Risultati della ricerca - Narayanappa Gayathri

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  1. 1
    Infective myositis

    Infective myositis di Narayanappa Gayathri, Bevinahalli N. Nandeesh

    Pubblicazione 2021
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  2. 2
    Infective myositis

    Infective myositis di Narayanappa, Gayathri, Nandeesh, Bevinahalli Nanjegowda

    Pubblicazione 2021
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  3. 3
    Lipid storage myopathy with clinical markers of Marfan syndrome: A rare association

    Lipid storage myopathy with clinical markers of Marfan syndrome: A rare association di Ramakrishnan, Subasree, Narayanappa, Gayathri, Christopher, Rita

    Pubblicazione 2012
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  4. 4
    Coexistence of central nucleus, cores, and rods: Diagnostic relevance

    Coexistence of central nucleus, cores, and rods: Diagnostic relevance di Dhinakaran, Sathiyabama, Kumar, Rashmi Santhosh, Thakkar, Ravindra, Narayanappa, Gayathri

    Pubblicazione 2016
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  5. 5
    Macrophagic Myofasciitis: A Report of Two South Indian Infants

    Macrophagic Myofasciitis: A Report of Two South Indian Infants di Gowda, Vykuntaraju K, Srinivasan, Varunvenkat M, Muthane, Yasha, Narayanappa, Gayathri

    Pubblicazione 2020
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  6. 6
    Sporadic amyotrophic lateral sclerosis (SALS) – skeletal muscle response to cerebrospinal fluid from SALS patients in a rat model

    Sporadic amyotrophic lateral sclerosis (SALS) – skeletal muscle response to cerebrospinal fluid from SALS patients in a rat model di Shanmukha, Shruthi, Narayanappa, Gayathri, Nalini, Atchayaram, Alladi, Phalguni Anand, Raju, Trichur R.

    Pubblicazione 2018
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  7. 7
    Myelopathy in Two Brothers with Respiratory Chain Disorder–Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association

    Myelopathy in Two Brothers with Respiratory Chain Disorder–Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association di Chandra, Sadanandavalli Retnaswami, Padmanabha, Hansashree, Gupta, Manisha, Pruthi, Nupur, Narayanappa, Gayathri, Christopher, Rita

    Pubblicazione 2020
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  8. 8
    Lipid Storage Myopathy with Ketonuria: A Case of Fatty Acid Oxidation–Related Myopathy and Encephalopathy due to Multiple Acyl-CoA Dehydrogenase Deficiency

    Lipid Storage Myopathy with Ketonuria: A Case of Fatty Acid Oxidation–Related Myopathy and Encephalopathy due to Multiple Acyl-CoA Dehydrogenase Deficiency di Chandra, Sadanandavalli R., Christopher, Rita, Narayanappa, Gayathri, Ramanujam, Nitin C., Katragadda, Pavan, Huddar, Akshata, Jha, Shreyashi

    Pubblicazione 2018
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  9. 9
    Clinical, Electrophysiological, Imaging, and Ultrastructural Description in 68 Patients With Neuronal Ceroid Lipofuscinoses and Its Subtypes

    Clinical, Electrophysiological, Imaging, and Ultrastructural Description in 68 Patients With Neuronal Ceroid Lipofuscinoses and Its Subtypes di Rakesh Jadav, Sanjib Sinha, T.C. Yasha, Hanumanthapura R. Aravinda, Narayanappa Gayathri, Shilpa Rao, Parayil Sankaran Bindu, P Satishchandra

    Pubblicazione 2013
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  10. 10
    Utility of Immunohistochemistry and Western Blot in Profiling Clinically Suspected Cases of Congenital Muscular Dystrophy

    Utility of Immunohistochemistry and Western Blot in Profiling Clinically Suspected Cases of Congenital Muscular Dystrophy di Mhatre, Radhika, Sekar, Deepha, Ponmalar, Jessiena, Nagappa, Madhu, Veeramani, Preethish-Kumar, Polavarapu, Kiran, Vengalil, Seena, Atchayaram, Nalini, Narayanappa, Gayathri

    Pubblicazione 2021
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  11. 11
    Neuronal Ceroid Lipofuscinosis: Clinical and Laboratory Profile in Children from Tertiary Care Centre in South India

    Neuronal Ceroid Lipofuscinosis: Clinical and Laboratory Profile in Children from Tertiary Care Centre in South India di Gowda, Vykuntaraju K., Vegda, Hemadri, Sugumar, Kiruthiga, Narayanappa, Gayathri, Srinivasan, Varunvenkat M., Santhoshkumar, Rashmi, Bhat, Maya, Balu, Sam, Naveen, Mohan Rao

    Pubblicazione 2020
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  12. 12
    Mitochondrial Alterations and Oxidative Stress in an Acute Transient Mouse Model of Muscle Degeneration

    Mitochondrial Alterations and Oxidative Stress in an Acute Transient Mouse Model of Muscle Degeneration di Renjini Ramadasan-Nair, Narayanappa Gayathri, Sudha Mishra, B. Sunitha, Rajeswara Babu Mythri, Atchayaram Nalini, Yashwanth Subbannayya, Harsha Gowda, Ullas Kolthur‐Seetharam, M. M. Srinivas Bharath

    Pubblicazione 2013
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  13. 13
    Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex

    Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex di Kapoor, Saketh, Shah, Mohd Hussain, Singh, Nivedita, Rather, Mohammad Iqbal, Bhat, Vishwanath, Gopinath, Sindhura, Bindu, Parayil Sankaran, Taly, Arun B., Sinha, Sanjib, Nagappa, Madhu, Bharath, Rose Dawn, Mahadevan, Anita, Narayanappa, Gayathri, Chickabasaviah, Yasha T., Kumar, Arun

    Pubblicazione 2016
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  14. 14
    Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome

    Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome di Sanjiban Chakrabarty, Periyasamy Govindaraj, Bindu Parayil Sankaran, Madhu Nagappa, Shama Prasada Kabekkodu, Pradyumna Jayaram, Sandeep Mallya, Sekar Deepha, J.N. Jessiena Ponmalar, Hanumanthapura R. Arivinda, Angamuthu K. Meena, Rajan Kumar Jha, Sanjib Sinha, Narayanappa Gayathri, Arun B. Taly, Kumarasamy Thangaraj, Kapaettu Satyamoorthy

    Pubblicazione 2021
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  15. 15
    Neuromuscular disease genetics in under-represented populations: increasing data diversity

    Neuromuscular disease genetics in under-represented populations: increasing data diversity di Lindsay A. Wilson, William L. Macken, Luke Perry, Christopher J. Record, Katherine Schon, Rodrigo Siqueira Soares Frezatti, Sharika Raga, K. Satyam Naidu, Özlem Yayıcı Köken, İpek Polat, Musambo M Kapapa, Natalia Dominik, Stéphanie Efthymiou, Heba Morsy, Melissa Nel, Mahmoud R. Fassad, Fei Gao, Krutik Patel, Maryke Schoonen, Michelle Bisschoff, Armand Vorster, Hallgeir Jonvik, Ronel Human, Elsa Lubbe, Malebo Nonyane, Seena Vengalil, Saraswati Nashi, Kosha Srivastava, Richard J.L.F. Lemmers, Alisha Reyaz, Rinkle Mishra, Ana Töpf, Christina Trainor, Elizabeth Steyn, Amokelani C. Mahungu, Patrick J. van der Vliet, Ahmet Cevdet Ceylan, Semra Hız Kurul, Büşranur Çavdarlı, Cavidan Nur Semerci Gündüz, Gülay Güleç Ceylan, Madhu Nagappa, Karthik Bharadwaj Tallapaka, Periyasamy Govindaraj, Silvère M. van der Maarel, Narayanappa Gayathri, Bevinahalli N. Nandeesh, Somwe Wa Somwe, David Bearden, Michelle Kvalsund, Gita Ramdharry, Yavuz Oktay, Uluç Yiş, Haluk Topaloğlu, Anna Sárközy, Enrico Bugiardini, Franclo Henning, Jo M. Wilmshurst, Jeannine M. Heckmann, Robert McFarland, Robert W. Taylor, Izelle Smuts, Francois H. van der Westhuizen, Cláudia Ferreira da Rosa Sobreira, Pedro José Tomaselli, Wilson Marques, Rohit Bhatia, Ashwin Dalal, M.V. Padma Srivastava, Sireesha Yareeda, Atchayaram Nalini, Venugopalan Y. Vishnu, Kumarasamy Thangaraj, Volker Straub, Rita Horváth, Patrick F. Chinnery, Robert D. S. Pitceathly, Francesco Muntoni, Henry Houlden, Jana Vandrovcová, Mary M. Reilly, Michael G. Hanna

    Pubblicazione 2023
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