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Pragalatha Kumar

Showing results (1-10 of 6) with videos related to

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International Journal of Trichology|April 30, 2016
Carvajal SyndromeSahana M Srinivas, Pragalatha Kumar, G V Basavaraja
International Journal of Dermatology|February 28, 2024
Lack of association of Stevens-Johnson syndrome/toxic epidermal necrolysis due to aromatic anticonvulsants and HLA-B alleles in South Indian childrenSahana M Srinivas, Vykuntaraju K Gowda, Aruna Gowdra, et al.
Indian Dermatology Online Journal|February 20, 2026
Clinico-Etiological Study of Purpura Fulminans: Experience from a Tertiary-Care Children HospitalShaziya Kalam, Sahana M Srinivas, M L Keshavamurthy, et al.
Journal of Pediatric Genetics|August 22, 2022
A Treatable Cause of Myelopathy: Biotinidase Deficiency Presenting as Acute Flaccid ParalysisVykuntaraju K Gowda, Chetan Kerur, Dhananjaya K Vamyanmane, et al.
Proteomics|January 11, 2024
Identification of a rare [<sup>G</sup>γ(<sup>A</sup>γδβ)<sup>0</sup>] -thalassemia using tandem mass spectrometryAnikha Bellad, Kannan Rangiah, Gajanan Sathe, et al.
Indian Pediatrics|March 12, 2024
Indian Academy of Pediatrics Consensus Statement on Diagnosis and Management of Bone and Joint Infections in ChildrenBhaskar Shenoy, Tanu Singhal, Vijay Yewale, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
International Journal of Trichology|April 30, 2016
Carvajal SyndromeSahana M Srinivas, Pragalatha Kumar, G V Basavaraja
International Journal of Dermatology|February 28, 2024
Lack of association of Stevens-Johnson syndrome/toxic epidermal necrolysis due to aromatic anticonvulsants and HLA-B alleles in South Indian childrenSahana M Srinivas, Vykuntaraju K Gowda, Aruna Gowdra, et al.
Indian Dermatology Online Journal|February 20, 2026
Clinico-Etiological Study of Purpura Fulminans: Experience from a Tertiary-Care Children HospitalShaziya Kalam, Sahana M Srinivas, M L Keshavamurthy, et al.
Journal of Pediatric Genetics|August 22, 2022
A Treatable Cause of Myelopathy: Biotinidase Deficiency Presenting as Acute Flaccid ParalysisVykuntaraju K Gowda, Chetan Kerur, Dhananjaya K Vamyanmane, et al.
Proteomics|January 11, 2024
Identification of a rare [<sup>G</sup>γ(<sup>A</sup>γδβ)<sup>0</sup>] -thalassemia using tandem mass spectrometryAnikha Bellad, Kannan Rangiah, Gajanan Sathe, et al.
Indian Pediatrics|March 12, 2024
Indian Academy of Pediatrics Consensus Statement on Diagnosis and Management of Bone and Joint Infections in ChildrenBhaskar Shenoy, Tanu Singhal, Vijay Yewale, et al.
Pageof 1