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Andreina Bordoni

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Dario Ronchi; Monica Sciacco; Binghui Shen; Yate-Ching Yuan; Li Zheng; Andreina Bordoni; Nereo Bresolin; Stefania Corti; Alessio Di Fonzo; Elisa Fassone; Maria Teresa Ferrò; Massimiliano Filosto; Hongzhi Li; Weiqiang Lin; Changwei Liu; Francesca Magri; Maurizio Moggio; Serena Pagliarani; Lorenzo Peverelli; Michela Ranieri; Mafalda Rizzuti; Giacomo Pietro Comi
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability.
Marianna Ciccolella; Giacomo Pietro Comi; Stefania Corti; Adele D'Amico; Monica Nizzardo; Stefania Petrini; Teresa Rizza; Cristiano Rizzo; Dario Ronchi; Giulia Tozzi; Andreina Bordoni; Rosalba Carrozzo; Michela Catteruccia; Enrico Bertini
Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutations.
Francesca Magri; Maurizio Moggio; Laura Napoli; Monica Sciacco; Roberto Del Bo; Sara Bonato; Andreina Bordoni; Nereo Bresolin; Erika Brighina; Patrizia Ciscato; Stefania Corti; Maria Grazia D'Angelo; Francesco Fortunato; Sandra Gandossini; Alessandra Govoni; Valeria Lucchini; Giacomo P Comi
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients.

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All Publications

2013: Dario Ronchi; Monica Sciacco; Binghui Shen; Yate-Ching Yuan; Li Zheng; Andreina Bordoni; Nereo Bresolin; Stefania Corti; Alessio Di Fonzo; Elisa Fassone; Maria Teresa Ferrò; Massimiliano Filosto; Hongzhi Li; Weiqiang Lin; Changwei Liu; Francesca Magri; Maurizio Moggio; Serena Pagliarani; Lorenzo Peverelli; Michela Ranieri; Mafalda Rizzuti; Giacomo Pietro Comi
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability.
American journal of human genetics 2013;92(2):293-300.
2013: Marianna Ciccolella; Giacomo Pietro Comi; Stefania Corti; Adele D'Amico; Monica Nizzardo; Stefania Petrini; Teresa Rizza; Cristiano Rizzo; Dario Ronchi; Giulia Tozzi; Andreina Bordoni; Rosalba Carrozzo; Michela Catteruccia; Enrico Bertini
Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutations.
Journal of medical genetics 2013;50(2):104-7.
2012: Francesca Magri; Maurizio Moggio; Laura Napoli; Monica Sciacco; Roberto Del Bo; Sara Bonato; Andreina Bordoni; Nereo Bresolin; Erika Brighina; Patrizia Ciscato; Stefania Corti; Maria Grazia D'Angelo; Francesco Fortunato; Sandra Gandossini; Alessandra Govoni; Valeria Lucchini; Giacomo P Comi
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients.
Neuromuscular disorders : NMD 2012;22(11):934-43.
2012: Michela Ranieri; Giulietta Riboldi; Dario Ronchi; Maura Servida; Andreina Bordoni; Nereo Bresolin; Irene Colombo; Giacomo P Comi; Alessandra Cosi; Roberto Del Bo; Francesca Magri; Maurizio Moggio; Stefania Corti
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families.
Journal of the neurological sciences 2012;315(1-2):146-9.
2012: Dario Ronchi; Monica Sciacco; Maura Servida; Andreina Bordoni; Nereo Bresolin; Patrizia Ciscato; Stefania Corti; Alessandra Cosi; Alessio Di Fonzo; Elisa Fassone; Maurizio Moggio; Monika Raimondi; Michela Ripolone; Mafalda Rizzuti; Giacomo P Comi
The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairment.
European journal of human genetics : EJHG 2012;20(3):357-60.
2011: Dario Ronchi; Monica Sciacco; Andreina Bordoni; Nereo Bresolin; Patrizia Ciscato; Martina Collotta; Irene Colombo; Stefania Corti; Alessandra Cosi; Alessio Di Fonzo; Elisa Fassone; Valeria Lucchini; Maurizio Moggio; Laura Napoli; Mafalda Rizzuti; Giacomo P Comi
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia.
Journal of the neurological sciences 2011;308(1-2):173-6.
2011: Francesca Magri; Maurizio Moggio; Gandossini Sandra; Monica Sciacco; Silvana Tedeschi; Yvan Torrente; Anna Carla Turconi; Sara Bonato; Andreina Bordoni; Nereo Bresolin; Patrizia Ciscato; Stefania Corti; Domenico Coviello; Maria Grazia D'Angelo; Roberto Del Bo; Francesco Fortunato; Serena Ghezzi; Alessandra Govoni; Costanza Lamperti; Valeria Lucchini; Giacomo Pietro Comi
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up.
Journal of neurology 2011;258(9):1610-23.
2011: Dario Ronchi; Marco Ronzoni; Monica Sciacco; Maura Servida; Andreina Bordoni; Nereo Bresolin; Martina Collotta; Stefania Corti; Alessandra Cosi; Alessio Di Fonzo; Elisa Fassone; Valeria Lucchini; Marco Mattioli; Maurizio Moggio; Mafalda Rizzuti; Giacomo P Comi
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutation.
Biochemical and biophysical research communications 2011;412(2):245-8.
2011: Dario Ronchi; Monica Sciacco; Davide Tonduti; Pierangelo Veggiotti; Angela Berardinelli; Andreina Bordoni; Sophie Cagdas; Giuseppe Capovilla; Martina Collotta; Alessandra Cosi; Francesco Fortunato; Maurizio Moggio; Simona Orcesi; Mafalda Rizzuti; Giacomo P Comi
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation: a case report.
BMC neurology 2011;11():85.
2011: Francesca Magri; Roberto Del Bo; Maria G D'Angelo; Alessandra Govoni; Serena Ghezzi; Sandra Gandossini; Monica Sciacco; Patrizia Ciscato; Andreina Bordoni; Silvana Tedeschi; Francesco Fortunato; Valeria Lucchini; Matteo Cereda; Stefania Corti; Maurizio Moggio; Nereo Bresolin; Giacomo P Comi
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing.
BMC medical genetics 2011;12():37.
2010: Veronica Crugnola; Costanza Lamperti; Valeria Lucchini; Dario Ronchi; Lorenzo Peverelli; Alessandro Prelle; Monica Sciacco; Andreina Bordoni; Elisa Fassone; Francesco Fortunato; Stefania Corti; Vincenzo Silani; Nereo Bresolin; Salvatore Di Mauro; Giacomo P Comi; Maurizio Moggio
Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosis.
Archives of neurology 2010;67(7):849-54.
2010: Dario Ronchi; Roberta Virgilio; Andreina Bordoni; Elisa Fassone; Monica Sciacco; Patrizia Ciscato; Maurizio Moggio; Alessandra Govoni; Stefania Corti; Nereo Bresolin; Giacomo P Comi
The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment.
Journal of the neurological sciences 2010;292(1-2):107-10.
2009: Costanza Lamperti; Sabrina Lucchiari; Alessandro Prelle; M Ripolone; Sabrina Salani; Andreina Bordoni; Nereo Bresolin; A Cappellini; C Colombo; Giacomo P Comi; V Crugnola; Gigliola Fagiolari; M E Fruguglietti; Maurizio Moggio
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 gene.
Journal of inherited metabolic disease 2009;32 Suppl 1():S161-8.
2009: Roberta Virgilio; Dario Ronchi; Andreina Bordoni; Elisa Fassone; Sara Bonato; Chiara Donadoni; Giuseppe Torgano; Maurizio Moggio; Stefania Corti; Nereo Bresolin; Giacomo P Comi
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study.
Journal of the neurological sciences 2009;281(1-2):85-92.
2009: Alessio Di Fonzo; Dario Ronchi; Tiziana Lodi; Elisa Fassone; Marco Tigano; Costanza Lamperti; Stefania Corti; Andreina Bordoni; Francesco Fortunato; Monica Nizzardo; Laura Napoli; Chiara Donadoni; Sabrina Salani; Francesca Saladino; Maurizio Moggio; Nereo Bresolin; Iliana Ferrero; Giacomo P Comi
The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency.
American journal of human genetics 2009;84(5):594-604.
2009: Stefania Corti; Chiara Donadoni; Dario Ronchi; Andreina Bordoni; Francesco Fortunato; Domenico Santoro; Roberto Del Bo; Valeria Lucchini; Veronica Crugnola; Dimitra Papadimitriou; Sabrina Salani; Maurizio Moggio; Nereo Bresolin; Giacomo P Comi
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction.
Journal of the neurological sciences 2009;276(1-2):170-4.
2008: Peter Seibel; Chiara Di Nunno; Christian Kukat; Ingo Schäfer; Roberto Del Bo; Andreina Bordoni; Giacomo P Comi; Astrid Schön; Ferdinando Capuano; Dominga Latorre; Gaetano Villani
Cosegregation of novel mitochondrial 16S rRNA gene mutations with the age-associated T414G variant in human cybrids.
Nucleic acids research 2008;36(18):5872-81.
2008: Stefania Corti; Monica Nizzardo; Martina Nardini; Chiara Donadoni; Sabrina Salani; Dario Ronchi; Francesca Saladino; Andreina Bordoni; Francesco Fortunato; Roberto Del Bo; Dimitra Papadimitriou; Federica Locatelli; Giorgia Menozzi; Sandra Strazzer; Nereo Bresolin; Giacomo P Comi
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophy.
The Journal of clinical investigation 2008;118(10):3316-30.
2008: Stefania Corti; Andreina Bordoni; D Ronchi; Olimpia Musumeci; Mohammed Aguennouz; Antonio Toscano; Costanza Lamperti; Nereo Bresolin; Giacomo P Comi
Clinical features and new molecular findings in Carnitine Palmitoyltransferase II (CPT II) deficiency.
Journal of the neurological sciences 2008;266(1-2):97-103.
2008: Michela Guglieri; Francesca Magri; Maria Grazia D'Angelo; Alessandro Prelle; Lucia Morandi; Carmelo Rodolico; Rachele Cagliani; Marina Mora; Francesco Fortunato; Andreina Bordoni; Roberto Del Bo; Serena Ghezzi; Serena Pagliarani; Sabrina Lucchiari; Sabrina Salani; Chiara Zecca; Costanza Lamperti; Dario Ronchi; Mohammed Aguennouz; Patrizia Ciscato; Claudia Di Blasi; Alessandra Ruggieri; Isabella Moroni; Anna Turconi; Antonio Toscano; Maurizio Moggio; Nereo Bresolin; Giacomo P Comi
Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients.
Human mutation 2008;29(2):258-66.
2007: Olimpia Musumeci; Mohammed Aguennouz; Giacomo P Comi; Carmelo Rodolico; Massimo Autunno; Andreina Bordoni; Silvia Baratta; Franco Taroni; Giuseppe Vita; Antonio Toscano
Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency.
Neuromuscular disorders : NMD 2007;17(11-12):960-3.
2006: Manuela Sironi; Uberto Pozzoli; Giacomo P Comi; Stefania Riva; Andreina Bordoni; Nereo Bresolin; Dilip K Nag
A region in the dystrophin gene major hot spot harbors a cluster of deletion breakpoints and generates double-strand breaks in yeast.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2006;20(11):1910-2.
2006: Sara Galbiati; Andreina Bordoni; Dimitra Papadimitriou; Antonio Toscano; Carmelo Rodolico; Efi Katsarou; Monica Sciacco; Anastasia Garufi; Alessandro Prelle; M 'hammed Aguennouz; Maria Bonsignore; Crimi Marco; Andrea Martinuzzi; Nereo Bresolin; Alexandros Papadimitriou; Giacomo P Comi
New mutations in TK2 gene associated with mitochondrial DNA depletion.
Pediatric neurology 2006;34(3):177-85.
2006: Stefania Corti; Federica Locatelli; Dimitra Papadimitriou; Chiara Donadoni; Roberto Del Bo; Crimi Marco; Andreina Bordoni; Francesco Fortunato; Sandra Strazzer; Giorgia Menozzi; Sabrina Salani; Nereo Bresolin; Giacomo P Comi
Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1.
Human molecular genetics 2006;15(2):167-87.
2005: Monica Sciacco; Alessandro Prelle; Gigliola Fagiolari; Andreina Bordoni; Crimi Marco; Alessio Di Fonzo; Patrizia Ciscato; Costanza Lamperti; Elisabetta D'Adda; Stefano Jann; Nereo Bresolin; Giacomo P Comi; Maurizio Moggio
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy.
Journal of the neurological sciences 2005;239(1):21-4.
2005: Crimi Marco; Andreina Bordoni; Giorgia Menozzi; Laura Riva; Francesco Fortunato; Sara Galbiati; Roberto Del Bo; Uberto Pozzoli; Nereo Bresolin; Giacomo P Comi
Skeletal muscle gene expression profiling in mitochondrial disorders.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2005;19(7):866-8.
2004: Crimi Marco; Alexandros Papadimitriou; Sara Galbiati; Phani Palamidou; Francesco Fortunato; Andreina Bordoni; Urania Papandreou; Dimitra Papadimitriou; Georgios M Hadjigeorgiou; Eurydiki Drogari; Nereo Bresolin; Giacomo P Comi
A new mitochondrial DNA mutation in ND3 gene causing severe Leigh syndrome with early lethality.
Pediatric research 2004;55(5):842-6.
2004: Crimi Marco; Sara Galbiati; Monica Sciacco; Andreina Bordoni; Maria Grazia Natali; Massimo Raimondi; Nereo Bresolin; Giacomo P Comi
Mitochondrial-DNA nucleotides G4298A and T10010C as pathogenic mutations: the confirmation in two new cases.
Mitochondrion 2004;3(5):279-83.
2003: Federica Locatelli; Stefania Corti; Chiara Donadoni; Michela Guglieri; F Capra; Sandra Strazzer; Sabrina Salani; Roberto Del Bo; Francesco Fortunato; Andreina Bordoni; Giacomo P Comi
Neuronal differentiation of murine bone marrow Thy-1- and Sca-1-positive cells.
Journal of hematotherapy & stem cell research 2003;12(6):727-34.
2003: Monica Sciacco; Alessandro Prelle; Elisabetta D'Adda; Costanza Lamperti; Andreina Bordoni; Mario Rango; Crimi Marco; Giacomo P Comi; Nereo Bresolin; Maurizio Moggio
Familial mtDNA T8993C transition causing both the NARP and the MILS phenotype in the same generation. A morphological, genetic and spectroscopic study.
Journal of neurology 2003;250(12):1498-500.
2003: Alessio Di Fonzo; Andreina Bordoni; Crimi Marco; Galbiati Sara; Roberto Del Bo; Nereo Bresolin; Giacomo P Comi
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions.
Human mutation 2003;22(6):498-9.
2003: Crimi Marco; Roberto Del Bo; Sara Galbiati; Monica Sciacco; Andreina Bordoni; Nereo Bresolin; Giacomo P Comi
Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion.
European journal of human genetics : EJHG 2003;11(11):896-8.
2003: Roberto Del Bo; Andreina Bordoni; Monica Sciacco; Alessio Di Fonzo; Sara Galbiati; Crimi Marco; Nereo Bresolin; Giacomo P Comi
Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domain.
Neurology 2003;61(7):903-8.
2003: Roberto Del Bo; Crimi Marco; Monica Sciacco; Giulia Malferrari; Andreina Bordoni; Laura Napoli; Alessandro Prelle; Ida Biunno; Maurizio Moggio; Nereo Bresolin; Guglielmo Scarlato; Giacomo Pietro Comi
High mutational burden in the mtDNA control region from aged muscles: a single-fiber study.
Neurobiology of aging 2003;24(6):829-38.
2003: Crimi Marco; Sara Galbiati; Isabella Moroni; Andreina Bordoni; Maria Paola Perini; Eleonora Lamantea; Monica Sciacco; Massimo Zeviani; Ida Biunno; Maurizio Moggio; Guglielmo Scarlato; Giacomo P Comi
A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome.
Neurology 2003;60(11):1857-61.
2003: Crimi Marco; Sara Galbiati; Maria Paola Perini; Andreina Bordoni; Giulia Malferrari; Monica Sciacco; Ida Biunno; Sandra Strazzer; Maurizio Moggio; Nereo Bresolin; Giacomo P Comi
A mitochondrial tRNA(His) gene mutation causing pigmentary retinopathy and neurosensorial deafness.
Neurology 2003;60(7):1200-3.
2002: Crimi Marco; Monica Sciacco; Sara Galbiati; Andreina Bordoni; Giulia Malferrari; Roberto Del Bo; Ida Biunno; Nereo Bresolin; Giacomo P Comi
A collection of 33 novel human mtDNA homoplasmic variants.
Human mutation 2002;20(5):409.
2002: Roberto Del Bo; Andreina Bordoni; Filippo Martinelli Boneschi; Crimi Marco; Monica Sciacco; Nereo Bresolin; Guglielmo Scarlato; Giacomo P Comi
Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients.
Journal of the neurological sciences 2002;202(1-2):85-91.
2002: Eleonora Lamantea; Valeria Tiranti; Andreina Bordoni; Antonio Toscano; Francesco Bono; Serenella Servidei; Alex Papadimitriou; Hans Spelbrink; Laura Silvestri; Giorgio Casari; Giacomo P Comi; Massimo Zeviani
Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.
Annals of neurology 2002;52(2):211-9.
2002: Alessandro Prelle; Lucia Tancredi; Monica Sciacco; Luca Chiveri; Giacomo P Comi; Alessandro Battistel; Paola Bazzi; Filippo Martinelli Boneschi; Vincenzo Bagnardi; Patrizia Ciscato; Andreina Bordoni; Francesco Fortunato; Sandra Strazzer; Nereo Bresolin; Guglielmo Scarlato; Maurizio Moggio
Retrospective study of a large population of patients with asymptomatic or minimally symptomatic raised serum creatine kinase levels.
Journal of neurology 2002;249(3):305-11.
2001: Laura Napoli; Andreina Bordoni; M Zeviani; Georgios M Hadjigeorgiou; Monica Sciacco; Valeria Tiranti; AE Terentiou; Maurizio Moggio; Alexandros Papadimitriou; Guglielmo Scarlato; Giacomo P Comi
A novel missense adenine nucleotide translocator-1 gene mutation in a Greek adPEO family.
Neurology 2001;57(12):2295-8.
2001: Monica Sciacco; Alessandro Prelle; Giacomo P Comi; Laura Napoli; Alessandro Battistel; Nereo Bresolin; Lucia Tancredi; Costanza Lamperti; Andreina Bordoni; Gigliola Fagiolari; Patrizia Ciscato; Luca Chiveri; Maria Paola Perini; Francesco Fortunato; L Adobbati; S Messina; Antonio Toscano; Filippo Martinelli Boneschi; Alexandros Papadimitriou; Guglielmo Scarlato; Maurizio Moggio
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation.
Journal of neurology 2001;248(9):778-88.
2001: Giacomo P Comi; Francesco Fortunato; Sabrina Lucchiari; Andreina Bordoni; Alessandro Prelle; Stefano Jann; A Keller; Patrizia Ciscato; Sara Galbiati; Luca Chiveri; Yvan Torrente; Guglielmo Scarlato; Nereo Bresolin
Beta-enolase deficiency, a new metabolic myopathy of distal glycolysis.
Annals of neurology 2001;50(2):202-7.
1999: Georgios M Hadjigeorgiou; Giacomo P Comi; Andreina Bordoni; J Shen; Y T Chen; Sabrina Salani; Antonio Toscano; Francesco Fortunato; Sabrina Lucchiari; Nereo Bresolin; Carmelo Rodolico; M G Piscaglia; L Franceschina; Alexandros Papadimitriou; Guglielmo Scarlato
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa.
Journal of inherited metabolic disease 1999;22(6):762-3.
1998: L Franceschina; Sabrina Salani; Andreina Bordoni; Monica Sciacco; Laura Napoli; Giacomo P Comi; Alessandro Prelle; Francesco Fortunato; Georgios M Hadjigeorgiou; E Farina; Nereo Bresolin; M G D'Angelo; Guglielmo Scarlato
A novel mitochondrial tRNA(Ile) point mutation in chronic progressive external ophthalmoplegia.
Journal of neurology 1998;245(11):755-8.
1998: Alexandros Papadimitriou; Giacomo P Comi; Georgios M Hadjigeorgiou; Andreina Bordoni; Monica Sciacco; Laura Napoli; Alessandro Prelle; Maurizio Moggio; Gigliola Fagiolari; Nereo Bresolin; Sabrina Salani; IE Anastasopoulos; G Giassakis; R Divari; Guglielmo Scarlato
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.
Neurology 1998;51(4):1086-92.
1998: Giacomo P Comi; Andreina Bordoni; Sabrina Salani; L Franceschina; Monica Sciacco; Alessandro Prelle; Francesco Fortunato; M Zeviani; Laura Napoli; Nereo Bresolin; Maurizio Moggio; CD Ausenda; J W Taanman; Guglielmo Scarlato
Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.
Annals of neurology 1998;43(1):110-6.
1996: CD Ausenda; Nereo Bresolin; A De Liso; Maria Grazia D'Angelo; Maurizio Moggio; Roberto Del Bo; A Gallanti; G P Comi; Yvan Torrente; Andreina Bordoni; Guglielmo Scarlato
In vivo biolistic technique in control and mdx dystrophic mice.
Muscle & nerve 1996;19(7):912-4.
1995: I Moroni; E F Gonano; G P Comi; Vincenzo Tegazzin; Alessandro Prelle; Andreina Bordoni; Nereo Bresolin; Guglielmo Scarlato
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility.
Journal of neurology 1995;242(3):127-33.
1994: A Fassati; S Tedeschi; Andreina Bordoni; P Amboni; C Curcio; Nereo Bresolin; Guglielmo Scarlato
Rapid direct diagnosis of deletions carriers of Duchenne and Becker muscular dystrophies.
Lancet 1994;344(8918):302-3.
1994: L Bet; Maurizio Moggio; G P Comi; Claudio Mariani; Alessandro Prelle; N Checcarelli; Andreina Bordoni; Nereo Bresolin; Elio Scarpini; Guglielmo Scarlato
Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseases.
Journal of neurology 1994;241(8):511-6.
1994: N Checcarelli; Alessandro Prelle; Maurizio Moggio; G Comi; Nereo Bresolin; Alexandros Papadimitriou; G Fagiolari; Andreina Bordoni; Guglielmo Scarlato
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy.
Journal of the neurological sciences 1994;123(1-2):74-9.
1994: A Fassati; Andreina Bordoni; P Amboni; Francesco Fortunato; G Fagiolari; Nereo Bresolin; Alessandro Prelle; G Comi; Guglielmo Scarlato
Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile.
Journal of the neurological sciences 1994;123(1-2):140-6.
1994: G P Comi; Alessandro Prelle; Nereo Bresolin; Maurizio Moggio; A Bardoni; A Gallanti; Giuseppe Vita; Antonio Toscano; M T Ferro; Andreina Bordoni
Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates.
Brain : a journal of neurology 1994;117 ( Pt 1)():1-14.
1994: Alessandro Prelle; G Fagiolari; N Checcarelli; Maurizio Moggio; A Battistel; G P Comi; Paola Bazzi; Andreina Bordoni; Massimo Zeviani; Guglielmo Scarlato
Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber level.
Acta neuropathologica 1994;87(4):371-6.
1993: Alessandro Prelle; Maurizio Moggio; N Checcarelli; G Comi; Nereo Bresolin; A Battistel; Andreina Bordoni; Guglielmo Scarlato
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis.
Journal of the neurological sciences 1993;117(1-2):24-7.
1993: Giuseppe Vita; Antonio Toscano; Alessandro Prelle; Andreina Bordoni; N Checcarelli; Nereo Bresolin; A Baradello; Corrado Messina
Muscle mitochondria investigation in myotonic dystrophy.
European neurology 1993;33(6):423-7.
1991: Giovanni Meola; G Rotondo; M Velicogna; R Toppi; Valeria Sansone; Nereo Bresolin; G Comi; Andreina Bordoni; P Amati; CD Ausenda
[Expression of a defect in the respiratory chain in cultured human cells].
Rivista di neurologia 1991;61(4):122-34.
1990: Massimo Zeviani; Nereo Bresolin; Cinzia Gellera; Andreina Bordoni; M Pannacci; P Amati; M Moggio; Serenella Servidei; Guglielmo Scarlato; S DiDonato
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease.
American journal of human genetics 1990;47(6):904-14.
1990: Carola Ponzetto; Nereo Bresolin; Andreina Bordoni; Maurizio Moggio; Giovanni Meola; L Bet; Alessandro Prelle; Guglielmo Scarlato
Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues.
Journal of the neurological sciences 1990;96(2-3):207-10.