Reversible upper limb muscle weakness with selective loss of thick filamentsVATTEMI, G; TONIN, P; FILOSTO, M et al.Neurology. 2003, Vol 61, Num 6, pp 863-864, issn 0028-3878, 2 p.Article

Confirmation of FWT1 as a Wilms'tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1RAHMAN, N; ABIDI, F; DAVISON, V et al.Human genetics. 1998, Vol 103, Num 5, pp 547-556, issn 0340-6717Article

Critical illness myopathy and neuropathyLATRONICO, N; FENZI, F; RECUPERO, D et al.Lancet (British edition). 1996, Vol 347, Num 9015, pp 1579-1582, issn 0140-6736Article

Hereditary breast cancer : pathobiology, prognosis, and BRCA1 and BRCA2 gene linkageMARCUS, J. N; WATSON, P; PAGE, D. L et al.Cancer. 1996, Vol 77, Num 4, pp 697-709, issn 0008-543XArticle

Right hemisphere patients's judgements on emotionsSEMENZA, C; PASINI, M; ZETTIN, M et al.Acta neurologica scandinavica. 1986, Vol 74, Num 1, pp 43-50, issn 0001-6314Article

Effects of GM₁ ganglioside in cerebrovascular diseases: a double-blind trial in 40 casesBATTISTIN, L; CESARI, A; GALLIGIONI, F et al.European neurology. 1985, Vol 24, Num 5, pp 343-351, issn 0014-3022Article

Genetic and physical characterization of trimethoprim resistance plasmids from Shigella sonnei and Shigella flexneriTONIN, P. N; GRANT, R. B.Canadian journal of microbiology. 1987, Vol 33, Num 10, pp 905-913, issn 0008-4166Article

Botulinum toxin treatment of apraxia of eyelid opening in progressive supranuclear palsy : Report of two casesPICCIONE, F; MANCINI, E; TONIN, P et al.Archives of physical medicine and rehabilitation. 1997, Vol 78, Num 5, pp 525-529, issn 0003-9993Article

Eyelid ptosis from sympathetic nerve dysfunction mistaken as myopathy : a simple test to identify this conditionTOMELLERI, G; VATTEMI, G; FILOSTO, M et al.Journal of neurology, neurosurgery and psychiatry. 2007, Vol 78, Num 6, pp 632-634, issn 0022-3050, 3 p.Article

The role of muscle biopsy in investigating isolated muscle painFILOSTO, M; TONIN, P; VATTEMI, G et al.Neurology. 2007, Vol 68, Num 3, pp 181-186, issn 0028-3878, 6 p.Article

Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophyVATTEMI, G; TOMELLERI, G; FILOSTO, M et al.Neuropathology and applied neurobiology (Print). 2005, Vol 31, Num 1, pp 45-52, issn 0305-1846, 8 p.Article

Critically ill patients : immunological evidence of inflammation in muscle biopsyBAZZI, P; MOGGIO, M; CHECCARELLI, N et al.Clinical neuropathology. 1999, Vol 18, Num 1, pp 23-30, issn 0722-5091Article

Mutations in BRCA1 and BRCA2 in breast cancer families: Are there more breast cancer-susceptibility genes?SEROVA, O. M; MAZOYER, S; PUGET, N et al.American journal of human genetics. 1997, Vol 60, Num 3, pp 486-495, issn 0002-9297Article

Mutation analysis of the BRCA1 gene in 23 families with cases of cancer of the breast, ovary, and multiple other sitesDUROCHER, F; TONIN, P; SHATTUCK-EIDENS, D et al.Journal of medical genetics. 1996, Vol 33, Num 10, pp 814-819, issn 0022-2593Article

Common origins of BRCA1 mutations in Canadian breast and ovarian cancer familiesSIMARD, J; TONIN, P; LIU, Q et al.Nature genetics. 1994, Vol 8, Num 4, pp 392-398, issn 1061-4036Article

The gene for hereditary breast-ovarian cancer, BRCA1, maps distal of EDH17B2 in chromosome region 17q12-q21TONIN, P; SEROVA, O; SIMARD, J et al.Human molecular genetics (Print). 1994, Vol 3, Num 9, pp 1679-1682, issn 0964-6906Article

The effects of long-term rehabilitation therapy on poststroke hemiplegic patientsDAM, M; TONIN, P; CASSON, S et al.Stroke (1970). 1993, Vol 24, Num 8, pp 1186-1191, issn 0039-2499Article

Phenotypic and molecular characterization of inducible human neuroblastoma cell linesYEGER, H; BAUMAL, R; PAWLIN, G et al.Differentiation (London). 1988, Vol 39, Num 3, pp 216-227, issn 0301-4681Article

Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer familiesOSHER, D. J; DE LEENEER, K; ARSENEAU, J et al.British journal of cancer. 2012, Vol 106, Num 8, pp 1460-1463, issn 0007-0920, 4 p.Article

Calpain 3 deficiency presenting as fibre type disproportionVATTEMI, G; TONIN, P; NERI, M et al.Neuropathology and applied neurobiology (Print). 2009, Vol 35, Num 6, pp 614-617, issn 0305-1846, 4 p.Article

P300-based brain computer interface : Reliability and performance in healthy and paralysed participantsPICCIONE, F; GIORGI, F; TONIN, P et al.Clinical neurophysiology. 2006, Vol 117, Num 3, pp 531-537, issn 1388-2457, 7 p.Article

Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mitochondrial diseasesFILOSTO, M; TONIN, P; VATTEMI, G et al.Neuropathology and applied neurobiology (Print). 2003, Vol 29, Num 1, pp 52-59, issn 0305-1846, 8 p.Article

A high proportion of mutations in the BRCA1 gene in German breast/ovarian cancer families with clustering of mutations in the 3'third of the geneJUAN DONG; CHANG-CLAUDE, J; YIXIN WU et al.Human genetics. 1998, Vol 103, Num 2, pp 154-161, issn 0340-6717Article

Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21RAHMAN, N; ARBOUR, L; TONIN, P et al.Nature genetics. 1996, Vol 13, Num 4, pp 461-463, issn 1061-4036Article

Mutations analysis of the BRCA2 gene in 49 site-specific breast cancer familiesPHELAN, C. M; LANCASTER, J. M; FAUCHER, M.-C et al.Nature genetics. 1996, Vol 13, Num 1, pp 120-122, issn 1061-4036Article