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Number of items: 96.

A

Ahmed, M; Miller, A; Hanna, MG; Greensmith, L; (2011) Investigating the effects of pharmacological up-regulation of the heat shock response on protein degradation pathways in an in-vitro model of sporadic inclusion body myositis. In: NEUROMUSCULAR DISORDERS. (pp. S26 - S27). PERGAMON-ELSEVIER SCIENCE LTD

Ahmed, Z; Asi, YT; Lees, AJ; Revesz, T; Holton, JL; (2011) Investigating the role of oligodendroglial precursor cells in multiple system atrophy and progressive supranuclear palsy. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 21 - 21). WILEY-BLACKWELL PUBLISHING, INC

Allen, G.F.G.; (2011) The neurochemical consequences of aromatic L-amino acid decarboxylase deficiency. Doctoral thesis , UCL (University College London). Green open access
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Anzak, A; Tan, H; Pogosyan, A; Ling, H; Lees, AJ; Brown, P; (2011) Improvements in rate of development and magnitude of force with intense auditory stimuli in patients with Parkinson's disease. European Journal of Neuroscience , 34 (1) pp. 124-132.

B

Bandopadhyay, R; Mamais, A; Lashley, T; Griffiths, C; Goswami, N; Holton, JL; Revesz, T; (2011) The role of 4E-BP1, a putative LRRK2 interactor in the pathology of IPD and in G2019S LRRK2 mutation cases. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 21 - 21). WILEY-BLACKWELL PUBLISHING, INC

Brady, S; Squier, W; Hilton-Jones, D; Sewry, C; Holton, JL; (2011) Inclusion body myositis: A diagnostic challenge. In: (Proceedings) 16th International Congress of the World-Muscle-Society. (pp. pp. 732-733). PERGAMON-ELSEVIER SCIENCE LTD

Burge, J; Hanna, MG; (2011) Muscle Channelopathies. pp. 96-102. 10.1002/9781119973331.ch13.

Burge, J; Horga, A; Griggs, RC; Hanna, MG; HYP HOP Investigators, ; (2011) Double-blind, placebo-controlled, parallel group, phase Ill study comparing dichlorphenamide vs. placebo for the treatment of periodic paralysis (HYP HOP trial). In: NEUROMUSCULAR DISORDERS. (pp. S13 - S13). PERGAMON-ELSEVIER SCIENCE LTD

C

Casper, CJ; Warner, TT; Taanman, JW; Nathwani, AC; (2011) Generation of iPS-derived dopaminergic neurons as an in-vitro model of Rapid-Onset Dystonia Parkinsonism. HUMAN GENE THERAPY , 22 (10) A42 - A43.

Coop, M; (2011) Untitled. GEOTECHNIQUE LETTERS , 1 p. 1. 10.1680/geolett.11.00013.

Crehan, H; Pocock, JM; Hardy, J; (2011) THE ROLE OF MICROGLIAL COMPLEMENT RECEPTOR 1 (CR1) IN ALZHEIMER'S DISEASE. In: GLIA. (pp. S135 - S135). WILEY-BLACKWELL

D

Deriziotis, P; Andre, R; Smith, DM; Goold, R; Kinghorn, KJ; Kristiansen, M; Nathan, JA; ... Tabrizi, SJ; + view all (2011) Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry. EMBO J , 30 (15) 3065 - 3077. 10.1038/emboj.2011.224.

Djamshidian, A; O'Sullivan, SS; Wittmann, BC; Lees, AJ; Averbeck, BB; (2011) Novelty seeking behaviour in Parkinson's disease. Neuropsychologia

Dunn, L.M.; (2011) Characterisation of leucine-rich repeat kinase-2 regulation and kinase function. Doctoral thesis , UCL (University College London). Green open access
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Durran, S; Matthews, E; Rayan, DLR; Sud, R; Polke, J; Haworth, A; Holton, JL; ... Hanna, MG; + view all (2011) Genetic heterogeneity and mechanisms of phenotypic variability in human skeletal muscle channelopathies - a new S4 mutation not associated with HypoPP. In: NEUROMUSCULAR DISORDERS. (pp. S13 - S13). PERGAMON-ELSEVIER SCIENCE LTD

F

Fawcett, K; Murphy, SM; Polke, J; Reilly, MM; Houlden, H; (2011) TRPV4 mutations and functional characterisation in a cohort of patients with hereditary neuropathy. In: NEUROMUSCULAR DISORDERS. (pp. S16 - S16). PERGAMON-ELSEVIER SCIENCE LTD

Fawcett, K; Murphy, SM; Reilly, MM; Houlden, H; (2011) TRPV4 MUTATIONS AND FUNCTIONAL CHARACTERISATION IN A COHORT OF PATIENTS WITH HEREDITARY NEUROPATHY. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. S36 - S36). WILEY-BLACKWELL

Fletcher, E.V.; (2011) Alternative splicing in SCN1A: biophysical consequences for NaV1.1 channels. Doctoral thesis , UCL (University College London). Green open access
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G

Gray, A; Malik, B; Montague, K; Dick, J; Hanna, MG; Greensmith, L; (2011) Investigating pathophysiology and therapeutic strategies in a mouse model of spinal and bulbar muscular atrophy (SBMA). In: NEUROMUSCULAR DISORDERS. (pp. S10 - S10). PERGAMON-ELSEVIER SCIENCE LTD

H

Hardy, J; (2011) Read all about it! NEW SCI , 211 (2822) 22 - 23.

Holmstrom, KM; Gourine, AV; Abramov, AY; (2011) A Novel Role for Polyphosphate in Astrocyte Signalling. In: (Proceedings) 55th Annual Meeting of the Biophysical-Society. (pp. p. 562). CELL PRESS

I

Innes, A; Kalmar, B; Houlden, H; Reilly, MM; Greensmith, L; (2011) Characterisation of novel mutations within heat shock protein 27 causing motor axonopathies. In: NEUROMUSCULAR DISORDERS. (pp. S3 - S3). PERGAMON-ELSEVIER SCIENCE LTD

K

Kalmar, B; Innes, A; Rossor, AM; Houlden, H; Schiavo, G; Reilly, MM; Greensmith, L; (2011) ASSESSMENT OF FUNCTIONAL IMPAIRMENTS IN CELLULAR MODELS OF MUTANT HSPB1 INDUCED NEUROPATHIES. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. S62 - S63). WILEY-BLACKWELL

Koepke, J; Haag, C; Feldbrügge, M; Kaffarnik, F; Zarnack, K; Luscombe, NM; König, J; ... Begerow, D; + view all (2011) The RNA-binding protein Rrm4 is essential for efficient secretion of endochitinase Cts1. Molecular and Cellular Proteomics , 10 (12) 10.1074/mcp.M111.011213.

Kojovic, M; Sheerin, UM; Wood, N; Houlden, H; Hardy, J; Bhatia, KP; (2011) Young onset parkinsonism due to alpha synuclein gene multiplication in a consanguineous family - A case report. In: (Proceedings) 15th International Congress of Parkinsons Disease and Movement Disorders. (pp. S310-S311). WILEY-BLACKWELL

Konig, J; Zarnack, K; Rot, G; Curk, T; Kayikci, M; Zupan, B; Turner, DJ; ... Ule, J; + view all (2011) iCLIP--transcriptome-wide mapping of protein-RNA interactions with individual nucleotide resolution. Journal of visualized experiments : JoVE (50)

Kovac, S; Domijan, A; Walker, MC; Abramov, AY; (2011) PROLONGED SEIZURE ACTIVITY IMPAIRS MITOCHONDRIAL BIOENERGETICS AND INDUCES CELL DEATH. In: (Proceedings) 3rd London-Innsbruck Colloquium on Status Epilepticus. (pp. p. 85). WILEY-BLACKWELL

Kovac, S; Domijan, A-M; Walker, MC; Abramov, AY; (2011) ROLE OF MITOCHONDRIAL FUNCTION IN SEIZURE-INDUCED NEURONAL CELL DEATH. In: (Proceedings) 29th International Epilepsy Congress. (pp. p. 45). WILEY-BLACKWELL

Kuo, LT; Tsai, SY; Groves, MJ; An, SF; Scaravilli, F; (2011) Gene Expression Profile in Rat Dorsal Root Ganglion Following Sciatic Nerve Injury and Systemic Neurotrophin-3 Administration. J MOL NEUROSCI , 43 (3) 503 - 515. 10.1007/s12031-010-9473-3.

L

Lashley, T; Holton, JL; Revesz, T; (2011) TDP-43 pathology may occur in the BRI2 gene-related dementias. ACTA NEUROPATHOL , 121 (4) 559 - 560. 10.1007/s00401-011-0811-5.

Laura, M; Eichler, FS; Hornemann, T; Polke, J; Davis, M; Bull, K; Houlden, H; (2011) HEREDITARY SENSORY AND AUTONOMIC NEUROPATHY TYPE 1: CORRELATION OF SEVERITY AND PLASMA ATYPICAL DEOXY-SPHYNGOID BASES. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. S72 - S73). WILEY-BLACKWELL

Lees, A; (2011) The Hurricane Port. [Book]. Mainstream Digital

Lees, AJ; (2011) CAN THERAPY MODIFY NATURAL EVOLUTION OF PARKINSON'S DISEASE? - CONTRA. In: (pp. p. 17).

Lees, AJ; (2011) THE NOSOLOGY OF PARKINSON'S DISEASE. In: (pp. p. 638).

Lindgren, HS; Rylander, D; Iderberg, H; Andersson, M; O'Sullivan, SS; Williams, DR; Lees, AJ; (2011) Putaminal upregulation of FosB/ΔFosB-like immunoreactivity in Parkinson's disease patients with Dyskinesia. Journal of Parkinson's Disease , 1 (4) pp. 347-357. 10.3233/JPD-2011-11068.

Ling, H; Bhidayasiri, R; (2011) Reduced Serum Caeruloplasmin Levels in Non-Wilsonian Movement Disorders. EUROPEAN NEUROLOGY , 66 (3) pp. 123-127. 10.1159/000330538.

Ling, H; Braschinsky, M; Taba, P; Luus, SM; Doherty, K; Hotter, A; Poewe, W; (2011) Decades of Delayed Diagnosis in 4 Levodopa-Responsive Young-Onset Monogenetic Parkinsonism Patients. MOVEMENT DISORD , 26 (7) 1337 - 1340. 10.1002/mds.23563.

Ling, H; Braschinsky, M; Taba, P; Lüüs, S-M; Doherty, K; Hotter, A; Poewe, W; (2011) Decades of delayed diagnosis in 4 levodopa-responsive young-onset monogenetic parkinsonism patients. Movement Disorders

Ling, H; Braschinsky, M; Taba, P; Lüüs, SM; Doherty, K; Hotter, A; Poewe, W; (2011) Decades of delayed diagnosis in 4 levodopa-responsive young-onset monogenetic parkinsonism patients. Movement Disorders , 26 (7) pp. 1337-1340. 10.1002/mds.23563.

Ling, H; Massey, L; Lunn, M; Lees, A; (2011) A rare cause of L-Dopa responsive parkinsonism: The answer lies in the eyes. In: (pp. S341-S341).

Ling, H; Polke, JM; Sweeney, MG; Haworth, A; Sandford, CA; Heales, SJ; Wood, NW; ... Lees, AJ; + view all (2011) An intragenic duplication in guanosine triphosphate cyclohydrolase-1 gene in a dopa-responsive dystonia family. Movement Disorders , 26 (5) pp. 905-909.

Liu, YT; Murphy, SM; Houlden, H; Reilly, MM; (2011) Neurofilament light chain polypeptide gene (NEFL) mutations in autosomal dominant or sporadic Charcot-Marie-Tooth disease. In: NEUROMUSCULAR DISORDERS. (pp. S17 - S17). PERGAMON-ELSEVIER SCIENCE LTD

Loublier, S; Bayot, A; Rak, M; El-Khoury, R; Bénit, P; Rustin, P; (2011) The NDUFB6 subunit of the mitochondrial respiratory chain complex I is required for electron transfer activity: a proof of principle study on stable and controlled RNA interference in human cell lines. Biochem Biophys Res Commun , 414 (2) pp. 367-372. 10.1016/j.bbrc.2011.09.078.

Léveillé, N; Elkon, R; Davalos, V; Vrielink, JO; Le Sage, C; Melo, CA; Esteller, M; ... Ule, J; + view all (2011) Selective inhibition of microRNA accessibility by RBM38 is required for p53 activity. Nature Communications , 2 (1) 10.1038/ncomms1519.

M

Maennikkoe, R; Flanagan, SE; Sim, X; Segal, D; Hussain, K; Ellard, S; Hattersley, AT; (2011) Mutations of the Same Conserved Glutamate Residue in NBD2 of the Sulfonylurea Receptor 1 Subunit of the K-ATP Channel Can Result in Either Hyperinsulinism or Neonatal Diabetes. DIABETES , 60 (6) pp. 1813-1822. 10.2337/db10-1583.

Mattsson, N; Olsson, B; Andreasson, U; Portelius, E; Zetterberg, H; (2011) Found in translation: a blood-based test for Niemann-Pick type C1. Biomark Med , 5 (2) 201-. 10.2217/bmm.11.10.

Mattsson, N; Olsson, B; Andreasson, U; Portelius, E; Zetterberg, H; (2011) Growth factors in Parkinson's disease. Biomark Med , 5 (2) pp. 201-202.

Mattsson, N; Olsson, B; Andreasson, U; Portelius, E; Zetterberg, H; (2011) It is all about clearance. Biomark Med , 5 (2) 202-.

Mattsson, N; Olsson, B; Andreasson, U; Portelius, E; Zetterberg, H; (2011) Troponin T: more than acute myocardial infarction. Biomark Med , 5 (2) 203-.

Mattsson, N; Olsson, B; Andreasson, U; Portelius, E; Zetterberg, H; (2011) A new member in the biomarker discovery toolbox. Biomark Med , 5 (2) 202-.

Meschia, JF; Nalls, MA; Rich, SS; Singleton, A; Hardy, JA; Brott, TG; Brown, RD; ... SWISS Investigators, ; + view all (2011) Genome-wide Search for Ischemic Stroke Genes: The Siblings with Ischemic Stroke Study (SWISS). In: STROKE. (pp. E269 - E269). LIPPINCOTT WILLIAMS & WILKINS

Miller, A; Ahmed, M; Hanna, MG; Greensmith, L; (2011) The effects of arimoclomol on pathological outcome measures of inclusion body myositis in vitro. In: NEUROMUSCULAR DISORDERS. (pp. S27 - S27). PERGAMON-ELSEVIER SCIENCE LTD

Morrow, JM; Dewar, EL; Ramdharry, GM; Laura, M; Yousry, TA; Hanna, MG; Reilly, MM; (2011) ISOMETRIC AND ISOKINETIC LOWER LIMB STRENGTH IN CHARCOT-MARIE-TOOTH DISEASE 1A. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. S90 - S90). WILEY-BLACKWELL

Morrow, JM; Matthews, E; Rayan, DLR; Amer, I; Fischmann, A; Sinclair, CDJ; Thornton, JS; ... Hanna, MG; + view all (2011) Magnetic resonance imaging in the non-dystrophic myotonias. In: NEUROMUSCULAR DISORDERS. (pp. S5 - S5). PERGAMON-ELSEVIER SCIENCE LTD

Morrow, JM; Sinclair, CDJ; Fischmann, A; Thornton, JS; Laura, M; Yousry, TA; Hanna, MG; (2011) QUANTITATIVE MAGNETIC RESONANCE IMAGING OF MUSCLE IN CHARCOT-MARIE-TOOTH DISEASE 1A-A POTENTIAL OUTCOME MEASURE. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. S90 - S90). WILEY-BLACKWELL

Murphy, S; Laura, M; Blake, J; Polke, J; Bremner, F; Reilly, MM; (2011) Conduction block and tonic pupils in Charcot-Marie-Tooth disease caused by a Myelin Protein Zero p.Ile112Thr mutation. Neuromouscular Disorders , 21 pp. 223-226.

Murphy, S; Polke, J; Manji, H; Blake, J; Sweeney, M; Brandner, S; Reilly, MM; (2011) A novel mutation in the nerve-specific 5′UTR of the GJB1 gene causes X-linked Charcot-Marie-Tooth Disease. Journal of the Peripheral Nervous System , 16 pp. 65-70.

Murphy, S; Reilly, MM; (2011) Amyloid neuropathies. Advances in Clinical Neuroscience and Rehabilitation , 11 (1) pp. 16-19.

Murphy, SM; Siskind, C; Ovens, R; Polke, J; Laura, M; Houlden, H; Murphy, RPJ; ... Reilly, MM; + view all (2011) X-inactivation pattern in females with CMTX1. In: NEUROMUSCULAR DISORDERS. (pp. S18 - S18). PERGAMON-ELSEVIER SCIENCE LTD

Murphy, SM; Siskind, CE; Ovens, R; Polke, J; Laura, M; Houlden, H; Murphy, RPJ; ... Reilly, MM; + view all (2011) X-INACTIVATION PATTERN IN FEMALES WITH CMTX1. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. S94 - S94). WILEY-BLACKWELL

N

Nesbitt, V; Pitceathly, RDS; Rahman, S; Hanna, MG; McFarland, R; Turnbull, DM; (2011) A3243G-more than just MELAS! In: NEUROMUSCULAR DISORDERS. (pp. S21 - S21). PERGAMON-ELSEVIER SCIENCE LTD

Nesbitt, V; Pitceathly, RDS; Rahman, S; Poulton, J; Turnbull, DM; Hanna, MG; McFarland, R; (2011) The MRC Centre for Translational Research in Neuromuscular Disease: Mitochondrial Disease Patient Cohort Study UK. In: NEUROMUSCULAR DISORDERS. (pp. S29 - S30). PERGAMON-ELSEVIER SCIENCE LTD

Noyce, AJ; Gilpin, P; Howard, R; Lees, AJ; Silviera-Moriyama, L; (2011) Severe dysphagia preceding Parkinson's disease. In: (Proceedings) 15th International Congress of Parkinsons Disease and Movement Disorders. (pp. S195-S196). WILEY-BLACKWELL

Nunes, A; Pressey, SNR; Cooper, JD; Soriano, S; (2011) Loss of amyloid precursor protein in a mouse model of Niemann-Pick type C disease exacerbates its phenotype and disrupts tau homeostasis. NEUROBIOL DIS , 42 (3) 349 - 359. 10.1016/j.nbd.2011.01.028.

O

O'Sullivan, SS; Johnson, M; Williams, DR; Revesz, T; Holton, JL; Lees, AJ; Perry, EK; (2011) The effect of drug treatment on neurogenesis in Parkinson's disease. Movement Disorders , 26 (1) pp. 45-50. 10.1002/mds.23340.

O'Sullivan, SS; Johnson, M; Williams, DR; Revesz, T; Holton, JL; Lees, AJ; Perry, EK; (2011) The effect of drug treatment on neurogenesis in Parkinson's disease. Mov Disord , 26 (1) pp. 45-50. 10.1002/mds.23340.

O'Sullivan, SS; Lees, AJ; (2011) Dopamine Dysregulation Syndrome. pp. 202-214. 10.1002/9781444397970.ch19.

P

Pandraud, A; Murphy, SM; Laura, M; Reilly, MM; Houlden, H; (2011) Genetic modifying factors for the common form of CMT1A due to the chromosome 17 duplication and other causes of CMT1 in non-CMT1A patients. In: NEUROMUSCULAR DISORDERS. (pp. S18 - S18). PERGAMON-ELSEVIER SCIENCE LTD

Phukan, J; Warner, TT; (2011) Other Dystonias. In: Oxford Textbook of Movement Disorders. Oxford University Press

Pitceathly, RDS; Fassone, E; Taanman, JW; Sadowski, M; Fratter, C; Mudanohwo, EE; Woodward, CE; ... Rahman, S; + view all (2011) Kearns-Sayre syndrome caused by defective R1/p53R2 assembly. NEUROMUSCULAR DISORDERS , 21 S21 - S21.

Pitceathly, RDS; Fassone, E; Taanman, JW; Sadowski, M; Fratter, C; Mudanohwo, EE; Woodward, CE; ... Rahman, S; + view all (2011) Kearns-Sayre syndrome caused by defective R1/p53R2 assembly. J MED GENET , 48 (9) 610 - 617. 10.1136/jmg.2010.088328.

Pocock, J; Davenport, C; Jebelli, J; Sevastou, I; Hooper, C; (2011) P53-ACTIVATED PATHWAYS IN MICROGLIA: GOOD OR BAD FOR THE BRAIN? In: GLIA. (pp. S25 - S26). WILEY-BLACKWELL

Portaro, S; Sweeney, MG; Matthews, E; Sud, R; Musumeci, O; Rodolico, C; Vita, G; ... Hanna, M; + view all (2011) Clinical and molecular genetic studies of a cohort of Italian patients with muscle channelopathies. In: (Proceedings) 21st Meeting of the European-Neurological-Society. (pp. p. 246). SPRINGER HEIDELBERG

R

Rajakulendran, S; Paisan-Ruiz, C; Houlden, H; (2011) Thinning of the Corpus Callosum and Cerebellar Atrophy is Correlated with Phenotypic Severity in a Family with Spastic Paraplegia Type 11. J CLIN NEUROL , 7 (2) 102 - 104. 10.3988/jcn.2011.7.2.102. Gold open access

Rayan, DLR; Haworth, A; Sud, R; Burge, J; Portaro, S; Toscano, A; Hanna, MG; (2011) Large scale chloride channel gene DNA rearrangements are an important cause of recessive myotonia congenita - implications for diagnostic screening. In: NEUROMUSCULAR DISORDERS. (pp. S14 - S15). PERGAMON-ELSEVIER SCIENCE LTD

Rayan, DLR; Matthews, E; Barreto, G; Tan, SV; Dewar, L; Burge, J; Barohn, R; ... CINCH Grp, ; + view all (2011) Assessing the efficacy of Mexiletine in UK patients with non-dystrophic myotonia. In: NEUROMUSCULAR DISORDERS. (pp. S14 - S14). PERGAMON-ELSEVIER SCIENCE LTD

Rayan, DLR; Matthews, E; Rajakulendran, S; Barreto, G; Tan, SV; Dewar, L; Burge, J; ... CINCH Grp, ; + view all (2011) Genotype-phenotype correlation and longitudinal three year natural history study in the non-dystrophic myotonias in the UK. In: NEUROMUSCULAR DISORDERS. (pp. S14 - S14). PERGAMON-ELSEVIER SCIENCE LTD

Rayan, DLR; Rajakulendran, S; Barreto, G; Tan, SV; Dewar, L; Griggs, RC; Hanna, MG; (2011) Genotype-phenotype correlation and longitudinal study of Andersen-Tawil Syndrome in the UK. In: NEUROMUSCULAR DISORDERS. (pp. S14 - S14). PERGAMON-ELSEVIER SCIENCE LTD

Revesz, T; Rostagno, A; Plant, G; Lashley, T; Frangione, B; Ghiso, J; Holton, JL; (2011) Inherited Amyloidoses and Neurodegeneration: Familial British Dementia and Familial Danish Dementia. pp. 439-445. 10.1002/9781444341256.ch46.

Rinaldi, S; Pitceathly, RDS; Roberts, ME; (2011) A dizzy and disorientated DJ. Pract Neurol , 11 (4) pp. 252-255. 10.1136/practneurol-2011-000065.

Rodrigues, M; de la Torre, BG; Rádis-Baptista, G; Santos, NC; Andreu, D; (2011) Efficient Cellular Delivery of β-Galactosidase Mediated by NrTPs, a New Family of Cell-Penetrating Peptides. Bioconjugate Chemistry , 22 (11) pp. 2339-2344. 10.1021/bc200421z.

Ross, OA; Soto-Ortolaza, AI; Verbeeck, C; Rich, SS; Singleton, A; Hardy, JA; Brott, TG; ... SWISS Investigators, ; + view all (2011) Results of NOTCH3 Sequencing in Siblings with Ischemic Stroke Study Probands. In: STROKE. (pp. E269 - E269). LIPPINCOTT WILLIAMS & WILKINS

Rossor, A; Houlden, H; Reilly, MM; (2011) A clinical study of the hereditary neuropathies due to mutations in the small heat shock proteins. In: NEUROMUSCULAR DISORDERS. (pp. S18 - S19). PERGAMON-ELSEVIER SCIENCE LTD

S

Sailer, A; Scholz, SW; Gibbs, JR; Johnson, JO; Wood, NW; Hernandez, D; Hardy, J; ... Houlden, H; + view all (2011) EXOME SEQUENCING AS A RAPID AND COST EFFICIENT DIAGNOSTIC METHOD IN NEUROGENETIC DISORDERS. In: EUROPEAN JOURNAL OF NEUROLOGY. (pp. 552 - 552). WILEY-BLACKWELL

Schrag, A; Hobart, J; Selai, C; Quinn, N; Lees, AJ; Litvan, I; Lang, A; ... Burn, D; + view all (2011) Measuring quality of life in progressive supranuclear palsy: The PSP-QoL. pp. 52-59. 10.1017/CBO9780511975363.006.

Sinclair, CDJ; Morrow, JM; Fischmann, A; Hanna, MG; Reilly, MM; Yousry, TA; Golay, X; (2011) MRI shows increased tibial nerve size in CMT1A. In: NEUROMUSCULAR DISORDERS. (pp. S28 - S28). PERGAMON-ELSEVIER SCIENCE LTD

Sinclair, CDJ; Morrow, JM; Fischmann, A; Hanna, MG; Reilly, MM; Yousry, TA; Golay, X; (2011) Skeletal muscle MRI-determined fat fraction and myometric strength in inclusion body myositis and Charcot-Marie-Tooth disease Type 1A. In: NEUROMUSCULAR DISORDERS. (pp. S5 - S5). PERGAMON-ELSEVIER SCIENCE LTD

Sinclair, CDJ; Morrow, JM; Hanna, MG; Reilly, MM; Yousry, TA; Golay, X; Thornton, JS; (2011) Improved magnetization transfer MRI of skeletal muscle in myopathy and neuropathy. In: NEUROMUSCULAR DISORDERS. (pp. S29 - S29). PERGAMON-ELSEVIER SCIENCE LTD

Siskind, C; Murphy, S; Ovens, R; Polke, J; Reilly, MM; Shy, ME; (2011) Phenotype expression in women with CMT1X. Journal of the Peripheral Nervous System , 16 (2) pp. 102-107.

Soreq, Bergman, Greenberg, Israel, Soreq, LSHBDSGIZSH; (2011) METHODS OF DIAGNOSING PARKINSON'S DISEASE.

Spillane, JE; Hanna, MG; Kullmann, DM; (2011) Synaptic mechanisms in P/Qdeficient neuromuscular junctions. In: NEUROMUSCULAR DISORDERS. (pp. S15 - S15). PERGAMON-ELSEVIER SCIENCE LTD

Statland, J; Wang, Y; Bundy, B; Trivedi, J; Herbelin, L; Pandya, S; Martens, W; ... Barohn, R; + view all (2011) A Quantitative Measure of Handgrip Myotonia in Patients with Non-Dystrophic Myotonia. In: (Proceedings) 63rd AAN Annual Meeting. (pp. A531-A531). LIPPINCOTT WILLIAMS & WILKINS

Stevens, J; Llewelyn, JG; Taylor, AMR; Wood, NW; (2011) Ataxia in a young patient. Pract Neurol , 11 (5) pp. 319-322. 10.1136/practneurol-2011-000097.

W

Wall, M; Mattsson, N; Zetterberg, H; Blennow, K; (2011) [Automated cerebrospinal fluid cell count. A valuable contribution to diagnostics of brain diseases]. Lakartidningen , 108 (40) pp. 1972-1973.

Willis, T; Hollingsworth, KG; Sveen, ML; Morrow, JM; Sinclair, CDJ; Thornton, JS; Vandenheede, J; ... Straub, V; + view all (2011) Assessing muscle pathology by MRI in LGMD2I. In: NEUROMUSCULAR DISORDERS. (pp. S4 - S5). PERGAMON-ELSEVIER SCIENCE LTD

Willis, TA; Hollingsworth, KG; Sveen, ML; Morrow, J; Vandenheede, J; Strojkovic, T; Eagle, M; ... Straub, V; + view all (2011) Quantitative MRI in LGMD2I; a longitudinal study. In: (Proceedings) 16th International Congress of the World-Muscle-Society. (pp. p. 667). PERGAMON-ELSEVIER SCIENCE LTD

This list was generated on Sun Jun 17 01:55:28 2018 BST.