Your search returned 13 results.

Results
	1.	Root resorption in elderly patients. [electronic resource] by Aguilar, P E Aguilar, A P Rolleri, M F Ubios, A M Producer: 20040826 In: Acta odontologica latinoamericana : AOL vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	2.	A 'de novo' point mutation of the low-density lipoprotein receptor gene in an Italian subject with primary hypercholesterolemia. [electronic resource] by Cassanelli, S Bertolini, S Rolleri, M De Stefano, F Casarino, L Elicio, N Naselli, A Calandra, S Producer: 19980911 In: Clinical genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia. [electronic resource] by Bertolini, S Cassanelli, S Garuti, R Ghisellini, M Simone, M L Rolleri, M Masturzo, P Calandra, S Producer: 19990316 In: Arteriosclerosis, thrombosis, and vascular biology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Occurrence of multiple aberrantly spliced mRNAs of the LDL-receptor gene upon a donor splice site mutation that causes familial hypercholesterolemia (FHBenevento). [electronic resource] by Lelli, N Garuti, R Ghisellini, M Tiozzo, R Rolleri, M Aimale, V Ginocchio, E Naselli, A Bertolini, S Calandra, S Producer: 19951010 In: Journal of lipid research vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	5.	Pseudodominance of lipoprotein lipase (LPL) deficiency due to a nonsense mutation (Tyr302>Term) in exon 6 of LPL gene in an Italian family from Sardinia (LPL(Olbia)). [electronic resource] by Bertolini, S Simone, M L Pes, G M Ghisellini, M Rolleri, M Bellocchio, A Elicio, N Masturzo, P Calandra, S Producer: 20000512 In: Clinical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A new missense mutation (Cys297-->Phe) of the low density lipoprotein receptor in Italian patients with familial hypercholesterolemia (FHTrieste). [electronic resource] by Lelli, N Garuti, R Pedrazzi, P Ghisellini, M Simone, M L Tiozzo, R Cattin, L Valenti, M Rolleri, M Bertolini, S Producer: 19940602 In: Human genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Apolipoprotein E epsilon 4 allele frequency is not increased in progressive supranuclear palsy. [electronic resource] by Tabaton, M Rolleri, M Masturzo, P Cammarata, S Angelini, G Hansen, L A Saitoh, T Petersen, R B Perry, G Richey, P Producer: 19951017 In: Neurology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Four novel partial deletions of LDL-receptor gene in Italian patients with familial hypercholesterolemia. [electronic resource] by Bertolini, S Garuti, R Lelli, W Rolleri, M Tiozzo, R M Ghisellini, M Simone, M L Masturzo, P Elicio, N C Stefanutti, C Producer: 19950620 In: Arteriosclerosis, thrombosis, and vascular biology vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Influence of beta(0)-thalassemia on the phenotypic expression of heterozygous familial hypercholesterolemia : a study of patients with familial hypercholesterolemia from Sardinia. [electronic resource] by Deiana, L Garuti, R Pes, G M Carru, C Errigo, A Rolleri, M Pisciotta, L Masturzo, P Cantafora, A Calandra, S Bertolini, S Producer: 20000128 In: Arteriosclerosis, thrombosis, and vascular biology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Hypocomplementemic type II membranoproliferative glomerulonephritis in a male patient with familial lecithin-cholesterol acyltransferase deficiency due to two different allelic mutations. [electronic resource] by Sessa, A Battini, G Meroni, M Daidone, G Carnera, I Brambilla, P L Viganò, G Giordano, F Pallotti, F Torri Tarelli, L Calabresi, L Rolleri, M Bertolini, S Producer: 20011011 In: Nephron vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Two Italian kindreds carrying the Arg136-->Ser mutation of the Apo E gene: development of premature and severe atherosclerosis in the presence of epsilon 2 as second allele. [electronic resource] by Rolleri, M Vivona, N Emmanuele, G Cefalù, A B Pisciotta, L Guido, V Noto, D Fiore, B Barbagallo, C M Notarbartolo, A Travali, S Bertolini, S Averna, M R Producer: 20031208 In: Nutrition, metabolism, and cardiovascular diseases : NMCD vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patients. [electronic resource] by Cefalù, A B Barbagallo, C M Sesti, E Caldarella, R Polizzi, F Marino, G Noto, D Rolleri, M Travali, S Scalisi, G Notarbartolo, A Corsini, A Bertolini, S Averna, M R Producer: 20020724 In: Clinical and experimental medicine vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotype. [electronic resource] by Bertolini, S Cantafora, A Averna, M Cortese, C Motti, C Martini, S Pes, G Postiglione, A Stefanutti, C Blotta, I Pisciotta, L Rolleri, M Langheim, S Ghisellini, M Rabbone, I Calandra, S Producer: 20001012 In: Arteriosclerosis, thrombosis, and vascular biology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)