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Items: 1 to 20 of 63

1.

The Assisted Dying Bill is not a UK bill.

Stephenson DA.

BMJ. 2015 Sep 8;351:h4768. doi: 10.1136/bmj.h4768. No abstract available.

PMID:
26350226
2.

Disrupted SOX10 function causes spongiform neurodegeneration in gray tremor mice.

Anderson SR, Lee I, Ebeling C, Stephenson DA, Schweitzer KM, Baxter D, Moon TM, LaPierre S, Jaques B, Silvius D, Wegner M, Hood LE, Carlson G, Gunn TM.

Mamm Genome. 2015 Feb;26(1-2):80-93. doi: 10.1007/s00335-014-9548-5. Epub 2014 Nov 16.

3.

Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemia.

Lee MJ, Chien KL, Chen MF, Stephenson DA, Su TC.

Clin Chim Acta. 2013 Feb 1;416:31-5. doi: 10.1016/j.cca.2012.10.054. Epub 2012 Nov 23.

PMID:
23178747
4.

Novel technique of total pancreatectomy before autologous islet transplants in chronic pancreatitis patients.

Desai CS, Stephenson DA, Khan KM, Jie T, Gruessner AC, Rilo HL, Gruessner RW.

J Am Coll Surg. 2011 Dec;213(6):e29-34. doi: 10.1016/j.jamcollsurg.2011.09.008. Epub 2011 Oct 13. No abstract available.

PMID:
21996486
5.

Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings.

Jacobi H, Hauser TK, Giunti P, Globas C, Bauer P, Schmitz-Hübsch T, Baliko L, Filla A, Mariotti C, Rakowicz M, Charles P, Ribai P, Szymanski S, Infante J, van de Warrenburg BP, Dürr A, Timmann D, Boesch S, Fancellu R, Rola R, Depondt C, Schöls L, Zdzienicka E, Kang JS, Ratzka S, Kremer B, Stephenson DA, Melegh B, Pandolfo M, Tezenas du Montcel S, Borkert J, Schulz JB, Klockgether T.

Cerebellum. 2012 Mar;11(1):155-66. doi: 10.1007/s12311-011-0292-z.

PMID:
21701895
6.

Phosphatase and tensin homologue on chromosome 10 (PTEN) directs prostaglandin E2-mediated fibroblast responses via regulation of E prostanoid 2 receptor expression.

Sagana RL, Yan M, Cornett AM, Tsui JL, Stephenson DA, Huang SK, Moore BB, Ballinger MN, Melonakos J, Kontos CD, Aronoff DM, Peters-Golden M, White ES.

J Biol Chem. 2009 Nov 20;284(47):32264-71. doi: 10.1074/jbc.M109.004796. Epub 2009 Oct 6.

7.

SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia.

Schmitz-Hübsch T, Giunti P, Stephenson DA, Globas C, Baliko L, Saccà F, Mariotti C, Rakowicz M, Szymanski S, Infante J, van de Warrenburg BP, Timmann D, Fancellu R, Rola R, Depondt C, Schöls L, Zdzienicka E, Kang JS, Döhlinger S, Kremer B, Melegh B, Filla A, Klockgether T.

Neurology. 2008 Aug 12;71(7):486-92. doi: 10.1212/01.wnl.0000324863.76290.19.

PMID:
18695159
8.

Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.

Schmitz-Hübsch T, Coudert M, Bauer P, Giunti P, Globas C, Baliko L, Filla A, Mariotti C, Rakowicz M, Charles P, Ribai P, Szymanski S, Infante J, van de Warrenburg BP, Dürr A, Timmann D, Boesch S, Fancellu R, Rola R, Depondt C, Schöls L, Zdienicka E, Kang JS, Döhlinger S, Kremer B, Stephenson DA, Melegh B, Pandolfo M, di Donato S, du Montcel ST, Klockgether T.

Neurology. 2008 Sep 23;71(13):982-9. doi: 10.1212/01.wnl.0000325057.33666.72. Epub 2008 Aug 6.

PMID:
18685131
9.

HMBS mutations in Chinese patients with acute intermittent porphyria.

Yang CC, Kuo HC, You HL, Wang J, Huang CC, Liu CY, Lan MY, Stephenson DA, Lee MJ.

Ann Hum Genet. 2008 Sep;72(Pt 5):683-6. doi: 10.1111/j.1469-1809.2008.00463.x.

10.

Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum.

Lee MJ, Cheng TW, Hua MS, Pan MK, Wang J, Stephenson DA, Yang CC.

J Neurol Neurosurg Psychiatry. 2008 May;79(5):607-9. doi: 10.1136/jnnp.2007.136390. No abstract available.

PMID:
18408091
11.

Recent developments in neurofibromatosis type 1.

Lee MJ, Stephenson DA.

Curr Opin Neurol. 2007 Apr;20(2):135-41. Review.

PMID:
17351482
12.

Characterization of a familial case with primary erythromelalgia from Taiwan.

Lee MJ, Yu HS, Hsieh ST, Stephenson DA, Lu CJ, Yang CC.

J Neurol. 2007 Feb;254(2):210-4. Epub 2007 Feb 8.

PMID:
17294067
13.

Modulation of monocyte function by activated protein C, a natural anticoagulant.

Stephenson DA, Toltl LJ, Beaudin S, Liaw PC.

J Immunol. 2006 Aug 15;177(4):2115-22.

14.

Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1.

Lee MJ, Su YN, You HL, Chiou SC, Lin LC, Yang CC, Lee WC, Hwu WL, Hsieh FJ, Stephenson DA, Yu CL.

Hum Mutat. 2006 Aug;27(8):832.

PMID:
16835897
15.

Performance of galanin transgenic mice in the 5-choice serial reaction time attentional task.

Wrenn CC, Turchi JN, Schlosser S, Dreiling JL, Stephenson DA, Crawley JN.

Pharmacol Biochem Behav. 2006 Mar;83(3):428-40. Epub 2006 Apr 19.

PMID:
16626795
16.

Economic evaluation of gemcitabine in the treatment of pancreatic cancer in the UK.

Aristides M, Lees M, Botwood N, McKendrick J, Stephenson DA, Maniadakis N.

Eur J Health Econ. 2003 Sep;4(3):216-21. Epub 2003 Jul 1.

PMID:
15609188
17.

Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene.

Lee MJ, Stephenson DA, Groves MJ, Sweeney MG, Davis MB, An SF, Houlden H, Salih MA, Timmerman V, de Jonghe P, Auer-Grumbach M, Di Maria E, Scaravilli F, Wood NW, Reilly MM.

Hum Mol Genet. 2003 Aug 1;12(15):1917-25.

PMID:
12874111
18.

The impact of antidepressants on sleep and anxiety: a comparative study of fluoxetine and dothiepin using the Leeds Sleep Evaluation Questionnaire.

Stephenson DA, Harris B, Davies RH, Mullin JM, Richardson E, Boardman H, Meanley D, Banerjee A.

Hum Psychopharmacol. 2000 Oct;15(7):529-534.

PMID:
12404623
19.

Quantitative trait loci affecting prion incubation time in mice.

Stephenson DA, Chiotti K, Ebeling C, Groth D, DeArmond SJ, Prusiner SB, Carlson GA.

Genomics. 2000 Oct 1;69(1):47-53.

PMID:
11013074
20.

Report and abstracts of the Sixth International Workshop on chromosome 9.

Chadwick BP, Campbell LJ, Jackson CL, Ozelius L, Slaugenhaupt SA, Stephenson DA, Edwards JH, Wiest J, Povey S.

Ann Hum Genet. 1999 Mar;63(Pt 2):101-24.

PMID:
10738523

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