Ngā hua rapu kaituhi

1

Mitochondrial disorders mā Massimo Zeviani

I whakaputaina 2004

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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2

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

I whakaputaina 2009

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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3

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

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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4

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

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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5

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

I whakaputaina 2018

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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6

Strategies for fighting mitochondrial diseases mā Carlo Viscomi, Massimo Zeviani

I whakaputaina 2020

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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7

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

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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8

Mitochondrial Retinopathies mā Massimo Zeviani, Valério Carelli

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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9

Mitochondrial Neurodegeneration mā Massimo Zeviani, Carlo Viscomi

I whakaputaina 2022

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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10

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

I whakaputaina 2015

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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11

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

I whakaputaina 2017

Whiwhi kuputuhi katoa
Artigo

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12

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

I whakaputaina 2020

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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13

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

I whakaputaina 2015

Whiwhi kuputuhi katoa
Revisão

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14

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

I whakaputaina 1984

Whiwhi kuputuhi katoa
Artigo

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15

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

I whakaputaina 2006

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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16

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

I whakaputaina 1996

Whiwhi kuputuhi katoa
Artigo

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17

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

I whakaputaina 2006

Whiwhi kuputuhi katoa
Artigo

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I tiakina i:
18

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

I whakaputaina 1997

Whiwhi kuputuhi katoa
Artigo

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19

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

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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20

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

I whakaputaina 2015

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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Ngā hua rapu - Massimo Zeviani

Mitochondrial disorders mā Massimo Zeviani

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

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

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

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

Strategies for fighting mitochondrial diseases mā Carlo Viscomi, Massimo Zeviani

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

Mitochondrial Retinopathies mā Massimo Zeviani, Valério Carelli

Mitochondrial Neurodegeneration mā Massimo Zeviani, Carlo Viscomi

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

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

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

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

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

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

Complex I deficiency is Associated with 3243G:C Mitochondrial DNA in Osteosarcoma Cell Cybrids mā 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) mā 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 mā 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 mā Ivano Di Meo, Silvia Marchet, Costanza Lamperti, Massimo Zeviani, Carlo Viscomi

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

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