A. Lèbre
发表
M. Leboyer,
C. Benkelfat,
J. Allilaire,
2002,
Neuropsychopharmacology.
C. Ross,
A. Dürr,
A. Brice,
2001,
Annals of neurology.
Robert W. Taylor,
H. Prokisch,
A. Rötig,
2014,
Orphanet Journal of Rare Diseases.
V. Desquiret-Dumas,
D. Bonneau,
P. Amati‐Bonneau,
2015,
The international journal of biochemistry & cell biology.
C. Duyckaerts,
J. Hauw,
V. Meininger,
2004,
Acta Neuropathologica.
A. Munnich,
N. Boddaert,
F. Brunelle,
2014,
Journal of Medical Genetics.
A. Munnich,
N. Boddaert,
F. Brunelle,
2014,
Revue neurologique.
A. Munnich,
N. Boddaert,
A. Rötig,
2010,
Mitochondrion.
A. Munnich,
E. Leshinsky‐Silver,
D. Lev,
2009,
Molecular genetics and metabolism.
I. Scheffer,
H. Mefford,
A. Munnich,
2019,
Human mutation.
F. Rivier,
R. Touraine,
A. Chabli,
2013,
Orphanet Journal of Rare Diseases.
C. Duyckaerts,
A. Brice,
J. Camonis,
2011,
Neurobiology of Disease.
Y. Agid,
M. Vidailhet,
A. Durr,
1999,
Brain : a journal of neurology.
A. Afenjar,
N. Philip,
D. Lacombe,
2018,
Clinical genetics.
L. Christa,
C. Barnérias,
I. Desguerre,
2018,
Journal of Inherited Metabolic Disease.
F. Grange,
A. Lèbre,
O. Beaudoux,
2022,
Molecular Diagnosis & Therapy.
Y. Agid,
G. Yvert,
T. Klockgether,
1997,
Human molecular genetics.
Nephronophthisis in Young Adults Phenocopying Thrombotic Microangiopathy and Severe Nephrosclerosis.
L. Raymond,
A. Lèbre,
A. Karras,
2020,
Clinical journal of the American Society of Nephrology : CJASN.
R. Salomon,
C. Antignac,
B. Knebelmann,
2010,
Clinical journal of the American Society of Nephrology : CJASN.
A. Munnich,
D. Galanaud,
N. Boddaert,
2010,
Journal of Medical Genetics.
Y. Agid,
A. Dürr,
A. Brice,
1997,
American journal of human genetics.
J. Weissenbach,
H. Cann,
S. Meier-Ewert,
1998,
Genomics.
V. Procaccio,
B. Vialettes,
C. Jardel,
2020,
Annales d'endocrinologie.
A. Rötig,
I. Durand-zaleski,
C. Florentz,
2013,
Journal of Medical Genetics.
A. Munnich,
N. Boddaert,
A. Rötig,
2010,
Epilepsia.
J. Thevenon,
R. Nabbout,
D. Ville,
2022,
European journal of medical genetics.
A. Biraben,
F. Bartolomei,
P. Striano,
2018,
Genetics in Medicine.
C. Bris,
D. Goudenège,
V. Desquiret-Dumas,
2018,
Genetics in Medicine.
A. Afenjar,
N. Philip,
V. Cormier-Daire,
2019,
Genetics in Medicine.
A. Munnich,
A. Rötig,
C. Guillermet,
2012,
Biochimica et biophysica acta.
A. Munnich,
N. Boddaert,
A. Rötig,
2011,
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.
A. Munnich,
A. Rötig,
D. Rabier,
2009,
Journal of Inherited Metabolic Disease.
A. Munnich,
D. Seidenwurm,
N. Boddaert,
2008,
Molecular genetics and metabolism.
Resveratrol attenuates oxidative stress in mitochondrial Complex I deficiency: Involvement of SIRT3.
Robert W. Taylor,
A. Slama,
A. Lèbre,
2016,
Free radical biology & medicine.
A. Lèbre,
G. Yeşil,
T. Güran,
2014,
American journal of medical genetics. Part A.
A. Munnich,
A. Rötig,
A. Lèbre,
2009,
Journal of pediatric hematology/oncology.
A. Munnich,
N. Boddaert,
A. Rötig,
2009,
Molecular genetics and metabolism.
J. Weissenbach,
H. Cann,
S. Meier-Ewert,
1996,
Human molecular genetics.
A. Lèbre,
M. Doco‐Fenzy,
M. Labrousse,
2019,
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.
P. Fergelot,
M. Tartaglia,
G. Merla,
2022,
International journal of molecular sciences.
C. Schneider,
S. Dedieu,
O. Bouché,
2018,
Oncotarget.
H. Galehdari,
T. Frebourg,
R. Maroofian,
2020,
European journal of medical genetics.
T. Coşkun,
R. Topaloğlu,
A. Gürgey,
2008,
The Turkish journal of pediatrics.
Coenzyme Q is effective on anemia in a patient with sideroblastic anemia and mitochondrial myopathy.
B. Eymard,
A. Lèbre,
R. Girot,
2010,
Blood.
R. Touraine,
J. Mandel,
J. Thevenon,
2020,
Journal of Medical Genetics.
A. Munnich,
M. Zilbovicius,
D. Seidenwurm,
2010,
Journal of neuroradiology. Journal de neuroradiologie.
I. Scheffer,
H. Mefford,
A. Munnich,
2020,
Epilepsia.
A. Brice,
A. Lèbre,
2003,
Cytogenetic and Genome Research.
A. Lèbre,
2003
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Y. Agid,
A. Dürr,
A. Brice,
1998,
Human molecular genetics.
V. Beneš,
A. Munnich,
N. Boddaert,
2011,
Human mutation.
C. Duyckaerts,
J. Hauw,
A. Dürr,
2003,
Neurobiology of Disease.
C. Duyckaerts,
J. Hauw,
G. Yvert,
2002,
Brain : a journal of neurology.
A. Durr,
A. Brice,
G. Stevanin,
2003,
Brain : a journal of neurology.
V. Cottin,
A. Lèbre,
M. Doco‐Fenzy,
2020,
Biology.
E. Letavernier,
L. Raymond,
J. Boffa,
2022,
Kidney international reports.
A. Munnich,
A. Rötig,
C. Bole-Feysot,
2012,
Molecular genetics and metabolism.
N. Soufir,
F. Grange,
A. Lèbre,
2018,
Journal of the European Academy of Dermatology and Venereology : JEADV.
C. Richelme,
J. Pouget,
A. Chaussenot,
2013,
European Journal of Human Genetics.
A. Munnich,
N. Boddaert,
A. Rötig,
2012,
Mitochondrion.
C. Bris,
D. Goudenège,
V. Desquiret-Dumas,
2017,
Neurology: Genetics.
D. Goudenège,
V. Desquiret-Dumas,
D. Bonneau,
2022
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C. Duyckaerts,
A. Brice,
G. Stevanin,
2001,
Human molecular genetics.
A. Lèbre,
O. Beaudoux,
E. Canivet,
2021,
American journal of medical genetics. Part A.
V. Cottin,
J. Traclet,
F. Thivolet-Béjui,
2020,
European Respiratory Journal.
Y. Agid,
M. Ruberg,
C. Duyckaerts,
2000,
Brain : a journal of neurology.
C. Duyckaerts,
A. Brice,
J. Camonis,
2001,
Human molecular genetics.
C. Antignac,
A. Bensman,
A. Lèbre,
2009,
European Journal of Human Genetics.
N. Drouot,
A. Durr,
M. Koenig,
2013,
Orphanet Journal of Rare Diseases.
F. Rivier,
P. Meyer,
A. Lèbre,
2017
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V. Cormier-Daire,
A. Lèbre,
M. le Merrer,
2008,
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
A. Afenjar,
N. Philip,
V. Cormier-Daire,
2019,
Genetics in Medicine.
Anne de Saint Martin,
A. Biraben,
F. Bartolomei,
2018,
Genetics in Medicine.
D. Galanaud,
N. Boddaert,
A. Rötig,
2010,
Journal of Medical Genetics.