A.L. Taratuto

1.8k total citations
35 papers, 552 citations indexed

About

A.L. Taratuto is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, A.L. Taratuto has authored 35 papers receiving a total of 552 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 8 papers in Neurology. Recurrent topics in A.L. Taratuto's work include Muscle Physiology and Disorders (6 papers), Genetic Neurodegenerative Diseases (4 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). A.L. Taratuto is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Genetic Neurodegenerative Diseases (4 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). A.L. Taratuto collaborates with scholars based in Argentina, France and United States. A.L. Taratuto's co-authors include J Monges, Gustavo Sevlever, R. Leiguarda, H.A. Molina, Marcelo L. Berthier, Sergio Starkstein, S. DiMauro, M. Saccoliti, Héctor Freilij and L.M. Jost and has published in prestigious journals such as Journal of Clinical Oncology, Neurology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

A.L. Taratuto

34 papers receiving 530 citations

Peers

A.L. Taratuto

EPIDE

PMH

PHYSI

Ana Martı́nez de Aragón Spain

Tommy Stödberg Sweden

Masato Mori Japan

Yoshito Ishizaki Japan

Nobutsune Ishikawa Japan

José Pedro Vieira Portugal

B. O. Berg United States

Hisashi Kawawaki Japan

Alan M. Aron United States

Marie Vincent France

Ana Martı́nez de Aragón Spain

A.L. Taratuto

242 ×0.9

63 ×0.8

68 ×0.9

EPIDE

38 ×0.5

PMH

29 ×0.4

PHYSI

Citations per year, relative to A.L. Taratuto A.L. Taratuto (= 1×) peers Ana Martı́nez de Aragón

Countries citing papers authored by A.L. Taratuto

Since Specialization

Citations

This map shows the geographic impact of A.L. Taratuto's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by A.L. Taratuto with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A.L. Taratuto more than expected).

Fields of papers citing papers by A.L. Taratuto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A.L. Taratuto. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by A.L. Taratuto. The network helps show where A.L. Taratuto may publish in the future.

Co-authorship network of co-authors of A.L. Taratuto

This figure shows the co-authorship network connecting the top 25 collaborators of A.L. Taratuto. A scholar is included among the top collaborators of A.L. Taratuto based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with A.L. Taratuto. A.L. Taratuto is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Girard, Emmanuelle, Karine Poulard, Guy Brochier, et al.. (2021). CONGENITAL MYOPATHIES – NEMALINE MYOPATHIES. Neuromuscular Disorders. 31. S61–S62. 1 indexed citations

Taratuto, A.L., Hasan O. Akman, M. Saccoliti, et al.. (2010). Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: Muscle biopsy and autopsy findings, biochemical and molecular genetic studies. Neuromuscular Disorders. 20(12). 783–790. 21 indexed citations

Taratuto, A.L., M. Saccoliti, Fabiana Lubieniecki, et al.. (2009). G.P.1.07 Progressive muscle biopsies morphological changes in long-term follow-up of multiminicore disease related to RYR1 gene. Neuromuscular Disorders. 19(8-9). 558–558. 3 indexed citations

Taratuto, A.L., Alberto Dubrovsky, & José Corderí. (2009). G.P.8.03 Misleading muscle biopsies in late onset Pompe’s disease. Neuromuscular Disorders. 19(8-9). 591–592. 1 indexed citations

Taratuto, A.L., et al.. (2008). EGFR/AKT pathways alterations in gliomas. Journal of Clinical Oncology. 26(15_suppl). 2061–2061.

Barroso, Fábio, Martín Nogués, Ramón Leiguarda, & A.L. Taratuto. (2007). G.P.8.09 Exercise intolerance and rippling syndrome in caveolinopathy. Neuromuscular Disorders. 17(9-10). 812–813. 2 indexed citations

Lubieniecki, Fabiana, Soledad Monges, Alberto Dubrovsky, et al.. (2007). G.P.5.01 Inflammatory or ‘congenital myopathy’ type findings in muscle biopsies of patients with LMNA mutations. Neuromuscular Disorders. 17(9-10). 797–797. 2 indexed citations

Dubrovsky, Alberto, et al.. (2007). C.P.4.11 Ragged red fibres finding in muscle biopsy of dynamin 2-related centronuclear myopathy. Neuromuscular Disorders. 17(9-10). 881–882. 2 indexed citations

Mancuso, Michelangelo, Leonardo Salviati, Sabrina Sacconi, et al.. (2002). Mitochondrial DNA depletion. Neurology. 59(8). 1197–1202. 124 indexed citations

10.

Ruggieri, Víctor, Fabiana Lubieniecki, Francisco Meli, et al.. (2001). Merosin-positive congenital muscular dystrophy with mental retardation, microcephaly and central nervous system abnormalities unlinked to the Fukuyama muscular dystrophy and muscular–eye–brain loci: report of three siblings. Neuromuscular Disorders. 11(6-7). 570–578. 11 indexed citations

11.

Pomata, Hugo, Roberto González, Marcelo Bartuluchi, et al.. (2000). Extratemporal epilepsy in children: candidate selection and surgical treatment. Child s Nervous System. 16(12). 842–850. 26 indexed citations

12.

Russo, Ricardo, et al.. (2000). Primary angiitis of the central nervous system presenting as a mass lesion in a child.. PubMed. 27(5). 1297–8. 13 indexed citations

13.

Taratuto, A.L., et al.. (1999). Merosin-deficient congenital muscular dystrophy associated with abnormal cerebral cortical gyration: an autopsy study. Neuromuscular Disorders. 9(2). 86–94. 30 indexed citations

14.

Dubrovsky, Alberto, A.L. Taratuto, Gustavo Sevlever, et al.. (1995). Duchenne muscular dystrophy and myotonic dystrophy in the same patient. American Journal of Medical Genetics. 55(3). 342–348. 5 indexed citations

15.

Sevlever, Gustavo, et al.. (1995). CHEMORESISTANCE MARKERS IN CNS TUMORS. Journal of Neuropathology & Experimental Neurology. 54(3). 420–420. 1 indexed citations

16.

Taratuto, A.L., et al.. (1991). Leptomyxid amoeba encephalitis: report of the first case in Argentina. Transactions of the Royal Society of Tropical Medicine and Hygiene. 85(1). 77–77. 43 indexed citations

17.

Berthier, Marcelo L., R. Leiguarda, Sergio Starkstein, Gustavo Sevlever, & A.L. Taratuto. (1991). Alzheimer's disease in a patient with posterior cortical atrophy.. Journal of Neurology Neurosurgery & Psychiatry. 54(12). 1110–1111. 71 indexed citations

18.

Taratuto, A.L., et al.. (1990). Giant axonal neuropathy (GAN): an immunohistochemical and ultrastructural study report of a Latin American case. Acta Neuropathologica. 80(6). 680–683. 7 indexed citations

19.

Taratuto, A.L., Gustavo Sevlever, & Marcela Schultz. (1987). MONOCLONAL ANTIBODIES IN SUPERFICIAL DESMOPLASTIC CEREBRAL ASTROCYTOMA ATTACHED TO DURA IN INFANTS. Journal of Neuropathology & Experimental Neurology. 46(3). 395–395. 2 indexed citations

20.

Taratuto, A.L., et al.. (1985). Primary rhabdomyosarcoma of brain and cerebellum. Acta Neuropathologica. 66(2). 98–104. 16 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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