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International Journal of Trichology
|
April 30, 2016
Carvajal Syndrome
Sahana 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 children
Sahana 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 Hospital
Shaziya 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 Paralysis
Vykuntaraju 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 spectrometry
Anikha 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 Children
Bhaskar Shenoy, Tanu Singhal, Vijay Yewale, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
International Journal of Trichology
|
April 30, 2016
Carvajal Syndrome
Sahana 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 children
Sahana 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 Hospital
Shaziya 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 Paralysis
Vykuntaraju 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 spectrometry
Anikha 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 Children
Bhaskar Shenoy, Tanu Singhal, Vijay Yewale, et al.
Page
of 1