C. Gellera: search on Z-Library

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1

Calvinist Metaphysics and the Eucharist in the Early Seventeenth Century

Gellera, Giovanni

Journal:

British Journal for the History of Philosophy

Year:

2013

Language:

english

File:

PDF, 189 KB

english, 2013

2

Contexts of religious tolerance: New perspectives from early modern Britain and beyond

Maurer, Christian, Gellera, Giovanni

Journal:

Global Intellectual History

Year:

2020

File:

PDF, 1.34 MB

2020

3

A novel SOD1 mutation in a young amyotrophic lateral sclerosis patient with a very slowly progressive clinical course

Eleni Georgoulopoulou, Cinzia Gellera, Cinzia Bragato, Patrizia Sola, Annalisa Chiari, Chiara Bernabei, Jessica Mandrioli

Journal:

Year:

2010

Language:

english

File:

PDF, 370 KB

english, 2010

4

LAS removal and biodegradation in a wastewater treatment plant

L. Cavalli, A. Gellera, A. Landone

Journal:

Environmental Toxicology and Chemistry

Year:

1993

Language:

english

File:

PDF, 590 KB

english, 1993

5

Preferential expression of mutantABCD1allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms

Ettore Salsano, Silvia Tabano, Silvia M Sirchia, Patrizia Colapietro, Barbara Castellotti, Cinzia Gellera, Marco Rimoldi, Viviana Pensato, Caterina Mariotti, Davide Pareyson, Monica Miozzo, Graziella

Journal:

Orphanet Journal of Rare Diseases

Year:

2012

Language:

english

File:

PDF, 287 KB

english, 2012

6

Co-occurrence of amyotrophic lateral sclerosis and Charcot-Marie-Tooth disease type 2A in a patient with a novel mutation in the mitofusin-2 gene

Chiara Marchesi, Claudia Ciano, Ettore Salsano, Lorenzo Nanetti, Micaela Milani, Cinzia Gellera, Franco Taroni, Gian Maria Fabrizi, Antonino Uncini, Davide Pareyson

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 88 KB

english, 2011

7

Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2

Elide Mantuano, Silvia Romano, Liana Veneziano, Cinzia Gellera, Barbara Castellotti, Sara Caimi, Daniela Testa, Margherita Estienne, Giovanna Zorzi, Marianna Bugiani, Yusuf A. Rajabally, Maria J Garcì

Journal:

Journal of the Neurological Sciences

Year:

2010

Language:

english

File:

PDF, 246 KB

english, 2010

8

SETXmutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein

Nanetti, Lorenzo, Cavalieri, Simona, Pensato, Viviana, Erbetta, Alessandra, Pareyson, Davide, Panzeri, Marta, Zorzi, Giovanna, Antozzi, Carlo, Moroni, Isabella, Gellera, Cinzia, Brusco, Alfredo, Mario

Journal:

Orphanet Journal of Rare Diseases

Year:

2013

Language:

english

File:

PDF, 559 KB

english, 2013

9

Large Pathogenic Expansions in the SCA2 and SCA7 Genes Can Be Detected by Fluorescent Repeat-Primed Polymerase Chain Reaction Assay

Cagnoli, Claudia, Stevanin, Giovanni, Michielotto, Chiara, Gerbino Promis, Giovanni, Brussino, Alessandro, Pappi, Patrizia, Durr, Alexandra, Dragone, Elisa, Viemont, Michelle, Gellera, Cinzia, Brice,

Journal:

The Journal of Molecular Diagnostics

Year:

2006

Language:

english

File:

PDF, 468 KB

english, 2006

10

Stance instability in preclinical SCA1 mutation carriers: A 4-year prospective posturography study

Nanetti, Lorenzo, Alpini, Dario, Mattei, Valentina, Castaldo, Anna, Mongelli, Alessia, Brenna, Greta, Gellera, Cinzia, Mariotti, Caterina

Journal:

Year:

2017

Language:

english

File:

PDF, 308 KB

english, 2017

11

Kv7.3 Compound Heterozygous Variants in Early Onset Encephalopathy Reveal Additive Contribution of C-Terminal Residues to PIP2-Dependent K+ Channel Gating

Ambrosino, Paolo, Freri, Elena, Castellotti, Barbara, Soldovieri, Maria Virginia, Mosca, Ilaria, Manocchio, Laura, Gellera, Cinzia, Canafoglia, Laura, Franceschetti, Silvana, Salis, Barbara, Iraci, Nu

Journal:

Molecular Neurobiology

Year:

2018

Language:

english

File:

PDF, 2.64 MB

english, 2018

12

Expanding The Central Nervous System Disease Spectrum Associated WITH Flnc Mutation

Previtali, Stefano C., Scarlato, Marina, Vezzulli, Paolo, Ruggieri, Alessandra, Velardo, Daniele, Benedetti, Sara, Torini, Giacomo, Colombo, Bruno, Maggi, Lorenzo, Bella, Daniela Di, Gellera, Cinzia,

Journal:

Year:

2019

Language:

english

File:

PDF, 1.09 MB

english, 2019

13

Frequency and distribution of polyQ disease intermediate-length repeat alleles in healthy Italian population

Mongelli, Alessia, Magri, Stefania, Salvatore, Elena, Rizzo, Elena, De Rosa, Anna, Fico, Tommasina, Gatti, Marta, Gellera, Cinzia, Taroni, Franco, Mariotti, Caterina, Nanetti, Lorenzo

Journal:

Neurological Sciences

Year:

2020

Language:

english

File:

PDF, 617 KB

english, 2020

14

Family and molecular data for a fine analysis of age at onset in Huntington disease

F. Squitieri, G. Sabbadini, P. Mandich, C. Gellera, E. Di Maria, E. Bellone, B. Castellotti, E. Nargi, U. de Grazia, M. Frontali, A. Novelletto

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 138 KB

english, 2000

15

The gender effect in juvenile Huntington disease patients of Italian origin

Milena Cannella, Cinzia Gellera, Vittorio Maglione, Patrizia Giallonardo, Giuliana Cislaghi, Maria Muglia, Aldo Quattrone, Francesco Pierelli, Stefano Di Donato, Ferdinando Squitieri

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2004

Language:

english

File:

PDF, 87 KB

english, 2004

16

Paraoxonase gene mutations in amyotrophic lateral sclerosis

Nicola Ticozzi, Ashley Lyn LeClerc, Pamela J. Keagle, Jonathan D. Glass, Anne-Marie Wills, Marka van Blitterswijk, Daryl A. Bosco, Ildefonso Rodriguez-Leyva, Cinzia Gellera, Antonia Ratti, Franco Taro

Journal:

Annals of Neurology

Year:

2010

Language:

english

File:

PDF, 132 KB

english, 2010

17

Normalization of short-chain acylcoenzyme a dehydrogenase after riboflavin treatment in a girl with multiple acylcoenzyme a dehydrogenase—deficient myopathy

Dr. Stefano Didonato, Cinzia Gellera, Dionisio Peluchetti, Graziella Uziel, Antonella Antonelli, Giacomo Lus, Marco Rimoldi

Journal:

Annals of Neurology

Year:

1989

Language:

english

File:

PDF, 867 KB

english, 1989

18

Measures of 104 faint common motion pairs of LUYTEN'S NLTT catalogue on prints of the Palomar Sky Survey

Journal:

Astronomische Nachrichten

Year:

1987

Language:

english

File:

PDF, 713 KB

english, 1987

19

Photographic measurements of 320 double stars of POURTEAU remeasured 50 years after their discovery

Journal:

Astronomische Nachrichten

Year:

1990

Language:

english

File:

PDF, 449 KB

english, 1990

20

High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis

Lucia Corrado, A. Ratti, C. Gellera, E. Buratti, B. Castellotti, Y. Carlomagno, N. Ticozzi, L. Mazzini, L. Testa, F. Taroni, F. E. Baralle, V. Silani, S. D'Alfonso

Journal:

Year:

2009

Language:

english

File:

PDF, 183 KB

english, 2009

21

Myoclonic dystonia as unique presentation of isolated vitamin E deficiency in a young patient

Lucia Angelini, Anna Erba, Caterina Mariotti, Cinzia Gellera, Claudia Ciano, Nardo Nardocci

Journal:

Movement Disorders

Year:

2002

Language:

english

File:

PDF, 4.11 MB

english, 2002

22

Brain diffusion-weighted imaging in Friedreich's ataxia

Giovanni Rizzo, Caterina Tonon, Maria Lucia Valentino, David Manners, Filippo Fortuna, Cinzia Gellera, Antonella Pini, Alessandro Ghezzo, Agostino Baruzzi, Claudia Testa, Emil Malucelli, Bruno Barbiro

Journal:

Movement Disorders

Year:

2011

Language:

english

File:

PDF, 271 KB

english, 2011

23

Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysis

Ferdinando Squitieri, Alfredo Berardelli, Eleonora Nargi, Barbara Castellotti, Caterina Mariotti, Milena Cannella, Maria Luisa Lavitrano, Ugo De Grazia, Cinzia Gellera, Stefano Ruggieri

Journal:

Clinical Genetics

Year:

2000

Language:

english

File:

PDF, 135 KB

english, 2000

24

The gene coding for PGC-1α modifies age at onset in Huntington's Disease

Patrick Weydt, Selma M Soyal, Cinzia Gellera, Stefano DiDonato, Claus Weidinger, Hannes Oberkofler, G Bernhard Landwehrmeyer, Wolfgang Patsch

Journal:

Molecular Neurodegeneration

Year:

2009

Language:

english

File:

PDF, 472 KB

english, 2009

25

Kennedy's disease: clinical and molecular study of two Italian families

D. Pareyson, B. Castellotti, S. Botti, C. A. Defanti, C. Gellera, F. Taroni, A. Sghirlanzoni

Journal:

Neurological Sciences

Year:

1995

Language:

english

File:

PDF, 376 KB

english, 1995

26

Myoadenylate deaminase deficiency in twins with recessive olivopontocerebellar atrophy

G. Uziel, F. Cornelio, C. Gellera, G. Perego, M. Rimoldi, S. Donato

Journal:

Neurological Sciences

Year:

1986

Language:

english

File:

PDF, 402 KB

english, 1986

27

Spinocerebellar ataxia type 17 (SCA17): Oculomotor phenotype and clinical characterization of 15 Italian patients

C. Mariotti, D. Alpini, R. Fancellu, P. Soliveri, M. Grisoli, S. Ravaglia, C. Lovati, V. Fetoni, G. Giaccone, A. Castucci, F. Taroni, C. Gellera, S. Di Donato

Journal:

Journal of Neurology

Year:

2007

Language:

english

File:

PDF, 361 KB

english, 2007

28

Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): a new case and review of the literature

Lorenzo Nanetti, Roberto Fancellu, Chiara Tomasello, Cinzia Gellera, Davide Pareyson, Caterina Mariotti

Journal:

Journal of Neurology

Year:

2009

Language:

english

File:

PDF, 117 KB

english, 2009

29

Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I:SCA1andSCA2are the most common genotypes

Davide Pareyson, Cinzia Gellera, Barbara Castellotti, Antonella Antonelli, Maria Concetta Riggio, Franca Mazzucchelli, Floriano Girotti, Vladimiro Pietrini, Caterina Mariotti, S. Di Donato

Journal:

Journal of Neurology

Year:

1999

Language:

english

File:

PDF, 58 KB

english, 1999

30

Efficacious vitamin E treatment in a child with ataxia with isolated vitamin E deficiency

Laura Doria-Lamba, Elisa De Grandis, Elisabetta Cristiani, Isabella Fiocchi, Luciano Montaldi, Paolo Grosso, Cinzia Gellera

Journal:

European Journal of Pediatrics

Year:

2006

Language:

english

File:

PDF, 56 KB

english, 2006

31

Genetic analysis of candidate genes modifying the age-at-onset in Huntington’s disease

Silke Metzger, Peter Bauer, Jürgen Tomiuk, Franco Laccone, Stefano DiDonato, Cinzia Gellera, Caterina Mariotti, Herwig W. Lange, Helga Weirich-Schwaiger, Gregor K. Wenning, Klaus Seppi, Bela Melegh, V

Journal:

Year:

2006

Language:

english

File:

PDF, 317 KB

english, 2006

32

The S18Y polymorphism in theUCHL1gene is a genetic modifier in Huntington’s disease

Silke Metzger, Peter Bauer, Juergen Tomiuk, Franco Laccone, Stefano Didonato, Cinzia Gellera, Paola Soliveri, Herwig W. Lange, Helga Weirich-Schwaiger, Gregor K. Wenning, Bela Melegh, Victoria Havasi,

Journal:

Year:

2006

Language:

english

File:

PDF, 95 KB

english, 2006

33

Frataxin gene point mutations in Italian Friedreich ataxia patients

Cinzia Gellera, Barbara Castellotti, Caterina Mariotti, Rossana Mineri, Viviana Seveso, Stefano DiDonato, Franco Taroni

Journal:

Year:

2007

Language:

english

File:

PDF, 253 KB

english, 2007

34

Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis

Cinzia Gellera, Claudia Colombrita, Nicola Ticozzi, Barbara Castellotti, Cinzia Bragato, Antonia Ratti, Franco Taroni, Vincenzo Silani

Journal:

Year:

2008

Language:

english

File:

PDF, 247 KB

english, 2008

35

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families

C. Mariotti, C. Gellera, M. Rimoldi, R. Mineri, G. Uziel, G. Zorzi, D. Pareyson, G. Piccolo, D. Gambi, S. Piacentini, F. Squitieri, R. Capra, B. Castellotti, S. Di Donato

Journal:

Neurological Sciences

Year:

2004

Language:

english

File:

PDF, 153 KB

english, 2004

36

The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias

S. Di Donato, C. Gellera, C. Mariotti

Journal:

Neurological Sciences

Year:

2001

Language:

english

File:

PDF, 170 KB

english, 2001

37

Cognitive and psychiatric characterization of patients with Huntington's disease and their at-risk relatives

P. Soliveri, D. Monza, S. Piacentini, D. Paridi, C. Nespolo, C. Gellera, C. Mariotti, A. Albanese, F. Girotti

Journal:

Neurological Sciences

Year:

2002

Language:

english

File:

PDF, 38 KB

english, 2002

38

Spinocerebellar ataxia type 28: A novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis

Caterina Mariotti, Alfredo Brusco, Daniela Di Bella, Claudia Cagnoli, Marco Seri, Cinzia Gellera, Stefano Di Donato, Franco Taroni

Journal:

Year:

2008

Language:

english

File:

PDF, 227 KB

english, 2008

39

Clinical and molecular findings in the first identified Italian family with dentatorubral-pallidoluysian atrophy

F. Villain, C. Gellera, R. Spreafico, B. Castellotti, M. Casazza, F. Carrara, G. Avanzini

Journal:

Acta Neurologica Scandinavica

Year:

1998

Language:

english

File:

PDF, 406 KB

english, 1998

40

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

Zeviani, Massimo, Servidei, Serenella, Gellera, Cinzia, Bertini, Enrico, DiMauro, Salvatore, DiDonato, Stefano

Journal:

Year:

1989

File:

PDF, 339 KB

1989

41

Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world

Lund, Annastiina, Udd, Bjarne, Juvonen, Vesa, Andersen, Peter M, Cederquist, Kristina, Davis, Mark, Gellera, Cinzia, Kölmel, Christina, Ronnevi, Lars-Olof, Sperfeld, Anne-Dorte

Journal:

European Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 598 KB

english, 2001

42

A Simple Multiplex Real-Time PCR Methodology for the SMN1 Gene Copy Number Quantification

Passon, Nadia, Pozzo, Federico, Molinis, Cristiano, Bregant, Elisa, Gellera, Cinzia, Damante, Giuseppe, Lonigro, Renata I.

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2009

Language:

english

File:

PDF, 140 KB

english, 2009

43

Evidence for two distinct mitochondrial malic enzymes in human skeletal muscle: purification and properties of the NAD(P)+-dependent enzyme

Franco Taroni, Cinzia Gellera, Stefano Di Donato

Journal:

Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology

Year:

1987

Language:

english

File:

PDF, 772 KB

english, 1987

44

Biological abnormalities of peripheral A2A receptors in a large representation of polyglutamine disorders and Huntington's disease stages

K. Varani, A.-C. Bachoud-Lévi, C. Mariotti, A. Tarditi, M.P. Abbracchio, V. Gasperi, P.A. Borea, G. Dolbeau, C. Gellera, A. Solari, A. Rosser, J. Naji, O. Handley, M. Maccarrone, Marc Peschanski, S. D

Journal:

Neurobiology of Disease

Year:

2007

Language:

english

File:

PDF, 303 KB

english, 2007

45

cDNA cloning and mitochondrial import of the β-subunit of the human electron-transfer flavoprotein

Gaetano FINOCCHIARO, Irma COLOMBO, Barbara GARAVAGLIA, Cinzia GELLERA, Giulio VALDAMERI, Nicoletta GARBUGLIO, Stefano DIDONATO

Journal:

Year:

1993

Language:

english

File:

PDF, 763 KB

english, 1993

46

Assignment of the Human Carnitine Palmitoyltransferase II Gene (CPT1) to Chromosome 1p32

Cinzia Gellera, Elisabetta Verderio, Giovanna Floridia, Gaetano Finocchiaro, Laura Montermini, Patrizia Cavadini, Orsetta Zuffardi, Franco Taroni

Journal:

Year:

1994

File:

PDF, 205 KB

1994

47

A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interference

Maria Stella Lombardi, Leonie Jaspers, Christine Spronkmans, Cinzia Gellera, Franco Taroni, Emilio Di Maria, Stefano Di Donato, William F. Kaemmerer

Journal:

Experimental Neurology

Year:

2009

Language:

english

File:

PDF, 454 KB

english, 2009

48

No association of DPP6 with amyotrophic lateral sclerosis in an Italian population

Isabella Fogh, Sandra D’Alfonso, Cinzia Gellera, Antonia Ratti, Cristina Cereda, Silvana Penco, Lucia Corrado, Gianni Sorarù, Barbara Castellotti, Cinzia Tiloca, Stella Gagliardi, Lorena Cozzi, Michel

Journal:

Neurobiology of Aging

Year:

2011

Language:

english

File:

PDF, 106 KB

english, 2011

49

ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counseling

Cinzia Gellera, Nicola Ticozzi, Viviana Pensato, Lorenzo Nanetti, Alessia Castucci, Barbara Castellotti, Giuseppe Lauria, Franco Taroni, Vincenzo Silani, Caterina Mariotti

Journal:

Neurobiology of Aging

Year:

2012

Language:

english

File:

PDF, 657 KB

english, 2012

50

Paroxysmal exercise-induced dyskinesia with self-limiting partial epilepsy: A novel GLUT-1 mutation with benign phenotype

Tommaso Bovi, Alfonso Fasano, Ina Juergenson, Cinzia Gellera, Barbara Castellotti, Elena Fontana, Michele Tinazzi

Journal:

Parkinsonism & Related Disorders

Year:

2011

Language:

english

File:

PDF, 449 KB

english, 2011