A. Chidambaram

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A rare case of metapneumovirus-induced rhabdomyolysis and multi-organ dysfunction in a 4-year-old child

N. Parameswaran, R. Bhowmick, D. Gunasekaran, 2020, Paediatrics and international child health.

Assessment of neurological sequelae and new‐onset symptoms in the long‐term follow‐up of paediatric Guillain–Barre syndrome: A longitudinal study from India

Kiruthiga Sugumar, D. Gunasekaran, A. Chidambaram, 2022, Journal of paediatrics and child health.

A 5-year-old girl with bony deformities and disproportionate short stature: Answers

S. Krishnamurthy, Pediredla Karunakar, A. Chidambaram, 2021, Pediatric Nephrology.

Nephrocalcinosis in a 3-year-old child with hypocalcemia: Answers

R. Venkatesh Babu, Benjamin M. Sagayaraj, A. Chidambaram, 2022, Pediatric Nephrology.

Etiology, Comorbidities, and Rate of Progression of Pediatric Chronic Kidney Disease: A Cohort Study

S. Parameswaran, S. Krishnamurthy, Kiruthiga Sugumar, 2022, Indian Journal of Pediatrics.

A rare cause of severe hypertension with hypokalemic metabolic alkalosis in a 14-year-old girl: Questions

S. Krishnamurthy, B. Dubashi, S. Kamalanathan, 2020, Pediatric Nephrology.

Severe acute kidney injury in a 3-year-old boy with fever and pleural effusion: Answers

S. Sistla, S. Krishnamurthy, Pediredla Karunakar, 2020, Pediatric Nephrology.

Severe acute kidney injury in a 3-year-old boy with fever and pleural effusion: Questions

S. Sistla, S. Krishnamurthy, Pediredla Karunakar, 2020, Pediatric Nephrology.

Hypokalemic paralysis and discolored teeth in a 12-year-old girl: Answers

S. Krishnamurthy, Pediredla Karunakar, A. Chidambaram, 2021, Pediatric Nephrology.

Paradoxical upgrading reaction following treatment of disseminated tuberculosis-associated haemophagocytic lymphohistiocytosis in an infant without HIV: a case report and review of the literature

Kiruthiga Sugumar, J. Ramamoorthy, T. Selvan, 2022, Paediatrics and international child health.

A novel mutation of adenosine deaminase causing SCID presenting as hemophagocytic lymphohistiocytosis with acute kidney injury

N. Parameswaran, J. Ramamoorthy, A. Chidambaram, 2020, British journal of haematology.

A 5-year-old boy with refractory rickets, polyuria, and hypokalemic metabolic alkalosis: Answers

S. Krishnamurthy, J. Ramamoorthy, D. Gunasekaran, 2020, Pediatric Nephrology.

A 5-year-old boy with refractory rickets, polyuria, and hypokalemic metabolic alkalosis: Questions

S. Krishnamurthy, J. Ramamoorthy, D. Gunasekaran, 2020, Pediatric Nephrology.

MLASA-1: A Rare Cause of Myopathy with Sideroblastic Anemia

Benjamin M. Sagayaraj, A. Chidambaram, K. Vidhyasagar, 2022, Annals of Indian Academy of Neurology.

A child with tetany, convulsions, and nephrocalcinosis: Answers

S. Krishnamurthy, Pediredla Karunakar, A. Chidambaram, 2020, Pediatric Nephrology.

A rare case of severe hypertension with hypokalemic metabolic alkalosis in a 14-year-old girl: Answers

S. Krishnamurthy, B. Dubashi, S. Kamalanathan, 2020, Pediatric Nephrology.

Haematohidrosis in a 12-year-old boy: blood, sweat and tears

C. Delhikumar, Suresh Mekala, N. Parameswaran, 2021, Paediatrics and international child health.

A rare cause of stroke in young children: minor head trauma associated with mineralising lenticulostriate angiopathy in three patients

C. Delhikumar, S. Krishnamurthy, Kiruthiga Sugumar, 2022, Paediatrics and international child health.

Neutrophil-Lymphocyte Ratio for Predicting Coronary Artery Lesions in Children With Kawasaki Disease

J. Ramamoorthy, A. Chidambaram, A. Anantharaj, 2023, Indian Pediatrics.

A Novel Chromosomal Aberration in the Pathogenesis of Transient Leukemia of Down Syndrome

N. Mondal, N. Plakkal, J. Ramamoorthy, 2021, Indian Journal of Pediatrics.

Renal stones in an infant with microcephaly and spastic quadriparesis: Answers

A. Kasinathan, S. Krishnamurthy, Pediredla Karunakar, 2019, Pediatric Nephrology.

Renal stones in an infant with microcephaly and spastic quadriparesis: Questions

A. Kasinathan, S. Krishnamurthy, Pediredla Karunakar, 2019, Pediatric nephrology (Berlin, West).

Pyridoxine Therapy: Not Just the Dose, the Duration Matters Too

A. Kasinathan, T. Selvan, R. Gulati, 2020, Journal of Pediatric Genetics.

Recurrent Skin Ulcers with Facial Dysmorphism and Sinopulmonary Infections: Thinking Beyond Hyper-IgE Syndrome

U. Dutta, Kiruthiga Sugumar, J. Ramamoorthy, 2022, Journal of Pediatric Genetics.

Macrophage Activation Syndrome in a Patient with Prolidase Deficiency: a Rare Genetic Disorder Associated with Elevated IgE and Lupus-Like Syndrome

J. Ramamoorthy, D. Gunasekaran, A. Chidambaram, 2021, Journal of Clinical Immunology.

Dysregulated immune system secondary to novel heterozygous mutation of CIITA gene presenting with recurrent infections and Systemic lupus erythematosus

S. Krishnamurthy, J. Ramamoorthy, Pediredla Karunakar, 2020 .

Anticoagulation strategies for pediatric continuous renal replacement therapy

K. Nallasamy, A. Chidambaram, Ankit Mangla, 2024, Journal of Pediatric Critical Care.