Suchergebnisse - Narayanappa Gayathri
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Infective myositis von Narayanappa Gayathri, Bevinahalli N. Nandeesh
Veröffentlicht 2021Revisão -
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Infective myositis von Narayanappa, Gayathri, Nandeesh, Bevinahalli Nanjegowda
Veröffentlicht 2021Text -
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Myelopathy in Two Brothers with Respiratory Chain Disorder–Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association von Chandra, Sadanandavalli Retnaswami, Padmanabha, Hansashree, Gupta, Manisha, Pruthi, Nupur, Narayanappa, Gayathri, Christopher, Rita
Veröffentlicht 2020Text -
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Lipid Storage Myopathy with Ketonuria: A Case of Fatty Acid Oxidation–Related Myopathy and Encephalopathy due to Multiple Acyl-CoA Dehydrogenase Deficiency von Chandra, Sadanandavalli R., Christopher, Rita, Narayanappa, Gayathri, Ramanujam, Nitin C., Katragadda, Pavan, Huddar, Akshata, Jha, Shreyashi
Veröffentlicht 2018Text -
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Clinical, Electrophysiological, Imaging, and Ultrastructural Description in 68 Patients With Neuronal Ceroid Lipofuscinoses and Its Subtypes von Rakesh Jadav, Sanjib Sinha, T.C. Yasha, Hanumanthapura R. Aravinda, Narayanappa Gayathri, Shilpa Rao, Parayil Sankaran Bindu, P Satishchandra
Veröffentlicht 2013Artigo -
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Utility of Immunohistochemistry and Western Blot in Profiling Clinically Suspected Cases of Congenital Muscular Dystrophy von Mhatre, Radhika, Sekar, Deepha, Ponmalar, Jessiena, Nagappa, Madhu, Veeramani, Preethish-Kumar, Polavarapu, Kiran, Vengalil, Seena, Atchayaram, Nalini, Narayanappa, Gayathri
Veröffentlicht 2021Text -
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Neuronal Ceroid Lipofuscinosis: Clinical and Laboratory Profile in Children from Tertiary Care Centre in South India von Gowda, Vykuntaraju K., Vegda, Hemadri, Sugumar, Kiruthiga, Narayanappa, Gayathri, Srinivasan, Varunvenkat M., Santhoshkumar, Rashmi, Bhat, Maya, Balu, Sam, Naveen, Mohan Rao
Veröffentlicht 2020Text -
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Mitochondrial Alterations and Oxidative Stress in an Acute Transient Mouse Model of Muscle Degeneration von 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
Veröffentlicht 2013Artigo -
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Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex von 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
Veröffentlicht 2016Text -
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Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome von 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
Veröffentlicht 2021Artigo -
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Neuromuscular disease genetics in under-represented populations: increasing data diversity von 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
Veröffentlicht 2023Artigo
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Ähnliche Schlagworte
Medicine
Pathology
Biology
Disease
Gene
Genetics
Atrophy
Biochemistry
Bioinformatics
Cell biology
Chemistry
Computer science
Degeneration (medical)
Dermatology
Encephalopathy
Genetic testing
Internal medicine
Lactic acidosis
Lipofuscin
MELAS syndrome
Medical genetics
Mitochondrial DNA
Mitochondrial disease
Mitochondrial myopathy
Mitochondrion
Myoclonus
Myositis
Neurology
Neuromuscular disease
Neuronal ceroid lipofuscinosis