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Transgenic mouse models and human neurodegenerative disordersDENG, Han-Xiang; SIDDIQUE, Teepu.Archives of neurology (Chicago). 2000, Vol 57, Num 12, pp 1695-1702, issn 0003-9942Article

Cholinergic denervation in a pure multi-infarct state: Observations on CADASILMESULAM, Marsel; SIDDIQUE, Teepu; COHEN, Bruce et al.Neurology. 2003, Vol 60, Num 7, pp 1183-1185, issn 0028-3878, 3 p.Article

Genetic aspects of amyotrophic lateral sclerosisSIDDIQUE, Teepu; LALANI, Irfan.Advances in neurology. 2002, Vol 88, pp 21-32, issn 0091-3952, 12 p.Article

OCULOMOTOR INVOLVEMENT IN MYOTONIC DYSTROPHY TYPE 2AJROUD-DRISS, Senda; SUFIT, Robert; SIDDIQUE, Teepu et al.Muscle & nerve. 2008, Vol 38, Num 4, pp 1326-1329, issn 0148-639X, 4 p.Article

Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouseLIJUN WANG; DENG, Han-Xiang; GRISOTTI, Gabriella et al.Human molecular genetics (Print). 2009, Vol 18, Num 9, pp 1642-1651, issn 0964-6906, 10 p.Article

International Symposium on Amyotrophic Lateral Sclerosis/Motor Neurone DiseaseDE JONG, Vianney; SWASH, Michael; SIDDIQUE, Teepu et al.Journal of the neurological sciences. 1997, Vol 152, issn 0022-510X, 102 p., SUP1Conference Proceedings

Ventilatory support : Japanese experienceHAYASHI, H.Journal of the neurological sciences. 1997, Vol 152, pp S97-S100, issn 0022-510X, SUP1Conference Paper

Home care of patients with amyotrophic lateral sclerosis (ALS)KRIVICKAS, L. S; SHOCKLEY, L; MITSUMOTO, H et al.Journal of the neurological sciences. 1997, Vol 152, pp S82-S89, issn 0022-510X, SUP1Conference Paper

The use of transgenic mouse models of amyotrophic lateral sclerosis in preclinical drug studiesGURNEY, M. E.Journal of the neurological sciences. 1997, Vol 152, pp S67-S73, issn 0022-510X, SUP1Conference Paper

A brief quality-of-life measure for ALS clinical trials based on a subset of items from the sickness impact profileMCGUIRE, D; GARRISON, L; ARMON, C et al.Journal of the neurological sciences. 1997, Vol 152, pp S18-S22, issn 0022-510X, SUP1Conference Paper

Toxicity of cysteine and cysteine sulphinic acid to human neuronal cell-linesPARSONS, R. B; WARING, R. H; RAMSDEN, D. B et al.Journal of the neurological sciences. 1997, Vol 152, pp S62-S66, issn 0022-510X, SUP1Conference Paper

Amyotrophic lateral sclerosis : lessons in trial design from recent trialsBORASIO, G. D.Journal of the neurological sciences. 1997, Vol 152, pp S23-S28, issn 0022-510X, SUP1Conference Paper

Polysomnographic studies in amyotrophic lateral sclerosisDAVID, W. S; BUNDLIE, S. R; MAHDAVI, Z et al.Journal of the neurological sciences. 1997, Vol 152, pp S29-S35, issn 0022-510X, SUP1Conference Paper

CONFIRMATION OF THE SEVERE PHENOTYPIC EFFECT OF SERINE AT CODON 41 OF THE SUPEROXIDE DISMUTASE 1 GENESUBRAMONY, S. H; ASHIZAWA, Tetsuo; LANGFORD, Leigh et al.Muscle & nerve. 2011, Vol 44, Num 4, pp 499-502, issn 0148-639X, 4 p.Article

Factors influencing a patient's decision regarding riluzole : an early experienceRUDNICKI, S. A.Journal of the neurological sciences. 1997, Vol 152, pp S80-S81, issn 0022-510X, SUP1Conference Paper

Fasciculations : what do we know of their significance?DESAI, J; SWASH, M.Journal of the neurological sciences. 1997, Vol 152, pp S43-S48, issn 0022-510X, SUP1Conference Paper

MR spectroscopy in amyotrophic lateral sclerosis/motor neuron diseasePIORO, E. P.Journal of the neurological sciences. 1997, Vol 152, pp S49-S53, issn 0022-510X, SUP1Conference Paper

Performance of the Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS) in multicenter clinical trialsCEDARBAUM, J. M; STAMBLER, N.Journal of the neurological sciences. 1997, Vol 152, pp S1-S9, issn 0022-510X, SUP1Conference Paper

Differential Involvement of Optineurin in Amyotrophic Lateral Sclerosis With or Without SOD1 MutationsDENG, Han-Xiang; BIGIO, Eileen H; SUFIT, Robert et al.Archives of neurology (Chicago). 2011, Vol 68, Num 8, pp 1057-1061, issn 0003-9942, 5 p.Article

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementiaDENG, Han-Xiang; CHEN, Wenjie; HUJUN JIANG et al.Nature (London). 2011, Vol 477, Num 7363, pp 211-215, issn 0028-0836, 5 p.Article

Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutationsMACKENZIE, Ian R. A; BIGIO, Eileen H; EISEN, Andrew et al.Annals of neurology. 2007, Vol 61, Num 5, pp 427-434, issn 0364-5134, 8 p.Article

Presence of dendritic cells, MCP-1, and activated microglia/macrophages in amyotrophic lateral sclerosis spinal cord tissueHENKEL, Jenny S; ENGELHARDT, Joseph I; SIKLOS, Laszlo et al.Annals of neurology. 2004, Vol 55, Num 2, pp 221-235, issn 0364-5134, 15 p.Article

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22HOSLER, Betsy A; SIDDIQUE, Teepu; HUNG, Wu-Yen et al.JAMA, the journal of the American Medical Association. 2000, Vol 284, Num 13, pp 1664-1669, issn 0098-7484Article

Prion protein codon 129 genotype prevalence is altered in primary progressive aphasiaXIAOHONG LI; ROWLAND, Lewis P; WEINTRAUB, Sandra et al.Annals of neurology. 2005, Vol 58, Num 6, pp 858-864, issn 0364-5134, 7 p.Article