E. Brusse
发表
E. Brusse,
2011
.
J. V. van Swieten,
E. Brusse,
J. A. Maat-Kievit,
2006,
Clinical genetics.
P. Heutink,
B. Oostra,
J. V. van Swieten,
2006,
Movement disorders : official journal of the Movement Disorder Society.
W. Linssen,
C. Straathof,
Ludo W van der Pol,
2019,
Clinical genetics.
G. Schaaf,
Jeroen A. A. Demmers,
L. Verdijk,
2016,
Circulation. Cardiovascular genetics.
E. Aronica,
C. Saris,
R. D. de Haan,
2020,
Rheumatology.
D. Rizopoulos,
M. Kruijshaar,
E. Brusse,
2017,
Neurology.
A. Khrunin,
S. Limborska,
S. Pajusalu,
2022,
Human mutation.
G. Drost,
J. D. de Vries,
M. Tijssen,
2020,
Parkinsonism & related disorders.
J. T. Dunnen,
B. Oostra,
B. P. Warrenburg,
2013,
Human mutation.
E. Aronica,
I. V. van Langen,
C. Langerhorst,
2008,
Neurology.
G. Schaaf,
W. Pijnappel,
R. Verdijk,
2015,
Acta neuropathologica communications.
M. P. van den Berg,
P. Doevendans,
E. Ippel,
2012,
Netherlands Heart Journal.
E. Brusse,
B. Jacobs,
A. J. van der Kooi,
2018,
Journal of the peripheral nervous system : JPNS.
W. Hop,
L. H. van den Berg,
M. Vermeulen,
2010,
Journal of Neurology, Neurosurgery & Psychiatry.
B. Oostra,
G. Visser,
A. Bertoli-Avella,
2009,
neurogenetics.
A. V. van Norden,
B. Kleine,
J. Verschuuren,
2012,
Neurology.
M. Lucchetta,
D. Pareyson,
A. Schenone,
2009,
The Lancet Neurology.
Gijs van Tulder,
Marleen de Bruijne,
H. Tiddens,
2022,
European Radiology.
D. Rizopoulos,
J. Hogrel,
P. Laforêt,
2019,
Neurology.
L. H. van den Berg,
M. Vermeulen,
T. van Gelder,
2013,
Journal of Neurology, Neurosurgery & Psychiatry.
A. Vulto,
W. Pijnappel,
E. Brusse,
2019,
Neuromuscular Disorders.
P. van Paassen,
A. ten Brinke,
G. D'Haens,
2022,
Annals of the Rheumatic Diseases.
S. Nejentsev,
C. Allaart,
W. Lems,
2022,
The Lancet Rheumatology.
Maintenance IV immunoglobulin treatment in chronic inflammatory demyelinating polyradiculoneuropathy
E. Brusse,
B. Jacobs,
A. J. van der Kooi,
2017,
Journal of the peripheral nervous system : JPNS.
J. Kros,
E. Hoorn,
J. V. van Laar,
2010,
Thorax.
E. Brusse,
A. Eggink,
C. D. van der Marel,
2018,
International journal of obstetric anesthesia.
P. Nijssen,
E. Brusse,
R. Roos,
2002,
Movement disorders : official journal of the Movement Disorder Society.
M. Lequin,
G. Mancini,
D. Halley,
2008,
Archives of neurology.
E. Brusse,
A. T. van der Ploeg,
M. Wagenmakers,
2022,
Orphanet Journal of Rare Diseases.
Esther van den Berg,
E. Brusse,
R. Muetzel,
2021,
Journal of inherited metabolic disease.
E. Brusse,
M. Wagenmakers,
J. Langendonk,
2020,
JIMD reports.
Hester F. Lingsma,
D. Nieboer,
E. Brusse,
2020,
European journal of neurology.
Marleen de Bruijne,
H. Tiddens,
P. Ciet,
2017,
Neuromuscular Disorders.
A. V. van Norden,
M. Dijkgraaf,
B. Kleine,
2010,
The Lancet Neurology.
M. Kruijshaar,
E. Brusse,
A. T. van der Ploeg,
2013,
Orphanet Journal of Rare Diseases.
R. R. Hagen,
S. Nejentsev,
P. van Paassen,
2022,
The Lancet Rheumatology.
Elmar Krieger,
Peter Heutink,
Ben A. Oostra,
2003
.
B. Oostra,
J. V. van Swieten,
G. Breedveld,
2004,
Journal of Medical Genetics.
B. V. van Engelen,
N. Voermans,
H. Jungbluth,
2022,
Practical Neurology.
G. Schaaf,
E. Brusse,
F. Sage,
2012
.
Wim G. M. Janssen,
Gijs van Tulder,
Marleen de Bruijne,
2021,
Neuromuscular Disorders.
S. Heymans,
H. Brunner,
F. Asselbergs,
2020,
Human mutation.
Elmar Krieger,
Peter Heutink,
E. Krieger,
2003,
American journal of human genetics.
H. Smeets,
B. J. van den Bosch,
B. Poll-The,
2009,
Journal of Medical Genetics.
C. Straathof,
N. Voermans,
E. Brusse,
2016,
Muscle & nerve.
G. Schaaf,
W. Pijnappel,
R. Verdijk,
2015,
Acta neuropathologica communications.
W. Linssen,
C. Straathof,
N. Voermans,
2019,
Neuromuscular Disorders.
Gijs van Tulder,
Marleen de Bruijne,
P. Wielopolski,
2021,
Orphanet Journal of Rare Diseases.
C. Roelen,
E. Brusse,
M. Michels,
2020,
Neuromuscular Disorders.
P. van Paassen,
F. Bemelman,
G. D'Haens,
2023,
Journal of Autoimmunity.
R. Lewis,
H. Lingsma,
E. Brusse,
2021,
European journal of neurology.
J. Wokke,
N. Voermans,
E. Brusse,
2013,
Nederlands tijdschrift voor geneeskunde.
F. Mattace-Raso,
E. Sijbrands,
M. Kruijshaar,
2014,
Journal of Inherited Metabolic Disease.
P. Lijnzaad,
G. Schaaf,
W. Pijnappel,
2022,
Journal of inherited metabolic disease.
P. van Paassen,
A. ten Brinke,
F. Bemelman,
2023,
BMC Infectious Diseases.
W. D. den Dunnen,
C. Cupidi,
J. V. van Swieten,
2020,
Neurology: Genetics.
W. Hop,
M. Kruijshaar,
D. Güngör,
2013,
Molecular genetics and metabolism.
Home-based enzyme replacement therapy in children and adults with Pompe disease; a prospective study
E. Brusse,
A. T. van der Ploeg,
H. Huidekoper,
2023,
Orphanet Journal of Rare Diseases.
H. Duivenvoorden,
J. V. van Swieten,
M. Brusse-Keizer,
2011,
Neurology.
E. Brusse,
C. Tijssen,
2001
.
B. Engelen,
P. Laforêt,
N. Voermans,
2013,
Muscle & nerve.
M. Kruijshaar,
E. Brusse,
A. T. van der Ploeg,
2023,
BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy.
C. Allaart,
P. van Paassen,
A. ten Brinke,
2022,
BMC Medicine.
W. Hop,
M. Kruijshaar,
D. Güngör,
2013,
BMC Musculoskeletal Disorders.
M. Lequin,
G. Mancini,
D. Halley,
2008,
Archives of neurology.