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Showing results (91-100 of 166) with videos related to

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Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|March 7, 2013
Systemic AA amyloidosis as a unique manifestation of a combined mutation of TNFRSF1A and MEFV genesOana M Mereuta, Simone Baldovino, Edoardo Errichiello, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|May 29, 2012
An ALS case with a novel D90N-SOD1 heterozygous missense mutationAndrea Calvo, Antonio Ilardi, Cristina Moglia, et al.
Human Genetics|September 12, 2000
Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) geneR Rabionet, L Zelante, N López-Bigas, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 10, 2014
A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year courseAntonio Canosa, Andrea Calvo, Cristina Moglia, et al.
Human Genetics|February 28, 2003
No evidence of fetal DNA persistence in maternal plasma after pregnancyMaddalena Smid, Silvia Galbiati, Antonia Vassallo, et al.
British Journal of Haematology|July 10, 2001
Severe and long-lasting disruption of T-cell receptor diversity in human myeloma after high-dose chemotherapy and autologous peripheral blood progenitor cell infusionS Mariani, M Coscia, J Even, et al.
Human Genetics|October 1, 1993
Small frameshift deletions within the COL4A5 gene in juvenile-onset Alport syndromeA Renieri, M Seri, L Galli, et al.
Lupus|January 12, 2012
NEMO syndrome (incontinentia pigmenti) and systemic lupus erythematosus: a new disease associationG B Piccoli, R Attini, F N Vigotti, et al.
BMC Nephrology|February 23, 2012
Chronic kidney disease, severe arterial and arteriolar sclerosis and kidney neoplasia: on the spectrum of kidney involvement in MELAS syndromeGiorgina Barbara Piccoli, Laura Davico Bonino, Paola Campisi, et al.
Blood|February 1, 1990
Recurrent mutations and three novel rearrangements in the factor VIII gene of hemophilia A patients of Italian descentL Casula, S Murru, M Pecorara, et al.
Pageof 17

Showing results (91-100 of 166) with videos related to

Sort By:
Pageof 17
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|March 7, 2013
Systemic AA amyloidosis as a unique manifestation of a combined mutation of TNFRSF1A and MEFV genesOana M Mereuta, Simone Baldovino, Edoardo Errichiello, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|May 29, 2012
An ALS case with a novel D90N-SOD1 heterozygous missense mutationAndrea Calvo, Antonio Ilardi, Cristina Moglia, et al.
Human Genetics|September 12, 2000
Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) geneR Rabionet, L Zelante, N López-Bigas, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 10, 2014
A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year courseAntonio Canosa, Andrea Calvo, Cristina Moglia, et al.
Human Genetics|February 28, 2003
No evidence of fetal DNA persistence in maternal plasma after pregnancyMaddalena Smid, Silvia Galbiati, Antonia Vassallo, et al.
British Journal of Haematology|July 10, 2001
Severe and long-lasting disruption of T-cell receptor diversity in human myeloma after high-dose chemotherapy and autologous peripheral blood progenitor cell infusionS Mariani, M Coscia, J Even, et al.
Human Genetics|October 1, 1993
Small frameshift deletions within the COL4A5 gene in juvenile-onset Alport syndromeA Renieri, M Seri, L Galli, et al.
Lupus|January 12, 2012
NEMO syndrome (incontinentia pigmenti) and systemic lupus erythematosus: a new disease associationG B Piccoli, R Attini, F N Vigotti, et al.
BMC Nephrology|February 23, 2012
Chronic kidney disease, severe arterial and arteriolar sclerosis and kidney neoplasia: on the spectrum of kidney involvement in MELAS syndromeGiorgina Barbara Piccoli, Laura Davico Bonino, Paola Campisi, et al.
Blood|February 1, 1990
Recurrent mutations and three novel rearrangements in the factor VIII gene of hemophilia A patients of Italian descentL Casula, S Murru, M Pecorara, et al.
Pageof 17