epileptogenic tuber and correlates with interictal spike frequency.

Fedi M, Reutens DC, Andermann F, Okazawa H, Boling W, White C, Dubeau F, Nakai A, Gross DW, Andermann E, Diksic M. Fedi M, et al. Epilepsy Res. 2003 Jan;52(3):203-13. doi: 10.1016/s0920-1211(02)00216-4. Epilepsy Res. 2003. PMID: 12536053

9

Neuropsychological function in patients with a single gene mutation associated with autosomal dominant nocturnal frontal lobe epilepsy.

Wood AG, Saling MM, Fedi M, Berkovic SF, Scheffer IE, Benjamin C, Reutens DC. Wood AG, et al. Among authors: fedi m. Epilepsy Behav. 2010 Apr;17(4):531-5. doi: 10.1016/j.yebeh.2010.01.168. Epub 2010 Feb 26. Epilepsy Behav. 2010. PMID: 20189461

10

Reduced striatal D1 receptor binding in autosomal dominant nocturnal frontal lobe epilepsy.

Fedi M, Berkovic SF, Scheffer IE, O'Keefe G, Marini C, Mulligan R, Gong S, Tochon-Danguy H, Reutens DC. Fedi M, et al. Neurology. 2008 Sep 9;71(11):795-8. doi: 10.1212/01.wnl.0000316192.52731.77. Epub 2008 Aug 6. Neurology. 2008. PMID: 18685138

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