M. García-Silva
发表
F. Castelló,
M. Martínez,
E. Vázquez,
2000,
The American journal of clinical nutrition.
J. Arenas,
Miguel Ángel Martín,
M. García-Silva,
2005,
Pediatric Nephrology.
T. Hennet,
G. Matthijs,
P. Briones,
2004,
Journal of Inherited Metabolic Disease.
A. Ribes,
P. Briones,
M. García-Silva,
2010,
Journal of Inherited Metabolic Disease.
N. Blau,
V. Ramaekers,
A. Ormazabal,
2008,
Neurology.
C. Pérez-Cerdá,
M. Couce,
A. Fernández-Marmiesse,
2016,
Journal of Human Genetics.
J. García-Peñas,
E. Rivas,
A. Ferreiro,
2005,
Pediatric neurology.
C. Pérez-Cerdá,
M. Martínez-Pardo,
M. Ugarte,
2019,
Clinical genetics.
C. Pérez-Cerdá,
B. Merinero,
M. Ugarte,
2019,
European Journal of Human Genetics.
J. Arenas,
Miguel Ángel Martín,
F. Martínez-Azorín,
2016,
neurogenetics.
J. Arenas,
Miguel Ángel Martín,
A. Delmiro,
2013,
Human mutation.
B. Cormand,
A. Macaya,
M. García-Silva,
2011,
Headache.
B. Cormand,
A. Macaya,
M. García-Silva,
2011
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Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases
C. Pérez-Cerdá,
M. Martínez-Pardo,
M. Couce,
2014,
Orphanet Journal of Rare Diseases.
P. Navas,
E. Ruiz-Pesini,
E. Trevisson,
2016,
Mitochondrion.
M. Couce,
J. Campistol,
Á. H. Ameijeiras,
2016
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M. Couce,
G. Pintos-Morell,
E. Guillén-Navarro,
2021,
Orphanet Journal of Rare Diseases.
E. Ruiz-Pesini,
A. Ormazabal,
R. Artuch,
2014,
Orphanet Journal of Rare Diseases.
M. Morales-Conejo,
C. Pedrón‐Giner,
M. García-Silva,
2022,
Nutrients.
C. Vrinten,
G. Ceccarini,
A. Federico,
2020,
Orphanet Journal of Rare Diseases.
E. Ruiz-Pesini,
A. Ormazabal,
R. Artuch,
2010
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A. Camacho-Salas,
M. García-Silva,
E. Martín‐Hernández,
2017,
Journal of Pediatric Neurology.
Paolo Gasparini,
Brigitte Vollmer,
Massimo Zeviani,
2004,
American journal of human genetics.
A. Ribes,
J. Arenas,
B. Garavaglia,
1997,
Pediatric neurology.
J. Arenas,
A. Muñoz,
F. Mateos,
1999,
Neuroradiology.
R. Wevers,
S. Wopereis,
P. Demacker,
2003,
Clinical chemistry.
F. Martínez-Azorín,
M. García-Silva,
M. Rodríguez-García,
2021,
Neuromuscular Disorders.
J. Arenas,
A. Delmiro,
F. Martínez-Azorín,
2017,
Clinical genetics.
A. Ribes,
J. Arenas,
P. Briones,
1994,
The Journal of pediatrics.
S. Seneca,
T. Gabaldón,
J. Arenas,
2009,
Mitochondrion.
M. Pineda,
J. Jaeken,
P. Briones,
2001,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
E. Ruiz-Pesini,
A. Ormazabal,
R. Artuch,
2011,
Mitochondrion.
M. Krieger,
W. Annaert,
G. Matthijs,
2007,
Human molecular genetics.
A. Lucia,
J. Arenas,
A. Santos-Lozano,
2016,
Clinical nutrition.
N. Baena,
G. Antiñolo,
S. Gökben,
2019,
Scientific Reports.
N. Baena,
G. Antiñolo,
Gábor Csányi,
2017,
Scientific Reports.
N. Baena,
G. Antiñolo,
S. Gökben,
2017,
Scientific Reports.
Joaquín Dopazo,
Frederic Tort,
Paz Briones,
2013,
Molecular genetics and metabolism.
M. Morán,
M. García-Silva,
M. Martín,
2017,
Clinical Nutrition.
S. Beltran,
F. Tort,
A. Ribes,
2019,
Human mutation.
J. Arenas,
Miguel Ángel Martín,
F. Martínez-Azorín,
2015,
neurogenetics.
A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome
J. Arenas,
Miguel Ángel Martín,
A. Delmiro,
2013,
BMC Nephrology.
Ronald J A Wanders,
Antonia Ribes,
Magdalena Ugarte,
2005,
Pediatric Research.
Miguel Ángel Martín,
M. García-Silva,
A. Martínez de Aragón,
2021,
JIMD reports.
M. Pineda,
E. Vázquez,
M. García-Silva,
1999,
Revista de neurología (Ed. impresa).
J. Arredondo,
M. Cervera,
B. Bornstein,
2012,
Mitochondrion.
C. Pérez-Cerdá,
B. Merinero,
M. Ugarte,
2019,
European Journal of Human Genetics.
N. Baena,
G. Antiñolo,
S. Gökben,
2017,
Scientific Reports.
J. Arenas,
M. García-Silva,
Y. Campos,
2012,
Mitochondrion.