E-LIB Suche - Ergebnisse für: Tajsharghi, H

1

P.246Drosophila model of myosin myopathy rescued by overexp..:

Tajsharghi, H. ; Dahl-Halvarsson, M. ; Olive, M....
Neuromuscular Disorders. 29 (2019) - p. S138-S139 , 2019

Link: https://doi.org/10.1016/..

2

P.276Childhood-onset spinal muscular atrophy or juvenile am..:

Sedghi, M. ; Moslemi, A. ; Olive, M....
Neuromuscular Disorders. 29 (2019) - p. S148 , 2019

Link: https://doi.org/10.1016/..

3

Ryanodine receptor type 3 (RYR3) as a novel gene associated..:

Nilipour, Y. ; Nafissi, S. ; Tjust, A. E....
European Journal of Neurology. 25 (2018) 6 - p. 841-847 , 2018

Link: https://doi.org/10.1111/..

4

TOR1A variants cause a severe arthrogryposis with developme..:

Kariminejad, A. ; Dahl-Halvarsson, M. ; Ravenscroft, G....
Neuromuscular Disorders. 27 (2017) - p. S243 , 2017

Link: https://doi.org/10.1016/..

5

Ryanodine receptor type 3 (RYR3) as a novel gene associated..:

Nilipour, Y. ; Nafissi, S. ; Varasteh, V....
Neuromuscular Disorders. 26 (2016) - p. S137 , 2016

Link: https://doi.org/10.1016/..

6

Lethal multiple pterygium syndrome associated with mutation..:

Kariminejad, A. ; Ghaderi-Sohi, S. ; Hossein-Nejad Nedai, H...
Neuromuscular Disorders. 25 (2015) - p. S257 , 2015

Link: https://doi.org/10.1016/..

7

G.P.153:

Tajsharghi, H. ; Hammans, S. ; Lindberg, C....
Neuromuscular Disorders. 24 (2014) 9-10 - p. 847 , 2014

Link: https://doi.org/10.1016/..

8

O.5 Mutations in MuRF1 and MuRF3 cause a novel protein aggr..:

Olivé, M. ; Abdul-Hussein, S. ; Oldfors, A....
Neuromuscular Disorders. 23 (2013) 9-10 - p. 740-741 , 2013

Link: https://doi.org/10.1016/..

9

P.9.16 The cause of developmental myopathy due to the embry..:

Pokrzywa, M. ; Ghobadpour, M. ; Abdul-Hussein, S...
Neuromuscular Disorders. 23 (2013) 9-10 - p. 788 , 2013

Link: https://doi.org/10.1016/..

10

G.O.2 Hereditary myopathy with early respiratory failure as..:

Hedberg, C. ; Ohlsson, M. ; Brådvik, B....
Neuromuscular Disorders. 22 (2012) 9-10 - p. 873 , 2012

Link: https://doi.org/10.1016/..

11

Myopathies associated with β-tropomyosin mutations:

Tajsharghi, H. ; Ohlsson, M. ; Palm, L..
Neuromuscular Disorders. 22 (2012) 11 - p. 923-933 , 2012

Link: https://doi.org/10.1016/..

12

P1.39 Transfection of cultured myoblast with mutant β-tropo..:

Abdul-Hussein, S. ; Moslemi, A.R. ; Tajsharghi, H.
Neuromuscular Disorders. 20 (2010) 9-10 - p. 612 , 2010

Link: https://doi.org/10.1016/..

13

P2.14 Familial myopathy with early respiratory failure and ..:

Ohlsson, M. ; Brådvik, B. ; Lindberg, C....
Neuromuscular Disorders. 20 (2010) 9-10 - p. 622 , 2010

Link: https://doi.org/10.1016/..

14

D.I.2 Myosin myopathies and distal arthrogryposis syndromes:

Oldfors, A. ; Tajsharghi, H. ; Kimber, E...
Neuromuscular Disorders. 20 (2010) 9-10 - p. 635 , 2010

Link: https://doi.org/10.1016/..

15

O.19 Inactivation of glycogen synthesis priming due to a mi..:

Moslemi, A.-R. ; Lindberg, C. ; Nilsson, J....
Neuromuscular Disorders. 20 (2010) 9-10 - p. 679 , 2010

Link: https://doi.org/10.1016/..