Canlyniadau Chwilio am Awdur

1

Mitochondrial disorders gan Massimo Zeviani

Cyhoeddwyd 2004

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Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
2

Disorders from perturbations of nuclear‐mitochondrial intergenomic cross‐talk gan Antonella Spinazzola, Massimo Zeviani

Cyhoeddwyd 2009

Cael y testun llawn Cael y testun llawn
Artigo

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
3

Altered Sulfide (H2S) Metabolism in Ethylmalonic Encephalopathy gan Valeria Tiranti, Massimo Zeviani

Cyhoeddwyd 2013

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Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
4

MtDNA‐maintenance defects: syndromes and genes gan Carlo Viscomi, Massimo Zeviani

Cyhoeddwyd 2017

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Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
5

Human diseases associated with defects in assembly of OXPHOS complexes gan Daniele Ghezzi, Massimo Zeviani

Cyhoeddwyd 2018

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Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
6

Strategies for fighting mitochondrial diseases gan Carlo Viscomi, Massimo Zeviani

Cyhoeddwyd 2020

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Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
7

Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions gan Margherita Protasoni, Massimo Zeviani

Cyhoeddwyd 2021

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Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
8

Mitochondrial Retinopathies gan Massimo Zeviani, Valério Carelli

Cyhoeddwyd 2021

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Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
9

Mitochondrial Neurodegeneration gan Massimo Zeviani, Carlo Viscomi

Cyhoeddwyd 2022

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Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
10

Nuclear gene mutations as the cause of mitochondrial complex III deficiency gan Erika Fernández‐Vizarra, Massimo Zeviani

Cyhoeddwyd 2015

Cael y testun llawn Cael y testun llawn
Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
11

Mitochondrial complex III Rieske Fe-S protein processing and assembly gan Erika Fernández‐Vizarra, Massimo Zeviani

Cyhoeddwyd 2017

Cael y testun llawn
Artigo

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
12

Mitochondrial disorders of the OXPHOS system gan Erika Fernández‐Vizarra, Massimo Zeviani

Cyhoeddwyd 2020

Cael y testun llawn Cael y testun llawn
Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
13

Emerging concepts in the therapy of mitochondrial disease gan Carlo Viscomi, Emanuela Bottani, Massimo Zeviani

Cyhoeddwyd 2015

Cael y testun llawn
Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
14

Myofibrillar-protein isoforms and sarcoplasmic-reticulum Ca2+-transport activity of single human muscle fibres gan G. Salviati, Romeo Betto, Daniela Danieli‐Betto, Massimo Zeviani

Cyhoeddwyd 1984

Cael y testun llawn
Artigo

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
15

Mitochondrial medicine: A metabolic perspective on the pathology of oxidative phosphorylation disorders gan Jan Smeitink, Massimo Zeviani, Douglass M. Turnbull, Howard T. Jacobs

Cyhoeddwyd 2006

Cael y testun llawn Cael y testun llawn
Revisão

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
16

Complex I deficiency is Associated with 3243G:C Mitochondrial DNA in Osteosarcoma Cell Cybrids gan Donald R. Dunbar, Pamela Moonie, Massimo Zeviani, Ian Holt

Cyhoeddwyd 1996

Cael y testun llawn
Artigo

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
17

Nonsense mutation in pseudouridylate synthase 1 (PUS1) in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia (MLASA) gan Erika Fernández‐Vizarra, Angela Berardinelli, Lucia Valente, Valeria Tiranti, Massimo Zeviani

Cyhoeddwyd 2006

Cael y testun llawn
Artigo

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
18

Expression of the SMN Gene, the Spinal Muscular Atrophy Determining Gene, in the Mammalian Central Nervous System gan Giorgio Battaglia, Alessandra P. Princivalle, Francesca Forti, Carlotta Lizier, Massimo Zeviani

Cyhoeddwyd 1997

Cael y testun llawn
Artigo

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
19

AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome gan Ivano Di Meo, Silvia Marchet, Costanza Lamperti, Massimo Zeviani, Carlo Viscomi

Cyhoeddwyd 2017

Cael y testun llawn Cael y testun llawn
Artigo

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:
20

Loss of apoptosis-inducing factor critically affects MIA40 function gan Katharina Meyer, Sabrina Buettner, Daniele Ghezzi, Massimo Zeviani, Daniele Bano, Pierluigi Nicotera

Cyhoeddwyd 2015

Cael y testun llawn Cael y testun llawn
Artigo

Ychwanegu at ffefrynnau

Wedi'i Gadw mewn:

Canlyniadau Chwilio - Massimo Zeviani

Mitochondrial disorders gan Massimo Zeviani

Disorders from perturbations of nuclear‐mitochondrial intergenomic cross‐talk gan Antonella Spinazzola, Massimo Zeviani

Altered Sulfide (H2S) Metabolism in Ethylmalonic Encephalopathy gan Valeria Tiranti, Massimo Zeviani

MtDNA‐maintenance defects: syndromes and genes gan Carlo Viscomi, Massimo Zeviani

Human diseases associated with defects in assembly of OXPHOS complexes gan Daniele Ghezzi, Massimo Zeviani

Strategies for fighting mitochondrial diseases gan Carlo Viscomi, Massimo Zeviani

Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions gan Margherita Protasoni, Massimo Zeviani

Mitochondrial Retinopathies gan Massimo Zeviani, Valério Carelli

Mitochondrial Neurodegeneration gan Massimo Zeviani, Carlo Viscomi

Nuclear gene mutations as the cause of mitochondrial complex III deficiency gan Erika Fernández‐Vizarra, Massimo Zeviani

Mitochondrial complex III Rieske Fe-S protein processing and assembly gan Erika Fernández‐Vizarra, Massimo Zeviani

Mitochondrial disorders of the OXPHOS system gan Erika Fernández‐Vizarra, Massimo Zeviani

Emerging concepts in the therapy of mitochondrial disease gan Carlo Viscomi, Emanuela Bottani, Massimo Zeviani

Myofibrillar-protein isoforms and sarcoplasmic-reticulum Ca2+-transport activity of single human muscle fibres gan G. Salviati, Romeo Betto, Daniela Danieli‐Betto, Massimo Zeviani

Mitochondrial medicine: A metabolic perspective on the pathology of oxidative phosphorylation disorders gan Jan Smeitink, Massimo Zeviani, Douglass M. Turnbull, Howard T. Jacobs

Complex I deficiency is Associated with 3243G:C Mitochondrial DNA in Osteosarcoma Cell Cybrids gan Donald R. Dunbar, Pamela Moonie, Massimo Zeviani, Ian Holt

Nonsense mutation in pseudouridylate synthase 1 (PUS1) in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia (MLASA) gan Erika Fernández‐Vizarra, Angela Berardinelli, Lucia Valente, Valeria Tiranti, Massimo Zeviani

Expression of the SMN Gene, the Spinal Muscular Atrophy Determining Gene, in the Mammalian Central Nervous System gan Giorgio Battaglia, Alessandra P. Princivalle, Francesca Forti, Carlotta Lizier, Massimo Zeviani

AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome gan Ivano Di Meo, Silvia Marchet, Costanza Lamperti, Massimo Zeviani, Carlo Viscomi

Loss of apoptosis-inducing factor critically affects MIA40 function gan Katharina Meyer, Sabrina Buettner, Daniele Ghezzi, Massimo Zeviani, Daniele Bano, Pierluigi Nicotera

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