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	21.	Muscle energy metabolism in female DMD/BMD carriers: a 31P-MR spectroscopy study. [electronic resource] by Barbiroli, B Funicello, R Ferlini, A Montagna, P Zaniol, P Producer: 19920507 In: Muscle & nerve vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Expression, regulation and localisation of dystrophin isoforms in human foetal skeletal and cardiac muscle. [electronic resource] by Torelli, S Ferlini, A Obici, L Sewry, C Muntoni, F Producer: 20000214 In: Neuromuscular disorders : NMD vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	[The multitest in evaluating cellular immunity]. [electronic resource] by Bettoli, V Selvi, M Ferlini, A Pasi, F Patrizi, A Producer: 19900326 In: Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia vol. 124 Availability: No items available. Save to lists Add to cart (remove)
	24.	The effect of ofloxacin on the immune system of elderly patients. [electronic resource] by Munno, I Arpinelli, F Benedetti, M Spoglianti, R Ferlini, A Producer: 19900615 In: The Journal of antimicrobial chemotherapy vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	X-linked dilated cardiomyopathy and the dystrophin gene. [electronic resource] by Ferlini, A Sewry, C Melis, M A Mateddu, A Muntoni, F 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)
	26.	X-linked muscular dystrophies: studies through functional assay and DNA polymorphisms. [electronic resource] by Romeo, G Rocchi, M Roncuzzi, L Ferlini, A Nobile, C Rugolo, M Producer: 19880120 In: Advances in neurology vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	27.	Capillary electrophoresis of polymerase chain reaction-amplified products in polymer networks: the case of Kennedy's disease. [electronic resource] by Nesi, M Righetti, P G Patrosso, M C Ferlini, A Chiari, M Producer: 19941026 In: Electrophoresis vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy. [electronic resource] by Ferlini, A Galié, N Merlini, L Sewry, C Branzi, A Muntoni, F Producer: 19981224 In: American journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	31P-NMR spectroscopy of skeletal muscle in Becker dystrophy and DMD/BMD carriers. Altered rate of phosphate transport. [electronic resource] by Barbiroli, B Funicello, R Iotti, S Montagna, P Ferlini, A Zaniol, P Producer: 19920826 In: Journal of the neurological sciences vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Prenatal diagnosis of Duchenne muscular dystrophy by comparative genomic hybridization. [electronic resource] by Bovolenta, M Rimessi, P Dolcini, B Ravani, A Ferlini, A Gualandi, F Producer: 20100914 In: Clinical genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy? [electronic resource] by D'Alessandro, M Naom, I Ferlini, A Sewry, C Dubowitz, V Muntoni, F Producer: 19991110 In: Human genetics vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Electromyographic findings in transthyretin (TTR)-related familial amyloid polyneuropathy (FAP). [electronic resource] by Montagna, P Marchello, L Plasmati, R Ferlini, A Patrosso, M C Salvi, F Producer: 19961220 In: Electroencephalography and clinical neurophysiology vol. 101 Availability: No items available. Save to lists Add to cart (remove)
	33.	Molecular strategies in genetic diagnosis of transthyretin-related hereditary amyloidosis. [electronic resource] by Ferlini, A Fini, S Salvi, F Patrosso, M C Vezzoni, P Forabosco, A Producer: 19920827 In: FASEB journal : official publication of the Federation of American Societies for Experimental Biology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Seven novel additional small mutations and a new alternative splicing in the human dystrophin gene detected by heteroduplex analysis and restricted RT-PCR heteroduplex analysis of illegitimate transcripts. [electronic resource] by Barbieri, A M Soriani, N Ferlini, A Michelato, A Ferrari, M Carrera, P Producer: 19970102 In: European journal of human genetics : EJHG vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Predictors of cardiac arrhythmic events in non coronary artery disease patients. [electronic resource] by Balla, C Vitali, F Brieda, A Gualandi, F Ferlini, A Bertini, M Ferrari, R Producer: 20200127 In: BMC cardiovascular disorders vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR. [electronic resource] by Feriotto, G Ferlini, A Ravani, A Calzolari, E Mischiati, C Bianchi, N Gambari, R Producer: 20011212 In: Human mutation vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Discrimination of peripheral polyneuropathies caused by TTR variant or diabetes in the same pedigree through protein studies. [electronic resource] by Ferlini, A Romeo, G Tassinari, C A Saraiva, M J Costa, P P Salvi, F Producer: 19880120 In: Advances in neurology vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	38.	Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosis. [electronic resource] by Patrosso, M C Salvi, F De Grandis, D Vezzoni, P Jacobson, D R Ferlini, A Producer: 19980624 In: American journal of medical genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Calpain 3 deficiency presenting as fibre type disproportion. [electronic resource] by Vattemi, G Tonin, P Neri, M Marini, M Gualandi, F Guglielmi, V Ferlini, A Tomelleri, G Producer: 20100204 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)
	40.	Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele. [electronic resource] by Gualandi, E Ravani, A Berto, A Burdo, S Trevisi, P Ferlini, A Martini, A Calzolari, E Producer: 20041231 In: Acta oto-laryngologica. Supplementum no. 552 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 95 results.