213 related articles for article (PubMed ID: 21614992)
1. Congenital myasthenic syndrome: a case report.
Ceylan A; Tuncer O; Sayin R; Peker E; Caksen H; Sari S
Genet Couns; 2011; 22(1):75-8. PubMed ID: 21614992
[TBL] [Abstract][Full Text] [Related]
2. Congenital myasthenia gravis.
Nizamani NB; Talpur KI; Memon MN
J Coll Physicians Surg Pak; 2013 Jul; 23(7):517-8. PubMed ID: 23823963
[TBL] [Abstract][Full Text] [Related]
3. Congenital myasthenic syndrome: a rare, potentially treatable cause of respiratory failure in a "floppy" infant.
McConkey PP; Mullens AJ
Anaesth Intensive Care; 2000 Feb; 28(1):82-6. PubMed ID: 10701044
[TBL] [Abstract][Full Text] [Related]
4. Temporary diazepam responsive apneic attacks and congenital myasthenic syndrome.
Yis U; Kurul SH; Oztura I; Ozden O; Akinci G; Dirik E
J Child Neurol; 2009 Jul; 24(7):895-8. PubMed ID: 19289695
[TBL] [Abstract][Full Text] [Related]
5. Congenital myasthenic syndrome: presentation, electrodiagnosis, and muscle biopsy.
Gurnett CA; Bodnar JA; Neil J; Connolly AM
J Child Neurol; 2004 Mar; 19(3):175-82. PubMed ID: 15119478
[TBL] [Abstract][Full Text] [Related]
6. Congenital myasthenic syndromes and transient myasthenia gravis.
Gajda A; Szabó H; Gergev G; Karcagi V; Szabó N; Endreffy E; Túri S; Sztriha L
Ideggyogy Sz; 2013 May; 66(5-6):200-3. PubMed ID: 23909021
[TBL] [Abstract][Full Text] [Related]
7. Unique presentation of rapidly fluctuating symptoms in a child with congenital myasthenic syndrome due to RAPSN mutation.
Kumar A; Asghar S; Kavanagh R; Wicklund MP
Muscle Nerve; 2018 Oct; 58(4):E23-E24. PubMed ID: 30028532
[No Abstract] [Full Text] [Related]
8. Congenital myasthenic syndromes.
Engel AG
Handb Clin Neurol; 2008; 91():285-331. PubMed ID: 18631848
[No Abstract] [Full Text] [Related]
9. Refinement of the clinical phenotype in musk-related congenital myasthenic syndromes.
Mihaylova V; Salih MA; Mukhtar MM; Abuzeid HA; El-Sadig SM; von der Hagen M; Huebner A; Nürnberg G; Abicht A; Müller JS; Lochmüller H; Guergueltcheva V
Neurology; 2009 Dec; 73(22):1926-8. PubMed ID: 19949040
[No Abstract] [Full Text] [Related]
10. Congenital myasthenic syndrome due to a genetic mutation.
Tsalta-Mladenov M; Levkova M; Georgieva D; Andonova S
J Am Assoc Nurse Pract; 2023 Aug; 35(8):519-523. PubMed ID: 37141567
[TBL] [Abstract][Full Text] [Related]
11. β2-Adrenergic receptor agonists ameliorate the adverse effect of long-term pyridostigmine on neuromuscular junction structure.
Vanhaesebrouck AE; Webster R; Maxwell S; Rodriguez Cruz PM; Cossins J; Wickens J; Liu WW; Cetin H; Cheung J; Ramjattan H; Palace J; Beeson D
Brain; 2019 Dec; 142(12):3713-3727. PubMed ID: 31633155
[TBL] [Abstract][Full Text] [Related]
12. Presentation and management of congenital myasthenic syndrome with a homozygous Agrin variant (Pro1448Leu).
Singh S; Govindarajan R
Clin Neurol Neurosurg; 2020 Dec; 199():106277. PubMed ID: 33059315
[No Abstract] [Full Text] [Related]
13. [Differential congenital myasthenia syndrome diagnosis].
Spuler S; Lehmann TN; Engel AG
Nervenarzt; 2004 Feb; 75(2):141-4. PubMed ID: 14770284
[TBL] [Abstract][Full Text] [Related]
14. Update on juvenile myasthenia gravis.
Liew WK; Kang PB
Curr Opin Pediatr; 2013 Dec; 25(6):694-700. PubMed ID: 24141560
[TBL] [Abstract][Full Text] [Related]
15. Management of myasthenic conditions: nonimmune issues.
Argov Z
Curr Opin Neurol; 2009 Oct; 22(5):493-7. PubMed ID: 19593127
[TBL] [Abstract][Full Text] [Related]
16. Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1.
Finlayson S; Palace J; Belaya K; Walls TJ; Norwood F; Burke G; Holton JL; Pascual-Pascual SI; Cossins J; Beeson D
J Neurol Neurosurg Psychiatry; 2013 Oct; 84(10):1119-25. PubMed ID: 23447650
[TBL] [Abstract][Full Text] [Related]
17. [Respiratory arrests caused by congenital myasthenia gravis syndrome].
Byring RF; Ohno K; Pihko H; Gustafsson B; Hackman P; Engel A; Udd B
Duodecim; 2002; 118(22):2323-6. PubMed ID: 12523110
[No Abstract] [Full Text] [Related]
18. Therapeutic strategies for congenital myasthenic syndromes.
Lee M; Beeson D; Palace J
Ann N Y Acad Sci; 2018 Jan; 1412(1):129-136. PubMed ID: 29381222
[TBL] [Abstract][Full Text] [Related]
19. Congenital myasthenic syndrome due to rapsyn deficiency: A case report with a new mutation and compound heterozygosity.
Espinoza IO; Reynoso C; Chávez G; Engel AG
Medwave; 2019 Jun; 19(5):e7645. PubMed ID: 31226102
[TBL] [Abstract][Full Text] [Related]
20. Congenital myasthenic syndromes.
Eymard B; Hantaï D; Estournet B
Handb Clin Neurol; 2013; 113():1469-80. PubMed ID: 23622369
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]