M. Rimoldi - Concepedia

Author

M. Rimoldi

Fondazione IRCCS Istituto Neurologico Carlo Besta ORCID

Also Known As

M Rimoldi, M. Rimoldi, Martina Rimoldi

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Fondazione IRCCS Istituto Neurologico Carlo Besta University of Milan Mario Negri Institute for Pharmacological Research Bambino Gesù Children's Hospital Istituti di Ricovero e Cura a Carattere Scientifico

About

M. Rimoldi is an author at Fondazione IRCCS Istituto Neurologico Carlo Besta specializing in medicine, metabolism, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	25	1.3K
2	Biochemistry	8	8	280
3	Health Sciences	3	3	43
4	Social Sciences	3	3	42
5	Cell Biology	1	1	48

M. Rimoldi

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR) Massimo Zeviani, Cinzia Gellera, Carlo Antozzi, The Lancet Mitochondrial MyopathyMendelian DisorderGenetic DisorderGeneticsMitochondrial Dna Trnaleu	1991	383
Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families Caterina Mariotti, Cinzia Gellera, M. Rimoldi, Neurological Sciences Mendelian DisorderGenetic DisorderInherited Metabolic DiseaseGenetic EpidemiologyNovel Mutations	2004	154
Respiratory chain and mitochondrial DNA in muscle and brain in Parkinson's disease patients Stefano DiDonato, Massimo Zeviani, P. Giovannini, Neurology	1993	98
Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymes Cinzia Gellera, Graziella Uziel, M. Rimoldi, Neurology	1990	96
Propionylcarnitine excretion in propionic and methylmalonic acidurias: a cause of carnitine deficiency Stefano Di Donato, M. Rimoldi, Barbara Garavaglia, Clinica Chimica Acta UrologyPhysiologyPropionylcarnitine ExcretionCarnitine DeficiencyMethylmalonic Acidurias	1984	89
Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho transformants Valeria Tiranti, M. Munaro, Doriana Sandonà, Human Molecular Genetics	1995	83
Late‐onset riboflavin‐responsive myopathy with combined multiple acyl coenzyme A dehydrogenase and respiratory chain deficiency Carlo Antozzi, Barbara Garavaglia, Marina Mora, Neurology	1994	76
Cytochrome-C-oxidase deficiency in muscles of a floppy infant without mitochondrial myopathy M. Rimoldi, E. Bottacchi, Loreto Rossi, Journal of Neurology Mitochondrial MyopathyMuscle FunctionBiochemistryMitochondrial FunctionMedicine	1982	75
Fulminant Leigh syndrome and sudden unexpected death in a family with the T9176C mutation of the mitochondrial ATPase 6 gene Carlo Dionisi‐Vici, Sara Seneca, Massimo Zeviani, Journal of Inherited Metabolic Disease	1998	68
Identification of new mutations in the <i>ETHE1</i> gene in a cohort of 14 patients presenting with ethylmalonic encephalopathy Rossana Mineri, M. Rimoldi, Alberto Burlina, Journal of Medical Genetics	2008	66

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