Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ankur K, Jindal"'
Autor:
Alex Fonollosa, Ester Carreño, Antonio Vitale, Ankur K. Jindal, Athimalaipet V. Ramanan, Laura Pelegrín, Borja Santos-Zorrozua, Verónica Gómez-Caverzaschi, Luca Cantarini, Claudia Fabiani, José Hernández-Rodríguez
Publikováno v:
Frontiers in Ophthalmology, Vol 4 (2024)
Autoinflammatory diseases include disorders with a genetic cause and also complex syndromes associated to polygenic or multifactorial factors. Eye involvement is present in many of them, with different extent and severity. The present review covers o
Externí odkaz:
https://doaj.org/article/c283f09795a145e8887ed850a2ce3783
Autor:
Divya Ilanchoorian, J S Thakur, Rajesh Vijayvergiya, Ankur K Jindal, Aravind Gandhi, Vivek Sagar
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 12, Iss 12, Pp 3254-3261 (2023)
Background: Rheumatic heart disease/Rheumatic fever is a non – communicable disease being a major neglected health problem. Recurrent attacks of rheumatic fever can have catastrophic outcomes, therefore regular administration of antibiotics is reco
Externí odkaz:
https://doaj.org/article/a3e4fdc247d942558d20f2473bd6a31f
Autor:
Pratap K Patra, Aaqib Z Banday, Ankur K Jindal, Dharmagat Bhattarai, Nilamani Patra, Uma N Saikia, Anju Gupta, Deepti Suri
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 11, Iss 6, Pp 3280-3286 (2022)
Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome after the use of first-line antitubercular drugs (ATDs) is rare and literature regarding DRESS syndrome due to ATDs is scarce in children. We report a young boy with tuberculosis
Externí odkaz:
https://doaj.org/article/b1e1198a99514220abc522ad9a6d0167
Publikováno v:
Genes and Diseases, Vol 7, Iss 1, Pp 12-25 (2020)
Primary immunodeficiency diseases (PIDs) refer to a heterogenous group of disorders characterized clinically by increased susceptibility to infections, autoimmunity and increased risk of malignancies.These group of disorders present with clinical man
Externí odkaz:
https://doaj.org/article/1404df1786c74864a614d05a82e96bd7
Publikováno v:
Indian Dermatology Online Journal, Vol 11, Iss 1, Pp 94-98 (2020)
There is a common belief among the laity and even physicians that sun exposure is a useful source of vitamin D. However, despite the fact that sun exposure occurs almost throughout the year in India, vitamin D deficiency is widely prevalent. Although
Externí odkaz:
https://doaj.org/article/307063b97e114827940665419cbec1b0
Autor:
Deepti Suri, Rashmi Rikhi, Ankur K. Jindal, Amit Rawat, Murugan Sudhakar, Pandiarajan Vignesh, Anju Gupta, Anit Kaur, Jyoti Sharma, Jasmina Ahluwalia, Prateek Bhatia, Alka Khadwal, Revathi Raj, Ramya Uppuluri, Mukesh Desai, Prasad Taur, Ambreen A. Pandrowala, Vijaya Gowri, Manisha R. Madkaikar, Harsha Prasada Lashkari, Sagar Bhattad, Harish Kumar, Sanjeev Verma, Kohsuke Imai, Shigeaki Nonoyama, Osamu Ohara, Koon W. Chan, Pamela P. Lee, Yu Lung Lau, Surjit Singh
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundWiskott Aldrich syndrome (WAS) is characterized by bleeding manifestations, recurrent infections, eczema, autoimmunity, and malignancy. Over the last decade, improved awareness and better in-house diagnostic facilities at several centers in
Externí odkaz:
https://doaj.org/article/40f9e91155324dac9955f31d9057e303
Publikováno v:
Indian Dermatology Online Journal, Vol 8, Iss 6, Pp 391-405 (2017)
Primary immunodeficiency disorders (PIDs) are a group of disorders affecting the capability to fight against infection. These include defects in T cells and B cells affecting cell-mediated and humoral immunity, respectively, combined humoral and cell
Externí odkaz:
https://doaj.org/article/5c0ccccf1c964572b19145cbd275fb0c
Publikováno v:
Pediatric and Developmental Pathology. 25:345-350
Wiskott-Aldrich Syndrome (WAS) is an inherited disorder characterized by the classical triad of eczema, micro-thrombocytopenia, and immune deficiency. This disease affects the hematopoietic cells to a variable extent. The spectrum of clinical and lab
Publikováno v:
Journal of paediatrics and child health. 54(11)