دوره 4، شماره 1 - ( 10-1396 )                   جلد 4 شماره 1 صفحات 38-35 | برگشت به فهرست نسخه ها


XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Shervin Badv R, Memarian S, Ghahvechi M, Farshad Moghaddam H, Saidi M, Mohsenipour R, et al . A Case Report of Congenital Myasthenia Gravis Presenting With Respiratory Distress. Caspian.J.Neurol.Sci 2018; 4 (1) :35-38
URL: http://cjns.gums.ac.ir/article-1-218-fa.html
A Case Report of Congenital Myasthenia Gravis Presenting With Respiratory Distress. مجله علوم اعصاب کاسپین 1396; 4 (1) :38-35

URL: http://cjns.gums.ac.ir/article-1-218-fa.html


متن کامل [PDF 688 kb]   (1382 دریافت)     |   چکیده (HTML)  (3236 مشاهده)
متن کامل:   (1262 مشاهده)
نوع مطالعه: پژوهشي | موضوع مقاله: تخصصي
دریافت: 1396/3/17 | پذیرش: 1396/6/24 | انتشار: 1396/10/11

فهرست منابع
1. Sarnat HB. Disorders of neuromuscular transmission and of motor neurons. In: Kliegman RM, Stanton BF, St. Geme JW, Schor NF, Behrman RE, et al., editors. Nelson Textbook of Pediatrics. Philadelphia: Saunders; 2016.
2. Muppidi S, Wolfe GI, Barohn RJ. Diseases of the neuromuscular junction. In: Swaiman KF, Ashwal S, Ferriero DM, Schor NF, editors. Swaiman's Pediatric Neurology. Amsterdam: Elsevier Inc; 2012. [DOI:10.1016/B978-1-4377-0435-8.00094-9]
3. Bodensteiner JB. The evaluation of the hypotonic infant. Semin Pediatr Neurol. 2008; 15(1):10–20. doi: 10.1016/j.spen.2008.01.003 [DOI:10.1016/j.spen.2008.01.003]
4. Romaneli MT das N, Castro CCT de S, Fraga A de MA, Lomazi EA, Nucci A, Tresoldi AT. Evento com aparente risco de morte recorrente como manifestação inicial de síndrome miastênica congênita. Rev Paul Pediatr. 2013; 31(1):121–3. doi: 10.1590/s0103-05822013000100019 [DOI:10.1590/S0103-05822013000100019]
5. Waseem M, Gernsheimer J, Park TK, Jara F, Erickson E. A floppy infant. Int J Case Rep Imag. 2013;4(1):66. doi: 10.5348/ijcri-2013-01-262-cr-16 [DOI:10.5348/ijcri-2013-01-262-CR-16]
6. Lorenzoni PJ, Scola RH, Gervini BL, Kay CSK, Werneck LC. Electrophysiological study in synaptic congenital myasthenic syndrome: End-plate acetylcholinesterase deficiency. Arq Neuropsiquiatr. 2009; 67(2b):502–4. doi: 10.1590/s0004-282x2009000300024 [DOI:10.1590/S0004-282X2009000300024]
7. Pyle A, Nightingale HJ, Griffin H, Abicht A, Kirschner J, Baric I, et al. Respiratory chain deficiency in nonmitochondrial disease. Neurol Genet. 2015; 1(1):e6. doi:10.1212/nxg.0000000000000006 [DOI:10.1212/NXG.0000000000000006]
8. Robb SA, Muntoni F, Simonds AK. Respiratory management of congenital myasthenic syndromes in childhood: Workshop 8th December 2009, UCL Institute of Neurology, London, UK. Neuromuscul Disord. 2010; 20(12):833–8. doi: 10.1016/j.nmd.2010.08.002 [DOI:10.1016/j.nmd.2010.08.002]
9. Mihaylova V, Müller JS, Vilchez JJ, Salih MA, Kabiraj MM, D'Amico A, et al. Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes. Brain. 2008; 131(3):747–59. doi: 10.1093/brain/awm325 [DOI:10.1093/brain/awm325]

ارسال نظر درباره این مقاله : نام کاربری یا پست الکترونیک شما:
CAPTCHA

بازنشر اطلاعات
Creative Commons License این مقاله تحت شرایط Creative Commons Attribution-NonCommercial 4.0 International License قابل بازنشر است.

کلیه حقوق این وب سایت متعلق به مجله علوم اعصاب کاسپین می باشد.

طراحی و برنامه نویسی : یکتاوب افزار شرق

© 2023 CC BY-NC 4.0 | Caspian Journal of Neurological Sciences

Designed & Developed by : Yektaweb