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Mitochondrion|December 23, 2015
Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature agingArumugam Paramasivam, Angamuthu Kannan Meena, Lalitha Pedaparthi, et al.
Acta Cytologica|August 16, 2008
Utility of fine needle aspiration cytology in mediastinal lesions: a clinicopathologic study of 1617 cases from a single institutionDeepa Goel, Aruna K Prayaga, Challa Sundaram, et al.
Journal of Neuro-Oncology|August 27, 2015
Incidence and spectrum of paraneoplastic neurological syndromes: single center studyMeena A Kanikannan, Y Sirisha, Megha S Uppin, et al.
Phytotherapy Research : PTR|December 24, 2005
Protective effect of Spirulina against doxorubicin-induced cardiotoxicityMahmood Khan, Jagdish Chandra Shobha, Iyyapu Krishna Mohan, et al.
Urology Annals|October 26, 2020
Differentiation of renal cell tumors with morphological cocktails using a minimal panel of immunohistochemical markersB Vishal Rao, Tejomayi Regulavalasa, Daphne Fonseca, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 1, 2011
Contribution of muscle biopsy and genetics to the diagnosis of chronic progressive external opthalmoplegia of mitochondrial originChalla Sundaram, A K Meena, Megha S Uppin, et al.
Indian Journal of Surgical Oncology|October 3, 2022
Post-treatment Residual Clinicopathological Outcomes in Testicular Germ Cell TumoursRanjitha Vodigenahalli Nagaraj, B Vishal Rao, Jayakarthik Yoganarsimha, et al.
European Journal of Clinical Investigation|October 10, 2013
Distinct genetic aberrations in oesophageal adeno and squamous carcinomaRamaswamy Pandilla, Viswakalyan Kotapalli, Swarnalata Gowrishankar, et al.
Urology Annals|February 24, 2022
The core four - A panel of immunohistochemistry markers to diagnose and subtype testicular germ cell tumorsV N Ranjitha, Rashmi Khemani, B Vishal Rao, et al.
Investigative Ophthalmology & Visual Science|May 16, 2013
Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in IndiaNahid Akhtar Khan, Periyasamy Govindaraj, Nagasamy Soumittra, et al.
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