M. O'Callaghan
发表
S. Duarte,
J. Armstrong,
A. Roche,
2013,
PloS one.
M. Roselló,
C. Orellana,
M. Tejada,
2020,
Clinical genetics.
L. Pérez-Jurado,
B. Martínez-Delgado,
M. O'Callaghan,
2020,
Orphanet journal of rare diseases.
J. Armstrong,
M. O'Callaghan,
M. Pineda,
2019,
International journal of molecular sciences.
S. Brodie,
A. Gass,
J. Fallon,
2001,
American journal of human genetics.
M. O'Callaghan,
R. Artuch,
M. Pineda,
2011,
Journal of Inherited Metabolic Disease.
M. O'Callaghan,
M. Pineda,
M. Vilaseca,
2010,
Molecular genetics and metabolism.
M. O'Callaghan,
R. Artuch,
À. García‐Cazorla,
2015,
Expert review of neurotherapeutics.
M. O'Callaghan,
N. Raben,
J. McPherson,
2008,
Molecular genetics and metabolism.
C. Ortez,
M. O'Callaghan,
À. García‐Cazorla,
2016,
Seminars in pediatric neurology.
M. Mancuso,
S. Rahman,
M. O'Callaghan,
2020,
Journal of inherited metabolic disease.
F. Villarroya,
S. Kalko,
E. Ruiz-Pesini,
2016,
PloS one.
T. Huisman,
A. Poretti,
C. Ortez,
2019,
Parkinsonism & related disorders.
M. O'Callaghan,
M. Couce,
G. Pintos-Morell,
2018,
Molecular genetics and metabolism reports.
J. Armstrong,
M. O'Callaghan,
M. Andrade-Campos,
2017,
Orphanet Journal of Rare Diseases.
Robert W. Taylor,
J. A. Arranz,
F. Tort,
2016,
Mitochondrion (Amsterdam. Print).
P. Navas,
E. Ruiz-Pesini,
M. O'Callaghan,
2015,
European Journal of Human Genetics.
P. Navas,
E. Ruiz-Pesini,
E. Trevisson,
2016,
Mitochondrion.