Author/Creator: Giunti, P - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Giunti, P

1. 002 Detecting retinal changes in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) using optical coherence tomography (OCT). Issue 3 (9th February 2012)

Authors:: Giunti, P; Nethisinghe, S; Clayton, L M; Vermeer, S; Chapple, J P; Reilly, M M; Bremner, F
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 83:Issue 3(2012)
Page Start:: e1
Record Type:: Journal Article
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2. 121 ARSACS: a novel phenotype causing peripheral neuropathy, ataxia and spasticity with supranuclear gaze palsy, myoclonus and epilepsy. Issue 3 (9th February 2012)

Authors:: Stevens, J; Murphy, S M; Davagnanam, I; Phadke, R; Bremner, F; Anderson, G; Nethisinghe, S; Giunti, P; Reilly, M M
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 83:Issue 3(2012)
Page Start:: e1
Record Type:: Journal Article
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3. A panel of nine cerebrospinal fluid biomarkers may identify patients with atypical parkinsonian syndromes. Issue 11 (14th January 2015)

Authors:: Magdalinou, N K; Paterson, R W; Schott, J M; Fox, N C; Mummery, C; Blennow, K; Bhatia, K; Morris, H R; Giunti, P; Warner, T T; de Silva, R; Lees, A J; Zetterberg, H
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 86:Issue 11(2015)
Page Start:: 1240
Record Type:: Journal Article
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4. Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Cav2.1 causing episodic ataxia 2. Issue 6 (1st June 2004)

Authors:: Mantuano, E; Veneziano, L; Spadaro, M; Giunti, P; Guida, S; Leggio, M G; Verriello, L; Wood, N; Jodice, C; Frontali, M
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 6(2004)
Page Start:: e82
Record Type:: Journal Article
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5. NOVEL DE NOVO MUTATION CAUSING BENIGN HEREDITARY CHOREA WITH HYPOTHRYOIDISM AND A PITUITARY MASS. (29th November 2012)

Authors:: Burke, A; Mantuano, E; Bhatia, KP; Veneziano, L; Giunti, P
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 83(2012)Supplement 2
Page Start:: A11
Record Type:: Journal Article
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6. PAW32 ITPR1 gene deletion causes spinocerebellar ataxia 15/16: a genetic, clinical and radiological description of a novel kindred. Issue 11 (22nd October 2010)

Authors:: Novak, M; Davis, M; Li, A; Goold, R; Tabrizi, S J; Sweeney, M G; Houlden, H; Treacy, C; Giunti, P
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 81:Issue 11(2010)
Page Start:: e32
Record Type:: Journal Article
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