Al-Sarraj S - Search Results

1

Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration.

Rohrer JD, Lashley T, Schott JM, Warren JE, Mead S, Isaacs AM, Beck J, Hardy J, de Silva R, Warrington E, Troakes C, Al-Sarraj S, King A, Borroni B, Clarkson MJ, Ourselin S, Holton JL, Fox NC, Revesz T, Rossor MN, Warren JD. Rohrer JD, et al. Brain. 2011 Sep;134(Pt 9):2565-81. doi: 10.1093/brain/awr198. Brain. 2011. PMID: 21908872 Free PMC article.

2

Sporadic and familial dementia with ubiquitin-positive tau-negative inclusions: clinical features of one histopathological abnormality underlying frontotemporal lobar degeneration.

Godbolt AK, Josephs KA, Revesz T, Warrington EK, Lantos P, King A, Fox NC, Al Sarraj S, Holton J, Cipolotti L, Khan MN, Rossor MN. Godbolt AK, et al. Arch Neurol. 2005 Jul;62(7):1097-101. doi: 10.1001/archneur.62.7.1097. Arch Neurol. 2005. PMID: 16009765

3

Magnetic resonance imaging signatures of tissue pathology in frontotemporal dementia.

Whitwell JL, Josephs KA, Rossor MN, Stevens JM, Revesz T, Holton JL, Al-Sarraj S, Godbolt AK, Fox NC, Warren JD. Whitwell JL, et al. Arch Neurol. 2005 Sep;62(9):1402-8. doi: 10.1001/archneur.62.9.1402. Arch Neurol. 2005. PMID: 16157747

4

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.

Beck J, Rohrer JD, Campbell T, Isaacs A, Morrison KE, Goodall EF, Warrington EK, Stevens J, Revesz T, Holton J, Al-Sarraj S, King A, Scahill R, Warren JD, Fox NC, Rossor MN, Collinge J, Mead S. Beck J, et al. Brain. 2008 Mar;131(Pt 3):706-20. doi: 10.1093/brain/awm320. Epub 2008 Jan 29. Brain. 2008. PMID: 18234697 Free PMC article.

5

Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium.

Alafuzoff I, Arzberger T, Al-Sarraj S, Bodi I, Bogdanovic N, Braak H, Bugiani O, Del-Tredici K, Ferrer I, Gelpi E, Giaccone G, Graeber MB, Ince P, Kamphorst W, King A, Korkolopoulou P, Kovács GG, Larionov S, Meyronet D, Monoranu C, Parchi P, Patsouris E, Roggendorf W, Seilhean D, Tagliavini F, Stadelmann C, Streichenberger N, Thal DR, Wharton SB, Kretzschmar H. Alafuzoff I, et al. Brain Pathol. 2008 Oct;18(4):484-96. doi: 10.1111/j.1750-3639.2008.00147.x. Epub 2008 Mar 26. Brain Pathol. 2008. PMID: 18371174 Free PMC article.

6

Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene.

Rohrer JD, Warren JD, Omar R, Mead S, Beck J, Revesz T, Holton J, Stevens JM, Al-Sarraj S, Pickering-Brown SM, Hardy J, Fox NC, Collinge J, Warrington EK, Rossor MN. Rohrer JD, et al. Arch Neurol. 2008 Apr;65(4):506-13. doi: 10.1001/archneur.65.4.506. Arch Neurol. 2008. PMID: 18413474 Free PMC article.

7

Frontotemporal lobar degeneration with ubiquitinated tau-negative inclusions and additional alpha-synuclein pathology but also unusual cerebellar ubiquitinated p62-positive, TDP-43-negative inclusions.

King A, Al-Sarraj S, Shaw C. King A, et al. Neuropathology. 2009 Aug;29(4):466-71. doi: 10.1111/j.1440-1789.2008.00966.x. Epub 2008 Aug 18. Neuropathology. 2009. PMID: 18715271

8

Mixed brain pathologies in dementia: the BrainNet Europe consortium experience.

Kovacs GG, Alafuzoff I, Al-Sarraj S, Arzberger T, Bogdanovic N, Capellari S, Ferrer I, Gelpi E, Kövari V, Kretzschmar H, Nagy Z, Parchi P, Seilhean D, Soininen H, Troakes C, Budka H. Kovacs GG, et al. Dement Geriatr Cogn Disord. 2008;26(4):343-50. doi: 10.1159/000161560. Epub 2008 Oct 10. Dement Geriatr Cogn Disord. 2008. PMID: 18849605 Free article.

9

TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations.

Maekawa S, Leigh PN, King A, Jones E, Steele JC, Bodi I, Shaw CE, Hortobagyi T, Al-Sarraj S. Maekawa S, et al. Neuropathology. 2009 Dec;29(6):672-83. doi: 10.1111/j.1440-1789.2009.01029.x. Epub 2009 Jun 3. Neuropathology. 2009. PMID: 19496940

10

Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation.

Rohrer JD, Beck J, Warren JD, King A, Al Sarraj S, Holton J, Revesz T, Collinge J, Mead S. Rohrer JD, et al. J Neurol Neurosurg Psychiatry. 2009 Nov;80(11):1297-8. doi: 10.1136/jnnp.2008.169383. J Neurol Neurosurg Psychiatry. 2009. PMID: 19864668 No abstract available.

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