Juliana Gurgel‐Giannetti

Author

Universidade Federal de Minas Gerais ORCID

Also Known As

Gurgel-Giannetti, Juliana, J Gurgel-Giannetti, J. Gurgel-Giannetti, J. Gurgel‐Giannetti, J.G. Giannetti, Juliana G Giannetti, Juliana G. Giannetti, Juliana Giannetti, Juliana Gurgel Giannetti, Juliana Gurgel-Giannetti

112

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

Universidade Federal de Minas Gerais Universidade de São Paulo Columbia University Irving Medical Center Inserm National Institutes of Health

About

Juliana Gurgel‐Giannetti is an author at Universidade Federal de Minas Gerais specializing in medicine, neuropathology, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	377
2	Health Sciences	1	1	244
3	Social Sciences	1	1	28
4	Genetic Medicine	1	1	34
5	Molecular Medicine	1	1	16

Juliana Gurgel‐Giannetti

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Myocardial Delayed Enhancement by Magnetic Resonance Imaging in Patients With Muscular Dystrophy Marly Conceição Silva, Zilda Maria Alves Meira, Juliana Gurgel‐Giannetti, Journal of the American College of Cardiology Cardiac MuscleCardiomyopathyHealth SciencesMedical ImagingMyocardial Delayed Enhancement	2007	244
Consensus Statement on Standard of Care for Congenital Myopathies Ching H. Wang, James J. Dowling, Kathryn N. North, Journal of Child Neurology Neuromusculoskeletal DisorderRare DiseasesPediatric Orthopedic SurgeryMendelian DisorderCare Committee	2012	182
Myocardial Fibrosis Progression in Duchenne and Becker Muscular Dystrophy Marly Conceição Silva, Tiago Augusto Magalhães, Zilda Maria Alves Meira, JAMA Cardiology	2016	112
Central core disease due to recessive mutations in <i>RYR1</i> gene: Is it more common than described? Patrícia M. Kossugue, Júlia Filardi Paim, Monica M. Navarro, Muscle & Nerve	2007	52
A novel complex neurological phenotype due to a homozygous mutation in FDX2 Juliana Gurgel‐Giannetti, David S. Lynch, Anderson Rodrigues Brandão de Paiva, Brain Muscle TissueNeurodegenerative DiseasesMuscle BiopsyMendelian DisorderNeurological Disorder	2018	51
Novel De Novo Mutations in <i>KIF1A</i> as a Cause of Hereditary Spastic Paraplegia With Progressive Central Nervous System Involvement Leslie Hotchkiss, Sandra Donkervoort, M. Leach, Journal of Child Neurology	2016	49
Deletion of the RMGA and CHD2 genes in a child with epilepsy and mental deficiency Leonardo Pires Capelli, Ana Cristina Victorino Krepischi, Juliana Gurgel‐Giannetti, European Journal of Medical Genetics Developmental BiologyMendelian DisorderMental DeficiencyGenetic DisorderGenetics	2011	47
Efficacy of Caffeine in <scp>ADCY5</scp>‐Related Dyskinesia: A Retrospective Study Aurélie Méneret, Shekeeb S. Mohammad, Laura Cif, Movement Disorders	2022	46
Nebulin expression in patients with nemaline myopathy Juliana Gurgel‐Giannetti, Umbertina C. Reed, Marie‐Louise Bang, Neuromuscular Disorders Nebulin ExpressionDermatologyDegenerative DiseaseConnective Tissue Disease	2001	45
Intragenic variants in the <i>SMN1</i> gene determine the clinical phenotype in 5q spinal muscular atrophy Rodrigo de Holanda Mendonça, Ciro Matsui, Graziela Jorge Polido, Neurology Genetics	2020	42

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