B. Héron
发表
M. Vidailhet,
A. Durr,
M. Polak,
2012,
Journal of Neurology, Neurosurgery & Psychiatry.
C. Depienne,
G. Stevanin,
P. Pennamen,
2021,
European Journal of Human Genetics.
A. Smahi,
J. Casanova,
C. Picard,
2007,
Science.
N. Boddaert,
G. Aznar Laín,
G. Dellatolas,
2013,
Epilepsia.
G. Ponsot,
P. Lebon,
F. Rozenberg,
2003,
Neurology.
G. Ponsot,
A. Vital,
J. Julien,
1998,
Journal of the peripheral nervous system : JPNS.
M. Vincent,
B. Héron,
P. Bitoun,
2004,
American journal of human genetics.
C. Tilikete,
F. Lamari,
V. Deramecourt,
2018,
Orphanet Journal of Rare Diseases.
M. Patterson,
O. Morand,
R. Giugliani,
2020,
Journal of inherited metabolic disease.
P. Latour,
T. Levade,
A. Brassier,
2017,
Orphanet Journal of Rare Diseases.
M. Patterson,
M. Walterfang,
D. Ory,
2018,
Orphanet Journal of Rare Diseases.
F. Sedel,
P. Latour,
H. Maurey,
2012,
Orphanet Journal of Rare Diseases.
D. Zafeiriou,
O. Danos,
M. Tardieu,
2011,
American journal of medical genetics. Part A.
A. Fatemi,
M. Portero-Otín,
I. Ferrer,
2023,
The Journal of clinical investigation.
J. Casanova,
C. Picard,
F. Geissmann,
2006,
Science.
S. Lehéricy,
D. Galanaud,
N. Baumann,
2009,
Molecular genetics and metabolism.
I. Scheffer,
H. Mefford,
J. Cross,
2021,
Epilepsia.
F. Rivier,
C. Garel,
A. Afenjar,
2022,
Journal of Medical Genetics.
A. Munnich,
A. Durr,
C. Orssaud,
2016,
American journal of human genetics.
B. Echenne,
S. Auvin,
N. Dorison,
2014,
Human mutation.
A. Brice,
V. Drouin‐Garraud,
C. Thauvin,
2014,
Orphanet Journal of Rare Diseases.
A. Brassier,
M. Schiff,
B. Héron,
2022,
The Journal of pediatrics.
S. Auvin,
L. Pasquier,
C. Philippe,
2014,
Journal of Medical Genetics.
Y. Gillerot,
H. Brunner,
A. Verloes,
2006,
American journal of medical genetics. Part A.
B. Chabrol,
B. Héron,
V. Valayannopoulos,
2015,
Orphanet Journal of Rare Diseases.
S. Marret,
Abdellah Tebani,
B. Héron,
2018,
Journal of Translational Medicine.
E. van Binsbergen,
W. Dobyns,
N. Matsumoto,
2017,
Brain : a journal of neurology.
S. Parker,
A. Chakrapani,
B. Arnould,
2022,
Orphanet Journal of Rare Diseases.
J. Eisengart,
S. Parker,
R. Giugliani,
2021,
Molecular genetics and metabolism.
A. Afenjar,
C. Schaaf,
U. Grasshoff,
2022,
American journal of medical genetics. Part A.
F. Rozenberg,
X. De Tiège,
B. Héron,
2008,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
G. Ponsot,
P. Lebon,
F. Rozenberg,
2003,
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
G. Ponsot,
F. Rozenberg,
X. Tiège,
2005,
Developmental medicine and child neurology.
M. M. Morrow,
M. Shinawi,
D. Chitayat,
2021,
Pediatric neurology.
G. Chatellier,
N. Belmatoug,
A. Brassier,
2021,
Orphanet Journal of Rare Diseases.
A. Vanderver,
H. Brunner,
P. Fockens,
2019
.
M. Vezain,
S. Marret,
I. Marie,
2021,
Diagnostics.
M. Patterson,
B. Bembi,
T. Symonds,
2020,
Orphanet Journal of Rare Diseases.
D. Rabier,
J. Saudubray,
G. Touati,
2005,
Journal of Inherited Metabolic Disease.
L. Vercueil,
A. Afenjar,
S. Auvin,
2013,
Orphanet Journal of Rare Diseases.
A. Vanderver,
Y. Crow,
D. Lev,
2020,
Human mutation.
R. Hochstenbach,
Q. Waisfisz,
R. Person,
2019,
American journal of medical genetics. Part A.
C. Garel,
A. Afenjar,
A. Toutain,
2018,
Genetics in Medicine.
N. Boddaert,
A. Kaminska,
J. Pedespan,
2015,
European journal of medical genetics.
T. Clozel,
J. Casanova,
F. Rivier,
2010,
The Journal of pediatrics.
H. Corvol,
C. Mignot,
D. Doummar,
2021,
The Journal of pediatrics.
R. Vialle,
B. Fauroux,
N. Leboulanger,
2011,
Pediatric pulmonology.
S. Julia,
A. Afenjar,
A. Toutain,
2016,
Clinical genetics.
O. Boespflug-Tanguy,
P. de Lonlay,
A. Slama,
2017,
Molecular genetics and metabolism.
M. Strupp,
M. Walterfang,
H. Runz,
2021,
Orphanet Journal of Rare Diseases.
M. Patterson,
R. D. Da Riol,
M. Gautschi,
2021,
Journal of inherited metabolic disease.
R. Touraine,
F. Ramond,
A. Imbard,
2020,
Journal of inherited metabolic disease.
C. Lourenço,
B. Héron,
V. Valayannopoulos,
2016,
BMC Pediatrics.
S. Julia,
A. Afenjar,
A. Toutain,
2016,
Clinical genetics.
L. Christa,
C. Corne,
M. Milh,
2016,
JIMD Reports.
L. Christa,
C. Corne,
M. Milh,
2016,
JIMD reports.
S. Marret,
P. de Lonlay,
A. Brassier,
2017,
Clinica chimica acta; international journal of clinical chemistry.
M. Durán,
D. Rabier,
J. Saudubray,
2000,
Journal of Inherited Metabolic Disease.
S. Lehéricy,
D. Galanaud,
N. Baumann,
2009,
Molecular Genetics and Metabolism.
N. Boddaert,
G. Aznar Laín,
G. Dellatolas,
2013,
Epilepsia.
Ye Htet Aung,
S. Berkovic,
S. Petrou,
2019,
Annals of clinical and translational neurology.
P. van Endert,
A. Imbard,
P. Laforêt,
2022,
Neurology: Genetics.
C. Garel,
A. Afenjar,
A. Toutain,
2018,
Genetics in Medicine.
J. Thevenon,
L. Faivre,
C. Philippe,
2019,
American journal of medical genetics. Part A.