Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ravi Kiran Valasani"'
Autor:
Gopikrishnan Unnikrishnan, Kiran Polavarapu, Mainak Bardhan, Saraswati Nashi, Seena Vengalil, Veeramani Preethish-Kumar, Ravi Kiran Valasani, Akshata Huddar, Vikas Nishadham, Bevinahalli Nanjegowda Nandeesh, Atchayaram Nalini
Publikováno v:
Journal of Neuromuscular Diseases. :1-12
Background: The phenotypic spectrum of Fukutin-related protein (FKRP) mutations is highly variable and comprises of limb girdle muscular dystrophy (LGMD) R9 (previously LGMD 2I) and FKRP related congenital muscular dystrophies. Objective: To identify
Autor:
Vikas Nishadham, Shilpa Rao, Akshaya Saravanan, Karthik Kulanthaivelu, Seena Vengalil, Hema A. Venkatappa, Ravi Kiran Valasani, Mainak Bardhan, Nupur Pruti, Atchayaram Nalini, Anita Mahadevan
Publikováno v:
Clinical Neuropathology. 42:100-111
Autor:
Vikas Nishadham, Mainak Bardhan, Kiran Polavarapu, Seena Vengalil, Saraswati Nashi, Deepak Menon, Valakunja Harikrishna Ganaraja, Veeramani Preethish-Kumar, Ravi Kiran Valasani, Akshata Huddar, Gopi Krishnan Unnikrishnan, Abel Thomas, Akshaya Saravanan, Karthik Kulanthaivelu, Atchayaram Nalini, Bevinahalli Nanjegowda Nandeesh
Publikováno v:
Journal of Neuromuscular Diseases. 9:411-422
Background and Objectives: Thymic pathology is common in Myasthenia Gravis(MG) and plays a crucial role in its pathogenesis and clinical outcome. This study aims to discuss the clinicohistopathological spectrum of thymic lesions in MG. Methods: In th
Autor:
Mainak Bardhan, Ram Murthy Anjanappa, Kiran Polavarapu, Veeramani Preethish-Kumar, Seena Vengalil, Saraswati Nashi, Shamita Sanga, Hansashree Padmanabh, Ravi Kiran Valasani, Vikas Nishadham, Muddasu Keerthipriya, Thenral S. Geetha, Vedam Ramprasad, Gautham Arunachal, Priya Treesa Thomas, Moulinath Acharya, Atchayaram Nalini
Publikováno v:
neurogenetics. 23:187-202
Autor:
Mainak, Bardhan, Ram Murthy, Anjanappa, Kiran, Polavarapu, Veeramani, Preethish-Kumar, Seena, Vengalil, Saraswati, Nashi, Shamita, Sanga, Hansashree, Padmanabh, Ravi Kiran, Valasani, Vikas, Nishadham, Muddasu, Keerthipriya, Thenral S, Geetha, Vedam, Ramprasad, Gautham, Arunachal, Priya Treesa, Thomas, Moulinath, Acharya, Atchayaram, Nalini
Publikováno v:
Neurogenetics. 23(3)
The clinico-genetic architecture of sarcoglycanopathies in Indian patients is reported only as short series. In the present study, we aimed to investigate the clinical picture, genetic basis, and disease progression of patients genetically confirmed
Autor:
Ganaraja, Valakunja H., Polavarapu, Kiran, Bardhan, Mainak, Preethish-Kumar, Veeramani, Leena, Shingavi, Anjanappa, Ram M., Vengalil, Seena, Nashi, Saraswati, Arunachal, Gautham, Gunasekaran, Swetha, Mohan, Dhaarini, Raju, Sanita, Unnikrishnan, Gopikrishnan, Huddar, Akshata, Ravi-Kiran, Valasani, Thomas, Priya T., Nalini, Atchayaram
Publikováno v:
Global Medical Genetics; Mar2022, Vol. 9 Issue 1, p34-41, 8p
Autor:
Ganaraja VH; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Polavarapu K; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.; Division of Neurology, Department of Medicine, Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, The Ottawa Hospital, Ottawa, Canada., Bardhan M; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Preethish-Kumar V; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Leena S; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Anjanappa RM; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.; Division of Neurology, Department of Medicine, Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, The Ottawa Hospital, Ottawa, Canada., Vengalil S; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Nashi S; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Arunachal G; Department of Human Genetics, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Gunasekaran S; Department of Human Genetics, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Mohan D; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Raju S; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Unnikrishnan G; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Huddar A; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Ravi-Kiran V; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Thomas PT; Department of Psychiatric Social Work, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India., Nalini A; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.
Publikováno v:
Global medical genetics [Glob Med Genet] 2021 Nov 09; Vol. 9 (1), pp. 34-41. Date of Electronic Publication: 2021 Nov 09 (Print Publication: 2022).