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	21.	Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size? [electronic resource] by Fanin, M Freda, M P Vitiello, L Danieli, G A Pegoraro, E Angelini, C Producer: 19961218 In: Muscle & nerve vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Emotional Lability in MND: Relationship to cognition and psychopathology and impact on caregivers. [electronic resource] by Palmieri, A Abrahams, S Sorarù, G Mattiuzzi, L D'Ascenzo, C Pegoraro, E Angelini, C Producer: 20090504 In: Journal of the neurological sciences vol. 278 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	An X:autosome translocation stabilizes truncated dystrophin: implications for lack of truncated dystrophins in Duchenne muscular dystrophy. [electronic resource] by Fidzianska, A Morrone, A Pegoraro, E Ryniewicz, B Ilnicka, A Zammarchi, E Hoffman, E P Producer: 19951207 In: Neuropediatrics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Sphingomonas paucimobilis associated with localised calf myositis. [electronic resource] by Pegoraro, E Borsato, C Dal Bello, F Stramare, R Fanin, M Palu, G Angelini, C Producer: 20081015 In: Journal of neurology, neurosurgery, and psychiatry vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes. [electronic resource] by Fanin, M Nascimbeni, A C Aurino, S Tasca, E Pegoraro, E Nigro, V Angelini, C Producer: 20090622 In: Neurology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Walker-Warburg syndrome: neurologic features and muscle membrane structure. [electronic resource] by Kanoff, R J Curless, R G Petito, C Falcone, S Siatkowski, R M Pegoraro, E Producer: 19980415 In: Pediatric neurology vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	The glucocorticoid receptor N363S polymorphism and steroid response in Duchenne dystrophy. [electronic resource] by Bonifati, D M Witchel, S F Ermani, M Hoffman, E P Angelini, C Pegoraro, E Producer: 20061005 In: Journal of neurology, neurosurgery, and psychiatry vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Quality of life and motor impairment in ALS: Italian validation of ALSAQ. [electronic resource] by Palmieri, A Sorarù, G Lombardi, L D'Ascenzo, C Baggio, L Ermani, M Pegoraro, E Angelini, C Producer: 20100322 In: Neurological research vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation. [electronic resource] by Wang, J Pegoraro, E Menegazzo, E Gennarelli, M Hoop, R C Angelini, C Hoffman, E P Producer: 19950911 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant. [electronic resource] by Pegoraro, E Carelli, V Zeviani, M Cortelli, P Montagna, P Barboni, P Angelini, C Hoffman, E P Producer: 19961203 In: American journal of medical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	The blurred scenario of motor neuron disorders linked to Spatacsin mutations: a case report. [electronic resource] by Querin, G Bertolin, C Martinuzzi, A Bassi, M T Arnoldi, A Polo, A Pegoraro, E Sorarù, G Producer: 20151008 In: European journal of neurology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Epidemiology of ALS in Padova district, Italy, from 1992 to 2005. [electronic resource] by Cima, V Logroscino, G D'Ascenzo, C Palmieri, A Volpe, M Briani, C Pegoraro, E Angelini, C Soraru, G Producer: 20091019 In: European journal of neurology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Retrospective study on PET-SPECT imaging in a large cohort of myotonic dystrophy type 1 patients. [electronic resource] by Romeo, Vincenzo Pegoraro, E Squarzanti, F Sorarù, G Ferrati, C Ermani, M Zucchetta, P Chierichetti, F Angelini, C Producer: 20110928 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Duchenne muscular dystrophy and myotonic dystrophy in the same patient. [electronic resource] by Dubrovsky, A L Taratuto, A L Sevlever, G Schultz, M Pegoraro, E Hoop, R C Hoffman, E P Producer: 19950525 In: American journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	A new mutation in a family with cold-aggravated myotonia disrupts Na(+) channel inactivation. [electronic resource] by Wu, F F Takahashi, M P Pegoraro, E Angelini, C Colleselli, P Cannon, S C Hoffman, E P Producer: 20010607 In: Neurology vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Memory deficits and retrieval processes in ALS. [electronic resource] by Mantovan, M C Baggio, L Dalla Barba, G Smith, P Pegoraro, E Soraru', G Bonometto, P Angelini, C Producer: 20030616 In: European journal of neurology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Large-scale disruption of microtubule pathways in morphologically normal human spastin muscle. [electronic resource] by Molon, A Di Giovanni, S Chen, Y W Clarkson, P M Angelini, C Pegoraro, E Hoffman, E P Producer: 20040802 In: Neurology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Cognitive profile and MRI findings in limb-girdle muscular dystrophy 2I. [electronic resource] by Palmieri, A Manara, R Bello, L Mento, G Lazzarini, L Borsato, C Bortolussi, L Angelini, C Pegoraro, E Producer: 20111115 In: Journal of neurology vol. 258 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family. [electronic resource] by Capellari, S Vital, C Parchi, P Petersen, R B Ferrer, X Jarnier, D Pegoraro, E Gambetti, P Julien, J Producer: 19970903 In: Neurology vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression. [electronic resource] by Korade-Mirnics, Z Tarleton, J Servidei, S Casey, R R Gennarelli, M Pegoraro, E Angelini, C Hoffman, E P Producer: 19990708 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 81 results.