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Results: 1 to 20 of 49

1.

Self-organization in autonomous, recurrent, firing-rate CrossNets with quasi-Hebbian plasticity.

Walls TJ, Likharev KK.

IEEE Trans Neural Netw Learn Syst. 2014 Apr;25(4):819-24. doi: 10.1109/TNNLS.2013.2280904.

PMID:
24807958
2.

Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1.

Finlayson S, Palace J, Belaya K, Walls TJ, Norwood F, Burke G, Holton JL, Pascual-Pascual SI, Cossins J, Beeson D.

J Neurol Neurosurg Psychiatry. 2013 Oct;84(10):1119-25. doi: 10.1136/jnnp-2012-304716. Epub 2013 Feb 27.

PMID:
23447650
3.

Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates.

Belaya K, Finlayson S, Slater CR, Cossins J, Liu WW, Maxwell S, McGowan SJ, Maslau S, Twigg SR, Walls TJ, Pascual Pascual SI, Palace J, Beeson D.

Am J Hum Genet. 2012 Jul 13;91(1):193-201. doi: 10.1016/j.ajhg.2012.05.022. Epub 2012 Jun 27.

4.

Long-term risk of carotid restenosis in patients randomly assigned to endovascular treatment or endarterectomy in the Carotid and Vertebral Artery Transluminal Angioplasty Study (CAVATAS): long-term follow-up of a randomised trial.

Bonati LH, Ederle J, McCabe DJ, Dobson J, Featherstone RL, Gaines PA, Beard JD, Venables GS, Markus HS, Clifton A, Sandercock P, Brown MM; CAVATAS Investigators.

Lancet Neurol. 2009 Oct;8(10):908-17. doi: 10.1016/S1474-4422(09)70227-3. Epub 2009 Aug 28.

5.

Endovascular treatment with angioplasty or stenting versus endarterectomy in patients with carotid artery stenosis in the Carotid and Vertebral Artery Transluminal Angioplasty Study (CAVATAS): long-term follow-up of a randomised trial.

Ederle J, Bonati LH, Dobson J, Featherstone RL, Gaines PA, Beard JD, Venables GS, Markus HS, Clifton A, Sandercock P, Brown MM; CAVATAS Investigators.

Lancet Neurol. 2009 Oct;8(10):898-907. doi: 10.1016/S1474-4422(09)70228-5. Epub 2009 Aug 28.

6.

Pre- and post-synaptic abnormalities associated with impaired neuromuscular transmission in a group of patients with 'limb-girdle myasthenia'.

Slater CR, Fawcett PR, Walls TJ, Lyons PR, Bailey SJ, Beeson D, Young C, Gardner-Medwin D.

Brain. 2006 Aug;129(Pt 8):2061-76.

7.

Motor neuron disease in a patient with a mitochondrial tRNAIle mutation.

Borthwick GM, Taylor RW, Walls TJ, Tonska K, Taylor GA, Shaw PJ, Ince PG, Turnbull DM.

Ann Neurol. 2006 Mar;59(3):570-4.

PMID:
16358336
8.

Minimum prevalence of spinocerebellar ataxia 17 in the north east of England.

Craig K, Keers SM, Walls TJ, Curtis A, Chinnery PF.

J Neurol Sci. 2005 Dec 15;239(1):105-9. Epub 2005 Oct 11.

PMID:
16223509
9.

Lambert-Eaton myasthenic syndrome associated with thymitis.

Warren NM, Bennett M, Lai M, Forty J, Walls TJ.

Neurology. 2005 Jan 11;64(1):168-9. No abstract available.

PMID:
15642933
10.

Spectrum of movement disorders in neuroferritinopathy.

Crompton DE, Chinnery PF, Bates D, Walls TJ, Jackson MJ, Curtis AJ, Burn J.

Mov Disord. 2005 Jan;20(1):95-9.

PMID:
15390132
11.

Sub-acute presentation of Morvan's syndrome after thymectomy.

Cottrell DA, Blackmore KJ, Fawcett PR, Birchall D, Vincent A, Barnard S, Walls TJ.

J Neurol Neurosurg Psychiatry. 2004 Oct;75(10):1504-5. No abstract available.

12.

Reversible abnormalities of DWI in high-altitude cerebral edema.

Wong SH, Turner N, Birchall D, Walls TJ, English P, Schmid ML.

Neurology. 2004 Jan 27;62(2):335-6. No abstract available.

PMID:
14745087
13.

Quantum fluctuations in Josephson junction comparators.

Walls TJ, Filippov TV, Likharev KK.

Phys Rev Lett. 2002 Nov 18;89(21):217004. Epub 2002 Nov 5.

PMID:
12443446
14.

Normokalemic periodic paralysis revisited: does it exist?

Chinnery PF, Walls TJ, Hanna MG, Bates D, Fawcett PR.

Ann Neurol. 2002 Aug;52(2):251-2.

PMID:
12210802
15.

Divry-Van Bogaert syndrome in a female: relationship to Sneddon's syndrome and radiographic appearances.

Stone J, Bhattacharya J, Walls TJ.

Neuroradiology. 2001 Jul;43(7):562-4.

PMID:
11512587
16.

A novel autosomal dominant distal myopathy with early respiratory failure: clinico-pathologic characteristics and exclusion of linkage to candidate genetic loci.

Chinnery PF, Johnson MA, Walls TJ, Gibson GJ, Fawcett PR, Jamieson S, Fulthorpe JJ, Cullen M, Hudgson P, Bushby KM.

Ann Neurol. 2001 Apr;49(4):443-52.

PMID:
11310621
17.

Hereditary motor and sensory neuropathy type 1A associated with sensorineural deafness.

Stone J, Moran G, Walls TJ.

J Neurol Neurosurg Psychiatry. 1998 Sep;65(3):403. No abstract available.

18.

Recurrent strokes in a 34-year-old man.

Chinnery PF, Turnbull DM, Walls TJ, Reading PJ.

Lancet. 1997 Aug 23;350(9077):560. No abstract available.

PMID:
9284779
19.

Case report: multiple thoracic haemangiomas--a rare cause of spinal cord compression.

Worthy SA, Gholkar A, Walls TJ, Todd NV.

Br J Radiol. 1995 Jul;68(811):770-2.

PMID:
7640936
20.

Breathing pattern awake and asleep in patients with myotonic dystrophy.

Veale D, Cooper BG, Gilmartin JJ, Walls TJ, Griffith CJ, Gibson GJ.

Eur Respir J. 1995 May;8(5):815-8.

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