|
๐
|
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
18 auth.
R. Bashir,
S. Britton,
T. Strachan,
S. Keers,
E. Vafiadaki,
M. Lako,
I. Richard,
S. Marchand,
N. Bourg,
Z. Argov,
...
M. Sadeh,
I. Mahjneh,
G. Marconi,
M. Passos-Bueno,
E. S. Moreira,
M. Zatz,
J. Beckmann,
K. Bushby
|
9 |
1998 |
9
๐
|
|
๐
|
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
20 auth.
I. Eisenberg,
N. Avidan,
T. Potikha,
H. Hochner,
Miriam Chen,
T. Olender,
M. Barash,
M. Shemesh,
M. Sadeh,
G. Grabov-Nardini,
...
Inna Shmilevich,
A. Friedmann,
G. Karpati,
W. Bradley,
Lisa Baumbach,
D. Lancet,
E. B. Asher,
J. Beckmann,
Z. Argov,
S. Mitrani-Rosenbaum
|
8 |
2001 |
8
๐
|
|
๐
|
International consensus outcome measures for patients with idiopathic inflammatory myopathies. Development and initial validation of myositis activity and damage indices in patients with adult onset disease.
87 auth.
D. Isenberg,
E. Allen,
V. Farewell,
M. Ehrenstein,
M. Hanna,
I. Lundberg,
C. Oddis,
C. Pilkington,
P. Plotz,
D. Scott,
J. Vencovskรฝ,
R. Cooper,
L. Rider,
Frederick W. Miller,
E. Adams,
...
H. Alexanderson,
N. Armentrout,
Z. Argov,
R. Barohn,
S. Bowyer,
H. Brunner,
R. Burgos-Vargas,
J. Callen,
G. Cawkwell,
P. Cherin,
Yuen-Li Chung,
H. Chwaliลska-Sadowska,
R. Cooper,
M. Cronin,
K. Danko,
J. Davidson,
Peter B. Dent,
E. Dugan,
B. Feldman,
Richard Finkel,
I. Torre,
E. Genth,
E. Giannini,
G. Hengstman,
J. Hicks,
A. Huber,
H. Huppertz,
L. Imundo,
Kent J. Johnson,
J. Jorizzo,
L. Kagen,
J. Kissel,
M. Kleinโgitelman,
A. Kutzbach,
B. Lang,
M. Lassere,
C. Lindsley,
D. Lovell,
S. Maillard,
P. Malleson,
A. Martini,
T. Medsger,
K. Murray,
C. Oddis,
L. Pachman,
A. Paller,
M. D. Perez,
P. Plotz,
D. Pongratz,
A. Ravelli,
A. Reed,
R. Rennebohm,
N. Ruperto,
S. Rutkove,
Clyde Ryder,
J. Senรฉcal,
G. Serratrice,
J. Serratrice,
D. Sherry,
K. Sivakumar,
Yeong-Uk Song,
R. Sontheimer,
I. Targoff,
M. Turner,
Basiel van Engelen,
M. Villalba,
K. Vincent,
V. Werth,
P. White,
J. Witter,
R. Wortmann,
S. Ytterberg
|
8 |
2004 |
8
๐
|
|
๐ฆ
|
โRimmed vacuole myopathyโ sparing the quadriceps A unique disorder in iranian jews
Z. Argov,
R. Yarom
|
8 |
1984 |
8
๐ฆ
|
|
๐
|
Safety and Clinical Effects of Mesenchymal Stem Cells Secreting Neurotrophic Factor Transplantation in Patients With Amyotrophic Lateral Sclerosis: Results of Phase 1/2 and 2a Clinical Trials.
12 auth.
P. Petrou,
Y. Gothelf,
Z. Argov,
M. Gotkine,
Y. Levy,
I. Kassis,
...
A. Vaknin-Dembinsky,
T. Ben-Hur,
D. Offen,
O. Abramsky,
E. Melamed,
D. Karussis
|
7 |
2016 |
7
๐
|
|
๐ฆ
|
Disorders of neuromuscular transmission caused by drugs
Z. Argov,
F. Mastaglia
|
7 |
1979 |
7
๐ฆ
|
|
๐
|
Polymyositis: An overdiagnosed entity
24 auth.
F. Miller,
L. Rider,
P. Plotz,
S. Rutkove,
A. Pestronk,
R. Wortmann,
I. Lundberg,
Z. Argov,
D. Isenberg,
D. Lacomis,
...
C. Oddis,
W. Bradley,
G. Hengstman,
B. Engelen,
M. V. D. Meulen,
I. Bronner,
J. Hoogendijk,
H. Burger,
W. V. Venrooij,
A. Voskuyl,
H. Dinant,
W. Linssen,
J. Wokke,
M. Visser
|
7 |
2004 |
7
๐
|
|
๐
|
EFNS/ENS Guidelines for the treatment of ocular myasthenia
7 auth.
E. Kerty,
A. Elsais,
A. Elsais,
Z. Argov,
A. Evoli,
N. Gilhus,
...
N. Gilhus
|
7 |
2014 |
7
๐
|
|
๐
|
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)
19 auth.
L. Anderson,
R. Harrison,
R. Pogue,
E. Vafiadaki,
C. Pollitt,
K. Davison,
Jennifer A. Moss,
S. Keers,
A. Pyle,
P. Shaw,
...
I. Mahjneh,
Z. Argov,
C. Greenberg,
K. Wrogemann,
T. Bertorini,
H. Goebel,
J. Beckmann,
R. Bashir,
K. Bushby
|
7 |
2000 |
7
๐
|
|
๐ข
|
GNE myopathy: current update and future therapy
I. Nishino,
N. Carrillo-Carrasco,
Z. Argov
|
7 |
2014 |
7
๐ข
|
|
๐ฆ
|
Bioenergetic heterogeneity of human mitochondrial myopathies
Z. Argov,
W. Bank,
J. Maris,
P. Peterson,
B. Chance
|
7 |
1987 |
7
๐ฆ
|
