Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Marami Das"'
Autor:
Ashok Kumar Kayal, Munindra Goswami, Marami Das, Lakhshya Jyoti Basumatary, Suvorit Subhas Bhowmick, Baiakmenlang Synmon
Publikováno v:
Annals of Indian Academy of Neurology, Vol 20, Iss 1, Pp 41-50 (2017)
Background: The discovery of antibodies against aquaporin-4 and evolving concepts of noncompressive myelopathies in the 21st century have made a major impact on the etiological profile of these diseases, with few cases turning out to be idiopathic. O
Externí odkaz:
https://doaj.org/article/287e3a3f206a47baacd92846a06846f8
Autor:
Papori Borah, Vikas Sharma, Lakshya Jyoti Basumatary, Marami Das, Munindra Goswami, Ashok K Kayal
Publikováno v:
Annals of Indian Academy of Neurology, Vol 17, Iss 3, Pp 317-320 (2014)
Introduction: Moyamoya disease is a chronic progressive cerebrovascular disorder, characterized by stenosis or occlusion of bilateral internal carotid arteries (ICAs), anterior cerebral arteries (ACAs) and middle cerebral arteries (MCAs), accompanied
Externí odkaz:
https://doaj.org/article/0a2671bb75d94cef915a2f21daf2ac6b
Autor:
Vikas Sharma, Papori Borah, Lakshya J Basumatary, Marami Das, Munindra Goswami, Ashok K Kayal
Publikováno v:
Annals of Indian Academy of Neurology, Vol 17, Iss 3, Pp 298-302 (2014)
Introduction: Major categories of endocrine myopathy include those associated with: Adrenal dysfunction (as in Cushing′s disease or steroid myopathy); thyroid dysfunction (as in myxedema coma or thyrotoxic myopathy); vitamin D deficiency; parathyro
Externí odkaz:
https://doaj.org/article/cd5c05ae7246420aba6cc7bb5b522ea1
Publikováno v:
Annals of Indian Academy of Neurology, Vol 16, Iss 2, Pp 211-217 (2013)
Background: Acute hypokalemic paralysis, characterized by acute flaccid paralysis is primarily a calcium channelopathy, but secondary causes like renal tubular acidosis (RTA), thyrotoxic periodic paralysis (TPP), primary hyperaldosteronism, Gitelman
Externí odkaz:
https://doaj.org/article/29cf360139c9423eafb50d17db304bec
Publikováno v:
Annals of Indian Academy of Neurology, Vol 17, Iss 3, Pp 349-351 (2014)
It has been just 7 years since the discovery of anti-NMDAR encephalitis as distinct immune-mediated encephalitis and we have such cases being reported from our country. Herein, we describe a case of a 13-year-old girl who had relapsing encephalitis c
Externí odkaz:
https://doaj.org/article/5d1802dddc504c65af406ab94ecb4361
Publikováno v:
INDIAN JOURNAL OF APPLIED RESEARCH. :44-49
BACKGROUND Guillain-Barre syndrome (GBS) is a rare, immune mediated disorder which is associated with demyelination of peripheral nervous system and progressive muscle weakness, with an annual global incidence of approximately 1–2 per 100,000 perso
Publikováno v:
Annals of Indian Academy of Neurology. 25(3)
1. To study the clinical profile, progression and outcome of GBS during peripartum period in a tertiary care hospital. 2. To identify the determinants of outcome in GBS during peripartum period.Guillain-Barré Syndrome (GBS) is an acute, autoimmune d
Publikováno v:
INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH. :79-80
Multisystem inammatory disorder in children and adolescents associated with COVID 19 is a life threatening and emerging condition now. Our case, a 15 year old boy initially presented with acute abdominal pain mimicking acute appendicitis but later
Publikováno v:
International Journal of Scientific and Research Publications (IJSRP). 12:340
Publikováno v:
Indian Journal of Psychiatry