213 related articles for article (PubMed ID: 10211476)
1. Myopathy with hexagonally cross-linked tubular arrays: a new autosomal dominant or sporadic congenital myopathy.
Bourque PR; Lach B; Carpenter S; Rippstein P
Ann Neurol; 1999 Apr; 45(4):512-5. PubMed ID: 10211476
[TBL] [Abstract][Full Text] [Related]
2. Myopathy with hexagonally cross-linked crystalloid inclusions: delineation of a clinico-pathological entity.
Claeys KG; Pellissier JF; Garcia-Bragado F; Weis J; Urtizberea A; Poza JJ; Cobo AM; Stoltenburg G; Figarella-Branger D; Willems PJ; Depuydt CE; Kleiner W; Pouget J; Piraud M; Brochier G; Romero NB; Fardeau M; Goebel HH; Bönnemann CG; Voit T; Eymard B; Laforêt P
Neuromuscul Disord; 2010 Nov; 20(11):701-8. PubMed ID: 20637616
[TBL] [Abstract][Full Text] [Related]
3. [Familial form of centronuclear myopathy in the adult].
Pépin B; Mikol J; Goldstein B; Haguenau M; Godlewski S
Rev Neurol (Paris); 1976 Dec; 132(12):845-57. PubMed ID: 1013570
[TBL] [Abstract][Full Text] [Related]
4. [A case of progressive myopathy with tubular aggregates].
Kamakura K; Takeshita K; Sunohara N; Arahata K; Nonaka I
Rinsho Shinkeigaku; 1989 Jun; 29(6):769-73. PubMed ID: 2684470
[TBL] [Abstract][Full Text] [Related]
5. [Autosomal dominant distal myopathy with rimmed vacuoles and cytoplasmic inclusions: report of a family].
Uesaka Y; Nakamichi K; Kojima S; Ida M; Takagi A
Rinsho Shinkeigaku; 1997 Jan; 37(1):1-6. PubMed ID: 9146065
[TBL] [Abstract][Full Text] [Related]
6. Spheroid-cytoplasmic complexes in a congenital myopathy.
Halbig L; Goebel HH; Hopf HC; Moll R
Rev Neurol (Paris); 1991; 147(4):300-7. PubMed ID: 1648255
[TBL] [Abstract][Full Text] [Related]
7. Slowly progressive congenital myopathy with cytoplasmic bodies--report of two cases and a review of the literature.
Wolburg H; Schlote W; Langohr HD; Peiffer J; Reiher KH; Heckl RW
Clin Neuropathol; 1982; 1(2):55-66. PubMed ID: 6301720
[TBL] [Abstract][Full Text] [Related]
8. Dominantly inherited tubular aggregate myopathy.
Cameron CH; Allen IV; Patterson V; Avaria MA
J Pathol; 1992 Dec; 168(4):397-403. PubMed ID: 1484321
[TBL] [Abstract][Full Text] [Related]
9. [Familial myopathy with "cytoplasmic body" (or "spheroid") type inclusions, disclosed by respiratory insufficiency].
Chapon F; Viader F; Fardeau M; Tomé F; Daluzeau N; Berthelin C; Thénint JP; Lechevalier B
Rev Neurol (Paris); 1989; 145(6-7):460-5. PubMed ID: 2552561
[TBL] [Abstract][Full Text] [Related]
10. [A new non progressive myopathy with autosomal dominant transmission: nemaline myopathy].
Battin J; Vital C; Vallat JM; Fontan D
Nouv Presse Med; 1972 Apr; 1(16):1097. PubMed ID: 5035868
[No Abstract] [Full Text] [Related]
11. Congenital myopathy without specific features (minimal change myopathy).
Nonaka I; Nakamura Y; Tojo M; Sugita H; Ishikawa T; Awaya A; Sugiyama N
Neuropediatrics; 1983 Nov; 14(4):237-41. PubMed ID: 6657012
[TBL] [Abstract][Full Text] [Related]
12. [Slowly progressive myopathy with accumulation of tubular aggregates].
Figarella-Branger D; Pellissier JF; Perez-Castillo AM; Desnuelle C; Pouget J; Serratrice G
Rev Neurol (Paris); 1991; 147(8-9):586-94. PubMed ID: 1962068
[TBL] [Abstract][Full Text] [Related]
13. Nemaline (rod) myopathy: the need for histochemical evaluation of affected families.
Bender AN; Willner JP
Ann Neurol; 1978 Jul; 4(1):37-42. PubMed ID: 697323
[TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family.
Sobrido MJ; Fernández JM; Fontoira E; Pérez-Sousa C; Cabello A; Castro M; Teijeira S; Alvarez S; Mederer S; Rivas E; Seijo-Martínez M; Navarro C
Brain; 2005 Jul; 128(Pt 7):1716-27. PubMed ID: 15857933
[TBL] [Abstract][Full Text] [Related]
15. [A case of myotubular myopathy with autosomal dominant inheritance (author's transl)].
Wakabayashi Y; Arimura Y; Sawaguchi Y; Koike H; Yoshino Y
No To Shinkei; 1980 Jul; 32(7):715-22. PubMed ID: 7407023
[No Abstract] [Full Text] [Related]
16. Myofibrillar (desmin-related) myopathy: clinico-pathological spectrum in 3 cases and review of the literature.
Wanschit J; Nakano S; Goudeau B; Ströbel T; Rinner W; Wimmer G; Resch H; Jaksch M; Akiguchi I; Vicart P; Budka H
Clin Neuropathol; 2002; 21(5):220-31. PubMed ID: 12365725
[TBL] [Abstract][Full Text] [Related]
17. Progressive myopathy in trisomy 21.
Mielke U; Schimrigk K; Edlinger H
Neuropediatrics; 1988 Aug; 19(3):132-4. PubMed ID: 2975770
[TBL] [Abstract][Full Text] [Related]
18. Autosomal dominant distal myopathy with desmin storage: a clinicopathologic and electrophysiologic study of a large kinship.
Horowitz SH; Schmalbruch H
Muscle Nerve; 1994 Feb; 17(2):151-60. PubMed ID: 8114783
[TBL] [Abstract][Full Text] [Related]
19. Perinatal diagnosis of myotubular (centronuclear) myopathy: a case report.
Collins JE; Collins A; Radford MR; Weller RO
Clin Neuropathol; 1983; 2(2):79-82. PubMed ID: 6851300
[TBL] [Abstract][Full Text] [Related]
20. [Centronuclear myopathy. Apropos of a new case].
Dubois B; Martin JJ; Develter S; Guérin M; Loeuille GA; Debeugny P; Farriaux JP
Sem Hop; 1983 Feb; 59(8):561-5. PubMed ID: 6302904
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]