PMM2-CDG T237M Mutation in a Patient with Cerebral Palsy-Like Phenotypes Reported from South India by N. Sreedevi, N. Swapna, Santosh Maruthy, H.S. Meghavathi, Charles Sylvester

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Association of apolipoprotein ε4 allele with intellectual disability in children with cerebral palsy by N Sreedevi, N Swapna, Santosh Maruthy, Rajesh Kundapur, Charles Sylvester

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Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive [version 1; referees: 2 approve... by Desaraju Suresh Bhargav, N. Sreedevi, N. Swapna, Soumya Vivek, Srinivas Kovvali

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Association of Serum Cyclophilin A Levels with Severity of Coronary Artery Disease by Namilakonda Manaswini, Neelam N. Sreedevi, Sabitha Thummala, Kompella S.S. Saibaba, Noorjahan Mohammed, Oruganti Sai Satish

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Evaluation of serum cysteine-rich angiogenic inducer 61 for peripheral arterial disease in patients with type 2 diabetes mellitus by Nabila Rahman, Siraj Ahmed Khan, Sandeep Mahapatra, M Vijaya Bhaskar, K S. S. Sai Baba, M Noorjahan, N Sreedevi

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Evaluation of Galectin-3 as a Novel Diagnostic Biomarker in Patients with Heart Failure with Preserved Ejection Fraction by Jyothirmayi Kanukurti, Noorjahan Mohammed, N. N. Sreedevi, Siraj Ahmed Khan, K.S.S. Sai Baba, M. Vijaya Bhaskar, O. Sai Satish, Shaik Mohammad Naushad, Iyyapu Krishna Mohan

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