F. Bouhour
发表
Y. Péréon,
N. Zahr,
A. Béhin,
2021,
Neuromuscular Disorders.
F. Rivier,
F. Chapon,
C. Richelme,
2019,
Orphanet Journal of Rare Diseases.
C. Confavreux,
P. Krolak-Salmon,
F. Bouhour,
1999,
European Neurology.
Renan Sales Barros,
Hester F. Lingsma,
Ivo G. H. Jansen,
2018,
The Lancet. Neurology.
E. Broussolle,
F. Bouhour,
C. Vial,
2008,
European Neurology.
E. Broussolle,
P. Leblanc,
S. Lumbroso,
2020,
European Neurology.
S. Thobois,
P. Leblanc,
S. Lumbroso,
2020,
International journal of molecular sciences.
A. Vighetto,
C. Tilikete,
D. Michel,
2000,
Annals of neurology.
A. Echaniz-Laguna,
Y. Péréon,
J. Antoine,
2018,
Muscle & nerve.
F. Chapon,
T. Perez,
G. Bassez,
2020,
Journal of inherited metabolic disease.
F. Chapon,
G. Bassez,
D. Orlikowski,
2016,
Scientific Reports.
R. Schiffmann,
D. Rodriguez,
O. Boespflug-Tanguy,
2003,
American journal of human genetics.
M. Tarnopolsky,
Y. Chien,
J. Charrow,
2021,
The Lancet Neurology.
L. Féasson,
P. Petiot,
C. Broussolle,
2007,
Muscle & nerve.
P. Lozeron,
J. Pouget,
O. Dubourg,
2019,
Neurological Therapeutics.
J. Antoine,
E. Hachulla,
J. Azulay,
2018,
BioMed Research International.
D. Annane,
L. Kremer,
T. Stojkovic,
2021,
Neurology.
B. Byrne,
A. Pestronk,
M. Tarnopolsky,
2021,
The Lancet Neurology.
B. Flourié,
F. Bouhour,
G. Boschetti,
2010,
Inflammatory bowel diseases.
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution
I. Nelson,
R. Carlier,
P. Carlier,
2014,
Journal of Neurology, Neurosurgery & Psychiatry.
F. Bouhour,
C. Vial,
C. Caudie,
2011,
Annales de biologie clinique.
Michael T. McManus,
Renan Sales Barros,
Hester F. Lingsma,
2019,
The Lancet Neurology.
F. Chapon,
D. Orlikowski,
J. Hogrel,
2013,
Revue neurologique.
P. Laforêt,
K. Wahbi,
D. Duboc,
2014,
Neuromuscular Disorders.
G. L. Masson,
W. Löscher,
P. Vermersch,
2017,
The Lancet. Neurology.
P. Laforêt,
M. Michaud,
F. Bouhour,
2021,
European journal of neurology.
T. Stojkovic,
A. Béhin,
F. Bouhour,
2012,
Journal of Neurology.
S. Vukusic,
C. Confavreux,
F. Bouhour,
1999,
La Revue du praticien.
F. Bouhour,
P. Roche,
2021,
Revue neurologique.
P. Bergh,
N. Romero,
B. V. van Engelen,
2014,
Neurology.
N. Romero,
P. Laforêt,
B. Eymard,
2017,
Journal of Neurology.
Julie M. Woessner,
P. Hennequin,
Cécile Paris,
2021,
The Lancet Rheumatology.
C. Fischer,
S. Diabira,
R. Bougeard,
1999,
Acta Neurochirurgica.
P. Convers,
S. Rheims,
J. Antoine,
2022,
Muscle & nerve.
F. Magdinier,
J. Pouget,
N. Lévy,
2015,
Orphanet Journal of Rare Diseases.
F. Chapon,
E. Pegoraro,
A. Briand-Suleau,
2019,
Neurology.
F. Magdinier,
N. Lévy,
A. Echaniz-Laguna,
2020,
International journal of molecular sciences.
F. Chapon,
A. Geille,
G. Bassez,
2016,
PloS one.
T. Maisonobe,
A. Echaniz-Laguna,
J. Antoine,
2020,
Blood.
A. Echaniz-Laguna,
Y. Péréon,
P. Cintas,
2022,
European journal of neurology.
M. Janier,
J. Puymirat,
L. Hébert,
2012,
Journal of magnetic resonance imaging : JMRI.
F. Mauguière,
S. Vukusic,
C. Confavreux,
2009,
Brain : a journal of neurology.
F. Mauguière,
F. Sedel,
S. Vukusic,
2011,
Revue neurologique.
P. Lozeron,
Y. Péréon,
A. Magot,
2020,
European Journal of Neurology.
J. Antoine,
P. Gonnaud,
P. Petiot,
2007,
Annales de biologie clinique.
F. Bouhour,
J. Ninet,
A. Hot,
2007,
Clinical Rheumatology.
LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2
P. Latour,
T. Stojkovic,
C. Goizet,
2019,
European Journal of Human Genetics.
LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2
P. Latour,
T. Stojkovic,
C. Goizet,
2019,
European Journal of Human Genetics.
E. Broussolle,
I. Court-Fortune,
J. Antoine,
2013,
Respiratory Care.
F. Rivier,
C. Béroud,
F. Chapon,
2022,
Orphanet Journal of Rare Diseases.
R. Porcher,
É. Marijon,
A. Lazarus,
2019,
Circulation.
Y. Péréon,
P. Cintas,
M. Michaud,
2023,
Revue neurologique.
F. Ducray,
N. Costedoat-Chalumeau,
F. Bouhour,
2007,
Revue neurologique.
P. Lozeron,
Y. Péréon,
A. Magot,
2019,
European journal of neurology.
D. Orlikowski,
D. Hamroun,
A. Echaniz-Laguna,
2018,
Journal of Inherited Metabolic Disease.
I. Durieu,
F. Bouhour,
S. Durupt,
1999,
Presse medicale.
Nathalie,
N. Romero,
P. Laforêt,
2017
.
R. Porcher,
D. Annane,
S. Chevret,
2008,
Neurology.
F. Ducray,
F. Mauguière,
S. Vukusic,
2015,
Neurology.
F. Chapon,
J. Pouget,
A. Echaniz-Laguna,
2011
.
D. Guehl,
P. Burbaud,
P. Derost,
2018,
Parkinsonism & related disorders.
F. Bouhour,
R. Marignier,
E. Delmont,
2022,
Neurology: Neuroimmunology & Neuroinflammation.
F. Bérard,
G. Bassez,
D. Orlikowski,
2023,
Molecular genetics and metabolism.
F. Bouhour,
N. Fabien,
C. Vial,
2013,
Clinical laboratory.
A. Echaniz-Laguna,
Y. Péréon,
P. Latour,
2023,
European journal of neurology.
R. Écochard,
I. Poirot,
V. Tiffreau,
2013,
Annals of physical and rehabilitation medicine.
E. Broussolle,
P. Latour,
P. Gonnaud,
2009,
Revue neurologique.
N. le Forestier,
M. Reilly,
A. Echaniz-Laguna,
2023,
Neurology: Genetics.
Fatal myositis and myasthenia induced by atezolizumab for the treatment of hepatocellular carcinoma.
J. Dumortier,
F. Bouhour,
Marie Simon,
2021,
Clinics and research in hepatology and gastroenterology.
P. Latour,
T. Stojkovic,
S. Allouche,
2022,
Brain : a journal of neurology.
B. Eymard,
F. Bouhour,
P. Richard,
2010,
Journal of Medical Genetics.
F. Bouhour,
R. Froissart,
M. Hermier,
2022,
Genes.
V. Cottin,
F. Bouhour,
C. Vial,
2007
.
S. Thobois,
F. Bouhour,
S. Gerber,
2023,
EMBO molecular medicine.
Y. Chien,
B. Schoser,
S. Illarioshkin,
2021,
Molecular Genetics and Metabolism.
P. Petiot,
F. Bouhour,
R. Marignier,
2023,
Journal of Neurology.
P. Latour,
T. Stojkovic,
F. Bouhour,
2023,
European journal of human genetics : EJHG.
B. Flourié,
F. Bouhour,
G. Boschetti,
2010,
Inflammatory Bowel Diseases.
Michael T. McManus,
Renan Sales Barros,
Hester F. Lingsma,
2019,
The Lancet. Neurology.
A. Echaniz-Laguna,
P. Petiot,
F. Bouhour,
2023,
Journal of Neurology.
I. Durieu,
P. Petiot,
M. Robert,
2023,
Rheumatology.
M. Janier,
J. Puymirat,
L. Hébert,
2012,
Journal of magnetic resonance imaging : JMRI.
D. Hamroun,
P. Laforêt,
P. Cintas,
2023,
Neurology.