Ana Lía Taratuto - Concepedia

Author

Ana Lía Taratuto

Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia

Also Known As

ANA LIA TARATUTO, Ana L Taratuto, Ana L. Taratuto, Ana Lia Taratuto, Ana Lía Taratuto, Ana Taratuto, Taratuto, Ana

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia Garrahan Hospital Sorbonne Université Inserm Institut de Myologie

About

Ana Lía Taratuto is an author at Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia specializing in medicine, neuropathology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	24	1.3K
2	Cell Biology	4	4	153
3	Health Sciences	2	2	40
4	Social Sciences	2	2	216
5	Anatomy	1	1	16

Ana Lía Taratuto

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Superficial cerebral astrocytoma attached to dura: Report of six cases in infants Ana Lía Taratuto, J Monges, Pedro Lylyk, Cancer Pediatric Brain TumorsPathologySuperficial Cerebral AstrocytomaBrain LesionGlioma	1984	192
Subependymal giant cell astrocytoma in children with tuberous sclerosis Vicente Cuccia, Graciela Zúccaro, Fidel Sosa, Child s Nervous System Neuro-oncologyPediatric Brain TumorsNeurological DisorderHistopathologyPathology	2003	153
Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset Marc Bitoun, Jorge A. Bevilacqua, Bernard Prudhon, Annals of Neurology	2007	148
Early onset collagen VI myopathies: Genetic and clinical correlations Laura Briñas, Pascale Richard, Susana Quijano‐Roy, Annals of Neurology	2010	132
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy Vanessa Schartner, Norma B. Romero, Sandra Donkervoort, Acta Neuropathologica Congenital MyopathyMendelian DisorderDegenerative DiseaseGenetic Disorder	2016	132
Mutation Update and Genotype-Phenotype Correlations of Novel and Previously Described Mutations in<i>TPM2</i>and<i>TPM3</i>Causing Congenital Myopathies M. Marttila, Vilma‐Lotta Lehtokari, Steven B. Marston, Human Mutation	2014	108
myotilin Mutation Found in Second Pedigree with LGMD1A Michael A. Hauser, Cecı́lia Conde, Valeria Kowaljow, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsMolecular GeneticsMyotilin Mutation Found	2002	103
Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1 Joachim Schessl, Ana Lía Taratuto, Caroline A. Sewry, Brain Mitochondrial MyopathyMechanobiologyProgressive WeaknessAutoimmune DiseaseDisease Mechanism	2008	100
Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations Johann Böhm, Valérie Biancalana, Edoardo Malfatti, Brain Mitochondrial MyopathyChromatinDevelopmental AnomalyMendelian DisorderGenetic Disorder	2014	99
Muscle histopathology in nebulin-related nemaline myopathy: ultrastrastructural findings correlated to disease severity and genotype Edoardo Malfatti, Vilma‐Lotta Lehtokari, Johann Böhm, Acta Neuropathologica Communications	2014	91

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