|
π’
|
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy
10 auth.
P. V. Overveld,
R. Lemmers,
L. Sandkuijl,
Leo Enthoven,
S. Winokur,
F. Bakels,
...
G. Padberg,
G. V. Ommen,
R. Frants,
S. M. Maarel
|
8 |
2003 |
8
π’
|
|
π
|
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element.
11 auth.
J. Gabriels,
M. Beckers,
Hao Ding,
A. D. Vriese,
S. Plaisance,
S. M. Maarel,
...
G. Padberg,
R. Frants,
J. Hewitt,
D. Collen,
A. Belayew
|
8 |
1999 |
8
π
|
|
π’
|
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere
7 auth.
R. Lemmers,
P. D. Kievit,
L. Sandkuijl,
G. Padberg,
G. V. Ommen,
R. Frants,
...
S. M. Maarel
|
8 |
2002 |
8
π’
|
|
π
|
ProteomeBinders: planning a European resource of affinity reagents for analysis of the human proteome
39 auth.
M. Taussig,
O. Stoevesandt,
C. Borrebaeck,
A. Bradbury,
D. Cahill,
C. Cambillau,
A. Daruvar,
S. DΓΌbel,
J. Eichler,
Ronald Frank,
T. Gibson,
David E. Gloriam,
L. Gold,
F. Herberg,
H. Hermjakob,
...
J. Hoheisel,
T. Joos,
O. Kallioniemi,
M. Koegl,
Z. Konthur,
B. Korn,
E. Kremmer,
S. Krobitsch,
U. Landegren,
S. M. Maarel,
J. McCafferty,
S. Muyldermans,
P. Nygren,
S. Palcy,
A. PlΓΌckthun,
B. PoliΔ,
M. Przybylski,
P. Saviranta,
A. Sawyer,
D. Sherman,
A. Skerra,
M. Templin,
M. Ueffing,
M. UhlΓ©n
|
7 |
2007 |
7
π
|
|
π
|
Clinical features of facioscapulohumeral muscular dystrophy 2
17 auth.
J. D. Greef,
R. Lemmers,
P. CamaΓ±o,
J. Day,
S. Sacconi,
M. Dunand,
B. Engelen,
S. Kiuru-Enari,
G. Padberg,
A. L. Rosa,
...
C. Desnuelle,
Simone Spuler,
M. Tarnopolsky,
S. Venance,
R. Frants,
S. M. Maarel,
R. Tawil
|
7 |
2010 |
7
π
|
|
π¦
|
De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10.
11 auth.
S. M. Maarel,
G. Deidda,
R. Lemmers,
P. V. Overveld,
M. V. D. Wielen,
J. Hewitt,
...
L. Sandkuijl,
B. Bakker,
G. V. Ommen,
G. Padberg,
R. Frants
|
7 |
2000 |
7
π¦
|
|
π
|
The expanding field of IgG4βmediated neurological autoimmune disorders
9 auth.
M. Huijbers,
L. Querol,
E. Niks,
J. Plomp,
S. M. Maarel,
F. Graus,
...
J. Dalmau,
I. Illa,
J. Verschuuren
|
7 |
2015 |
7
π
|
|
π
|
Strength training and albuterol in facioscapulohumeral muscular dystrophy
8 auth.
E. L. Kooi,
O. Vogels,
R.R.L.J. van Asseldonk,
E. Lindeman,
J. Hendriks,
M. Wohlgemuth,
...
S. M. Maarel,
G. Padberg
|
7 |
2004 |
7
π
|
|
π
|
Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis.
11 auth.
R. Lemmers,
S. M. Maarel,
J. Deutekom,
M. V. D. Wielen,
G. Deidda,
H. Dauwerse,
...
J. Hewitt,
M. Hofker,
E. Bakker,
G. Padberg,
R. Frants
|
6 |
1998 |
6
π
|
|
π¬
|
171st ENMC International Workshop: Standards of care and management of facioscapulohumeral muscular dystrophy
R. Tawil,
S. M. Maarel,
G. Padberg,
B. Engelen
|
6 |
2010 |
6
π¬
|
|
π’
|
Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level
8 auth.
R. Klooster,
K. Straasheijm,
Bharati Shah,
J. Sowden,
R. Frants,
C. Thornton,
...
R. Tawil,
S. M. Maarel
|
6 |
2009 |
6
π’
|
