Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Edavazhippurath A"'
Autor:
Madathil Govindaraj, Geeta, Jain, Abhinav, Edavazhippurath, Athulya, Bhoyar, Rahul C., Dhanasooraj, Dhananjayan, Mishra, Anushree, Gupta, Vishu, Nair, Mohandas, Shiny, P.M., Uppuluri, Ramya, Kumar, Anoop, Kashyap, Atul, Ajith Kumar, V.T., Shankaran, Gireesh, Senthivel, Vigneshwar, Imran, Mohamed, Kumar Divakar, Mohit, Sawant, Sneha, Dalvi, Aparna, Madkaikar, Manisha, Raj, Revathi, Sivasubbu, Sridhar, Scaria, Vinod
Publikováno v:
In Human Immunology April 2022 83(4):335-345
Autor:
Madhu Chhanda Mohanty, Mukesh Desai, Ahmad Mohammad, Amita Aggarwal, Geeta Govindaraj, Sagar Bhattad, Harsha Prasada Lashkari, Liza Rajasekhar, Harish Verma, Arun Kumar, Unnati Sawant, Swapnil Yashwant Varose, Prasad Taur, Reetika Malik Yadav, Manogat Tatkare, Mevis Fernandes, Umair Bargir, Sanjukta Majumdar, Athulya Edavazhippurath, Jyoti Rangarajan, Ramesh Manthri, Manisha Ranjan Madkaikar
Publikováno v:
Vaccines, Vol 11, Iss 7, p 1211 (2023)
The emergence of vaccine-derived polioviruses (VDPVs) in patients with Primary Immunodeficiency (PID) is a threat to the polio-eradication program. In a first of its kind pilot study for successful screening and identification of VDPV excretion among
Externí odkaz:
https://doaj.org/article/9e7015778aa347ddb270543ed528e298
Autor:
Abhinav Jain, Geeta Madathil Govindaraj, Athulya Edavazhippurath, Nabeel Faisal, Rahul C Bhoyar, Vishu Gupta, Ramya Uppuluri, Shiny Padinjare Manakkad, Atul Kashyap, Anoop Kumar, Mohit Kumar Divakar, Mohamed Imran, Sneha Sawant, Aparna Dalvi, Krishnan Chakyar, Manisha Madkaikar, Revathi Raj, Sridhar Sivasubbu, Vinod Scaria
Publikováno v:
PLoS ONE, Vol 16, Iss 7, p e0254407 (2021)
X-linked agammaglobulinemia (XLA, OMIM #300755) is a primary immunodeficiency disorder caused by pathogenic variations in the BTK gene, characterized by failure of development and maturation of B lymphocytes. The estimated prevalence worldwide is 1 i
Externí odkaz:
https://doaj.org/article/b260bd1f9264470b8851b4de048cbdfb
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
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
Autor:
Madkaikar, Madhu Chhanda Mohanty, Mukesh Desai, Ahmad Mohammad, Amita Aggarwal, Geeta Govindaraj, Sagar Bhattad, Harsha Prasada Lashkari, Liza Rajasekhar, Harish Verma, Arun Kumar, Unnati Sawant, Swapnil Yashwant Varose, Prasad Taur, Reetika Malik Yadav, Manogat Tatkare, Mevis Fernandes, Umair Bargir, Sanjukta Majumdar, Athulya Edavazhippurath, Jyoti Rangarajan, Ramesh Manthri, Manisha Ranjan
Publikováno v:
Vaccines; Volume 11; Issue 7; Pages: 1211
The emergence of vaccine-derived polioviruses (VDPVs) in patients with Primary Immunodeficiency (PID) is a threat to the polio-eradication program. In a first of its kind pilot study for successful screening and identification of VDPV excretion among
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::d6c2deecb97f6e4cb281b8c85540f044
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Geeta Madathil Govindaraj, Abhinav Jain, Athulya Edavazhippurath, Rahul C. Bhoyar, Dhananjayan Dhanasooraj, Anushree Mishra, Vishu Gupta, Mohandas Nair, P.M. Shiny, Ramya Uppuluri, Anoop Kumar, Atul Kashyap, V.T. Ajith Kumar, Gireesh Shankaran, Vigneshwar Senthivel, Mohamed Imran, Mohit Kumar Divakar, Sneha Sawant, Aparna Dalvi, Manisha Madkaikar, Revathi Raj, Sridhar Sivasubbu, Vinod Scaria
Publikováno v:
Human Immunology. 83:335-345
X-linked agammaglobulinemia (XLA) is an X-linked recessive primary immunodeficiency disorder caused due to a pathogenic variant in the Bruton tyrosine (BTK) gene with an incidence of 1:379,000 live births and 1:190,000 male births. Patients affected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d1e6b2574223353e39c95738e9a14ea
https://doi.org/10.1016/j.humimm.2022.01.003
https://doi.org/10.1016/j.humimm.2022.01.003
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Mohammed Manakkattu Thekke Peedikayil, Vinod Scaria, Abhinav Jain, Fiji Madona Devassikutty, Athulya Edavazhippurath, Michael Chittettu Joseph, Geeta Madathil Govindaraj, Pulukool Sandhya
Publikováno v:
Pediatr Allergy Immunol Pulmonol
Introduction: The Centers for Disease Control and Prevention (CDC) has listed primary immunodeficiency disorders as being predisposed to severe coronavirus disease 2019 (COVID-19). However, patients affected with X-linked agammaglobulinemia (XLA) hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f934c21ec71e1e3cce3392d158f253fe
https://pubmed.ncbi.nlm.nih.gov/34495748
https://pubmed.ncbi.nlm.nih.gov/34495748