Ellison DW - Search Results

1

Hereditary sensory and autonomic neuropathy with anhidrosis (type IV).

Haworth AE, Thomas NH, Cook LJ, Ellison DW, Walker J. Haworth AE, et al. Among authors: ellison dw. J R Soc Med. 1998 Feb;91(2):84-6. doi: 10.1177/014107689809100210. J R Soc Med. 1998. PMID: 9602746 Free PMC article. No abstract available.

2

A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome.

Chalmers RM, Lamont PJ, Nelson I, Ellison DW, Thomas NH, Harding AE, Hammans SR. Chalmers RM, et al. Among authors: ellison dw. Neurology. 1997 Aug;49(2):589-92. doi: 10.1212/wnl.49.2.589. Neurology. 1997. PMID: 9270602

3

February 2001: A 74 year old man with a history over 3 months of increasing dyspnea and malaise.

Baldwin L, Poller D, Ellison D. Baldwin L, et al. Brain Pathol. 2001 Jul;11(3):389-90; 393. Brain Pathol. 2001. PMID: 11414480

4

Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine-->serine (L250S) substitution at codon 250 of the presenilin 1 gene.

Harvey RJ, Ellison D, Hardy J, Hutton M, Roques PK, Collinge J, Fox NC, Rossor MN. Harvey RJ, et al. J Neurol Neurosurg Psychiatry. 1998 Jan;64(1):44-9. doi: 10.1136/jnnp.64.1.44. J Neurol Neurosurg Psychiatry. 1998. PMID: 9436726 Free PMC article.

5

A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathy.

Hammans SR, Robinson DO, Moutou C, Kennedy CR, Dennis NR, Hughes PJ, Ellison DW. Hammans SR, et al. Among authors: ellison dw. Neuromuscul Disord. 2000 Feb;10(2):133-7. doi: 10.1016/s0960-8966(99)00073-5. Neuromuscul Disord. 2000. PMID: 10714588

6

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia Caused by a Novel R782G Mutation in CSF1R.

Foulds N, Pengelly RJ, Hammans SR, Nicoll JA, Ellison DW, Ditchfield A, Beck S, Ennis S. Foulds N, et al. Among authors: ellison dw. Sci Rep. 2015 May 15;5:10042. doi: 10.1038/srep10042. Sci Rep. 2015. PMID: 25975230 Free PMC article.

7

Cortical myoclonus and cerebellar pathology.

Tijssen MA, Thom M, Ellison DW, Wilkins P, Barnes D, Thompson PD, Brown P. Tijssen MA, et al. Among authors: ellison dw. Neurology. 2000 Mar 28;54(6):1350-6. doi: 10.1212/wnl.54.6.1350. Neurology. 2000. PMID: 10746609

8

Alexander disease: ventricular garlands and abnormalities of the medulla and spinal cord.

van der Knaap MS, Ramesh V, Schiffmann R, Blaser S, Kyllerman M, Gholkar A, Ellison DW, van der Voorn JP, van Dooren SJ, Jakobs C, Barkhof F, Salomons GS. van der Knaap MS, et al. Among authors: ellison dw. Neurology. 2006 Feb 28;66(4):494-8. doi: 10.1212/01.wnl.0000198770.80743.37. Neurology. 2006. PMID: 16505300

9

Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum.

Bhatia KP, Brown P, Gregory R, Lennox GG, Manji H, Thompson PD, Ellison DW, Marsden CD. Bhatia KP, et al. Among authors: ellison dw. Brain. 1995 Oct;118 ( Pt 5):1087-93. doi: 10.1093/brain/118.5.1087. Brain. 1995. PMID: 7496772 Review.

10

Targeting of CCK-2 receptor-expressing tumors using a radiolabeled divalent gastrin peptide.

Sosabowski JK, Matzow T, Foster JM, Finucane C, Ellison D, Watson SA, Mather SJ. Sosabowski JK, et al. J Nucl Med. 2009 Dec;50(12):2082-9. doi: 10.2967/jnumed.109.064808. Epub 2009 Nov 12. J Nucl Med. 2009. PMID: 19910426 Free article.

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