Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome von Govindaraj, Geeta Madathil, Jain, Abhinav, Peethambaran, Geetha, Bhoyar, Rahul C, Vellarikkal, Shamsudheen Karuthedath, Ganapati, Arvind, Sandhya, Pulukool, Edavazhippurath, Athulya, Dhanasooraj, Dhananjayan, Puthenpurayil, Jayakrishnan Machinary, Chakkiyar, Krishnan, Mishra, Anushree, Batra, Arushi, Punnen, Anu, Kumar, Sathish, Sivasubbu, Sridhar, Scaria, Vinod

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Factors contributing to the non-identification of bacterial meningitis in febrile infants: A case series study von Chakkiyar, Krishnan, Sabeel Abdulla, PR, Fiji, MD, Vinod Kumar, MS, Jayakrishnan, MP

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Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency [version 2; peer review: 2 approved, 1... von Govindaraj, Geeta Madathil, Karuthedath Vellarikkal, Shamsudheen, Jayarajan, Rijith, Ravi, Rowmika, Verma, Ankit, Chakkiyar, Krishnan, Jayakrishnan, Machinari Puthenpurayil, Arakkal, Riyaz, Raj, Revathi, Kunnaruvath, Rajeevan, Sivasubbu, Sridhar, Scaria, Vinod

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Pseudotumour cerebri due to phenytoin in a child von Sasidharan Pillai, Sabitha, Riyaz, Arakkal, Krishnan, Chakkiyar, Gireesh, Sankaran Nair

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The changing profile of neonatal pathogens and susceptibility pattern: prospective observational study from a tertiary center in South India von Chakkiyar, Krishnan, Kuzhiyil, Gireeshan Veluthedath, Sudhakaran, Maya, Mohammed, Shameem Anathan, Faisal, Nabeel Valappil, Nair, Mohandas

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Spectrum of clinical features and genetic variants in mevalonate kinase von Govindaraj, Geeta Madathil, Jain, Abhinav, Peethambaran, Geetha, Bhoyar, Rahul C, Vellarikkal, Shamsudheen Karuthedath, Ganapati, Arvind, Sandhya, Pulukool, Edavazhippurath, Athulya, Dhanasooraj, Dhananjayan, Puthenpurayil, Jayakrishnan Machinary, Chakkiyar, Krishnan, Mishra, Anushree, Batra, Arushi, Punnen, Anu, Kumar, Sathish, Sivasubbu, Sridhar, Scaria, Vinod

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Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency von Govindaraj, Geeta Madathil, Karuthedath Vellarikkal, Shamsudheen, Jayarajan, Rijith, Ravi, Rowmika, Verma, Ankit, Chakkiyar, Krishnan, Jayakrishnan, Machinari Puthenpurayil, Arakkal, Riyaz, Raj, Revathi, Sivasubbu, Sridhar, Scaria, Vinod

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Pseudotumour cerebri due to phenytoin in a child von Sasidharan Pillai, Sabitha, Riyaz, Arakkal, Krishnan, Chakkiyar, Gireesh, Sankaran Nair

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