339 related articles for article (PubMed ID: 23743156)
1. 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]
2. [Neonatal hypotonia of muscular origin: analysis of 50 cases].
Floriach-Robert M; Cabello A; Simón De Las Heras R; Mateos Beato F
Neurologia; 2001; 16(6):245-53. PubMed ID: 11423041
[TBL] [Abstract][Full Text] [Related]
3. The value of electromyography in the aetiological diagnosis of hypotonia in infants and toddlers.
Cetin E; Cuisset JM; Tiffreau V; Vallée L; Hurtevent JF; Thevenon A
Ann Phys Rehabil Med; 2009; 52(7-8):546-55. PubMed ID: 19713169
[TBL] [Abstract][Full Text] [Related]
4. The myopathology of floppy and hypotonic infants in Singapore.
Premasiri MK; Lee YS
Pathology; 2003 Oct; 35(5):409-13. PubMed ID: 14555385
[TBL] [Abstract][Full Text] [Related]
5. [Muscle biopsy in children: Usefulness in 2012].
Cuisset JM; Maurage CA; Carpentier A; Briand G; Thévenon A; Rouaix N; Vallée L
Rev Neurol (Paris); 2013; 169(8-9):632-9. PubMed ID: 23993361
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Electromyography (EMG) accuracy compared to muscle biopsy in childhood.
Rabie M; Jossiphov J; Nevo Y
J Child Neurol; 2007 Jul; 22(7):803-8. PubMed ID: 17715269
[TBL] [Abstract][Full Text] [Related]
8. Electromyography and biopsy correlation with suggested protocol for evaluation of the floppy infant.
David WS; Jones HR
Muscle Nerve; 1994 Apr; 17(4):424-30. PubMed ID: 8170489
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Nemaline congenital myopathy:clinical features and histopathological findings in nine patients].
Botelho CH; Carod-Artal FJ; Kalil RK
Rev Neurol; 2001 Feb 16-28; 32(4):309-14. PubMed ID: 11333383
[TBL] [Abstract][Full Text] [Related]
11. The floppy infant: contribution of genetic and metabolic disorders.
Prasad AN; Prasad C
Brain Dev; 2003 Oct; 25(7):457-76. PubMed ID: 13129589
[TBL] [Abstract][Full Text] [Related]
12. The hypotonic infant: case study of central core disease.
Castrodale V
Neonatal Netw; 2003; 22(1):53-9. PubMed ID: 12597091
[TBL] [Abstract][Full Text] [Related]
13. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
Smeyers P
Rev Neurol; 1999 Jan 16-31; 28(2):141-9. PubMed ID: 10101782
[TBL] [Abstract][Full Text] [Related]
14. A study of histopathological pattern of neuromuscular disorders with clinico-pathologic correlation.
Karim MS; Kamal M; Rahman AJ
Bangladesh Med Res Counc Bull; 2003 Apr; 29(1):11-22. PubMed ID: 14674616
[TBL] [Abstract][Full Text] [Related]
15. A large series of immunohistochemically confirmed cases of congenital muscular dystrophy seen over a period of one decade.
Nagappa M; Atchayaram N; Narayanappa G
Neurol India; 2013; 61(5):481-7. PubMed ID: 24262449
[TBL] [Abstract][Full Text] [Related]
16. Clinical and histologic changes in the follow-up of a congenital myopathy.
Camacho A; Villarejo A; Simón R; Mateos F; Cabello A
Pediatr Neurol; 2005 Aug; 33(2):139-41. PubMed ID: 16087062
[TBL] [Abstract][Full Text] [Related]
17. [Myotubular or centronuclear myopathy; report of a case and review of the literature].
Pereira de Sousa R; Miranda D; Perpetuo FO; Campos GB; Vuletin JC
Arq Neuropsiquiatr; 1977 Sep; 35(3):247-59. PubMed ID: 901263
[TBL] [Abstract][Full Text] [Related]
18. Spectrum of floppy children in Indian scenario.
Dua T; Das M; Kabra M; Bhatia M; Sarkar C; Arora S; Sharma MC; Kalra V
Indian Pediatr; 2001 Nov; 38(11):1236-43. PubMed ID: 11721063
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. The significance of type 1 fiber atrophy (hypotrophy) in childhood neuromuscular disorders.
Imoto C; Nonaka I
Brain Dev; 2001 Aug; 23(5):298-302. PubMed ID: 11504599
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]