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1دورية أكاديمية
المؤلفون: Hansashree Padmanabha, Rohan Mahale, Rita Christopher, Gautham Arunachal, Maya Bhat, Mahammad Samim Mondal, Ram Murthy Anjanappa, Ravindranadh Chowdhary Mundlamuri, Ravi Yadav, Seena Vengalil, Pooja Mailankody, Pavagada S Mathuranath, Sadanandavalli R Chandra, Atchayaram Nalini
المصدر: Annals of Indian Academy of Neurology, Vol 24, Iss 6, Pp 908-916 (2021)
مصطلحات موضوعية: hyperhomocysteinemia, metabolic myelopathy spastic paraparesis, mthfr (methylenetetrahydrofolate reductase) gene, remethylation disorders, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
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2
المؤلفون: 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
المصدر: neurogenetics. 23:187-202
مصطلحات موضوعية: Cellular and Molecular Neuroscience, Genetics, Genetics (clinical)
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3
المؤلفون: Saraswati Nashi, Kiran Polavarapu, Mainak Bardhan, Ram Murthy Anjanappa, Veeramani Preethish-Kumar, Seena Vengalil, Hansashree Padmanabha, Thenral S. Geetha, P. V. Prathyusha, Vedam Ramprasad, Aditi Joshi, Tanushree Chawla, Gopikirshnan Unnikrishnan, Pooja Sharma, Akshata Huddar, Bharathram Uppilli, Abel Thomas, Dipti Baskar, Susi Mathew, Deepak Menon, Gautham Arunachal, Mohammed Faruq, Kumarasamy Thangaraj, Atchayaram Nalini
المصدر: Neurogenetics.
مصطلحات موضوعية: Cellular and Molecular Neuroscience, Genetics, Genetics (clinical)
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4
المؤلفون: Veeramani Preethish-Kumar, Atchayaram Nalini, Rita Horvath, Nandeesh Bevinahalli, Ram Murthy Anjanappa, Saraswati Nashi, Mainak Bardhan, Seena Vengalil, Ichizo Nishino, Gautham Arunachal, Divya Nagabushana, Tanushree Chawla, Dhaarini Mohan, Kiran Polavarapu, Leena Shingavi
المصدر: Journal of Human Genetics. 66:813-823
مصطلحات موضوعية: 0301 basic medicine, Pathology, medicine.medical_specialty, Mutation, Muscle biopsy, medicine.diagnostic_test, business.industry, Muscle weakness, 030105 genetics & heredity, medicine.disease_cause, medicine.disease, Phenotype, 03 medical and health sciences, 030104 developmental biology, Genetics, medicine, Congenital muscular dystrophy, Missense mutation, Atypical Rett syndrome, Global developmental delay, medicine.symptom, business, Genetics (clinical)
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5
المؤلفون: 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
المصدر: Neurogenetics. 23(3)
مصطلحات موضوعية: Adult, Young Adult, Adolescent, Child, Preschool, Sarcoglycans, Disease Progression, Prevalence, Sarcoglycanopathies, Humans, Genetic Profile, Middle Aged, Child
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6
المصدر: Circulation. 144
مصطلحات موضوعية: Physiology (medical), Cardiology and Cardiovascular Medicine
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a4c4c30a786294070919fc8dfcf719da
https://doi.org/10.1161/circ.144.suppl_1.10472 -
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المؤلفون: Biju Viswanath, Ram Murthy Anjanappa, Sourav Nayak, Y.C.J. Reddy, Ravi Kumar Nadella, Anuranjan Anand, Vallikiran Manduva, Sanjeev Jain, Nagaraj S. Moily
المصدر: Bipolar Disorders. 22:70-78
مصطلحات موضوعية: Adult, Male, Untranslated region, Bipolar Disorder, Genetic Linkage, Biology, 03 medical and health sciences, 0302 clinical medicine, Chromosome (genetic algorithm), Genetic linkage, Exome Sequencing, medicine, Humans, Bipolar disorder, Allele, Exome, Biological Psychiatry, Exome sequencing, Adaptor Proteins, Signal Transducing, Family Health, Genetics, Haplotype, Membrane Proteins, medicine.disease, Pedigree, 030227 psychiatry, Cytoskeletal Proteins, Psychiatry and Mental health, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 6, Female, 030217 neurology & neurosurgery
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8
المؤلفون: Mainak, Bardhan, Kiran, Polavarapu, Nandeesh N, Bevinahalli, Preethish-Kumar, Veeramani, Ram Murthy, Anjanappa, Gautham, Arunachal, Leena, Shingavi, Seena, Vengalil, Saraswati, Nashi, Tanushree, Chawla, Divya, Nagabushana, Dhaarini, Mohan, Rita, Horvath, Ichizo, Nishino, Nalini, Atchayaram
المصدر: Journal of human genetics. 66(8)
مصطلحات موضوعية: Male, Infant, Muscular Dystrophies, Mitochondria, Phenotype, Child, Preschool, Mutation, Rett Syndrome, Choline Kinase, Humans, Female, Genetic Predisposition to Disease, Genetic Testing, Child, Muscle, Skeletal, Retrospective Studies
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9
المؤلفون: Kiran, Polavarapu, Mainak, Bardhan, Ram Murthy, Anjanappa, Seena, Vengalil, Veeramani, Preethish-Kumar, Leena, Shingavi, Tanushree, Chawla, Saraswati, Nashi, Dhaarini, Mohan, Gautham, Arunachal, Thenral S, Geetha, Vedam, Ramprasad, Atchayaram, Nalini
المصدر: Journal of Clinical Neurology (Seoul, Korea)
مصطلحات موضوعية: myopalladin, muscle, MYPN, cap myopathy, Original Article, nemaline rod myopathy
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::e71657a132931fd22a46eea96e7198ba
https://pubmed.ncbi.nlm.nih.gov/34184449 -
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المؤلفون: Veeramani Preethish Kumar, Kiran Polavarapu, Atchayaram Nalini, Seena Vengalil, Gopikrishnan Unnikrishnan, Saraswati Nashi, Akshata Huddar, Ram Murthy Anjanappa, Mainak Bardhan, Sanita Raju, Gautham Arunachal
المصدر: Journal of the Neurological Sciences. 429:119764
مصطلحات موضوعية: Oncology, medicine.medical_specialty, Neurology, business.industry, Internal medicine, Cohort, medicine, Neurology (clinical), business, Spectrum (topology)