F. Leturcq
发表
Luis Garcia,
Olivier Danos,
A. Goyenvalle,
2004,
Science.
F. Leturcq,
I. Desguerre,
J. Barbet,
2009,
Journal of neuropathology and experimental neurology.
F. Leturcq,
P. Landais,
P. Bougnères,
1993,
Diabetes Care.
D. Israeli,
R. Carlier,
J. Marsolier,
2017,
Neuromuscular Disorders.
L. Brunereau,
E. Malfatti,
I. Richard,
2021,
Neuromuscular Disorders.
E. Chouery,
A. Mégarbané,
G. Lefranc,
2021,
Journal of neuromuscular diseases.
K. Campbell,
M. Gautel,
I. Richard,
2007,
Annals of neurology.
S. Nelson,
M. Hegde,
A. Ferlini,
2019,
The Journal of pediatrics.
D. Annane,
G. Bassez,
R. Carlier,
2021,
Muscle & nerve.
F. Leturcq,
J. Kaplan,
G. Piluso,
2004,
American journal of medical genetics. Part A.
I. Richard,
N. Lévy,
F. Leturcq,
2010
.
I. Richard,
N. Lévy,
F. Leturcq,
2010,
Science Translational Medicine.
I. Nelson,
E. Malfatti,
N. Romero,
2018,
Journal of neuropathology and experimental neurology.
P. Soler-Palacín,
M. López-Trascasa,
F. Leturcq,
2012,
Orphanet Journal of Rare Diseases.
F. Leturcq,
J. Chelly,
C. Chiron,
2009,
PloS one.
M. Koenig,
M. Cossée,
J. Mandel,
2009,
Neuromuscular Disorders.
F. Leturcq,
H. Delage,
A. Drouet,
2002,
Presse medicale.
A. Laquérriere,
F. Leturcq,
S. Marret,
2021,
Scientific Reports.
D. Annane,
D. Orlikowski,
F. Leturcq,
2018,
The American journal of cardiology.
D. Annane,
D. Orlikowski,
F. Leturcq,
2017,
ESC heart failure.
Iñaki Inza,
Rubén Armañanzas,
Ana Cabello,
2008,
PloS one.
N. Romero,
N. Lévy,
F. Leturcq,
2006
.
M. Cossée,
F. Leturcq,
T. Stojkovic,
2016,
Neurology: Genetics.
C. Béroud,
D. Figarella-Branger,
G. Bassez,
2005,
Human mutation.
F. Leturcq,
J. Nectoux,
V. Tsatsaris,
2016,
Prenatal diagnosis.
F. Leturcq,
P. Laforêt,
T. Stojkovic,
2020,
médecine/sciences.
E. Pegoraro,
F. Leturcq,
P. Laforêt,
2015,
Neurology.
I. Nelson,
E. Malfatti,
N. Romero,
2015,
Neurology.
N. Romero,
D. Klatzmann,
R. Mulligan,
2012,
Brain : a journal of neurology.
C. Béroud,
D. Figarella-Branger,
F. Chapon,
2009,
Human mutation.
A. Toutain,
B. Echenne,
L. Kalaydjieva,
2000,
Neurology.
M. Cossée,
F. Leturcq,
S. Quijano-roy,
2022,
The Journal of molecular diagnostics : JMD.
M. Vidaud,
D. Vidaud,
F. Leturcq,
2018,
Clinical chemistry and laboratory medicine.
Gamma-Sarcoglycanopathy (LGMD 2C) with del 525t mutation: Report of the first familial case in Niger
F. Leturcq,
J. Urtizberea,
H. Moumouni,
2012
.
B. Dutrillaux,
F. Leturcq,
J. Kaplan,
1994,
Human Genetics.
A. Toutain,
N. Romero,
L. Pasquier,
2013,
European Journal of Human Genetics.
F. Muntoni,
V. Sardone,
E. Ricci,
2021,
Journal of neuropathology and experimental neurology.
F. Muntoni,
V. Sardone,
E. Ricci,
2021
.
A. Toutain,
L. Pasquier,
S. Mercier,
2013,
European Journal of Human Genetics.
A. Toutain,
F. Leturcq,
D. Babuty,
2007,
Neurology.
A. Chessel,
C. Béroud,
A. Boland,
2021,
Biomedicines.
F. Leturcq,
R. Gherardi,
D. Récan,
1995,
Journal of neurology, neurosurgery, and psychiatry.
T. Yousry,
J. Holton,
F. Leturcq,
2010,
Archives of neurology.
A. Munnich,
N. Romero,
F. Leturcq,
2001,
Neuromuscular Disorders.
K. Bushby,
N. Lévy,
F. Leturcq,
2011,
Clinical genetics.
P. Cluzel,
M. Cossée,
F. Leturcq,
2013,
International journal of cardiology.
A. Goyenvalle,
A. Vulin,
F. Fougerousse,
2004,
Medecine sciences : M/S.
F. Rivier,
A. Toutain,
B. Echenne,
2009,
Human molecular genetics.
N. Romero,
F. Leturcq,
B. Estournet,
2008,
Neuromuscular Disorders.
R. Weiss,
K. Flanigan,
C. Béroud,
2020,
Skeletal Muscle.
L. Servais,
J. Hogrel,
F. Leturcq,
2015,
Journal of neuromuscular diseases.
N. Lévy,
F. Leturcq,
G. Lattanzi,
2015
.
D. Figarella-Branger,
G. Bassez,
J. Pouget,
2007,
Archives of neurology.
N. Romero,
F. Leturcq,
L. Viollet,
2007,
Neurology.
K. Campbell,
I. Nonaka,
F. Leturcq,
1993,
American journal of human genetics.
P. Czernichow,
J. Hugnot,
F. Leturcq,
1992,
The Journal of clinical investigation.
Novel Exon-Skipping Therapeutic Approach for the DMD Gene Based on Asymptomatic Deletions of Exon 49
N. Philip,
N. Lévy,
F. Leturcq,
2022,
Genes.
R. Porcher,
D. Annane,
P. Ravaud,
2021,
European heart journal.
F. Muntoni,
R. Weiss,
K. Flanigan,
2020,
Journal of neuromuscular diseases.
D. Vidaud,
F. Leturcq,
J. Nectoux,
2022,
BJOG : an international journal of obstetrics and gynaecology.
Domenica Taruscio,
Emma Heslop,
Jes Rahbek,
2013,
Human mutation.
D. MacArthur,
M. Lek,
K. Claeys,
2017,
Journal of Neurology, Neurosurgery, and Psychiatry.
I. Nelson,
M. Cossée,
I. Richard,
2014,
European Journal of Human Genetics.
J. Beckmann,
I. Richard,
F. Leturcq,
1998,
Brain : a journal of neurology.
F. Leturcq,
J. Kaplan,
J. Chelly,
2008,
European Journal of Human Genetics.
J. Emparanza,
D. Figarella-Branger,
C. Bönnemann,
2005,
Brain : a journal of neurology.
J. Beckmann,
C. de Toma,
K. Campbell,
1997,
Annals of neurology.
J. Beckmann,
K. Campbell,
N. Romero,
1994,
Cell.
N. Lévy,
Jorge Oliveira,
F. Leturcq,
2011,
Neuromuscular Disorders.
J. Beckmann,
K. Campbell,
A. Toutain,
1996,
Human molecular genetics.
A. Toutain,
B. Echenne,
L. Kalaydjieva,
2000,
Neurology.
K. Campbell,
N. Romero,
F. Leturcq,
1997,
Neurology.
F. Leturcq,
J. Ben Chibani,
S. Laradi,
2000,
Annales de biologie clinique.
F. Muntoni,
S. Manilal,
F. Leturcq,
1998,
Human molecular genetics.
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
J. Beckmann,
K. Campbell,
N. Romero,
1995,
Nature Genetics.
F. Leturcq,
J. Chelly,
N. Deburgrave,
2014,
Neuromuscular Disorders.
K. Mamchaoui,
F. Leturcq,
F. Piétri-Rouxel,
2018,
Skeletal Muscle.
M. Cossée,
F. Leturcq,
J. Chelly,
2013,
European Journal of Human Genetics.
P. Soler-Palacín,
M. López-Trascasa,
F. Leturcq,
2012,
Orphanet Journal of Rare Diseases.
Christophe Béroud,
Jamel Chelly,
Mireille Claustres,
2009,
Human mutation.
M. Cossée,
F. Leturcq,
J. Chelly,
2008,
Human mutation.
M. Cossée,
M. Claustres,
F. Leturcq,
2016,
Journal of neuromuscular diseases.
F. Leturcq,
R. Ben Yaou,
2015,
Orphanet Journal of Rare Diseases.
C. Béroud,
I. Nelson,
A. Toutain,
2015,
Journal of neuromuscular diseases.
K. Flanigan,
P. Mangeot,
M. Peschanski,
2015,
Skeletal Muscle.
E. Malfatti,
N. Romero,
R. Carlier,
2019,
Neuromuscular Disorders.
N. Romero,
F. Leturcq,
T. Stojkovic,
2022,
Journal of neuromuscular diseases.
D. Annane,
S. Chevret,
D. Orlikowski,
2016,
PloS one.
C. Béroud,
F. Leturcq,
J. Kaplan,
2007,
Human mutation.
C. Béroud,
F. Leturcq,
J. Kaplan,
2004,
Neuromuscular Disorders.
L. Servais,
F. Leturcq,
I. Desguerre,
2020,
Annals of neurology.
L. Servais,
F. Leturcq,
P. Sabouraud,
2013,
Neuromuscular Disorders.
D. Vidaud,
C. Férec,
F. Leturcq,
2023,
medRxiv.
F. Leturcq,
N. Deburgrave,
Yuqing Wen,
2006,
Clinical Neurology and Neurosurgery.
N. Lévy,
F. Leturcq,
B. Eymard,
2006,
Clinical genetics.
M. Cossée,
J. Pouget,
N. Lévy,
2020,
Neuropathology and applied neurobiology.
C. Béroud,
F. Chapon,
V. Drouin‐Garraud,
2007,
Clinical genetics.
N. Romero,
D. Klatzmann,
J. Hogrel,
2004,
Human gene therapy.
F. Leturcq,
J. Kaplan,
D. Miličić,
2000,
Croatian medical journal.
Captain Haddock's health issues in the adventures of Tintin. Comparison with Tintin's health issues.
F. Leturcq,
L. Epelboin,
E. Caumes,
2016,
Presse medicale.
Dystrophin's central domain forms a complex filament that becomes disorganized by in-frame deletions
M. Baaden,
P. Roblin,
M. Czjzek,
2018,
The Journal of Biological Chemistry.
K. Campbell,
Y. Sunada,
F. Duclos,
1996,
FEBS letters.
V. Vié,
M. Claustres,
F. Leturcq,
2015,
Human molecular genetics.
F. Leturcq,
J. Kaplan,
L. Morandi,
1994,
The Journal of clinical investigation.
F. Leturcq,
J. Kaplan,
L. García,
2012,
Human molecular genetics.
L. Cuisset,
F. Leturcq,
J. Nectoux,
2023,
Neuromuscular Disorders.
K. Campbell,
F. Leturcq,
J. Kaplan,
1996,
Neuropediatrics.
K. Campbell,
F. Leturcq,
J. Kaplan,
1994,
Neuromuscular Disorders.
C. de Toma,
K. Campbell,
Y. Sunada,
1997,
Journal of medical genetics.
D. Annane,
S. Chevret,
D. Orlikowski,
2018,
PloS one.
K. Campbell,
F. Leturcq,
J. Kaplan,
1993,
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.
F. Leturcq,
P. Bougnères,
J. Carel,
1998,
Diabetes Care.
F. Rivier,
C. Béroud,
F. Chapon,
2022,
Orphanet Journal of Rare Diseases.
N. Romero,
R. Carlier,
F. Leturcq,
2017,
Muscle & nerve.
R. Porcher,
É. Marijon,
A. Lazarus,
2019,
Circulation.
F. Leturcq,
M. Szajnert,
N. Deburgrave,
2005,
European journal of haematology.
G. Bassez,
F. Leturcq,
P. Laforêt,
2021,
Journal of neuromuscular diseases.
F. Leturcq,
K. Azibi,
T. Voit,
1996,
Neuromuscular Disorders.
J. Beckmann,
F. Leturcq,
J. Kaplan,
1994,
Journal of medical genetics.
K. Campbell,
N. Romero,
F. Leturcq,
1994,
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.
F. Leturcq,
J. Kaplan,
2005,
Journal de la Societe de biologie.
G. Bassez,
T. Maisonobe,
F. Leturcq,
2021,
European journal of neurology.
T. Maisonobe,
F. Leturcq,
P. Laforêt,
2008,
Muscle & nerve.
K. Mamchaoui,
F. Leturcq,
F. Piétri-Rouxel,
2018,
Skeletal muscle.
F. Leturcq,
L. Epelboin,
P. Kozarsky,
2015,
Presse medicale.
J. Beckmann,
K. Campbell,
L. E. Lim,
1994,
Human molecular genetics.
F. Leturcq,
J. Kaplan,
P. Laforêt,
2012,
Neuromuscular Disorders.
F. Bouquet,
M. Cossée,
F. Leturcq,
2012,
Revue neurologique.
J. Pouget,
N. Lévy,
F. Leturcq,
2010,
Neuromuscular Disorders.
F. Leturcq,
P. Laforêt,
B. Eymard,
2004,
Heart.
E. Malfatti,
N. Romero,
I. Richard,
2020,
European journal of neurology.
M. Cossée,
F. Leturcq,
Y. Péréon,
2023,
Journal of Neurology.
F. Leturcq,
J. Kaplan,
H. Sorimachi,
2011,
Muscle & nerve.
J. Melki,
M. Cossée,
J. Pouget,
2018,
European Journal of Human Genetics.
K. Flanigan,
P. Mangeot,
M. Peschanski,
2015,
Skeletal Muscle.
R. Carlier,
F. Leturcq,
P. Laforêt,
2023,
European journal of neurology.
K. Bushby,
F. Leturcq,
F. Hanisch,
2007,
Neuromuscular Disorders.
N. Romero,
F. Leturcq,
J. Kaplan,
1997,
Neuromuscular Disorders.
F. Leturcq,
P. Bougnères,
J. Carel,
1998,
Diabetes Care.
M. Cossée,
F. Leturcq,
J. Chelly,
2008,
Human mutation.
P. Cluzel,
M. Cossée,
F. Leturcq,
2013,
International journal of cardiology.
M. Mattei,
N. Lévy,
F. Leturcq,
2008,
Neuromuscular Disorders.
D. Orlikowski,
F. Leturcq,
K. Wahbi,
2022
.
D. Orlikowski,
F. Leturcq,
K. Wahbi,
2022
.
D. Annane,
D. Orlikowski,
F. Leturcq,
2022
.