A. Gallanti

744 total citations
18 papers, 472 citations indexed

About

A. Gallanti is a scholar working on Molecular Biology, Clinical Biochemistry and Cell Biology. According to data from OpenAlex, A. Gallanti has authored 18 papers receiving a total of 472 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 4 papers in Cell Biology. Recurrent topics in A. Gallanti's work include Muscle Physiology and Disorders (6 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (4 papers). A. Gallanti is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (4 papers). A. Gallanti collaborates with scholars based in Italy and United States. A. Gallanti's co-authors include G. Scarlato, Nereo Bresolin, A. Prelle, Maurizio Moggio, Patrizia Ciscato, Nicoletta Checcarelli, Monica Sciacco, Giacomo P. Comi, Maria Teresa Bassi and Laura Adobbati and has published in prestigious journals such as Annals of Neurology, Acta Neuropathologica and Clinical Neurophysiology.

In The Last Decade

A. Gallanti

18 papers receiving 462 citations

Peers

Countries citing papers authored by A. Gallanti

Since Specialization

Citations

This map shows the geographic impact of A. Gallanti'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. Gallanti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Gallanti more than expected).

Fields of papers citing papers by A. Gallanti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. Gallanti. 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. Gallanti. The network helps show where A. Gallanti may publish in the future.

Co-authorship network of co-authors of A. Gallanti

This figure shows the co-authorship network connecting the top 25 collaborators of A. Gallanti. A scholar is included among the top collaborators of A. Gallanti 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. Gallanti. A. Gallanti is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	The genetic features of 24 patients affected by familial and sporadic hemiplegic migraine 2011 ·Neurological Sciences ·A. Gallanti, (unknown), A. Tonelli, Gennaro Bussone, Nereo Bresolin, C. Mariani, Maria Teresa Bassi	11
2	A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures 2008 ·Journal of the Neurological Sciences ·A. Gallanti, Alessandra Tonelli, (unknown), Gennaro Bussone, Nereo Bresolin, Maria Teresa Bassi	35
3	Migraine, stroke and patent foramen ovale: a dangerous trio? 2008 ·Journal of Cardiovascular Medicine ·Gianfranco Butera, Elio Clemente Agostoni, Giuseppe Biondi‐Zoccai, Nereo Bresolin, Lorenzo Fumagalli, Massimo Chessa, A. Gallanti, (unknown), Mário Carminati	4
4	Amino acid changes in the amino terminus of the Na,K‐adenosine triphosphatase alpha‐2 subunit associated to familial and sporadic hemiplegic migraine 2007 ·Clinical Genetics ·A. Tonelli, A. Gallanti, Anna Bersano, (unknown), Elena Ballabio, Giovanni Airoldi, Francesca Redaelli, L. Candelise, Nereo Bresolin, Maria Teresa Bassi	12
5	Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency 2003 ·Acta Neuropathologica ·A. Prelle, Monica Sciacco, (unknown), Gigliola Fagiolari, Giacomo P. Comi, Patrizia Ciscato, (unknown), Francesco Fortunato, Chiara Zecca, A. Gallanti, Luca Chiveri, Nereo Bresolin, G. Scarlato, Maurizio Moggio	28
6	Decreased EMG inhibition following electrical stimulation over muscle tendons in myopathies 2001 ·Clinical Neurophysiology ·Alberto Priori, Claudia Cinnante, Antonio Pesenti, A. Gallanti, A. Cappellari, G. Scarlato, Sergio Barbieri	4
7	Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiency 1993 ·Journal of Neurology ·Nereo Bresolin, Giacomo P. Comi, Francesco Fortunato, G. Meola, A. Gallanti, A Tajana, (unknown), (unknown), Paolino Ninfali, S. Pifferi, G. Scarlato	4
8	Dystrophin deficiency in a case of congenital myopathy 1992 ·Journal of Neurology ·A. Prelle, R. Medori, Maurizio Moggio, (unknown), A. Gallanti, G. Scarlato, E. Bonilla	13
9	Congenital myopathy associated with abnormal accumulation of desmin and dystrophin 1992 ·Neuromuscular Disorders ·A. Prelle, Maurizio Moggio, Giacomo P. Comi, A. Gallanti, Nicoletta Checcarelli, Nereo Bresolin, Patrizia Ciscato, Francesco Fortunato, G. Scarlato	35
10	Lack of anionic phospholipid calcium binding sites in duchenne muscular dystrophy 1992 ·Muscle & Nerve ·Maurizio Moggio, Gigliola Fagiolari, A. Prelle, A. Gallanti, Monica Sciacco, G. Scarlato	5
11	Desmin and Vimentin as markers of regeneration in muscle diseases 1992 ·Acta Neuropathologica ·A. Gallanti, A. Prelle, Maurizio Moggio, Patrizia Ciscato, Nicoletta Checcarelli, Monica Sciacco, (unknown), G. Scarlato	73
12	Congenital Myopathy with Type 2A Muscle Fiber Uniformity and Smallness 1992 ·Neuropediatrics ·A. Gallanti, A. Prelle, (unknown), Sergio Barbieri, S. Jann, Stefano Schiaffino, (unknown), Elio Scarpini, Gaia Pellegrini, Maurizio Moggio, G. Scarlato	3
13	Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patient 1991 ·Journal of the Neurological Sciences ·Nereo Bresolin, Paolo Martinelli, Bruno Barbiroli, P. Zaniol, Carlo D. Ausenda, P. Montagna, A. Gallanti, Giacomo P. Comi, G. Scarlato, E Lugaresi	56
14	Appearance and localization of dystrophin in normal human fetal muscle 1991 ·International Journal of Developmental Neuroscience ·A. Prelle, (unknown), Maurizio Moggio, A. Gallanti, Monica Sciacco, Nicoletta Checcarelli, Giacomo P. Comi, Elio Scarpini, E. Bonilla, G. Scarlato	11
15	Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trial 1990 ·Journal of the Neurological Sciences ·Nereo Bresolin, C. Doriguzzi, Carola Ponzetto, C. Angelini, Isabella Moroni, Enrico Castelli, (unknown), A. Binda, A. Gallanti, (unknown), G. Piccolo, Andrea Martinuzzi, Emma Ciafaloni, E. Arnaudo, (unknown), A. Carenzi, G. Scarlato	86
16	Cytochrome c oxidase during human fetal development 1989 ·International Journal of Developmental Neuroscience ·Maurizio Moggio, Nereo Bresolin, Elio Scarpini, Laura Adobbati, A. Prelle, A. Gallanti, (unknown), Francesco Fortunato, (unknown), G. Scarlato	6
17	Ultrastructural localization of calcium binding sites on human muscle cell surface 1989 ·Muscle & Nerve ·Maurizio Moggio, S. Jann, Laura Adobbati, A. Prelle, A. Gallanti, Gigliola Fagiolari, G. Pellegrini, G. Scarlato	6
18	Progressive cytochrome c oxidase deficiency in a case of earns‐sayre syndrome: Morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues 1987 ·Annals of Neurology ·Nereo Bresolin, Maurizio Moggio, (unknown), A. Gallanti, A. Prelle, Eduardo Nobile‐Orazio, Laura Adobbati, Claudio Ferrante, (unknown), G. Scarlato	80

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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