|
🐜
|
Prion-like domain mutations in hnRNPs cause multisystem proteinopathy and ALS
37 auth.
Hong-Joo Kim,
Nam Chul Kim,
Yong-Dong Wang,
Emily A. Scarborough,
Jennifer Moore,
Zamia Diaz,
K. MacLea,
Brian D. Freibaum,
Songqing Li,
A. Molliex,
A. Kanagaraj,
R. Carter,
K. Boylan,
Aleksandra M. Wojtas,
R. Rademakers,
...
J. Pinkus,
S. Greenberg,
J. Trojanowski,
B. Traynor,
Bradley N. Smith,
S. Topp,
A. Gkazi,
Jack W. Miller,
C. Shaw,
M. Kottlors,
J. Kirschner,
A. Pestronk,
Yun R Li,
A. F. Ford,
A. Gitler,
M. Benatar,
O. King,
V. Kimonis,
E. D. Ross,
C. Weihl,
J. Shorter,
J. Taylor
|
10 |
2013 |
10
🐜
|
|
🐜
|
Prion-like domain mutations in hnRNPs cause multisystem proteinopathy and ALS
37 auth.
Hong-Joo Kim,
Nam Chul Kim,
Yong-Dong Wang,
Emily A. Scarborough,
Jennifer Moore,
Zamia Diaz,
K. MacLea,
Brian D. Freibaum,
Songqing Li,
A. Molliex,
A. Kanagaraj,
R. Carter,
K. Boylan,
Aleksandra M. Wojtas,
R. Rademakers,
...
J. Pinkus,
S. Greenberg,
J. Trojanowski,
B. Traynor,
Bradley N. Smith,
S. Topp,
A. Gkazi,
Jack W. Miller,
C. Shaw,
M. Kottlors,
J. Kirschner,
A. Pestronk,
Yun R Li,
A. F. Ford,
A. Gitler,
M. Benatar,
O. King,
V. Kimonis,
E. D. Ross,
C. Weihl,
J. Shorter,
J. Taylor
|
7 |
2013 |
7
🐜
|
|
🦁
|
Elevated satellite cell number in Duchenne muscular dystrophy
M. Kottlors,
J. Kirschner
|
6 |
2010 |
6
🦁
|
|
🐜
|
Multiple symmetric lipomatosis
10 auth.
T. Klopstock,
M. Naumann,
B. Schalke,
F. Bischof,
P. Seibel,
M. Kottlors,
...
P. Eckert,
K. Reiners,
K. Toyka,
H. Reichmann
|
6 |
1994 |
6
🐜
|
|
🦁
|
Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiency
M. Kottlors,
M. Jaksch,
U. Ketelsen,
S. Weiner,
F. Glocker,
C. Lücking
|
5 |
2001 |
5
🦁
|
|
🦁
|
Facioscapulohumeral muscular dystrophy presenting with isolated axial myopathy and bent spine syndrome
M. Kottlors,
W. Kress,
G. Meng,
F. Glocker
|
5 |
2010 |
5
🦁
|
|
🦁
|
Polysegmental innervation of the medial paraspinal lumbar muscles
M. Kottlors,
F. Glocker
|
4 |
2008 |
4
🦁
|
|
🐬
|
A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
P. Seibel,
A. Flierl,
M. Kottlors,
H. Reichmann
|
4 |
1994 |
4
🐬
|
|
🦁
|
Late-onset autosomal dominant limb girdle muscular dystrophy and Paget's disease of bone unlinked to the VCP gene locus
11 auth.
M. Kottlors,
O. Moske-Eick,
A. Huebner,
S. Krause,
K. Mueller,
W. Kress,
...
R. Schwarzwald,
A. Bornemann,
V. Haug,
Markus Heitzer,
J. Kirschner
|
4 |
2010 |
4
🦁
|
|
🐬
|
Adult carnitine palmitoyltransferase II deficiency: Detection of characteristic carnitine esters in serum by tandem mass spectrometry
K. Gempel,
M. Kottlors,
M. Jaksch,
K. Gerbitz,
M. Bauer
|
3 |
1999 |
3
🐬
|
