Výsledky vyhledávání - Serenella Servidei
- Zobrazuji výsledky 1 - 20 z 29
- Přejít na další stránku
-
1
-
2
Vitamin D in Neurological Diseases Autor Domenico Plantone, Guido Primiano, Carlo Manco, Sara Locci, Serenella Servidei, Nicola De Stefano
Vydáno 2022Revisão -
3
-
4
-
5
-
6
Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency. Autor Ronald G. Haller, S. F. Lewis, R.W. Estabrook, S. DiMauro, Serenella Servidei, Daniel W. Foster
Vydáno 1989Artigo -
7
Prothrombin G20210A Mutant Genotype Is a Risk Factor for Cerebrovascular Ischemic Disease in Young Patients Autor Valerio De Stefano, Patrizia Chiusolo, Katia Paciaroni, Ida Casorelli, Elena Rossi, Marco Molinari, Serenella Servidei, Pietro Tonali, Giuseppe Leone
Vydáno 1998Artigo -
8
γ1- and γ2-Syntrophins, Two Novel Dystrophin-binding Proteins Localized in Neuronal Cells Autor Giulio Piluso, Massimiliano Mirabella, Enzo Ricci, Angela Belsito, Ciro Abbondanza, Serenella Servidei, Annibale Alessandro Puca, P. Tonali, Giovanni Alfredo Puca, Vincenzo Nigro
Vydáno 2000Artigo -
9
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases Autor Michelangelo Mancuso, C. Angelini, Enrico Bertini, Valério Carelli, Giacomo P. Comi, Carlo Minetti, Maurizio Moggio, Tiziana Mongini, Serenella Servidei, Paola Tonin, António Toscano, Graziella Uziel, Massimo Zeviani, Gabriele Siciliano
Vydáno 2012Revisão -
10
Impaired Skin Fibroblast Carnitine Uptake in Primary Systemic Carnitine Deficiency Manifested by Childhood Carnitine-Responsive Cardiomyopathy Autor Ingrid Tein, Darryl C. De Vivo, F Z Bierman, P Pulver, Linda J. De Meirleir, Ljerka Cvitanović-Šojat, Roberta A Pagon, Enrico Bertini, Carlo Dionisi‐Vici, Serenella Servidei, S. DiMauro
Vydáno 1990Revisão -
11
Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 Autor Jianping Zhou, Marcel Tawk, Francesco Danilo Tiziano, Julien Veillet, Mónica Bayés, Flora Nolent, Virginie Garcia, Serenella Servidei, Enrico Bertini, Francesc Castro-Giner, Yavuz Renda, Stéphane Carpentier, Nathalie Andrieu‐Abadie, Marta Gut, Thierry Levade, Haluk Topaloğlu, Judith Melki
Vydáno 2012Artigo -
12
Personalized Medicine in Mitochondrial Health and Disease: Molecular Basis of Therapeutic Approaches Based on Nutritional Supplements and Their Analogs Autor Vincenzo Tragni, Guido Primiano, Albina Tummolo, Lucas Cafferati Beltrame, Gianluigi La Piana, Maria Noemi Sgobba, Maria Maddalena Cavalluzzi, Giulia Paterno, Ruggiero Gorgoglione, Mariateresa Volpicella, Lorenzo Guerra, Domenico Marzulli, Serenella Servidei, Anna Grassi, Giuseppe Petrosillo, Giovanni Lentini, Ciro Leonardo Pierri
Vydáno 2022Revisão -
13
Macrophages excite muscle spindles with glutamate to bolster locomotion Autor Yuyang Yan, Nuria Antolin, Luming Zhou, Luyang Xu, Irene Lisa Vargas, Carlos Gómez, Guiping Kong, Ilaria Palmisano, Yi Yang, Jessica Chadwick, Franziska Mueller, Anthony M. J. Bull, Cristina Lo Celso, Guido Primiano, Serenella Servidei, Jean‐Françóis Perrier, Carmelo Bellardita, Simone Di Giovanni
Vydáno 2024Artigo -
14
Genotype-phenotype correlation in Pompe disease, a step forward Autor Paola De Filippi, Kolsoum Saeidi, Sabrina Ravaglia, Andrea Dardis, C. Angelini, Tiziana Mongini, Lucia Morandi, Maurizio Moggio, Antonio Di Muzio, Massimiliano Filosto, Bruno Bembi, Fabio Giannini, Giovanni Marrosu, Miriam Rigoldi, Paola Tonin, Serenella Servidei, Gabriele Siciliano, Annalisa Carlucci, Claudia Scotti, Mario Comelli, António Toscano, Cesare Danesino
Vydáno 2014Artigo -
15
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years Autor C. Angelini, Claudio Semplicini, Sabrina Ravaglia, Bruno Bembi, Serenella Servidei, Elena Pegoraro, Maurizio Moggio, Massimiliano Filosto, Elisabetta Sette, Grazia Crescimanno, Paola Tonin, Rossella Parini, Lucia Morandi, Maria Giovanna Marrosu, Giuseppe Greco, Olimpia Musumeci, Giuseppe Di Iorio, Gabriele Siciliano, Maria Alice Donati, Francesca Carubbi, Mario Ermani, Tiziana Mongini, António Toscano
Vydáno 2011Artigo -
16
The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway Autor Hsien-Yang Lee, Ying Xu, Yong Huang, Andrew H. Ahn, Georg Auburger, Massimo Pandolfo, Hubert Kwieciński, David A. Grimes, Anthony E. Lang, Jørgen E. Nielsen, Yuri Averyanov, Serenella Servidei, Andrzej Friedman, Patrick Van Bogaert, Marc Abramowicz, Michiko Kimura Bruno, Beatrice F. Sorensen, Ling Tang, Ying‐Hui Fu, Louis J. Ptáček
Vydáno 2004Artigo -
17
Mitochondrial disease and COVID-19: An international cohort study confirms risks and long-term outcomes Autor Chiara Pizzamiglio, Hallgeir Jonvik, Stefen Brady, Patrick F. Chinnery, Lucía Galán, Gráinne S. Gorman, Alejandro Horga, Rita Horváth, Mirian C. H. Janssen, Albert Lim, Michelangelo Mancuso, Robert McFarland, Mária Judit Molnár, Olimpia Musumeci, Victoria Nesbitt, Wladimir, Guido Primiano, Ernestina Santos, Serenella Servidei, Rhys H. Thomas, Michael G. Hanna, Pedro Machado, Robert D. S. Pitceathly
Vydáno 2021Artigo -
18
Factors associated with the severity of <scp>COVID</scp>‐19 outcomes in people with neuromuscular diseases: Data from the International Neuromuscular <scp>COVID</scp>‐19 Registry... Autor Chiara Pizzamiglio, Robert D. S. Pitceathly, Michael P. Lunn, Stefen Brady, Fabiola De Marchi, Lucía Galán, Jeannine M. Heckmann, Alejandro Horga, Mária Judit Molnár, Acary Sousa Bulle Oliveira, Wladimir Bocca Vieira de Rezende Pinto, Guido Primiano, Ernestina Santos, Benedikt Schoser, Serenella Servidei, Paulo Victor Sgobbi de Souza, Venugopalan Y. Vishnu, Michael G. Hanna, Mazen M. Dimachkie, Pedro Machado
Vydáno 2022Artigo -
19
Management of seizures in patients with primary mitochondrial diseases: consensus statement from the <scp>InterERNs</scp> Mitochondrial Working Group Autor Michelangelo Mancuso, Maria Papadopoulou, Yi Shiau Ng, Anna Ardissone, Marcello Bellusci, Enrico Bertini, Lidia Di Vito, Teresinha Evangelista, Carmen Fons, Omar Hikmat, Rita Horváth, Thomas Klopstock, Cornelia Kornblum, Costanza Lamperti, Laura Licchetta, Mária Judit Molnár, Kristin N. Varhaug, Mar O’Callaghan, Ronit Pressler, Manuel Schiff, Serenella Servidei, Nora Szabó, Gráinne S. Gorman, J. Helen Cross, Shamima Rahman
Vydáno 2024Artigo -
20
Biallelic <i>SQSTM1</i> mutations in early-onset, variably progressive neurodegeneration Autor Valentina Muto, Elisabetta Flex, Zachary A Kupchinsky, Guido Primiano, Hamid Galehdari, Mohammadreza Dehghani, Serena Cecchetti, Giovanna Carpentieri, Teresa Rizza, Neda Mazaheri, Alireza Sedaghat, Mohammad Yahya Vahidi Mehrjardi, Alice Traversa, Michela Di Nottia, Maria Kousi, Yalda Jamshidi, Andrea Ciolfi, Viviana Caputo, Reza Azizi Malamiri, Francesca Pantaleoni, Simone Martinelli, Aaron R. Jeffries, Jawaher Zeighami, Amir Sherafat, Daniela Di Giuda, Gholamreza Shariati, Rosalba Carrozzo, Nicholas Katsanis, Reza Maroofian, Serenella Servidei, Marco Tartaglia
Vydáno 2018Artigo
Vyhledávací nástroje:
Související témata
Medicine
Internal medicine
Biology
Gene
Genetics
Disease
Pediatrics
Biochemistry
Chemistry
Endocrinology
Mitochondrial DNA
Mutation
Mitochondrial disease
Phenotype
Coronavirus disease 2019 (COVID-19)
Engineering
Infectious disease (medical specialty)
Mechanical engineering
Mitochondrion
Myopathy
Physics
Psychiatry
Bioinformatics
Cell biology
Cohort
Creatine kinase
Encephalopathy
Genotype
Heart failure
Intensive care medicine