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January 30, 2024
Myriad complement defects in atypical hemolytic uremic syndrome and short term outcom...
Srinivasavaradan Govindarajan, Amit Rawat, Jitendra-Kumar Shandilya, et al.
August 09, 2023
Transmission patterns 
Sanghamitra Machhua, Ankur Jindal, Suprit Basu, et al.
June 08, 2023
Title of manuscript : Forme fruste of scleroderma and autoimmune hearing loss in a yo...
Munish Arora, Pallavi Nadig, Sanchi Chawla , et al.
July 16, 2020
Novel SERPING1 gene mutations and clinical experience of type 1 hereditary angioedema...
Ankur Jindal, Amit Rawat, Anit Kaur, et al.
September 11, 2020
Bridging diagnosis of a rare hematological disorder through genetic testing in a youn...
Himanshi Chaudhary, Sanjib Mondal, Ariba Zaidi, et al.
August 23, 2020
Myriad faces of X-linked agammaglobulinemia in a young boy
Murugan Sudhakar, Manpreet Arora, Lesa Dawman, et al.