Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jayakrishnan Machinary Puthenpurayil"'
Autor:
Madhu Chhanda Mohanty, Geeta Govindaraj, Mohammad Ahmad, Swapnil Y. Varose, Manogat Tatkare, Anita Shete, Savita Yadav, Yash Joshi, Pragya Yadav, Deepa Sharma, Arun Kumar, Harish Verma, Ankita P. Patil, Athulya Edavazhipurath, Dhananjayan Dhanasooraj, Sheena Othayoth Kandy, Jayakrishnan Machinary Puthenpurayil, Krishnan Chakyar, Kesavan Melarcode Ramanan, Manisha Madkaikar
Publikováno v:
Vaccines, Vol 12, Iss 7, p 759 (2024)
In order to maintain the polio eradication status, it has become evident that the surveillance of cases with acute flaccid paralysis and of environmental samples must be urgently supplemented with the surveillance of poliovirus excretions among indiv
Externí odkaz:
https://doaj.org/article/69554fab84c54428875bb73f1304ecc0
Autor:
Geeta Madathil Govindaraj, Abhinav Jain, Geetha Peethambaran, Rahul C Bhoyar, Shamsudheen Karuthedath Vellarikkal, Arvind Ganapati, Pulukool Sandhya, Athulya Edavazhippurath, Dhananjayan Dhanasooraj, Jayakrishnan Machinary Puthenpurayil, Krishnan Chakkiyar, Anushree Mishra, Arushi Batra, Anu Punnen, Sathish Kumar, Sridhar Sivasubbu, Vinod Scaria
Publikováno v:
PLoS ONE, Vol 15, Iss 8, p e0237999 (2020)
Hyper-IgD syndrome (HIDS, OMIM #260920) is a rare autosomal recessive autoinflammatory disorder caused by pathogenic variants in the mevalonate kinase (MVK) gene. HIDS has an incidence of 1:50,000 to 1:5,000, and is thought to be prevalent mainly in
Externí odkaz:
https://doaj.org/article/c8d44fc2ca07459f8f9d973e715de066
Autor:
Shamsudheen Karuthedath Vellarikkal, Sridhar Sivasubbu, Athulya Edavazhippurath, Arushi Batra, Dhananjayan Dhanasooraj, Abhinav Jain, Rahul C. Bhoyar, Arvind Ganapati, Geetha Peethambaran, Jayakrishnan Machinary Puthenpurayil, Anu Punnen, Geeta Madathil Govindaraj, Sathish Kumar, Pulukool Sandhya, Anushree Mishra, Krishnan Chakkiyar, Vinod Scaria
Publikováno v:
PLoS ONE, Vol 15, Iss 8, p e0237999 (2020)
PLoS ONE
PLoS ONE
Hyper-IgD syndrome (HIDS, OMIM #260920) is a rare autosomal recessive autoinflammatory disorder caused by pathogenic variants in the mevalonate kinase (MVK) gene. HIDS has an incidence of 1:50,000 to 1:5,000, and is thought to be prevalent mainly in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff6b82d0f3f3081e5e83a1a7eea0908c
https://doaj.org/article/c8d44fc2ca07459f8f9d973e715de066
https://doaj.org/article/c8d44fc2ca07459f8f9d973e715de066
Akademický článek
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Autor:
Jayakrishnan, Machinary Puthenpurayil1, Krishnakumar, Padinharath1 krikurp@gmail.com, Geeta, Madathil Govindaraj1, George, Biju1
Publikováno v:
Indian Journal of Community Medicine. Apr-Jun2021, Vol. 46 Issue 2, p350-351. 2p.
Akademický článek
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