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	1.	Absence of dystrophin and spectrin in regenerating muscle fibers from Becker dystrophy patients. [electronic resource] by Fanin, M Pegoraro, E Angelini, C Producer: 19940919 In: Journal of the neurological sciences vol. 123 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[Umbilical endometriosis]. [electronic resource] by SINISCALCO, O F ROA, R L PEGORARO, E Producer: 20030501 In: Prensa medica argentina vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	3.	Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern Italy. [electronic resource] by Fanin, M Hoffman, E P Angelini, C Pegoraro, E Producer: 20000822 In: Human mutation vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophy. [electronic resource] by Pegoraro, E Fanin, M Angelini, C Hoffman, E P Producer: 19990825 In: Neuromuscular disorders : NMD vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	LGMD2E patients risk developing dilated cardiomyopathy. [electronic resource] by Fanin, M Melacini, P Boito, C Pegoraro, E Angelini, C Producer: 20030819 In: Neuromuscular disorders : NMD vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Muscle histopathology in myasthenia gravis with antibodies against MuSK and AChR. [electronic resource] by Martignago, S Fanin, M Albertini, E Pegoraro, E Angelini, C Producer: 20090309 In: Neuropathology and applied neurobiology vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Novel sarcoglycan gene mutations in a large cohort of Italian patients. [electronic resource] by Boito, C Fanin, M Siciliano, G Angelini, C Pegoraro, E Producer: 20030805 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy. [electronic resource] by Pegoraro, E Fanin, M Trevisan, C P Angelini, C Hoffman, E P Producer: 20001207 In: Neurology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy. [electronic resource] by Fanin, M Pegoraro, E Matsuda-Asada, C Brown, R H Angelini, C Producer: 20010419 In: Neurology vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations. [electronic resource] by Duggan, D J Fanin, M Pegoraro, E Angelini, C Hoffman, E P Producer: 19970103 In: Journal of the neurological sciences vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Motor neuron disease in the Padua district of Italy: an epidemiological study. [electronic resource] by Briani, C Marcon, M Dam, M Beghi, E Pegoraro, E Angelini, C Producer: 19961126 In: Neuroepidemiology vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	MR imaging findings in children with merosin-deficient congenital muscular dystrophy. [electronic resource] by Caro, P A Scavina, M Hoffman, E Pegoraro, E Marks, H G Producer: 19990507 In: AJNR. American journal of neuroradiology vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	13.	Insights into the genetic epidemiology of spinal and bulbar muscular atrophy: prevalence estimation and multiple founder haplotypes in the Veneto Italian region. [electronic resource] by Bertolin, C Querin, G Martinelli, I Pennuto, M Pegoraro, E Sorarù, G Producer: 20190819 In: European journal of neurology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Steroids in muscular dystrophy: where do we stand? [electronic resource] by Dubrovsky, A L Angelini, C Bonifati, D M Pegoraro, E Mesa, L Producer: 19981106 In: Neuromuscular disorders : NMD vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	The role of AR polyQ tract in male breast carcinoma: lesson from an SBMA case. [electronic resource] by Querin, G Martinelli, I Bertolin, C Pegoraro, E Pennuto, M Sorarù, G Producer: 20180508 In: Annals of oncology : official journal of the European Society for Medical Oncology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Deflazacort in Duchenne dystrophy: study of long-term effect. [electronic resource] by Angelini, C Pegoraro, E Turella, E Intino, M T Pini, A Costa, C Producer: 19940602 In: Muscle & nerve vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance. [electronic resource] by Morrone, A Pegoraro, E Angelini, C Zammarchi, E Marconi, G Hoffman, E P Producer: 19970424 In: The Journal of clinical investigation vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypes. [electronic resource] by Angelini, C Fanin, M Pegoraro, E Freda, M P Cadaldini, M Martinello, F Producer: 19950105 In: Neuromuscular disorders : NMD vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28. [electronic resource] by Pegoraro, E Whitaker, J Mowery-Rushton, P Surti, U Lanasa, M Hoffman, E P Producer: 19970826 In: American journal of human genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Secular trends in nosocomial candidaemia in non-neutropenic patients in an Italian tertiary hospital. [electronic resource] by Luzzati, R Allegranzi, B Antozzi, L Masala, L Pegoraro, E Azzini, A Concia, E Producer: 20051212 In: Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases vol. 11 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.