156 related articles for article (PubMed ID: 12597091)
1. 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]
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. 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]
4. Central core disease.
Jungbluth H
Orphanet J Rare Dis; 2007 May; 2():25. PubMed ID: 17504518
[TBL] [Abstract][Full Text] [Related]
5. The floppy infant: a practical approach.
Zellweger H
Helv Paediatr Acta; 1983 Oct; 38(4):301-6. PubMed ID: 6360959
[TBL] [Abstract][Full Text] [Related]
6. [Neonatal hypotonia].
Erazo-Torricelli R
Rev Neurol; 2000 Aug 1-15; 31(3):252-62. PubMed ID: 10996927
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: muscle biopsy and autopsy findings, biochemical and molecular genetic studies.
Taratuto AL; Akman HO; Saccoliti M; Riudavets M; Arakaki N; Mesa L; Sevlever G; Goebel H; DiMauro S
Neuromuscul Disord; 2010 Dec; 20(12):783-90. PubMed ID: 20833045
[TBL] [Abstract][Full Text] [Related]
10. Undetected central core disease myopathy in an infant presenting for clubfoot surgery.
Zanette G; Robb N; Zadra N; Zanette L; Manani G
Paediatr Anaesth; 2007 Apr; 17(4):380-2. PubMed ID: 17359409
[TBL] [Abstract][Full Text] [Related]
11. The evaluation of the hypotonic infant.
Bodensteiner JB
Semin Pediatr Neurol; 2008 Mar; 15(1):10-20. PubMed ID: 18342256
[TBL] [Abstract][Full Text] [Related]
12. [Generalized neonatal hypotonia].
Alfonso I; Papazian O; Valencia P
Rev Neurol; 2003 Aug 1-15; 37(3):228-39. PubMed ID: 12938055
[TBL] [Abstract][Full Text] [Related]
13. Role of EMG in congenital hypotonia with favorable outcome.
Pisani F; Carboni P
Acta Biomed; 2005 Dec; 76(3):171-4. PubMed ID: 16676567
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Predictive value of electromyography in diagnosis and prognosis of the hypotonic infant.
Russell JW; Afifi AK; Ross MA
J Child Neurol; 1992 Oct; 7(4):387-91. PubMed ID: 1469246
[TBL] [Abstract][Full Text] [Related]
16. A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene.
Ferreiro A; Monnier N; Romero NB; Leroy JP; Bönnemann C; Haenggeli CA; Straub V; Voss WD; Nivoche Y; Jungbluth H; Lemainque A; Voit T; Lunardi J; Fardeau M; Guicheney P
Ann Neurol; 2002 Jun; 51(6):750-9. PubMed ID: 12112081
[TBL] [Abstract][Full Text] [Related]
17. "Floppy baby" (Oppenheim's disease, amyotonia congenital).
Hanson PA
Pediatr Ann; 1977 Mar; 6(3):194-202. PubMed ID: 322049
[No Abstract] [Full Text] [Related]
18. Novel presentation of central core disease with nemaline bodies (rods) in the setting of diploid/triploid mosaicism.
Shafi NB; Parker JC; Atkinson JB; Parker JR
Ann Clin Lab Sci; 2007; 37(2):177-81. PubMed ID: 17522375
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Midbrain disconnection: an aetiology of severe central neonatal hypotonia.
Bednarek N; Scavarda D; Mesmin F; Sabouraud P; Motte J; Morville P
Eur J Paediatr Neurol; 2005; 9(6):419-22. PubMed ID: 16055359
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
