Al-Sarraj S - Search Results

1

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.

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

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.

5

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

6

Riluzole treatment, survival and diagnostic criteria in Parkinson plus disorders: the NNIPPS study.

Bensimon G, Ludolph A, Agid Y, Vidailhet M, Payan C, Leigh PN; NNIPPS Study Group. Bensimon G, et al. Brain. 2009 Jan;132(Pt 1):156-71. doi: 10.1093/brain/awn291. Epub 2008 Nov 23. Brain. 2009. PMID: 19029129 Free PMC article. Clinical Trial.

7

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

8

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.

9

Abnormal TDP-43 expression is identified in the neocortex in cases of dementia pugilistica, but is mainly confined to the limbic system when identified in high and moderate stages of Alzheimer's disease.

King A, Sweeney F, Bodi I, Troakes C, Maekawa S, Al-Sarraj S. King A, et al. Neuropathology. 2010 Aug;30(4):408-19. doi: 10.1111/j.1440-1789.2009.01085.x. Epub 2010 Jan 19. Neuropathology. 2010. PMID: 20102526

10

Cognitive impairment in patients with multiple system atrophy and progressive supranuclear palsy.

Brown RG, Lacomblez L, Landwehrmeyer BG, Bak T, Uttner I, Dubois B, Agid Y, Ludolph A, Bensimon G, Payan C, Leigh NP; NNIPPS Study Group. Brown RG, et al. Brain. 2010 Aug;133(Pt 8):2382-93. doi: 10.1093/brain/awq158. Epub 2010 Jun 24. Brain. 2010. PMID: 20576697 Free article. Clinical Trial.

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