Genotype-phenotype spectrum of 130 unrelated Indian families with Mucopolysaccharidosis type II
Agrawal, Neha, Verma, Gaurav, Saxena, Deepti, Kabra, Madhulika, Gupta, Neerja, Mandal, Kausik, Moirangthem, Amita, Sheth, Jayesh, Puri, Ratna Dua, Bijarnia-Mahay, Sunita, Kapoor, Seema, Danda, Sumita, H, Sankar V., Datar, Chaitanya A., Ranganath, Prajnya, Shukla, Anju, Dalal, Ashwin, Srivastava, Priyanka, Devi, Radha Rama, Phadke, Shubha R.
Published in European journal of medical genetics (01.03.2022)
Published in European journal of medical genetics (01.03.2022)
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Identification and characterization of 20 novel pathogenic variants in 60 unrelated Indian patients with mucopolysaccharidoses type I and type II
Uttarilli, A., Ranganath, P., Matta, D., Md Nurul Jain, J., Prasad, K., Babu, A.S., Girisha, K.M., Verma, I.C., Phadke, S.R., Mandal, K., Puri, R.D., Aggarwal, S., Danda, S., Sankar, V.H., Kapoor, S., Bhat, M., Gowrishankar, K., Hasan, A.Q., Nair, M., Nampoothiri, S., Dalal, A.
Published in Clinical genetics (01.12.2016)
Published in Clinical genetics (01.12.2016)
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GALNS mutations in Indian patients with mucopolysaccharidosis IVA
Bidchol, Abdul Mueed, Dalal, Ashwin, Shah, Hitesh, S, Suryanarayana, Nampoothiri, Sheela, Kabra, Madhulika, Gupta, Neerja, Danda, Sumita, Gowrishankar, Kalpana, Phadke, Shubha R., Kapoor, Seema, Kamate, Mahesh, Verma, I.C., Puri, Ratna Dua, Sankar, V.H., Devi, A. Radha Rama, Patil, S.J., Ranganath, Prajnya, Jain, S. Jamal Md Nurul, Agarwal, Meenal, Singh, Ankur, Mishra, Pallavi, Tamhankar, Parag M., Gopinath, Puthiya Mundyat, Nagarajaram, H.A., Satyamoorthy, Kapaettu, Girisha, Katta Mohan
Published in American journal of medical genetics. Part A (01.11.2014)
Published in American journal of medical genetics. Part A (01.11.2014)
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Partial Androgen Insensitivity Syndrome: Incidentally Diagnosed in an Adolescent
Aparna, A. J., Riaz, I., Sankar, V H, Krishnannair, Devakumar Vasanthiamma
Published in Indian Pediatrics Case Reports (01.10.2023)
Published in Indian Pediatrics Case Reports (01.10.2023)
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Journal Article
Identification and characterization of 30 novel pathogenic variations in 69 unrelated Indian patients with Mucolipidosis Type II and Type III
Pasumarthi, Divya, Gupta, Neerja, Sheth, Jayesh, Jain, S. Jamal Md Nurul, Rungsung, Ikrormi, Kabra, Madhulika, Ranganath, Prajnya, Aggarwal, Shagun, Phadke, Shubha R, Girisha, Katta M., Shukla, Anju, Datar, Chaitanya, Verma, Ishwar C., Puri, Ratna Dua, Bhavsar, Riddhi, Mistry, Mehul, Sankar, V. H., Gowrishankar, Kalpana, Agrawal, Divya, Nair, Mohandas, Danda, Sumita, Soni, Jai Prakash, Dalal, Ashwin
Published in Journal of human genetics (01.11.2020)
Published in Journal of human genetics (01.11.2020)
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Recurrent and novel GLB1 mutations in India
Bidchol, Abdul Mueed, Dalal, Ashwin, Trivedi, Rakesh, Shukla, Anju, Nampoothiri, Sheela, Sankar, V.H., Danda, Sumita, Gupta, Neerja, Kabra, Madhulika, Hebbar, Shrikiran A., Bhat, Ramesh Y., Matta, Divya, Ekbote, Alka V., Puri, Ratna Dua, Phadke, Shubha R., Gowrishankar, Kalpana, Aggarwal, Shagun, Ranganath, Prajnya, Sharda, Sheetal, Kamate, Mahesh, Datar, Chaitanya A., Bhat, Kamalakshi, Kamath, Nutan, Shah, Hitesh, Krishna, Shuba, Gopinath, Puthiya Mundyat, Verma, Ishwar C., Nagarajaram, H.A., Satyamoorthy, Kapaettu, Girisha, Katta Mohan
Published in Gene (10.08.2015)
Published in Gene (10.08.2015)
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Comparing the Clinical Spectrum of Paediatric In-patients in pre-COVID-19, during COVID19 and post-COVID-19 Pandemic Periods in a Tertiary Level Teaching Centre
Anand, Veena, Vinitha, AO, Joseph, Susy, Sankar, VH, Yadev, IP
Published in Journal of clinical and diagnostic research (2024)
Published in Journal of clinical and diagnostic research (2024)
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Urorectal septum malformation presenting as nonimmune hydrops fetalis
Mandakini, Pradhan, Ashwin, Dalal, Manisha, R., Sankar, V. H., Niraj, Kumari, Narendra, Krishnani, Janak, Kishore
Published in Prenatal diagnosis (01.06.2006)
Published in Prenatal diagnosis (01.06.2006)
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Prenatal diagnosis in India is not limited to sex selection
Dalal, Ashwin B., Ranganath, Prajnya, Phadke, Shubha R., Kabra, Madhulika, Danda, Sumita, Puri, Ratna Dua, V.H., Sankar, Gupta, Neerja, Patil, S.J., Mandal, Kausik, Tamhankar, Parag, Aggarwal, Shagun, Agarwal, Meenal
Published in Genetics in medicine (01.01.2015)
Published in Genetics in medicine (01.01.2015)
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T1 and M1 polymorphism in glutathione S-transferase gene and coronary artery disease in North Indian population
Girisha, K M, Gilmour, A, Mastana, S, Singh, V P, Sinha, N, Tewari, S, Ramesh, V, Sankar, V H, Agrawal, S
Published in Indian journal of medical sciences (01.12.2004)
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Published in Indian journal of medical sciences (01.12.2004)
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Prevalence of exon 7/exon 8 deletion in patients with hypotonia and spinal muscular atrophy
Published in Indian journal of experimental biology
(01.10.2024)
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A hospital based comparative study of the first and second waves of Covid-19 related multi-system inflammatory syndrome in children
Sasidharan, Bindusha, Sugunan, Sheeja, Monica, K., Chinchilu, R. V., Niyas, H. R., Sankar, V. H.
Published in Sri Lanka journal of child health (05.09.2022)
Published in Sri Lanka journal of child health (05.09.2022)
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