Lorena Mosca : rechercher sur Z-Library

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1

Process design for green hydrogen production

Mosca, Lorena, Medrano Jimenez, Jose Antonio, Wassie, Solomon Assefa, Gallucci, Fausto, Palo, Emma, Colozzi, Michele, Taraschi, Stefania, Galdieri, Giulio

Journal:

International Journal of Hydrogen Energy

Année:

2019

Fichier:

PDF, 1.68 MB

2019

2

Process design for green hydrogen production

Mosca, Lorena, Medrano Jimenez, Jose Antonio, Wassie, Solomon Assefa, Gallucci, Fausto, Palo, Emma, Colozzi, Michele, Taraschi, Stefania, Galdieri, Giulio

Journal:

International Journal of Hydrogen Energy

Année:

2019

Langue:

english

Fichier:

PDF, 1.68 MB

english, 2019

3

Individuals with familial hypercholesterolemia and cardiovascular events have higher circulating Lp(a) levels

Pavanello, Chiara, Pirazzi, Carlo, Bjorkman, Kristina, Sandstedt, Joakim, Tarlarini, Claudia, Mosca, Lorena, Romeo, Stefano, Calabresi, Laura, Mancina, Rosellina Margherita

Journal:

Journal of Clinical Lipidology

Année:

2019

Langue:

english

Fichier:

PDF, 642 KB

english, 2019

4

Mutational Screening ofNOTCH3Gene Reveals Two Novel Mutations: Complexity of CADASIL Diagnosis

Mosca, Lorena, Rivieri, Francesca, Tanel, Raffaella, Bonfante, Aldo, Burlina, Alessandro, Manfredini, Emanuela, Primignani, Paola, Gesu, Giovanni P., Marocchi, Alessandro, Penco, Silvana

Journal:

Journal of Molecular Neuroscience

Année:

2014

Langue:

english

Fichier:

PDF, 1.06 MB

english, 2014

5

Phenotypic Heterogeneity in aSOD1G93D Italian ALS Family: An Example of Human Model to Study a Complex Disease

Silvana Penco, Christian Lunetta, Lorena Mosca, Eleonora Maestri, Francesca Avemaria, Claudia Tarlarini, Maria Cristina Patrosso, Alessandro Marocchi, Massimo Corbo

Journal:

Journal of Molecular Neuroscience

Année:

2011

Langue:

english

Fichier:

PDF, 130 KB

english, 2011

6

De NovoMGC4607Gene Heterozygous Missense Variants in a Child with Multiple Cerebral Cavernous Malformations

Lorena Mosca, Silvana Pileggi, Francesca Avemaria, Claudia Tarlarini, Maria Sole Cigoli, Valeria Capra, Patrizia De Marco, Marco Pavanello, Alessandro Marocchi, Silvana Penco

Journal:

Journal of Molecular Neuroscience

Année:

2012

Langue:

english

Fichier:

PDF, 382 KB

english, 2012

7

No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population

Claudia Ricci, Silvana Penco, Michele Benigni, Lorena Mosca, Claudia Tarlarini, Christian Lunetta, Fabio Giannini, Massimo Corbo, Stefania Battistini

Journal:

Neurobiology of Aging

Année:

2012

Langue:

english

Fichier:

PDF, 322 KB

english, 2012

8

Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject

Lorena Mosca, Christian Lunetta, Claudia Tarlarini, Francesca Avemaria, Eleonora Maestri, Mario Melazzini, Massimo Corbo, Silvana Penco

Journal:

Neurobiology of Aging

Année:

2012

Langue:

english

Fichier:

PDF, 418 KB

english, 2012

9

NOTCH3 gene mutations in subjects clinically suspected of CADASIL

Lorena Mosca, Raffaella Marazzi, Alfonso Ciccone, Ignazio Santilli, Anna Bersano, Valeria Sansone, Enrico Grosso, Giorgia Mandrile, Daniela Francesca Giachino, Laura Adobbati, Elisabetta Corengia, Eli

Journal:

Journal of the Neurological Sciences

Année:

2011

Langue:

english

Fichier:

PDF, 263 KB

english, 2011

10

Hypomorphic NOTCH3 mutation in an Italian family with CADASIL features

Moccia, Marcello, Mosca, Lorena, Erro, Roberto, Cervasio, Mariarosaria, Allocca, Roberto, Vitale, Carmine, Leonardi, Antonio, Caranci, Ferdinando, Del Basso-De Caro, Maria Laura, Barone, Paolo, Penco,

Journal:

Neurobiology of Aging

Année:

2015

Langue:

english

Fichier:

PDF, 912 KB

english, 2015

11

The Role of Laparoscopy in Newborns Affected by NEC

Leva, Ernesto, Di Cesare, Antonio, Canazza, Lorena, Arnoldi, Rossella, Macchini, Francesco, Rossi, Vincenzo, Colnaghi, Maria Rosa, Pugni, Lorenza, Mosca, Fabio, Torricelli, Maurizio

Journal:

Journal of Laparoendoscopic & Advanced Surgical Techniques

Année:

2010

Langue:

english

Fichier:

PDF, 1.67 MB

english, 2010

12

Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression

Avemaria, Francesca, Lunetta, Christian, Tarlarini, Claudia, Mosca, Lorena, Maestri, Eleonora, Marocchi, Alessandro, Melazzini, Mario, Penco, Silvana, Corbo, Massimo

Journal:

Amyotrophic Lateral Sclerosis

Année:

2011

Langue:

english

Fichier:

PDF, 83 KB

english, 2011

13

Genetic variability of the fructosamine 3-kinase gene in diabetic patients

Mosca, Lorena, Penco, Silvana, Patrosso, Maria C., Marocchi, Alessandro, Lapolla, Annunziata, Sartore, Giovanni, Chilelli, Nino C., Paleari, Renata, Mosca, Andrea

Journal:

Clinical Chemistry and Laboratory Medicine

Année:

2011

Langue:

english

Fichier:

PDF, 136 KB

english, 2011

14

Progressive Parkinsonism, Balance Difficulties, and Supranuclear Gaze Palsy

Erro, Roberto, Lees, Andrew J., Moccia, Marcello, Picillo, Marina, Penco, Silvana, Mosca, Lorena, Vitale, Carmine, Barone, Paolo

Journal:

Année:

2014

Langue:

english

Fichier:

PDF, 349 KB

english, 2014

15

Specialized Oral Diet Improved Clinical Outcome of a Patient with Severe Intestinal Insufficiency in a Late Postoperative Period: A Case Report in Clinical Nutrition

Lopes, Marina G.F., De-Freitas, Lorena A., Martins, Tatiana C.P., Mosca, Etelvina R.T., Silva, Ane A.S.C., De-Souza, Daurea A.

Journal:

Journal of the Academy of Nutrition and Dietetics

Année:

2016

Langue:

english

Fichier:

PDF, 736 KB

english, 2016

16

TBK1 mutations in Italian patients with amyotrophic lateral sclerosis: genetic and functional characterisation

Pozzi, Laura, Valenza, Fabiola, Mosca, Lorena, Dal Mas, Andrea, Domi, Teuta, Romano, Alessandro, Tarlarini, Claudia, Falzone, Yuri Matteo, Tremolizzo, Lucio, Sorarù, Gianni, Cerri, Federica, Ferraro,

Journal:

Journal of Neurology Neurosurgery & Psychiatry

Année:

2017

Langue:

english

Fichier:

PDF, 966 KB

english, 2017

17

Increase in DNA methylation in patients with amyotrophic lateral sclerosis carriers of not fully penetrant SOD1 mutations

Coppedè, Fabio, Stoccoro, Andrea, Mosca, Lorena, Gallo, Roberta, Tarlarini, Claudia, Lunetta, Christian, Marocchi, Alessandro, Migliore, Lucia, Penco, Silvana

Journal:

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Année:

2017

Langue:

english

Fichier:

PDF, 544 KB

english, 2017

18

ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis

Lattante, Serena, Pomponi, Maria Grazia, Conte, Amelia, Marangi, Giuseppe, Bisogni, Giulia, Patanella, Agata Katia, Meleo, Emiliana, Lunetta, Christian, Riva, Nilo, Mosca, Lorena, Carrera, Paola, Bee,

Journal:

Neurobiology of Aging

Année:

2017

Langue:

english

Fichier:

PDF, 553 KB

english, 2017

19

Mitochondrial DNA copy number and D-loop region methylation in carriers of amyotrophic lateral sclerosis gene mutations

Stoccoro, Andrea, Mosca, Lorena, Carnicelli, Vittoria, Cavallari, Ugo, Lunetta, Christian, Marocchi, Alessandro, Migliore, Lucia, Coppedè, Fabio

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 1.09 MB

english, 2018

20

HLA-DRB1*15 association with multiple sclerosis is confirmed in a multigenerational Italian family

Journal:

Functional Neurology

Année:

2017

Langue:

english

Fichier:

PDF, 125 KB

english, 2017

21

Abdominal pain and fever in a patient with Familial Periodic Fever: An extremely rare mutation of the TNF Receptor Superfamily Member 1A gene

Marini, Michele, Rausa, Emanuele, Coccolini, Federico, Bianco, Federica, Merli, Cecilia, Greco, S., Brucato, Antonio Luca, Mosca, Lorena, Surace, Alessandra, Sironi, Sandro, Campanati, Luca, Ansaloni,

Journal:

Journal of Peritoneum (and other serosal surfaces)

Année:

2018

Langue:

english

Fichier:

PDF, 551 KB

english, 2018

22

The role of clinical and neuroimaging features in the diagnosis of CADASIL

Bersano, Anna, Bedini, Gloria, Markus, Hugh Stephen, Vitali, Paolo, Colli-Tibaldi, Enrico, Taroni, Franco, Gellera, Cinzia, Baratta, Silvia, Mosca, Lorena, Carrera, Paola, Ferrari, Maurizio, Cereda, C

Journal:

Journal of Neurology

Année:

2018

Langue:

english

Fichier:

PDF, 1.28 MB

english, 2018

23

Identification of a novel NOTCH3 mutation in an Italian family affected by a mild form of CADASIL

Ferrante, Enrico, Mosca, Lorena, Erminio, Cristina, Penco, Silvana, Cavallari, Ugo

Journal:

Neurological Sciences

Année:

2019

Langue:

english

Fichier:

PDF, 1.53 MB

english, 2019

24

Neurofilament light chain and C reactive protein explored as predictors of survival in amyotrophic lateral sclerosis

De Schaepdryver, Maxim, Lunetta, Christian, Tarlarini, Claudia, Mosca, Lorena, Chio, Adriano, Van Damme, Philip, Poesen, Koen

Journal:

Journal of Neurology Neurosurgery & Psychiatry

Année:

2020

Langue:

english

Fichier:

PDF, 510 KB

english, 2020

25

Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS Cohort

Scarlino, Stefania, Domi, Teuta, Pozzi, Laura, Romano, Alessandro, Pipitone, Giovanni Battista, Falzone, Yuri Matteo, Mosca, Lorena, Penco, Silvana, Lunetta, Christian, Sansone, Valeria, Tremolizzo, L

Journal:

International Journal of Molecular Sciences

Année:

2020

Fichier:

PDF, 648 KB

2020

26

Urinary neopterin, a new marker of the neuroinflammatory status in amyotrophic lateral sclerosis

Lunetta, Christian, Lizio, Andrea, Gerardi, Francesca, Tarlarini, Claudia, Filippi, Massimo, Riva, Nilo, Tremolizzo, Lucio, Diamanti, Susanna, Dellanoce, Cinzia Carla, Mosca, Lorena, Sansone, Valeria

Journal:

Journal of Neurology

Année:

2020

Fichier:

PDF, 822 KB

2020

27

Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis

Stoccoro, Andrea, Smith, Adam R., Mosca, Lorena, Marocchi, Alessandro, Gerardi, Francesca, Lunetta, Christian, Cereda, Cristina, Gagliardi, Stella, Lunnon, Katie, Migliore, Lucia, CoppedÃ¨, Fabio

Journal:

Clinical Epigenetics

Année:

2020

Fichier:

PDF, 1.46 MB

2020

28

11 CâPK11195 PETâbased molecular study of microglia activation in SOD1 amyotrophic lateral sclerosis

Tondo, Giacomo, Iaccarino, Leonardo, Cerami, Chiara, Vanoli, Giovanna Emilia, Presotto, Luca, Masiello, Valeria, Coliva, Angela, Salvi, Fabrizio, Bartolomei, Ilaria, Mosca, Lorena, Lunetta, Christian,

Journal:

Annals of Clinical and Translational Neurology

Année:

2020

Fichier:

PDF, 909 KB

2020

29

[BMJ Publishing Group Ltd and European League Against Rheumatism Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12â15 June 2019 - ()] Abstracts Accepted for Publication - AB1106âPREVALENCE AND EPIDEMIOLOGY OF FAMILIAL MEDITERRANEAN FEVER AND TUMOR NECROSIS FACTORRECEPTOR-ASSOCIATED PERIODIC SYNDROME: RESULTS FROM AN ITALIAN CENTER

Talotta, Rossella, Mosca, Lorena, Rucci, Francesco, Brucato, Antonio, Atzeni, Fabiola, Perno, Carlo Federico, Scaglione, Francesco, Cavallari, Ugo

Année:

2019

Fichier:

PDF, 1.51 MB

2019