Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Sushil, Razdan"'
Autor:
Akshi Spolia, Arshia Angural, Varun Sharma, Shipra, Sushil Razdan, Manoj K. Dhar, Ankit Mahajan, Vijeshwar Verma, Kamal K. Pandita, Swarkar Sharma, Ekta Rai
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract Neurofibromatosis type 1 (NF1) is a multisystemic hereditary disorder associated with an increased risk of benign and malignant tumor formation predominantly on the skin, bone, and peripheral nervous system. It has been reported that out of
Externí odkaz:
https://doaj.org/article/528a8fdef95841a9bd8d7ce5e86460da
Publikováno v:
Saudi Journal for Health Sciences, Vol 12, Iss 3, Pp 188-194 (2023)
Background: The spectrum of neurological diseases encompasses a large number of disorders, including neuromuscular disorder (NMDs), ataxias, and muscular dystrophies. A detailed clinical examination, followed by electromyography and muscle biopsy, is
Externí odkaz:
https://doaj.org/article/c76ab63c30844fbd9f35c9bd5c4f699f
Autor:
Arshia Angural, Inderpal Singh, Ankit Mahajan, Pranav Pandoh, Manoj K Dhar, Sanjana Kaul, Vijeshwar Verma, Ekta Rai, Sushil Razdan, Kamal Kishore Pandita, Swarkar Sharma
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract Pantothenate kinase-associated neurodegeneration is a rare hereditary neurodegenerative disorder associated with nucleotide variation(s) in mitochondrial human Pantothenate kinase 2 (hPanK2) protein encoding PANK2 gene, and is characterized
Externí odkaz:
https://doaj.org/article/489c4bd2dfb94413be2ad62d69e5e0bb
Publikováno v:
Italian Journal of Medicine, Vol 10, Iss 1, Pp 62-66 (2015)
The original algorithmic approach, as outlined by de Kleijn and colleagues and practiced commonly, envisages performing computed tomography (CT) of chest, abdomen, and pelvis in patients with classical fever of unknown origin (FUO), in whom no potent
Externí odkaz:
https://doaj.org/article/2b1f6e3136a646af8bb0c7edc9a54d6f
Publikováno v:
Egyptian Rheumatology and Rehabilitation, Vol 42, Iss 2, Pp 100-102 (2015)
Polymyalgia rheumatica (PMR) is a connective tissue disorder of unknown aetiology. It is hypothesized that, in a genetically predisposed person, its pathogenesis is triggered by an environmental factor, possibly a hitherto unknown infectious agent. W
Externí odkaz:
https://doaj.org/article/785541a284a54a819ed29946517f0293
Publikováno v:
Annals of Indian Academy of Neurology, Vol 15, Iss 1, Pp 23-26 (2012)
Objective: To determine the Prevalence of mental retardation in children 3 to 10 years of age. Materials and Methods: The study was conducted in the framework of a population based, single centre, cross-sectional study at R.S.Pura town, 22 kms south-
Externí odkaz:
https://doaj.org/article/1b17631d9ad24c63914295731c5213a0
Autor:
Ekta Rai, Arshia Angural, Akshi Sapolia, Sushil Razdan, Kamal Kishore Pandita, Swarkar Sharma
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue-Supplement, Pp 250-250 (2017)
Rare disorders are poorly understood, most often remain uncharacterized or patients are misdiagnosed due to lack of specific clinical resources. Understanding the basics of inheritance is essential in such cases as it helps to figure out the plausibi
Externí odkaz:
https://doaj.org/article/319f7e3862df49748db2a0601cfb7097
Publikováno v:
Case Reports in Pulmonology, Vol 2014 (2014)
Churg-Strauss syndrome (CSS) is a rare cause of vasculitic neuropathy. Although rare and potentially fatal, Churg-Strauss syndrome (CSS) is easily diagnosable and treatable. The presence of bronchial asthma with peripheral neuropathy in a patient ale
Externí odkaz:
https://doaj.org/article/2283b5c4209546e3ae46f711981e1bb3
Autor:
Parthasarathy, Satishchandra, Chaturbhuj, Rathore, Anirudha, Apte, Abhishek, Kumar, Amlan, Mandal, Dushyant, Chauhan, Jagadish, Agadi, Jayanti, Gurumukhani, K, Asokan, K, Venkateshwarlu, Lokesh, Lingappa, Nagarjunakonda Venkata, Sundaracharya, Sudhir K, Jha, Sangeeta, Ravat, Sanjeev, Vk, Siddhartha, Garg, Sudhir Vadilal, Shah, Sundaram, Alagesan, Sushil, Razdan, Uma, Padhy, Vinay Kumar, Agarwal, Vinod, Arora, Bindu, Menon, Sujatha, Shetty, Deepa, Chodankar
Publikováno v:
Epilepsy & Behavior. 130:108671
To prospectively study the effectiveness and safety of clobazam as an add-on therapy in patients with epilepsy whose seizures are not adequately controlled with antiseizure medicine (ASM) monotherapy.We conducted a prospective, observational study at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a847921434c6f72372583df3c305677
https://doi.org/10.1016/j.yebeh.2022.108671
https://doi.org/10.1016/j.yebeh.2022.108671
Autor:
Sushil Razdan, Vijeshwar Verma, Manoj K. Dhar, Swarkar Sharma, Ekta Rai, Inderpal Singh, Pranav Pandoh, Arshia Angural, Sanjana Kaul, Ankit Mahajan, Kamal Kishore Pandita
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Scientific Reports
Scientific Reports
Pantothenate kinase-associated neurodegeneration is a rare hereditary neurodegenerative disorder associated with nucleotide variation(s) in mitochondrial human Pantothenate kinase 2 (hPanK2) protein encoding PANK2 gene, and is characterized by sympto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5100060b357e67bb3aac805030d84de
https://doaj.org/article/489c4bd2dfb94413be2ad62d69e5e0bb
https://doaj.org/article/489c4bd2dfb94413be2ad62d69e5e0bb