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Indian Journal of Pathology & Microbiology|April 14, 2021
Estimation of plasma and RBC acetylcholinesterase in children: An evaluation tool for Hirschsprung's disease?Neha Kuvelkar, Serena DSouza, K Vidhyashree, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
Floating-Harbor syndrome and polycystic kidneys associated with SRCAP mutationMichael Reschen, Usha Kini, Rebecca L Hood, et al.
Biomechanics and Modeling in Mechanobiology|May 22, 2026
Lumped parameter modeling of changes in liver hemodynamics due to cirrhosisEdith Luveina Joseph, Himanshi Saini, Usha Kini, et al.
Pediatric Surgery International|August 17, 2013
Skip segment Hirschsprung's disease: a case report and novel management techniqueB V Raghunath, Gowri Shankar, M Narendra Babu, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Etiological heterogeneity and clinical characteristics of metopic synostosis: Evidence from a tertiary craniofacial unitUsha Kini, Jane A Hurst, Jo C Byren, et al.
Journal of Pathology and Translational Medicine|July 16, 2025
What's new in medical renal pathology 2025: Updates on podocytopathy and immunofluorescence staining in medical kidneyAstrid Weins, Ibrahim Batal, Paola Romagnani, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 6, 2021
Diffuse C4d staining of peritubular capillaries in renal allograft following bamlanivimab therapyNattawat Klomjit, Mireille El Ters, Benjamin A Adam, et al.
Kidney International Reports|October 11, 2021
COVID-19 Vaccination and GlomerulonephritisNattawat Klomjit, Mariam Priya Alexander, Fernando C Fervenza, et al.
Clinical Case Reports|October 21, 2016
Activation of an exonic splice-donor site in exon 30 of CDK5RAP2 in a patient with severe microcephaly and pigmentary abnormalitiesAlistair T Pagnamenta, Malcolm F Howard, Samantha J L Knight, et al.
Human Mutation|March 25, 2018
A homozygous variant disrupting the PIGH start-codon is associated with developmental delay, epilepsy, and microcephalyAlistair T Pagnamenta, Yoshiko Murakami, Consuelo Anzilotti, et al.
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