159 related articles for article (PubMed ID: 36160617)
1. Congenital Myopathies: A Clinicopathological Study of 10 Cases in a Tertiary Care Hospital of North India.
Maheshwari S; Pant I; Bala K; Paradasani V
J Pediatr Neurosci; 2021; 16(3):184-195. PubMed ID: 36160617
[TBL] [Abstract][Full Text] [Related]
2. Congenital myopathies: a clinicopathological study of 25 cases.
Jain D; Sharma MC; Sarkar C; Gulati S; Kalra V; Singh S; Bhatia R
Indian J Pathol Microbiol; 2008; 51(4):474-80. PubMed ID: 19008569
[TBL] [Abstract][Full Text] [Related]
3. Spectrum of congenital myopathies: a single centre experience.
Uppin MS; Meena AK; Sundaram C
Neurol India; 2013; 61(3):254-9. PubMed ID: 23860144
[TBL] [Abstract][Full Text] [Related]
4. Coexistence of central nucleus, cores, and rods: Diagnostic relevance.
Dhinakaran S; Kumar RS; Thakkar R; Narayanappa G
Ann Indian Acad Neurol; 2016; 19(2):201-4. PubMed ID: 27293330
[TBL] [Abstract][Full Text] [Related]
5. Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion.
Lawlor MW; Dechene ET; Roumm E; Geggel AS; Moghadaszadeh B; Beggs AH
Hum Mutat; 2010 Feb; 31(2):176-83. PubMed ID: 19953533
[TBL] [Abstract][Full Text] [Related]
6. Congenital myopathies: clinical and immunohistochemical study.
Thaha F; Gayathri N; Nalini A
Neurol India; 2011; 59(6):879-83. PubMed ID: 22234203
[TBL] [Abstract][Full Text] [Related]
7. Comparison of clinical characteristics between congenital fiber type disproportion myopathy and congenital myopathy with type 1 fiber predominance.
Na SJ; Kim WK; Kim TS; Kang SW; Lee EY; Choi YC
Yonsei Med J; 2006 Aug; 47(4):513-8. PubMed ID: 16941741
[TBL] [Abstract][Full Text] [Related]
8. RYR1-Related Myopathies: Clinical, Histopathologic and Genetic Heterogeneity Among 17 Patients from a Portuguese Tertiary Centre.
Samões R; Oliveira J; Taipa R; Coelho T; Cardoso M; Gonçalves A; Santos R; Melo Pires M; Santos M
J Neuromuscul Dis; 2017; 4(1):67-76. PubMed ID: 28269792
[TBL] [Abstract][Full Text] [Related]
9. Nemaline rod myopathy: a rare form of myopathy.
Sharma MC; Gulati S; Atri S; Seth R; Kalra V; Das TK; Sarkar C
Neurol India; 2007; 55(1):70-4. PubMed ID: 17272906
[TBL] [Abstract][Full Text] [Related]
10. Congenital fiber type disproportion: a rare type of congenital myopathy: a report of four cases.
Sharma MC; Ralte AM; Atri SK; Gulati S; Kalra V; Sarkar C
Neurol India; 2004 Jun; 52(2):254-6. PubMed ID: 15269486
[TBL] [Abstract][Full Text] [Related]
11. Characterization of congenital myopathies at a Korean neuromuscular center.
Park YE; Shin JH; Kim HS; Lee CH; Kim DS
Muscle Nerve; 2018 Aug; 58(2):235-244. PubMed ID: 29669168
[TBL] [Abstract][Full Text] [Related]
12.
Avasthi KK; Agarwal S; Panigrahi I
J Pediatr Neurosci; 2019; 14(4):222-224. PubMed ID: 31908664
[TBL] [Abstract][Full Text] [Related]
13. Congenital myopathies with "diagnostic" pathological features.
Korényi-Both A; Korényi-Both I
J Med; 1987; 18(2):93-107. PubMed ID: 3323392
[TBL] [Abstract][Full Text] [Related]
14. Congenital myopathies.
D'Amico A; Bertini E
Curr Neurol Neurosci Rep; 2008 Jan; 8(1):73-9. PubMed ID: 18367042
[TBL] [Abstract][Full Text] [Related]
15. Congenital myopathies and muscular dystrophies.
Gilbreath HR; Castro D; Iannaccone ST
Neurol Clin; 2014 Aug; 32(3):689-703, viii. PubMed ID: 25037085
[TBL] [Abstract][Full Text] [Related]
16. A Systematic Review and Meta-Analysis of the Prevalence of Congenital Myopathy.
Huang K; Bi FF; Yang H
Front Neurol; 2021; 12():761636. PubMed ID: 34795634
[No Abstract] [Full Text] [Related]
17. Congenital myopathies: an update.
Claeys KG
Dev Med Child Neurol; 2020 Mar; 62(3):297-302. PubMed ID: 31578728
[TBL] [Abstract][Full Text] [Related]
18. Frequency and phenotype of patients carrying TPM2 and TPM3 gene mutations in a cohort of 94 patients with congenital myopathy.
Citirak G; Witting N; Duno M; Werlauff U; Petri H; Vissing J
Neuromuscul Disord; 2014 Apr; 24(4):325-30. PubMed ID: 24507666
[TBL] [Abstract][Full Text] [Related]
19. Clinical and skeletal muscle biopsy characteristics of 25 patients with floppy infant syndrome.
Bing Q; Hu J; Li N; Shen HR; Zhao Z
Clin Neuropathol; 2013; 32(6):471-9. PubMed ID: 23743156
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]