Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Anirudh J"'
Autor:
Anirudh J. Shetty, Liza Das, Satyam S. Jayant, Sanjay K. Bhadada, Rajender Kumar, Ajay Gulati, Surinder S. Rana, Harmandeep Singh, Uma N. Saikia, Arunanshu Behera, Bhagwant R. Mittal, Rama Walia, Pinaki Dutta
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 28, Iss 3, Pp 279-288 (2024)
Introduction: Insulinomas are rare, usually sporadic, and typically benign pancreatic neuroendocrine tumours. Pre-operative localization is challenging and evidence on comparative analysis of anatomic and scintigraphic modalities for pre-operative tu
Externí odkaz:
https://doaj.org/article/167c49ac2997487aac89839aacab3e2d
Autor:
Hardik Lalit Siroya, Mohit Juneja, Anirudh J. Rao, Sonal Chauhan, Dhananjaya Ishwar Bhat, Bhagavatula Indira Devi
Publikováno v:
Egyptian Journal of Neurosurgery, Vol 37, Iss 1, Pp 1-9 (2022)
Abstract Background Non-missile impalement spine injuries are quite uncommon. Most of these patients either present with impaling agent in situ or with a part of retained offending agent. Both the scenarios present unique management challenges especi
Externí odkaz:
https://doaj.org/article/e2665df1e6354e4388fed3e658469c91
Autor:
Anirudh J. Ullal, Hong Pham, Rajendra Singh, Peter Ross, Carrie A. Graham, Scott M. Norton, Miriam H. Nuffer, Debbie S. Burns, Allen E. Eckhardt, Maria Escolar, Deeksha Bali, Vamsee K. Pamula
Publikováno v:
Practical Laboratory Medicine, Vol 18, Iss , Pp - (2020)
Background: Decreased galactocerebrosidase (GALC) enzyme activity is causative for Krabbe disease, a lysosomal storage disorder with devastating neurodegenerative consequences. Quantitative fluorimetric assays for GALC activity in isolated blood and
Externí odkaz:
https://doaj.org/article/1864a58aeda24f8caccb00a7e9cd11c2
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 16, Iss 2, Pp 242-245 (2016)
Situs inversus totalis (SIT) is a rare autosomal recessive condition involving the complete lateral transposition of the organs. When individuals with this condition suffer from appendicitis, associated pain and symptoms are usually present on the le
Externí odkaz:
https://doaj.org/article/5e1c2a2650f04c80a9ffac13a6752b79
Autor:
Rajendra Singh, Shaileja Chopra, Carrie Graham, Melissa Langer, Rainer Ng, Anirudh J. Ullal, Vamsee K. Pamula
Publikováno v:
Diagnostics, Vol 10, Iss 5, p 294 (2020)
Interest in newborn screening for mucopolysaccharidoses (MPS) is growing, due in part to ongoing efforts to develop new therapies for these disorders and new screening assays to identify increased risk for the individual MPSs on the basis of deficien
Externí odkaz:
https://doaj.org/article/652f704710e94b98956e40db95c445c8
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 461-464 (2014)
Mucopolysaccharidosis type IVA or Morquio type-A disease is a hereditary lysosomal storage disorder caused by deficient activity of the lysosomal enzyme N-acetylgalactosamine-6-sulfate sulfatase (GALNS). The disease is caused by lysosomal accumulatio
Externí odkaz:
https://doaj.org/article/983ab154efdf41a5b25f3541b1882e80
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 465-467 (2014)
Mucopolysaccharidosis type VI or Maroteaux–Lamy syndrome is an autosomal recessive lysosomal storage disorder caused by deficiency of arylsulfatase B (ARS-B) enzyme activity. It results in mild to severe multi-organ system failure from accumulation
Externí odkaz:
https://doaj.org/article/eb6c36a4b46f4992b28907a701f27fd3
Autor:
Shetty, Anirudh J.1 (AUTHOR), Das, Liza1 (AUTHOR), Jayant, Satyam S.1 (AUTHOR), Bhadada, Sanjay K.1 (AUTHOR), Kumar, Rajender2 (AUTHOR), Gulati, Ajay3 (AUTHOR), Rana, Surinder S.4 (AUTHOR), Singh, Harmandeep2 (AUTHOR), Saikia, Uma N.5 (AUTHOR), Behera, Arunanshu6 (AUTHOR), Mittal, Bhagwant R.1 (AUTHOR), Walia, Rama1 (AUTHOR), Dutta, Pinaki1 (AUTHOR) drpinakidutta12@gmail.com
Publikováno v:
Indian Journal of Endocrinology & Metabolism. May/Jun2024, Vol. 28 Issue 3, p279-288. 10p.
Autor:
Ullal, Anirudh J., Pham, Hong, Singh, Rajendra, Ross, Peter, Graham, Carrie A., Norton, Scott M., Nuffer, Miriam H., Burns, Debbie S., Eckhardt, Allen E., Escolar, Maria, Bali, Deeksha, Pamula, Vamsee K.
Publikováno v:
In Practical Laboratory Medicine January 2020 18
Publikováno v:
Erciyes Medical Journal / Erciyes Tip Dergisi. 2022, Vol. 44 Issue 4, p434-436. 3p.