T. Voit
发表
Francesco Muntoni,
Hanns Lochmüller,
Alessandra Renieri,
2014,
European Journal of Human Genetics.
M. Veras,
G. Butler-Browne,
V. Mouly,
2015,
Skeletal Muscle.
M. Veras,
G. Butler-Browne,
V. Mouly,
2015,
Skeletal Muscle.
C. Ponting,
D. Bonthron,
E. Bertini,
2006,
Nature Genetics.
H. Goebel,
M. Cremer,
T. Voit,
1991,
Neuropediatrics.
R. Finkel,
E. Bertini,
S. Peltz,
2017,
The Lancet.
Susan C. Brown,
F. Muntoni,
T. Voit,
2003,
Human molecular genetics.
Francesco Muntoni,
William B. Dobyns,
Stanley F. Nelson,
2012,
Nature Genetics.
M. Narici,
D. Jones,
S. Sipilä,
2013,
Osteoporosis International.
Laetitia van Wittenberghe,
F. Mavilio,
T. Voit,
2016,
Molecular therapy. Methods & clinical development.
J. Smeitink,
T. Voit,
G. Hoffmann,
2005,
Journal of Inherited Metabolic Disease.
A. Lemainque,
C. Bönnemann,
N. Romero,
2002,
Annals of neurology.
F. Muntoni,
I. Barthélémy,
S. Blot,
2020,
Molecular therapy. Methods & clinical development.
G. Comi,
R. Finkel,
B. Wong,
2014,
Muscle & nerve.
A. Mayhew,
E. Mercuri,
K. Bushby,
2014
.
M. Willemsen,
T. Voit,
M. Willemsen,
2001,
FEBS letters.
T. Voit,
A. Verrips,
M. Willemsen,
2001,
Human molecular genetics.
K. Bushby,
F. Muntoni,
P. Jeannet,
2011,
Human molecular genetics.
L. Peltonen,
I. Richard,
T. Voit,
2001,
Neurology.
S. Züchner,
B. Dan,
P. van Damme,
2014,
neurogenetics.
H. Budka,
N. Romero,
G. Butler-Browne,
2013,
Neuromuscular Disorders.
F. Muntoni,
L. Servais,
T. Maisonobe,
2017,
Nature Communications.
V. Ricotti,
A. Mayhew,
F. Muntoni,
2019,
Neuromuscular Disorders.
L. Servais,
J. Hogrel,
P. Carlier,
2016,
Neurology.
L. Servais,
J. Hogrel,
S. Quijano-roy,
2015,
PloS one.
H. Reichmann,
H. Schroten,
T. Voit,
1994,
Acta paediatrica.
A. Nake,
H. Scheffer,
M. Willemsen,
2005,
Neuropediatrics.
S. Bensamoun,
L. Debernard,
F. Charleux,
2015
.
G. Dickson,
A. Mollard,
M. Wood,
2016,
Human molecular genetics.
G. Dickson,
A. Mollard,
M. Wood,
2015
.
H. Fehling,
T. Voit,
N. Rao,
2014
.
K. Davies,
A. Goyenvalle,
L. García,
2013,
Molecular therapy : the journal of the American Society of Gene Therapy.
K. Mamchaoui,
L. García,
S. Philippi,
2013,
Nucleic acids research.
T. N. Rao,
H. Fehling,
T. Voit,
2013,
Journal of Virology.
L. Servais,
J. Hogrel,
T. Voit,
2012
.
R. Kotin,
L. Servais,
J. Hogrel,
2014,
Molecular therapy : the journal of the American Society of Gene Therapy.
D. Israeli,
L. Servais,
I. Barthélémy,
2014,
The American journal of pathology.
L. Servais,
I. Barthélémy,
S. Blot,
2014
.
I. Harting,
F. Muntoni,
K. Zerres,
2005,
Nature Genetics.
Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy
C. Bönnemann,
P. Nürnberg,
G. Privé,
2010,
Brain : a journal of neurology.
L. Servais,
P. Carlier,
N. Azzabou,
2015,
NMR in biomedicine.
C. Roll,
T. Voit,
J. Erhard,
1997,
The Lancet.
Susan C. Brown,
K. Bushby,
F. Muntoni,
2004,
The American journal of pathology.
T. Voit,
A. Ballauff,
V. Engelbrecht,
1994,
European Journal of Pediatrics.
F. Muntoni,
T. Helliwell,
R. Appleton,
1995,
Neuropediatrics.
Susan C. Brown,
E. Mercuri,
F. Muntoni,
2003,
Annals of neurology.
F. Muntoni,
T. Voit,
F. Muntoni,
2005,
Neuromuscular Disorders.
R. Wanders,
T. Voit,
J. Schröder,
2004,
Acta Neuropathologica.
K. Hiller,
W. Buchalla,
Fabian Cieplik,
2021,
Frontiers in Medicine.
T. Voit,
U. Mellies,
H. Teschler,
2006,
Neuromuscular Disorders.
T. Voit,
U. Mellies,
H. Teschler,
2006,
Pediatric pulmonology.
C. Nienaber,
H. Goebel,
H. Lenard,
1988,
Neuropediatrics.
F. Muntoni,
T. Voit,
2004,
Neuromuscular Disorders.
J. Bourke,
K. Bushby,
F. Muntoni,
2004,
Annals of neurology.
H. Brunner,
J. van Reeuwijk,
H. van Bokhoven,
2007,
Human Genetics.
T. Voit,
E. Neuen‐Jacob,
B. Leube,
2001,
Neuromuscular Disorders.
B. Wong,
L. Servais,
T. Voit,
2014,
Neuromuscular Disorders.
F. Binkofski,
W. Heindel,
H. Kugel,
1996,
Genomics.
I. Nonaka,
I. Nishino,
H. Yoshikawa,
2002,
Biochemical and biophysical research communications.
L. Schaeffer,
C. Hourde,
A. Ferry,
2010,
The EMBO journal.
L. Schaeffer,
C. Hourde,
A. Ferry,
2009,
Neuromuscular Disorders.
P. Vreken,
A. V. van Kuilenburg,
M. Spraul,
2001,
Magnetic resonance in medicine.
A. V. van Kuilenburg,
L. Zoetekouw,
H. van Lenthe,
2004,
Human molecular genetics.
T. Voit,
2014,
Neuromuscular Disorders.
G. Gillessen‐kaesbach,
T. Voit,
A. Lackner,
2000,
American journal of medical genetics.
F. Brodsky,
A. Ferry,
Robyn Roth,
2014,
The Journal of cell biology.
K. Claeys,
N. Romero,
G. Faulkner,
2009,
Acta Neuropathologica.
E. Mercuri,
F. Muntoni,
M. Rutherford,
2006,
Archives of neurology.
F. Muntoni,
V. Dubowitz,
M. Rhodes,
2000,
American journal of human genetics.
T. Voit,
Thomas Voit,
1998,
Brain and Development.
R. Cohn,
T. Voit,
U. Wewer,
1998,
Neurology.
H. Katus,
O. Müller,
F. Weinberger,
2014,
Nature Communications.
C. Hourde,
T. Voit,
V. Mariot,
2020,
Molecular therapy. Nucleic acids.
A. Goyenvalle,
A. Vulin,
L. García,
2012,
Molecular therapy : the journal of the American Society of Gene Therapy.
K. Davies,
P. Kronqvist,
E. Engvall,
2003,
Human molecular genetics.
J. Léger,
T. Voit,
M. Fardeau,
1991,
FEBS letters.
T. Voit,
C. Wurthmann,
J. Klepper,
2008,
European Journal of Pediatrics.
W. Fogel,
H. Goebel,
M. Cremer,
1995,
Annals of the New York Academy of Sciences.
R. Finkel,
K. Bushby,
J. Jaiswal,
2020,
Annals of neurology.
J. Weissenbach,
T. Klockgether,
T. Voit,
1995,
American journal of human genetics.
A. Toutain,
B. Echenne,
L. Kalaydjieva,
2000,
Neurology.
T. Voit,
F. Leterrier,
2008,
Neuromuscular Disorders.
K. Claeys,
G. Faulkner,
T. Maisonobe,
2008,
Neuromuscular Disorders.
Jacqueline Palace,
K. Bushby,
F. Muntoni,
2012,
Journal of Neurology.
J. Weissenbach,
A. Dürr,
A. Brice,
2004,
Neurogenetics.
C. Hübner,
T. Voit,
K. Oexle,
1998
.
E. Hoffman,
S. Çırak,
T. Voit,
2016,
Journal of Human Genetics.
B. Wirth,
K. Zerres,
T. Voit,
2007
.
R. Lachmann,
M. Kroos,
T. Derks,
2016,
Orphanet Journal of Rare Diseases.
K. Davies,
C. Leumann,
A. Goyenvalle,
2015,
Nature Medicine.
V. Ricotti,
F. Muntoni,
L. Servais,
2018
.
F. Baas,
A. Starr,
D. Gresham,
2000,
Neuromuscular Disorders.
L. Kalaydjieva,
T. Voit,
J. Schröder,
1998,
Neuromuscular Disorders.
T. Voit,
U. Mellies,
H. Teschler,
2003,
Neuromuscular Disorders.
T. Voit,
U. Mellies,
C. Dohna-Schwake,
2006,
Neuromuscular Disorders.
T. Voit,
U. Mellies,
H. Teschler,
2005,
Neurology.
F. Ratjen,
T. Voit,
V. Straub,
2002,
The Journal of pediatrics.
J. J. Padilla,
R. Finkel,
P. Spagnolo,
2016,
Neuromuscular Disorders.
T. Voit,
M. Leinonen,
C. McDonald,
2018,
Journal of neuromuscular diseases.
H. van Bokhoven,
S. Çırak,
T. Voit,
2010,
Neurology.
B. Ilkovski,
N. Laing,
A. Koy,
2007,
Neuropediatrics.
E. Mercuri,
F. Muntoni,
T. Pierson,
2021,
Brain communications.
B. Eymard,
T. Stojkovic,
T. Voit,
2010,
Neuromuscular Disorders.
V. Dubowitz,
T. Voit,
C. Sewry,
1988,
Annals of neurology.
G. Herman,
T. Voit,
A. Amalfitano,
2009
.
F. Mastaglia,
P. Hedera,
N. Laing,
2005,
Journal of Neurology, Neurosurgery & Psychiatry.
M. Cremer,
H. Katus,
R. Cohn,
2000,
The Lancet.
R. Kotin,
R. Samulski,
S. Blot,
2012,
Journal of Virology.
H. Karch,
T. Voit,
H. Huppertz,
1993,
European Journal of Pediatrics.
H. Christen,
H. Goebel,
H. Lenard,
1998,
American journal of medical genetics.
L. García,
F. Weinberger,
T. Voit,
2013,
EMBO molecular medicine.
L. Popplewell,
G. Dickson,
T. Voit,
2016,
Human molecular genetics.
H. Lehr,
S. Marklund,
T. Voit,
1996,
Pediatric Research.
Tom H. Lindner,
Sebahattin Cirak,
F. von Deimling,
2005
.
F. Heinen,
T. Voit,
J. Klepper,
2002,
Journal of Inherited Metabolic Disease.
T. Voit,
R. Schmidt,
1993,
Neuropediatrics.
T. Voit,
V. Straub,
S. Richards,
2005,
Neuromuscular Disorders.
J. Lupski,
P. Brophy,
C. Boerkoel,
2002,
Annals of neurology.
Rafael J. Yáñez-Muñoz,
L. Popplewell,
K. Mamchaoui,
2013,
Human gene therapy.
R. Finkel,
P. Spagnolo,
N. Goemans,
2016,
Pediatric pulmonology.
R. Finkel,
N. Goemans,
C. Straathof,
2015,
The Lancet.
G. Butler-Browne,
V. Mouly,
A. Faussat,
2014,
Disease Models & Mechanisms.
F. Muntoni,
T. Voit,
P. Guicheney,
2009,
Neuromuscular Disorders.
W. Kress,
C. Hübner,
T. Voit,
1995,
The New England journal of medicine.
L. Servais,
J. Hogrel,
F. Leturcq,
2015,
Journal of neuromuscular diseases.
M. Schuelke,
E. Klopocki,
W. Kress,
2007,
Muscle & nerve.
C. Hübner,
T. Voit,
K. Oexle,
1996,
Human molecular genetics.
A. Spuler,
H. Knoblauch,
P. Nürnberg,
2010,
Annals of neurology.
G. Butler-Browne,
M. Ribeiro,
T. Voit,
2010,
Journal of Neuroimmunology.
I. Glass,
K. Gripp,
W. Dobyns,
2004,
Neuropediatrics.
Wiley Interscience,
T. Voit,
U. Mellies,
2008,
Pediatric pulmonology.
J. Léger,
T. Voit,
A. Robert,
1993,
Neuromuscular Disorders.
J. Léger,
T. Voit,
J. Léger,
1991,
The American journal of pathology.
T. Voit,
F. Pons,
J. Léger,
2007
.
M. Main,
E. Mazzone,
C. Palermo,
2014,
Neuromuscular Disorders.
R. Finkel,
K. Bushby,
K. Flanigan,
2008,
Neuromuscular Disorders.
A. Schulz,
J. Alroy,
H. Goebel,
1992,
Journal of neuropathology and experimental neurology.
A. Sonnenberg,
R. Cohn,
T. Voit,
1999,
Journal of the neurological sciences.
T. Voit,
V. Straub,
L. Klinge,
2005,
Neuropediatrics.
F. Muntoni,
M. Zatz,
N. Romero,
2005,
Neuromuscular Disorders.
T. Voit,
V. Straub,
R. Herrmann,
1996,
European Journal of Pediatrics.
C. Clark,
E. Mercuri,
K. Bushby,
2018,
Neurology.
F. Mastaglia,
P. Hedera,
N. Laing,
2004,
American journal of human genetics.
M. Ladd,
M. Forsting,
T. Egelhof,
2004,
Neuromuscular Disorders.
R. Finkel,
N. Goemans,
T. Voit,
2015
.
E. Mazzone,
A. Mayhew,
E. Mercuri,
2018,
Neuromuscular Disorders.
Soma Das,
G. Raca,
J. Coryell,
2003,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
E. Mercuri,
L. Servais,
C. Straathof,
2019,
Neuromuscular Disorders.
R. Cohn,
T. Voit,
U. Wewer,
1997,
Neuromuscular Disorders.
D. Wieczorek,
T. Voit,
J. Schaper,
2003,
Neuropediatrics.
T. Voit,
S. Nadalin,
C. Broelsch,
2006,
Pediatric transplantation.
A. Green,
D. Bonthron,
E. Bertini,
2007,
American journal of human genetics.
D. Barnes,
D. Bonthron,
H. Brunner,
2006,
Nature Genetics.
C. Woods,
J. Tolmie,
H. Brunner,
2000,
American journal of human genetics.
T. Voit,
A. Kohlschütter,
J. Klepper,
2004,
Prostaglandins, leukotrienes, and essential fatty acids.
C. Roll,
T. Voit,
M. Roggendorf,
1998,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
H. Reichmann,
T. Voit,
C. Thomas,
1991,
European Journal of Pediatrics.
William B. Dobyns,
A. James Barkovich,
Bernard S. Chang,
2004,
Science.
G. Gillessen‐kaesbach,
T. Voit,
L. Hanssler,
1999,
Clinical dysmorphology.
W. Dobyns,
H. Topaloglu,
T. Toda,
2003,
Clinical biochemistry.
C. Walsh,
H. Brunner,
B. van der Zwaag,
2002,
American journal of human genetics.
F. Muntoni,
H. Brunner,
W. Dobyns,
2004,
Journal of Medical Genetics.
Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders.
Michael D. Wilson,
F. Muntoni,
S. Pereira,
2016,
American journal of human genetics.
H. Goebel,
C. Bönnemann,
J. Schessl,
2010,
Neuropediatrics.
H. Goebel,
T. Voit,
E. Neuen‐Jacob,
2001,
Neuropediatrics.
K. Claeys,
T. Voit,
J. Schulz,
2014,
Neuromuscular Disorders.
Susan C. Brown,
G. Vrbóva,
F. Muntoni,
2007,
Proceedings of the National Academy of Sciences.
M. Blank,
T. Voit,
V. Straub,
2000,
Human molecular genetics.
M. Bahlo,
H. Goebel,
L. Kalaydjieva,
2015,
Neuromuscular Disorders.
A. Toutain,
B. Echenne,
L. Kalaydjieva,
2000,
Neurology.
F. Muntoni,
C. Bönnemann,
N. Romero,
2002,
American journal of human genetics.
M. Swash,
G. Bydder,
F. Muntoni,
2005,
Neurology.
J. Jais,
K. Claeys,
I. Nelson,
2016,
Revue neurologique.
H. Goebel,
T. Voit,
K. Jacobs,
1994,
Revue neurologique.
D. Israeli,
L. Servais,
I. Nelson,
2013,
PloS one.
V. Ricotti,
F. Muntoni,
L. Servais,
2014,
The Lancet Neurology.
K. Flanigan,
L. Servais,
T. Voit,
2013,
Neuromuscular Disorders.
M. Roberts,
K. Bushby,
T. Voit,
2008,
Neuromuscular Disorders.
V. Ricotti,
F. Muntoni,
L. Servais,
2020,
Epigenomics.
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
J. Beckmann,
K. Campbell,
N. Romero,
1995,
Nature Genetics.
D H Geschwind,
D B Calne,
D. Geschwind,
2004,
Neurology.
M. Bayés,
H. Brunner,
R. Gershoni-baruch,
2001,
Neurology.
H. Lenard,
T. Voit,
F. Majewski,
1993,
Pediatric neurology.
J. Sahel,
A. Bemelmans,
L. García,
2015,
Molecular therapy : the journal of the American Society of Gene Therapy.
H. Katus,
L. García,
O. Müller,
2013,
Molecular therapy. Nucleic acids.
N. Chatauret,
P. Ravassard,
T. Voit,
2011,
Human molecular genetics.
G. Gerken,
T. Voit,
C. Grasemann,
2005,
Journal of pediatric gastroenterology and nutrition.
S. Bione,
P. Tonali,
E. Ricci,
2000,
American journal of human genetics.
G. Gyapay,
N. Drouot,
C. Fizames,
1998,
Genome research.
L. Servais,
T. Voit,
Y. Audic,
2017,
Molecular therapy. Nucleic acids.
F. Muntoni,
S. Blumen,
A. Bigot,
2011,
Skeletal Muscle.
Effects of anticonvulsants on GLUT1-mediated glucose transport in GLUT1 deficiency syndrome in vitro
T. Voit,
J. Fischbarg,
A. Flörcken,
2003,
European Journal of Pediatrics.
E. Barrey,
J. Hogrel,
J. Thibaud,
2009,
Neuromuscular Disorders.
M. Scott,
J. Axelrod,
A. Bassuk,
2008,
American journal of human genetics.
T. Strom,
K. Bushby,
Jacqueline A Palace,
2011,
American journal of human genetics.
H. Lenard,
T. Voit,
M. Baethmann,
1996,
Acta paediatrica.
M. Rietschel,
G. Danieli,
K. Zerres,
1992,
Neuromuscular Disorders.
K. Claeys,
D. Figarella-Branger,
H. Goebel,
2010,
Neuromuscular Disorders.
T. Voit,
U. Mellies,
H. Teschler,
2001,
Neurology.
David Reversat,
Noura Azzabou,
Thomas Voit,
2014,
Journal of magnetic resonance imaging : JMRI.
T. Voit,
E. Neuen‐Jacob,
Hans-Christoph Diener,
2000,
Muscle & nerve.
E. Mercuri,
K. Bushby,
F. Muntoni,
2002,
Neuromuscular Disorders.
T. Voit,
A. Baltzer,
M. Goertzen,
1995,
Neuropediatrics.
A. Lamprecht,
H. Lenard,
T. Voit,
1992,
Neuropediatrics.
J. Azofeifa,
M. Cremer,
C. Hübner,
1995,
Human Genetics.
V. Ricotti,
F. Muntoni,
T. Voit,
2015,
Neuromuscular Disorders.
Hanns Lochmüller,
Thomas Voit,
P K Thomas,
2003,
Human mutation.
M. Verbeek,
M. Willemsen,
T. Voit,
2001,
Annals of neurology.
A. Mayhew,
E. Mercuri,
K. Bushby,
2015,
Neuromuscular Disorders.
K. Pelin,
S. Rudnik-Schöneborn,
V. Lehtokari,
2008,
European Journal of Human Genetics.
A. Schulz,
W. Friedrich,
U. Kornak,
2000,
Human molecular genetics.
V. Ricotti,
F. Muntoni,
L. Servais,
2022,
Human gene therapy.
Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy
Thomas Voit,
Jean-Yves Hogrel,
Laurent Servais,
2017,
Nature Communications.
Thomas Voit,
David Vissière,
Jean-Yves Hogrel,
2016,
PloS one.
F. Muntoni,
K. Flanigan,
K. Anthony,
2014,
Neurology.
M. Hurles,
F. Muntoni,
K. Campbell,
2013,
Brain : a journal of neurology.
W. Fogel,
H. Goebel,
H. Katus,
1995
.
F. Muntoni,
N. Romero,
H. Bokhoven,
2003,
Neuromuscular Disorders.
Ingeborg Krägeloh-Mann,
Francesco Muntoni,
Peter Nürnberg,
2008,
Nature Genetics.
Isabella Moroni,
Thomas Voit,
Hamid Galehdari,
2017,
American journal of human genetics.
Susan C. Brown,
C. Ponting,
E. Mercuri,
2001,
American journal of human genetics.
Susan C. Brown,
J. Burgunder,
K. Bushby,
2001,
Human molecular genetics.
M. Mizuno,
M. Takeuchi,
H. Topaloglu,
2001,
Developmental cell.
S. Heath,
J. Jais,
D. Zélénika,
2009,
American journal of human genetics.
R. Finkel,
A. Pestronk,
E. Mazzone,
2019,
Journal of Pharmacokinetics and Pharmacodynamics.
V. Ricotti,
F. Muntoni,
L. Servais,
2018,
Epigenomics.
L. Servais,
F. Leturcq,
P. Sabouraud,
2013,
Neuromuscular Disorders.
H. Karch,
T. Voit,
G. Horneff,
1993,
European Journal of Pediatrics.
V. Wahn,
A. Scheid,
T. Voit,
1986,
The Lancet.
D. Israeli,
L. Servais,
T. Voit,
2020,
bioRxiv.
A. Bigot,
K. Mamchaoui,
V. Mouly,
2016,
Skeletal Muscle.
A. Bigot,
G. Butler-Browne,
V. Mouly,
2012,
Journal of proteomics.
C. Lumenta,
T. Voit,
R. Weber,
1991,
Child's Nervous System.
C. Lumenta,
D. Körholz,
T. Voit,
1987,
Klinische Padiatrie.
J. Fyfe,
S. Raoul,
T. Voit,
2013,
Human gene therapy.
J. Lupski,
S. Berkovic,
A. Mégarbané,
2005,
Neurology.
H. Blom,
T. Voit,
G. Hoffmann,
2000,
Neuropediatrics.
Munhyang Lee,
Y. Hayashi,
I. Nishino,
2003,
Human molecular genetics.
T. Voit,
2001,
Neuropediatrics.
T. Voit,
V. Straub,
U. Mellies,
2004,
Neurology.
T. Voit,
R. Bittner,
R. Herrmann,
1997,
Acta Neuropathologica.
T. Voit,
J. Klepper,
2002,
European Journal of Pediatrics.
V. Dubowitz,
M. Dunn,
T. Voit,
1989,
Journal of the Neurological Sciences.
Susan C. Brown,
K. Bushby,
F. Muntoni,
2004
.
M. Ōsawa,
T. Voit,
Makio Kobayashi,
2004
.
H. Reichmann,
T. Voit,
C. Thomas,
1991,
European journal of pediatrics.
A. Sonnenberg,
R. Cohn,
T. Voit,
1999,
Journal of the Neurological Sciences.
A. Jauch,
M. Cremer,
T. Voit,
1992,
European Journal of Pediatrics.
J. Léger,
T. Voit,
V. Straub,
1992,
The Journal of cell biology.
M. Mizuguchi,
Kayoko Saito,
M. Ōsawa,
2004,
Brain and Development.
I. Nonaka,
I. Nishino,
H. Yoshikawa,
2002
.
K. Bushby,
T. Voit,
V. Straub,
2008
.
T. Voit,
V. Straub,
R. Falsaperla,
2002,
Neuromuscular Disorders.
F. Leturcq,
J. Kaplan,
L. García,
2012,
Human molecular genetics.
B. Wong,
L. Servais,
T. Lefèbvre,
2018,
Neuromuscular Disorders.
B. Wong,
L. Servais,
I. Richard,
2015,
Human molecular genetics.
K. Campbell,
F. Leturcq,
J. Kaplan,
1996,
Neuropediatrics.
J. Léger,
M. Cremer,
W. Kress,
1995,
Neuromuscular Disorders.
C. de Toma,
K. Campbell,
Y. Sunada,
1997,
Journal of medical genetics.
L. Servais,
J. Hogrel,
L. Guigand,
2016,
Human gene therapy.
V. Dubowitz,
M. Dunn,
T. Voit,
1988,
Journal of the Neurological Sciences.
Susan C. Brown,
F. Muntoni,
N. Romero,
2005,
Neuromuscular Disorders.
R. Cohn,
T. Voit,
U. Wewer,
1998,
Neurology.
T. Voit,
L. Anderson,
R. Herrmann,
1996,
Biochemical Society transactions.
C. Hourde,
T. Voit,
W. Duddy,
2021,
Journal of cachexia, sarcopenia and muscle.
K. Claeys,
N. Romero,
I. Husson,
2011,
European journal of medical genetics.
L. V. D. Heuvel,
J. Smeitink,
L. P. Van den Heuvel,
2000,
Biochemical and biophysical research communications.
Thomas Voit,
Christian Dohna-Schwake,
T. Voit,
2005,
Current opinion in neurology.
T. Voit,
U. Mellies,
H. Teschler,
2002,
Thorax.
F. Muntoni,
J. Melki,
S. Rudnik-Schöneborn,
2002,
Neuromuscular Disorders.
B. Wirth,
F. Hanefeld,
K. Zerres,
1996,
American journal of human genetics.
A. Ferry,
T. Voit,
M. Barkats,
2017,
Molecular therapy : the journal of the American Society of Gene Therapy.
T. Voit,
U. Mellies,
C. Dohna-Schwake,
2004,
Neuromuscular Disorders.
T. Voit,
U. Mellies,
H. Teschler,
2003,
European Respiratory Journal.
R. Wevers,
J. Smeitink,
S. Wopereis,
2005,
European Journal of Human Genetics.
P. Bénit,
D. Israeli,
L. Servais,
2020,
Scientific Reports.
H. Goebel,
A. Lamprecht,
H. Lenard,
1986,
European Journal of Pediatrics.
M. Narici,
D. Jones,
S. Sipilä,
2014,
AGE.
Apostolos Malatras,
William Duddy,
Matthew Thorley,
2015,
Nucleic Acids Res..
F. Muntoni,
L. Servais,
T. Maisonobe,
2017,
Nature Communications.
M. Ranke,
T. Voit,
F. Majewski,
1993,
European Journal of Pediatrics.
C. Lumenta,
T. Voit,
P. Lemburg,
1987,
Neuropediatrics.
D. Scherman,
D. Israeli,
K. Claeys,
2010,
The American journal of pathology.
Lee-Jen Wei,
G. Comi,
R. Finkel,
2020,
Journal of comparative effectiveness research.
G. Herman,
R. C. Rogers,
T. Voit,
2006,
The Journal of pediatrics.
R. Finkel,
B. Wirth,
E. Mercuri,
2005,
Neuromuscular Disorders.
T. Nakayama,
M. Funatsuka,
H. Oguni,
2005,
Brain and Development.
T. Voit,
D. D. De Vivo,
D. Webb,
2003,
Pediatric neurology.
P Ellen Grant,
Thomas Voit,
William B Dobyns,
2003,
Annals of neurology.
M. Blankenburg,
I. Tuxhorn,
C. Bönnemann,
2008
.
F. Leturcq,
K. Azibi,
T. Voit,
1996,
Neuromuscular Disorders.
A. Bigot,
K. Mamchaoui,
V. Mouly,
2016,
Skeletal Muscle.
B. Wong,
L. Servais,
T. Voit,
2015,
Neuromuscular Disorders.
V. Ricotti,
F. Muntoni,
L. Servais,
2020,
Journal of Neurology.
O. Dirsch,
M. Knaap,
T. Voit,
2005,
Journal of Inherited Metabolic Disease.
Noura Azzabou,
Jamie S. McPhee,
Thomas Voit,
2015,
AGE.
V. Ricotti,
R. Festenstein,
T. Voit,
2023,
Nature Medicine.
R. Cohn,
T. Voit,
B. Leube,
1999,
Neuromuscular Disorders.
Eric Barrey,
Thomas Voit,
Jean-Yves Hogrel,
2011,
BMC musculoskeletal disorders.
V. Dubowitz,
M. Dunn,
T. Voit,
1988,
Journal of the Neurological Sciences.
A. V. van Kuilenburg,
R. Wevers,
A. Ribes,
2006,
Nucleosides, nucleotides & nucleic acids.
A. V. van Kuilenburg,
R. Wevers,
E. Mayatepek,
2006,
Neuropediatrics.
J. J. Padilla,
P. Spagnolo,
C. Bönnemann,
2017,
Neuromuscular Disorders.
S. Züchner,
B. Dan,
Y. Parman,
2014,
neurogenetics.
P. Bénit,
D. Israeli,
M. Sanson,
2020,
Scientific Reports.
R. Finkel,
B. Wong,
S. Peltz,
2011,
Neuromuscular Disorders.
S. Krause,
S. Çırak,
T. Voit,
2006,
Biochemistry.
J. Sahel,
A. Bemelmans,
T. Voit,
2013,
PloS one.
J. Hogrel,
G. Butler-Browne,
P. Carlier,
2015,
AGE.
F. Leturcq,
J. Kaplan,
P. Laforêt,
2012,
Neuromuscular Disorders.
W. Dobyns,
H. Topaloglu,
T. Toda,
2003
.
L. Servais,
J. Hogrel,
S. Quijano-roy,
2015,
PloS one.
L. Servais,
B. Estournet,
T. Voit,
2010,
Neuromuscular Disorders.
A. Bigot,
G. Butler-Browne,
V. Mouly,
2012
.
Susan C. Brown,
E. Mercuri,
K. Bushby,
2004,
Neuropediatrics.
T. Voit,
L. Servais,
S. Quijano-roy,
2013,
Neuromuscular Disorders.
V. Ricotti,
E. Mercuri,
R. Festenstein,
2023,
Nature Medicine.
K. Claeys,
N. Romero,
B. Eymard,
2010,
Neuromuscular Disorders.
K. Devriendt,
E. Lerut,
T. Deconinck,
2013,
Neurology.
T. Voit,
U. Mellies,
H. Teschler,
2003,
Wiener klinische Wochenschrift.
L. Servais,
H. Cavé,
N. Romero,
2014,
Neuromuscular Disorders.
C. Verdier,
A. Bigot,
K. Mamchaoui,
2017,
Scientific Reports.
T. Voit,
2004,
Neuropediatrics.
T. Voit,
U. Wendel,
M. Baethmann,
2022
.
V. Wahn,
T. Voit,
R. Kries,
1987,
Neuropediatrics.
R. J. Ramamurthi,
S. Y. Kim,
H. Y. Wang,
2017,
The New England journal of medicine.
T. Voit,
B. Streubel,
H. Höger,
1994,
Neuropediatrics.
T. Voit,
R. Wessalowski,
L. Thomas,
1993,
The Pediatric infectious disease journal.
I. Scheffer,
Siddharth Srivastava,
B. Bourgeois,
2023,
JAMA neurology.
T. Voit,
R. Herrmann,
K. Meyer,
1996,
European journal of pediatrics.
F. Mastaglia,
P. Hedera,
N. Laing,
2022
.
T. Voit,
M. Fardeau,
F. Tomé,
1994,
Neuropediatrics.
J. Schroeder,
F. Muntoni,
A. Noegel,
2007,
Neuromuscular Disorders.
Katie,
M. Brin,
C. Rowe,
2014
.
R. Cohn,
T. Voit,
U. Wewer,
1997,
Neuromuscular disorders : NMD.
F. Brodsky,
A. Ferry,
Robyn Roth,
2014
.
K. Davies,
C. Leumann,
A. Goyenvalle,
2015,
Nature Medicine.
B. Wong,
L. Servais,
T. Lefèbvre,
2018,
Neuromuscular Disorders.
Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders.
F. Muntoni,
S. Pereira,
J. Dowling,
2016,
American journal of human genetics.
K. Devriendt,
E. Lerut,
T. Deconinck,
2013,
Neurology.
H. Katus,
O. Müller,
F. Weinberger,
2014,
Nature Communications.
T. Voit,
2015,
HMD Praxis der Wirtschaftsinformatik.
S. Çırak,
T. Voit,
T. Willer,
2010,
Neurology.
Jacqueline Palace,
K. Bushby,
F. Muntoni,
2012,
Journal of Neurology.
W. Fogel,
H. Goebel,
H. Katus,
1995
.