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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 8, 2008
Autosomal recessive tubular aggregate myopathy in an Indian family
Lekha Pandit, Gayathri Narayanappa, Irruvathur Gopalakrishna Bhat, et al.
Journal of Pediatric Neurosciences
|
February 3, 2021
Macrophagic Myofasciitis: A Report of Two South Indian Infants
Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Yasha Muthane, et al.
Neurology India
|
November 23, 2013
Mucolipidosis and progressive myoclonus epilepsy: a distinctive phenotype
Ramshekhar N Menon, Sujith Jagtap, Ravindra Thakkar, et al.
Journal of Neuromuscular Diseases
|
January 15, 2023
MLIP-Associated Myopathy: A Case Report and Review of the Literature
Fatema Al Amrani, Khalid Al-Thihli, Gayathri Narayanappa, et al.
Intervirology
|
June 29, 2018
Chikungunya Virus Interacts with Heat Shock Cognate 70 Protein to Facilitate Its Entry into Mosquito Cell Line
Ayushman Ghosh, Anita Desai, Vasanthapuram Ravi, et al.
Neurology India
|
March 15, 2017
Young onset Parkinsonism in a patient with familial central core disease
P Samuel Joseph, D M Syam Krishnan, Gayathri Narayanappa, et al.
Disease Models & Mechanisms
|
April 19, 2018
Sporadic amyotrophic lateral sclerosis (SALS) - skeletal muscle response to cerebrospinal fluid from SALS patients in a rat model
Shruthi Shanmukha, Gayathri Narayanappa, Atchayaram Nalini, et al.
Journal of Pediatric Neurosciences
|
May 22, 2020
Myelopathy in Two Brothers with Respiratory Chain Disorder-Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association
Sadanandavalli Retnaswami Chandra, Hansashree Padmanabha, Manisha Gupta, et al.
Journal of Pediatric Neurosciences
|
October 2, 2018
Lipid Storage Myopathy with Ketonuria: A Case of Fatty Acid Oxidation-Related Myopathy and Encephalopathy due to Multiple Acyl-CoA Dehydrogenase Deficiency
Sadanandavalli R Chandra, Rita Christopher, Gayathri Narayanappa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 25, 2004
Clinical features of adult GM1 gangliosidosis: report of three Indian patients and review of 40 cases
Uday Muthane, Yasha Chickabasaviah, Chris Kaneski, et al.
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of 4
Search research articles
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Showing results (11-20 of 34) with videos related to
Sort By:
Page
of 4
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 8, 2008
Autosomal recessive tubular aggregate myopathy in an Indian family
Lekha Pandit, Gayathri Narayanappa, Irruvathur Gopalakrishna Bhat, et al.
Journal of Pediatric Neurosciences
|
February 3, 2021
Macrophagic Myofasciitis: A Report of Two South Indian Infants
Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Yasha Muthane, et al.
Neurology India
|
November 23, 2013
Mucolipidosis and progressive myoclonus epilepsy: a distinctive phenotype
Ramshekhar N Menon, Sujith Jagtap, Ravindra Thakkar, et al.
Journal of Neuromuscular Diseases
|
January 15, 2023
MLIP-Associated Myopathy: A Case Report and Review of the Literature
Fatema Al Amrani, Khalid Al-Thihli, Gayathri Narayanappa, et al.
Intervirology
|
June 29, 2018
Chikungunya Virus Interacts with Heat Shock Cognate 70 Protein to Facilitate Its Entry into Mosquito Cell Line
Ayushman Ghosh, Anita Desai, Vasanthapuram Ravi, et al.
Neurology India
|
March 15, 2017
Young onset Parkinsonism in a patient with familial central core disease
P Samuel Joseph, D M Syam Krishnan, Gayathri Narayanappa, et al.
Disease Models & Mechanisms
|
April 19, 2018
Sporadic amyotrophic lateral sclerosis (SALS) - skeletal muscle response to cerebrospinal fluid from SALS patients in a rat model
Shruthi Shanmukha, Gayathri Narayanappa, Atchayaram Nalini, et al.
Journal of Pediatric Neurosciences
|
May 22, 2020
Myelopathy in Two Brothers with Respiratory Chain Disorder-Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association
Sadanandavalli Retnaswami Chandra, Hansashree Padmanabha, Manisha Gupta, et al.
Journal of Pediatric Neurosciences
|
October 2, 2018
Lipid Storage Myopathy with Ketonuria: A Case of Fatty Acid Oxidation-Related Myopathy and Encephalopathy due to Multiple Acyl-CoA Dehydrogenase Deficiency
Sadanandavalli R Chandra, Rita Christopher, Gayathri Narayanappa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 25, 2004
Clinical features of adult GM1 gangliosidosis: report of three Indian patients and review of 40 cases
Uday Muthane, Yasha Chickabasaviah, Chris Kaneski, et al.
Page
of 4