136 related articles for article (PubMed ID: 31740511)
1. Clinical Reasoning: Progressive proximal weakness in a 56-year-old man with bone pain.
Torabi T; Huttner A; Nowak RJ; Roy B
Neurology; 2019 Nov; 93(21):939-944. PubMed ID: 31740511
[No Abstract] [Full Text] [Related]
2. Distal myopathy and rapidly progressive dementia associated with a novel mutation in the VCP gene: Expanding inclusion body myopathy with early-onset Paget disease and frontotemporal dementia spectrum.
Falcão de Campos C; de Carvalho M
J Clin Neurosci; 2019 Jun; 64():8-10. PubMed ID: 30955949
[TBL] [Abstract][Full Text] [Related]
3. The multifaceted clinical presentation of VCP-proteinopathy in a Greek family.
Papadimas GK; Paraskevas GP; Zambelis T; Karagiaouris C; Bourbouli M; Bougea A; Walter MC; Schumacher NU; Krause S; Kapaki E
Acta Myol; 2017 Dec; 36(4):203-206. PubMed ID: 29770363
[TBL] [Abstract][Full Text] [Related]
4. Phenotypic variability in three families with valosin-containing protein mutation.
Spina S; Van Laar AD; Murrell JR; Hamilton RL; Kofler JK; Epperson F; Farlow MR; Lopez OL; Quinlan J; DeKosky ST; Ghetti B
Eur J Neurol; 2013 Feb; 20(2):251-8. PubMed ID: 22900631
[TBL] [Abstract][Full Text] [Related]
5. [Inclusion body myopathy with Paget's disease of bone and frontotemporal dementia].
Hayashi Y
Rinsho Shinkeigaku; 2013; 53(11):947-50. PubMed ID: 24291843
[TBL] [Abstract][Full Text] [Related]
6. A cross-sectional analysis of clinical evaluation in 35 individuals with mutations of the valosin-containing protein gene.
Plewa J; Surampalli A; Wencel M; Milad M; Donkervoort S; Caiozzo VJ; Goyal N; Mozaffar T; Kimonis V
Neuromuscul Disord; 2018 Sep; 28(9):778-786. PubMed ID: 30097247
[TBL] [Abstract][Full Text] [Related]
7. Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia.
Peyer AK; Kinter J; Hench J; Frank S; Fuhr P; Thomann S; Fischmann A; Kneifel S; Camaño P; López de Munain A; Sinnreich M; Renaud S
Neuromuscul Disord; 2013 Feb; 23(2):149-54. PubMed ID: 23140793
[TBL] [Abstract][Full Text] [Related]
8. The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice?
Clemen CS; Winter L; Strucksberg KH; Berwanger C; Türk M; Kornblum C; Florin A; Aguilar-Pimentel JA; Amarie OV; Becker L; Garrett L; Hans W; Moreth K; Neff F; Pingen L; Rathkolb B; Rácz I; Rozman J; Treise I; Fuchs H; Gailus-Durner V; de Angelis MH; Vorgerd M; Eichinger L; Schröder R
Biochem Biophys Res Commun; 2018 Sep; 503(4):2770-2777. PubMed ID: 30100055
[TBL] [Abstract][Full Text] [Related]
9. Muscle wasting, bone pain and cognitive decline: a unifying diagnosis.
St John L; Larner AJ
Br J Hosp Med (Lond); 2015 Oct; 76(10):602-3. PubMed ID: 26457944
[No Abstract] [Full Text] [Related]
10. p97/VCP at the intersection of the autophagy and the ubiquitin proteasome system.
Ju JS; Weihl CC
Autophagy; 2010 Feb; 6(2):283-5. PubMed ID: 20083896
[No Abstract] [Full Text] [Related]
11. Motor neuron involvement in multisystem proteinopathy: implications for ALS.
Benatar M; Wuu J; Fernandez C; Weihl CC; Katzen H; Steele J; Oskarsson B; Taylor JP
Neurology; 2013 May; 80(20):1874-80. PubMed ID: 23635965
[TBL] [Abstract][Full Text] [Related]
12. Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia.
Wang H; Wu S
Neuromuscul Disord; 2015 Mar; 25(3):273. PubMed ID: 25497399
[No Abstract] [Full Text] [Related]
13. 215th ENMC International Workshop VCP-related multi-system proteinopathy (IBMPFD) 13-15 November 2015, Heemskerk, The Netherlands.
Evangelista T; Weihl CC; Kimonis V; Lochmüller H;
Neuromuscul Disord; 2016 Aug; 26(8):535-47. PubMed ID: 27312024
[No Abstract] [Full Text] [Related]
14. Nuclear inclusions mimicking poly(A)-binding protein nuclear 1 inclusions in a case of inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia with a novel mutation in the valosin-containing protein gene.
Matsubara S; Shimizu T; Komori T; Mori-Yoshimura M; Minami N; Hayashi YK
Neuromuscul Disord; 2016 Jul; 26(7):436-40. PubMed ID: 27209344
[TBL] [Abstract][Full Text] [Related]
15. The Myoblast C2C12 Transfected with Mutant Valosin-Containing Protein Exhibits Delayed Stress Granule Resolution on Oxidative Stress.
Rodriguez-Ortiz CJ; Flores JC; Valenzuela JA; Rodriguez GJ; Zumkehr J; Tran DN; Kimonis VE; Kitazawa M
Am J Pathol; 2016 Jun; 186(6):1623-34. PubMed ID: 27106764
[TBL] [Abstract][Full Text] [Related]
16. [Multilocular Paget's disease in IBMPFD syndrome. A case report with 14-year follow-up].
Zajonz D; Langsieb C; Chavdarova L; Kellermann S; Baum P; Wickenhauser C; von Salis-Soglio G; Prietzel T
Orthopade; 2012 Jun; 41(6):482-7. PubMed ID: 22699758
[TBL] [Abstract][Full Text] [Related]
17. [A case of inclusion body myopathy with Paget's disease of bone and frontotemporal dementia (IBMPFD) showing clinical features of motor neuron disease].
Igari R; Wada M; Sato H; K Hayashi Y; Nishino I; Kato T
Rinsho Shinkeigaku; 2013; 53(6):458-64. PubMed ID: 23782824
[TBL] [Abstract][Full Text] [Related]
18. A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation.
Shinjo SK; Oba-Shinjo SM; Lerario AM; Marie SKN
Clin Rheumatol; 2018 Apr; 37(4):1129-1136. PubMed ID: 29127544
[TBL] [Abstract][Full Text] [Related]
19. [An advanced case of myopathy and dementia with a new mutation in the valosin-containing protein gene].
Kamiyama T; Sengoku R; Sasaki M; Hayashi Y; Nishino I; Mochio S; Iguchi Y
Rinsho Shinkeigaku; 2013; 53(6):465-9. PubMed ID: 23782825
[TBL] [Abstract][Full Text] [Related]
20. The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis.
Nalbandian A; Donkervoort S; Dec E; Badadani M; Katheria V; Rana P; Nguyen C; Mukherjee J; Caiozzo V; Martin B; Watts GD; Vesa J; Smith C; Kimonis VE
J Mol Neurosci; 2011 Nov; 45(3):522-31. PubMed ID: 21892620
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
