1.5 Abstract in rivista

1.5 Abstract in rivista: [1775] Home page tipologia

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Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 601 a 620 di 1.775

Unwanted stethoscopes’ hosts

2013-01-01 Messina, Gabriele; Ceriale, Emma; Burgassi, Sandra; Mariani, L.; Taddei, L.; Lenzi, D.; Manzi, P.

40 years of Italian suicide history: women are not the weak gender

2013-01-01 Messina, G.; Serafini, A.; Quercioli, C.; Gentile, A. M.; Fantozzi, P. L.; Nante, N.

Environmental contaminants in hospital settings and progress in disinfecting techniques

2013-01-01 Messina, G.; Ceriale, E.; Lenzi, D.; Burgassi, S.; Azzolini, E.; Manzi, P.

New diagnostic and therapeutic strategies in acute and chronic central serous corioretinopathy

2013-01-01 Fruschelli, Mario; Denaro, Rosario; Esposti, G.; Frezzotti, P.; Torchia, R.; Esposti, Pl

Vitamin D deficiency and arterial stiffness in isolated systolic hypertention: cause-effect relatioship or mere association with aging

2013-01-01 R., Nami; A., Tafa; C. R., Pondrelli; B., Franci; Campagna, MARIA STELLA; B., Lucani; A., Giambelluca; Gonnelli, Stefano

The Effects of Intravenous Aminobisphosphonates on Carotid Atherosclerosis could Be Influenced by the Changes in FGF23 Serum Levels

2013-01-01 Gonnelli, Stefano; Caffarelli, Carla; L., Tanzilli; M. D., Tomai Pitinca; A., Cadirni; Campagna, MARIA STELLA; M. B., Franci; Nuti, Ranuccio

Vascular risk factors in glaucoma: The results of a national survey

2004-01-01 Orzalesi, N.; Frezzotti, Paolo; OPTIME Study, Grp

Optic nerve fibre layer thickness in patients with CADASIL: an optical coherence tomography (OCT) study

2008-01-01 Rufa, Alessandra; Pretegiani, E.; Frezzotti, Paolo; Dotti, Maria; Federico, Antonio

Neuro-ophthalmologic aspects of CADASIL

2009-01-01 Rufa, A.; Frezzotti, P.; Rosini, F.; Pretegiani, E.; Stromillo, M. L.; Dotti, M. T.; Federico, A.

EBV-Bart-6-3p induces cell proliferation and escape of immunosurveillance in BL cell lines and primary tumours

2012-01-01 De Falco, G; Navari, M; Onnis, A; Di Lisio, L; Martinez, N; Leon, Ea; Montes-Moreno, S; Rogena, E; Bellan, C; Piris, Ma; Leoncini, L

Novel Genomic Alterations in MCL1 and ARID1A Identified in Pediatric Burkitt Lymphoma Using Targeted High-Throughput Sequencing

2012-01-01 Roth, Lisa Giulino; Wang, Kai; Macdonald, Theresa; Mathew, Susan; Tam, Yifang; Cronin, Maureen T.; Palmer, Gary; Lucena Silva, Norma; Pedrosa, Francisco; Pedrosa, Marcia; Teruya Feldstein, Julie; Bhagat, Govind; Alobeid, Bachir; Leoncini, Lorenzo; Bellan, Cristiana; Rogena, Emily; Rubin, Mark A.; Ribeiro, Raul; Yelensky, Roman; Tam, Wayne; Stephens, Philip; Cesarman, Ethel

Role of the Hypoxia-Inducible Factor-1alpha and Akt on hypoxia-induced migratory program in dendritic cells

2013-01-01 Filippi, I.; Aldinucci, C.; Pucci, A.; Sozzani, S.; Carraro, F.; Naldini, A.

Late-onset GM2-gangliosidosis in two siblings of Ashkenazi Jewish ancestry results from a mutation in the HEXA gene causing abnormal thermolability of Hexosaminidase A

1995-01-01 De Gasperi, R.; Gama Sosa, M. A.; Battistini, S.; Yeretsian, J.; Kolodny, E. H.

Molecular genetics of late-onset forms of Krabbe’s disease

1995-01-01 Kolodny, E. H.; Gama Sosa, M. A.; Battistini, S.; De Gasperi, R.

Substitution of alanine 531 with a threonine residue at the carboxy terminal end of the -chain is associated with thermolabile Hexosaminidase B in a Jewish family of Oriental ancestry

1995-01-01 Gama Sosa, M. A.; De Gasperi, R.; Grebner, E. E.; Mansfield, D.; Battistini, S.; Sartorato, E. L.; Raghavan, S. S.; Davis, J. G.; Kolodny, E. H

Multiple mutations in the galactocerebrosidase gene are associated with a very mild late-onset form of Globoid cell leukodystrophy

1997-01-01 Kolodny, E. H.; Gama Sosa, M. A.; Battistini, S.; Sartorato, E.; Raghavan, S.; De Gasperi, R.

Search for candidate genes in common Migraine in the Italian population

2000-01-01 Carrera, P.; Stenirri, S.; Battistini, S.; Ferrari, M.

Evidence for a founder effect for the Gly41Ser SOD1 gene mutation: report of four amyothrophic lateral sclerosis italian families from central Italy.

2003-01-01 Battistini, Stefania; G., Siciliano; R., Roggeri; A., Carducci; M., Mancuso; A., Del Corona; A., Rocchi; P., Carrera

Phenotipic-genotypic study of amyothrophic lateral sclerosis Italian families with the G41S SOD1 gene mutation.

2005-01-01 Giannini, Fabio; Battistini, Stefania; Ricci, Claudia; G., Greco; A., Del Corona; A., Rocchi; P., Carrera; G., Siciliano

The” D90A” still an enigma among SOD1 gene mutations. Report of three italian cases.

2005-01-01 Battistini, Stefania; Giannini, Fabio; G., Greco; Ricci, Claudia; E., Lotti; A., Del Corona; G., Siciliano; P., Carrera

Titolo	Data di pubblicazione	Autore(i)	Abstract
Unwanted stethoscopes’ hosts	1-gen-2013	Messina, Gabriele; Ceriale, Emma; Burgassi, Sandra; Mariani, L.; Taddei, L.; Lenzi, D.; Manzi, P.	-
40 years of Italian suicide history: women are not the weak gender	1-gen-2013	Messina, G.; Serafini, A.; Quercioli, C.; Gentile, A. M.; Fantozzi, P. L.; Nante, N.	-
Environmental contaminants in hospital settings and progress in disinfecting techniques	1-gen-2013	Messina, G.; Ceriale, E.; Lenzi, D.; Burgassi, S.; Azzolini, E.; Manzi, P.	-
New diagnostic and therapeutic strategies in acute and chronic central serous corioretinopathy	1-gen-2013	Fruschelli, Mario; Denaro, Rosario; Esposti, G.; Frezzotti, P.; Torchia, R.; Esposti, Pl	-
Vitamin D deficiency and arterial stiffness in isolated systolic hypertention: cause-effect relatioship or mere association with aging	1-gen-2013	R., Nami; A., Tafa; C. R., Pondrelli; B., Franci; Campagna, MARIA STELLA; B., Lucani; A., Giambelluca; Gonnelli, Stefano	-
The Effects of Intravenous Aminobisphosphonates on Carotid Atherosclerosis could Be Influenced by the Changes in FGF23 Serum Levels	1-gen-2013	Gonnelli, Stefano; Caffarelli, Carla; L., Tanzilli; M. D., Tomai Pitinca; A., Cadirni; Campagna, MARIA STELLA; M. B., Franci; Nuti, Ranuccio	-
Vascular risk factors in glaucoma: The results of a national survey	1-gen-2004	Orzalesi, N.; Frezzotti, Paolo; OPTIME Study, Grp	-
Optic nerve fibre layer thickness in patients with CADASIL: an optical coherence tomography (OCT) study	1-gen-2008	Rufa, Alessandra; Pretegiani, E.; Frezzotti, Paolo; Dotti, Maria; Federico, Antonio	-
Neuro-ophthalmologic aspects of CADASIL	1-gen-2009	Rufa, A.; Frezzotti, P.; Rosini, F.; Pretegiani, E.; Stromillo, M. L.; Dotti, M. T.; Federico, A.	-
EBV-Bart-6-3p induces cell proliferation and escape of immunosurveillance in BL cell lines and primary tumours	1-gen-2012	De Falco, G; Navari, M; Onnis, A; Di Lisio, L; Martinez, N; Leon, Ea; Montes-Moreno, S; Rogena, E; Bellan, C; Piris, Ma; Leoncini, L	-
Novel Genomic Alterations in MCL1 and ARID1A Identified in Pediatric Burkitt Lymphoma Using Targeted High-Throughput Sequencing	1-gen-2012	Roth, Lisa Giulino; Wang, Kai; Macdonald, Theresa; Mathew, Susan; Tam, Yifang; Cronin, Maureen T.; Palmer, Gary; Lucena Silva, Norma; Pedrosa, Francisco; Pedrosa, Marcia; Teruya Feldstein, Julie; Bhagat, Govind; Alobeid, Bachir; Leoncini, Lorenzo; Bellan, Cristiana; Rogena, Emily; Rubin, Mark A.; Ribeiro, Raul; Yelensky, Roman; Tam, Wayne; Stephens, Philip; Cesarman, Ethel	-
Role of the Hypoxia-Inducible Factor-1alpha and Akt on hypoxia-induced migratory program in dendritic cells	1-gen-2013	Filippi, I.; Aldinucci, C.; Pucci, A.; Sozzani, S.; Carraro, F.; Naldini, A.	-
Late-onset GM2-gangliosidosis in two siblings of Ashkenazi Jewish ancestry results from a mutation in the HEXA gene causing abnormal thermolability of Hexosaminidase A	1-gen-1995	De Gasperi, R.; Gama Sosa, M. A.; Battistini, S.; Yeretsian, J.; Kolodny, E. H.	-
Molecular genetics of late-onset forms of Krabbe’s disease	1-gen-1995	Kolodny, E. H.; Gama Sosa, M. A.; Battistini, S.; De Gasperi, R.	-
Substitution of alanine 531 with a threonine residue at the carboxy terminal end of the -chain is associated with thermolabile Hexosaminidase B in a Jewish family of Oriental ancestry	1-gen-1995	Gama Sosa, M. A.; De Gasperi, R.; Grebner, E. E.; Mansfield, D.; Battistini, S.; Sartorato, E. L.; Raghavan, S. S.; Davis, J. G.; Kolodny, E. H	-
Multiple mutations in the galactocerebrosidase gene are associated with a very mild late-onset form of Globoid cell leukodystrophy	1-gen-1997	Kolodny, E. H.; Gama Sosa, M. A.; Battistini, S.; Sartorato, E.; Raghavan, S.; De Gasperi, R.	-
Search for candidate genes in common Migraine in the Italian population	1-gen-2000	Carrera, P.; Stenirri, S.; Battistini, S.; Ferrari, M.	-
Evidence for a founder effect for the Gly41Ser SOD1 gene mutation: report of four amyothrophic lateral sclerosis italian families from central Italy.	1-gen-2003	Battistini, Stefania; G., Siciliano; R., Roggeri; A., Carducci; M., Mancuso; A., Del Corona; A., Rocchi; P., Carrera	-
Phenotipic-genotypic study of amyothrophic lateral sclerosis Italian families with the G41S SOD1 gene mutation.	1-gen-2005	Giannini, Fabio; Battistini, Stefania; Ricci, Claudia; G., Greco; A., Del Corona; A., Rocchi; P., Carrera; G., Siciliano	-
The” D90A” still an enigma among SOD1 gene mutations. Report of three italian cases.	1-gen-2005	Battistini, Stefania; Giannini, Fabio; G., Greco; Ricci, Claudia; E., Lotti; A., Del Corona; G., Siciliano; P., Carrera	-

Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 601 a 620 di 1.775

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