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Clinical Dysmorphology|May 29, 2000
Autosomal dominant ectrodactyly with sensorineural deafnessP Mishra, M Muranjan, B A BharuchaJournal of Tropical Pediatrics|October 30, 2004
Study of infant feeding practices: factors associated with faulty feedingChintan Parekh, S B Bavdekar, V ShaharaoThe Journal of Biological Chemistry|March 28, 1998
Characterization of the human serum trypanosome toxin, haptoglobin-related proteinM Muranjan, V Nussenzweig, S TomlinsonJournal of Postgraduate Medicine|January 10, 2024
Impact of COVID-19 pandemic on healthcare delivery for lysosomal storage disorders at a tertiary care public hospital in MumbaiM Muranjan, S Karande, S RajoriaCurrent Biology : CB|May 26, 1999
Receptor protein tyrosine phosphatase alpha activates Src-family kinases and controls integrin-mediated responses in fibroblastsJ Su, M Muranjan, J SapJournal of Postgraduate Medicine|March 16, 2026
Economic burden of Duchenne muscular dystrophy from a societal perspective in Mumbai, IndiaS Antony, M Muranjan, N J GogtayThe Journal of Biological Chemistry|February 25, 1990
Analysis of glucagon-receptor interactions on isolated canine hepatocytes. Formation of reversibly and irreversibly cell-associated hormoneD B Bharucha, H S TagerJournal of Postgraduate Medicine|February 2, 2018
Childhood cerebral X-linked adrenoleukodystrophy with atypical neuroimaging abnormalities and a novel mutationM Muranjan, S Karande, S Sankhe, et al.Journal of Postgraduate Medicine|April 21, 2023
Porphyrias: Uncommon disorders masquerading as common childhood diseasesA Chakraborty, M Muranjan, S Karande, et al.Journal of Postgraduate Medicine|March 9, 2017
Rare disease heralded by pulmonary manifestations: Avoiding pitfalls of an "asthma" labelS Bajaj, M Muranjan, S Karande, et al.Pageof 129