196 related articles for article (PubMed ID: 23044792)
1. Patient-specific protein aggregates in myofibrillar myopathies: laser microdissection and differential proteomics for identification of plaque components.
Feldkirchner S; Schessl J; Müller S; Schoser B; Hanisch FG
Proteomics; 2012 Dec; 12(23-24):3598-609. PubMed ID: 23044792
[TBL] [Abstract][Full Text] [Related]
2. How much mutant protein is needed to cause a protein aggregate myopathy in vivo? Lessons from an exceptional desminopathy.
Clemen CS; Fischer D; Reimann J; Eichinger L; Müller CR; Müller HD; Goebel HH; Schröder R
Hum Mutat; 2009 Mar; 30(3):E490-9. PubMed ID: 19105189
[TBL] [Abstract][Full Text] [Related]
3. Myofibrillar myopathies.
Selcen D; Engel AG
Handb Clin Neurol; 2011; 101():143-54. PubMed ID: 21496631
[TBL] [Abstract][Full Text] [Related]
4. Myofibrillar myopathies.
Selcen D
Curr Opin Neurol; 2010 Oct; 23(5):477-81. PubMed ID: 20664348
[TBL] [Abstract][Full Text] [Related]
5. Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathy.
Maerkens A; Kley RA; Olivé M; Theis V; van der Ven PF; Reimann J; Milting H; Schreiner A; Uszkoreit J; Eisenacher M; Barkovits K; Güttsches AK; Tonillo J; Kuhlmann K; Meyer HE; Schröder R; Tegenthoff M; Fürst DO; Müller T; Goldfarb LG; Vorgerd M; Marcus K
J Proteomics; 2013 Sep; 90():14-27. PubMed ID: 23639843
[TBL] [Abstract][Full Text] [Related]
6. Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients.
Selcen D; Ohno K; Engel AG
Brain; 2004 Feb; 127(Pt 2):439-51. PubMed ID: 14711882
[TBL] [Abstract][Full Text] [Related]
7. Myofibrillar myopathies.
Claeys KG; Fardeau M
Handb Clin Neurol; 2013; 113():1337-42. PubMed ID: 23622358
[TBL] [Abstract][Full Text] [Related]
8. Cytoskeletal derangements in hereditary myopathy with a desmin L345P mutation.
Carlsson L; Fischer C; Sjöberg G; Robson RM; Sejersen T; Thornell LE
Acta Neuropathol; 2002 Nov; 104(5):493-504. PubMed ID: 12410397
[TBL] [Abstract][Full Text] [Related]
9. [Myofibrillar myopathy].
Hayashi YK
Brain Nerve; 2011 Nov; 63(11):1179-88. PubMed ID: 22068470
[TBL] [Abstract][Full Text] [Related]
10. Myofibrillar myopathies: a clinical and myopathological guide.
Schröder R; Schoser B
Brain Pathol; 2009 Jul; 19(3):483-92. PubMed ID: 19563540
[TBL] [Abstract][Full Text] [Related]
11. Molecular pathology of myofibrillar myopathies.
Ferrer I; Olivé M
Expert Rev Mol Med; 2008 Sep; 10():e25. PubMed ID: 18764962
[TBL] [Abstract][Full Text] [Related]
12. Proteomic characterization of aggregate components in an intrafamilial variable FHL1-associated myopathy.
Feldkirchner S; Walter MC; Müller S; Kubny C; Krause S; Kress W; Hanisch FG; Schoser B; Schessl J
Neuromuscul Disord; 2013 May; 23(5):418-26. PubMed ID: 23489660
[TBL] [Abstract][Full Text] [Related]
13. Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study.
Claeys KG; van der Ven PF; Behin A; Stojkovic T; Eymard B; Dubourg O; Laforêt P; Faulkner G; Richard P; Vicart P; Romero NB; Stoltenburg G; Udd B; Fardeau M; Voit T; Fürst DO
Acta Neuropathol; 2009 Mar; 117(3):293-307. PubMed ID: 19151983
[TBL] [Abstract][Full Text] [Related]
14. [Myofibrillar myopathies].
Nakano S
Rinsho Shinkeigaku; 2012; 52(11):1151-3. PubMed ID: 23196546
[TBL] [Abstract][Full Text] [Related]
15. Biomechanical characterization of myofibrillar myopathies.
Winter L; Goldmann WH
Cell Biol Int; 2015 Apr; 39(4):361-3. PubMed ID: 25264173
[TBL] [Abstract][Full Text] [Related]
16. In vivo characterization of mutant myotilins.
Keduka E; Hayashi YK; Shalaby S; Mitsuhashi H; Noguchi S; Nonaka I; Nishino I
Am J Pathol; 2012 Apr; 180(4):1570-80. PubMed ID: 22349301
[TBL] [Abstract][Full Text] [Related]
17. Skeletal muscle biopsy analysis in reducing body myopathy and other FHL1-related disorders.
Malfatti E; Olivé M; Taratuto AL; Richard P; Brochier G; Bitoun M; Gueneau L; Laforêt P; Stojkovic T; Maisonobe T; Monges S; Lubieniecki F; Vasquez G; Streichenberger N; Lacène E; Saccoliti M; Prudhon B; Alexianu M; Figarella-Branger D; Schessl J; Bonnemann C; Eymard B; Fardeau M; Bonne G; Romero NB
J Neuropathol Exp Neurol; 2013 Sep; 72(9):833-45. PubMed ID: 23965743
[TBL] [Abstract][Full Text] [Related]
18. Exome sequencing identifies variants in two genes encoding the LIM-proteins NRAP and FHL1 in an Italian patient with BAG3 myofibrillar myopathy.
D'Avila F; Meregalli M; Lupoli S; Barcella M; Orro A; De Santis F; Sitzia C; Farini A; D'Ursi P; Erratico S; Cristofani R; Milanesi L; Braga D; Cusi D; Poletti A; Barlassina C; Torrente Y
J Muscle Res Cell Motil; 2016 Jun; 37(3):101-15. PubMed ID: 27443559
[TBL] [Abstract][Full Text] [Related]
19. Abnormal desmin protein in myofibrillar myopathies caused by desmin gene mutations.
Li M; Dalakas MC
Ann Neurol; 2001 Apr; 49(4):532-6. PubMed ID: 11310634
[TBL] [Abstract][Full Text] [Related]
20. Camptocormia as presenting sign in myofibrillar myopathy.
Renard D; Castelnovo G; Fernandez C; De Paula AM; Penttilä S; Suominen T; Udd B
Neuromuscul Disord; 2012 Nov; 22(11):987-9. PubMed ID: 22749474
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]