89 related articles for article (PubMed ID: 29508780)
1. Is infantile spinal muscular atrophy a disease of maturation arrest or a dynamic neurogenic atrophy of the skeletal muscle?
Gayathri N; Das S; Gourie-Devi M; Ramamohan Y; Sarala D
Neurol India; 1998; 46(3):216-224. PubMed ID: 29508780
[TBL] [Abstract][Full Text] [Related]
2. The developmental pattern of myotubes in spinal muscular atrophy indicates prenatal delay of muscle maturation.
Martínez-Hernández R; Soler-Botija C; Also E; Alias L; Caselles L; Gich I; Bernal S; Tizzano EF
J Neuropathol Exp Neurol; 2009 May; 68(5):474-81. PubMed ID: 19525895
[TBL] [Abstract][Full Text] [Related]
3. [Enzyme-and immuno-histochemistry of muscle biopsies in severe infantile spinal muscular atrophy].
Chen BF
Zhonghua Bing Li Xue Za Zhi; 1991 Mar; 20(1):38-40. PubMed ID: 2065375
[TBL] [Abstract][Full Text] [Related]
4. Acute infantile spinal muscular atrophy. Muscle apoptosis as a proposed pathogenetic mechanism.
Fidziańska A; Goebel HH; Warlo I
Brain; 1990 Apr; 113 ( Pt 2)():433-45. PubMed ID: 2328412
[TBL] [Abstract][Full Text] [Related]
5. Selective type II muscle fiber hypertrophy in severe infantile spinal muscular atrophy.
Kingma DW; Feeback DL; Marks WA; Bobele GB; Leech RW; Brumback RA
J Child Neurol; 1991 Oct; 6(4):329-34. PubMed ID: 1940135
[TBL] [Abstract][Full Text] [Related]
6. Polyethylene glycol-coupled IGF1 delays motor function defects in a mouse model of spinal muscular atrophy with respiratory distress type 1.
Krieger F; Elflein N; Saenger S; Wirthgen E; Rak K; Frantz S; Hoeflich A; Toyka KV; Metzger F; Jablonka S
Brain; 2014 May; 137(Pt 5):1374-93. PubMed ID: 24681663
[TBL] [Abstract][Full Text] [Related]
7. DNA fragmentation and BCL-2 expression in infantile spinal muscular atrophy.
Tews DS; Goebel HH
Neuromuscul Disord; 1996 Aug; 6(4):265-73. PubMed ID: 8887956
[TBL] [Abstract][Full Text] [Related]
8. Embryonic and foetal myosins in human skeletal muscle. The presence of foetal myosins in duchenne muscular dystrophy and infantile spinal muscular atrophy.
Fitzsimons RB; Hoh JF
J Neurol Sci; 1981; 52(2-3):367-84. PubMed ID: 7310440
[TBL] [Abstract][Full Text] [Related]
9. An autopsy case of spinal muscular atrophy type III (Kugelberg-Welander disease).
Kuru S; Sakai M; Konagaya M; Yoshida M; Hashizume Y; Saito K
Neuropathology; 2009 Feb; 29(1):63-7. PubMed ID: 18410269
[TBL] [Abstract][Full Text] [Related]
10. Neonatal spinal muscular atrophy with multiple contractures, bone fractures, respiratory insufficiency and 5q13 deletion.
García-Cabezas MA; García-Alix A; Martín Y; Gutiérrez M; Hernández C; Rodríguez JI; Morales C
Acta Neuropathol; 2004 May; 107(5):475-8. PubMed ID: 14968368
[TBL] [Abstract][Full Text] [Related]
11. [Clinical study of 83 cases with spinal muscular atrophy in children].
Li H; Wang HL; Shan CM
Zhonghua Er Ke Za Zhi; 2004 Oct; 42(10):762-4. PubMed ID: 16221347
[TBL] [Abstract][Full Text] [Related]
12. [Differential diagnosis in early muscular hypotonia: spinal atrophy].
Lukás Z; Zouhar A
Cesk Patol; 1992 Mar; 28(1):9-13. PubMed ID: 1596947
[TBL] [Abstract][Full Text] [Related]
13. [Changes of some proteins expression of the spinal cord and muscles in infantile spinal muscular atrophy].
Demirkapi N; Basseville M; Lagrange MC; Braun S; Gros F; Croizat B
Rev Neurol (Paris); 1994; 150(3):196-200. PubMed ID: 7863164
[TBL] [Abstract][Full Text] [Related]
14. Abnormalities in early markers of muscle involvement support a delay in myogenesis in spinal muscular atrophy.
Martínez-Hernández R; Bernal S; Alias L; Tizzano EF
J Neuropathol Exp Neurol; 2014 Jun; 73(6):559-67. PubMed ID: 24806300
[TBL] [Abstract][Full Text] [Related]
15. Centronuclear myopathy--morphological relation to developing human skeletal muscle: a clinicopathological evaluation.
Gayathri N; Das S; Vasanth A; Devi MG; Ramamohan Y; Santosh V; Yasha TC; Shankar SK
Neurol India; 2000 Mar; 48(1):19-28. PubMed ID: 10751809
[TBL] [Abstract][Full Text] [Related]
16. Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophy.
Omran H; Ketelsen UP; Heinen F; Sauer M; Rudnik-Schöneborn S; Wirth B; Zerres K; Kratzer W; Korinthenberg R
J Child Neurol; 1998 Jul; 13(7):327-31. PubMed ID: 9701481
[TBL] [Abstract][Full Text] [Related]
17. Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings.
Rudnik-Schöneborn S; Forkert R; Hahnen E; Wirth B; Zerres K
Neuropediatrics; 1996 Feb; 27(1):8-15. PubMed ID: 8677029
[TBL] [Abstract][Full Text] [Related]
18. Synaptic defects in type I spinal muscular atrophy in human development.
Martínez-Hernández R; Bernal S; Also-Rallo E; Alías L; Barceló MJ; Hereu M; Esquerda JE; Tizzano EF
J Pathol; 2013 Jan; 229(1):49-61. PubMed ID: 22847626
[TBL] [Abstract][Full Text] [Related]
19. Scapulo-peroneal muscular atrophy. Full autopsy report. Unusual findings in the anterior horn of the spinal cord. Lipid storage in muscle.
Probst A; Ulrich J; Kaeser HE; Heitz P
Eur Neurol; 1977; 16(1-6):181-96. PubMed ID: 615710
[TBL] [Abstract][Full Text] [Related]
20. Vascular Defects and Spinal Cord Hypoxia in Spinal Muscular Atrophy.
Somers E; Lees RD; Hoban K; Sleigh JN; Zhou H; Muntoni F; Talbot K; Gillingwater TH; Parson SH
Ann Neurol; 2016 Feb; 79(2):217-30. PubMed ID: 26506088
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]