Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Meena A Kannan"'
Autor:
Swetha Tandra, Balakrishna Ramavath, Rukmini Mridula Kandadai, S A Jabeen, Meena A Kannan, Rupam Borgohain
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 1, Pp 54-58 (2020)
Background: Deep brain stimulation (DBS) is an accepted modality of treatment in patients with Parkinson's disease (PD). Although DBS was approved in advanced PD, it is being done in early PD as well. It was mainly developed to help the patients of P
Externí odkaz:
https://doaj.org/article/9e73d990491b416ea5a7d72d9f25f6a1
Autor:
Sundaram Challa, Monalisa Hui, Saumya Jakati, Megha Shantveer Uppin, Liza Rajasekhar, Meena Angamuthu Kannan, Lokesh Lingappa, Murthy Murali Krishna Jagarlapudi
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 62, Iss 1, Pp 61-66 (2019)
Background: Juvenile idiopathic inflammatory myopathies (JIIM) are rare and heterogeneous. Subtype identification is important for treatment. Materials and Methods: Patients below 18 years diagnosed as idiopathic inflammatory myopathy (IIM) according
Externí odkaz:
https://doaj.org/article/3a07e6afb24f4026a58ba0e532d159f8
Autor:
Swethalakshmi Narla, Megha S Uppin, M K Murthy Jagarlapudi, Sundaram Challa, Meena A Kannan, Saumya Jakati
Publikováno v:
Neurology India. 69(3)
Background: Sporadic inclusion body myositis (s-IBM) is rare in India. Aim: The aim of this study was to diagnose s-IBM according to the European Neuromuscular Center (ENMC) IBM research diagnostic criteria 2011. Materials and Methods: A retrospectiv
Autor:
Lokesh Lingappa, Liza Rajasekhar, Murthy Murali Krishna Jagarlapudi, Monalisa Hui, Meena A Kannan, Sundaram Challa, Megha S Uppin, Saumya Jakati
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 62, Iss 1, Pp 61-66 (2019)
Background: Juvenile idiopathic inflammatory myopathies (JIIM) are rare and heterogeneous. Subtype identification is important for treatment. Materials and Methods: Patients below 18 years diagnosed as idiopathic inflammatory myopathy (IIM) according
Publikováno v:
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology, Vol 19, Iss 3, Pp 356-359 (2016)
Annals of Indian Academy of Neurology, Vol 19, Iss 3, Pp 356-359 (2016)
Background and Purpose: Muscle biopsy features of congenital muscular dystrophies (CMD) vary from usual dystrophic picture to normal or nonspecific myopathic picture or prominent fibrosis or striking inflammatory infiltrate, which may lead to diagnos
Publikováno v:
Neurology India. 66(4)
Aim: To study C4d expression as a marker of complement activation in the diagnosis of dermatomyositis Material and Methods: Muscle biopsies from patients diagnosed as definite dermatomyositis (10), nonspecific myositis associated with connective tiss
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Autor:
Rupam Borgohain, Rukmini Mridula Kandadai, Sundaram Challa, Meena A Kannan, S A Jabeen, Megha S Uppin
Publikováno v:
Neurology India. 63(1)
Background: Paraneoplastic vasculitic neuropathy (PVN) is a rare paraneoplastic syndrome. It is characterized by non-systemic subacute vasculitic neuropathy. It is most commonly associated with small cell lung cancers (SCLC) and lymphomas. PVN presen
Autor:
Rupam Borgohain, Vishnupriya Rao Paturi, Meena A Kannan, Sailaja Sarva, S A Jabeen, Rukmini Mridula Kandadai
Publikováno v:
Neurology India. 62(6)
Background: Neuropathy is often an associated feature woth long-standing type II diabetes mellitus. Neuropathy may occur even in subjects with impaired glucose tolerance. Objective: To study the prevalence of neuropathy using different electrophysiol
Clinico pathological study of adult dermatomyositis: Importance of muscle histology in the diagnosis
Publikováno v:
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology, Vol 18, Iss 2, Pp 194-199 (2015)
Annals of Indian Academy of Neurology, Vol 18, Iss 2, Pp 194-199 (2015)
Aims: To study the histological features on muscle biopsy and correlate them with clinical features, other laboratory data in adult patients to make a diagnosis of dermatomyositis (DM), applying the European Neuromuscular center (ENMC) criteria. Mate