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Megalencephaly-capillary malformation syndrome: a report of two cases

Sri Lanka journal of child health, 2020-09, Vol.49 (3), p.284

2020

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Clinical profile and role of serology in pediatric acute febrile illness: Experience from a tertiary care hospital in South India

Clinical epidemiology and global health, 2021-10, Vol.12, p.100898, Article 100898

2021

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Multilocus disease-causing genomic variations for Mendelian disorders: role of systematic phenotyping and implications on genetic counselling

European journal of human genetics : EJHG, 2021-12, Vol.29 (12), p.1774-1780

2021

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Refractory microcytic hypochromic anemia with type I diabetes mellitus and reversible cardiac hemochromatosis in congenital hypotransferrinemia

Pediatric hematology oncology journal, 2024-03, Vol.9 (1), p.37-39

2024

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Hemolytic uremic syndrome in children: Clinical characteristics and predictors of outcome

Clinical epidemiology and global health, 2024-09, Vol.29, p.101715, Article 101715

2024

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Primary chylous ascites in children: Rare cause of a common presentation

Sri Lanka journal of child health, 2019-12, Vol.48 (4), p.359

2019

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Waldmann's Disease (Primary Intestinal Lymphangiectasia) with Atrial Septal Defect

Journal of clinical and diagnostic research, 2017-04, Vol.11 (4), p.SD03-SD04

2017

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Interleukin-6 versus C-reactive Protein as Markers for Early Detection of Bacteremia in Febrile Neutropenia in Pediatric Population

Indian journal of medical and paediatric oncology, 2020-09, Vol.41 (5), p.702-706

2020

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Guillain-barré syndrome: a clinical study of twenty children

Journal of clinical and diagnostic research, 2015-01, Vol.9 (1), p.SC09-SC12

2015

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Colonic Arteriovenous Malformation in a Child with Klippel Trenaunay Weber Syndrome

Journal of clinical and diagnostic research, 2017-12, Vol.11 (12), p.SL01

2017

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A novel mutation (c.121‑13T>A) in the polypyrimidine tract of the splice acceptor site of intron 2 causes exon 3 skipping in mitochondrial acetoacetyl-CoA thiolase gene

Molecular medicine reports, 2017-06, Vol.15 (6), p.3879-3884

2017

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Avascular Necrosis of Femoral Head in a Child with Beta Thalassaemia Major

Journal of clinical and diagnostic research, 2016-09, Vol.10 (9), p.SL03-SL03

2016

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Super-Refractory Status Epilepticus: A Therapeutic Challenge in Paediatrics

Journal of clinical and diagnostic research, 2017-08, Vol.11 (8), p.SR01-SR04

2017

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Alopecia Areata and Demyelination as Paraneoplastic Manifestation in Paediatric Hodgkin's Lymphoma

International journal of hematology- oncology and stem cell research, 2018-04, Vol.12 (2), p.98-102

2018

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Cutaneous creeping eruption in a child

Nasza dermatologia online, 2016-01, Vol.7 (1), p.119-120

2016

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Transient cutaneous hyperpigmentation of extremities following dengue fever

Nasza dermatologia online, 2014-07, Vol.5 (3), p.298-299

2014

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Clinical profile and predictors of severity in children with scrub typhus admitted to paediatric intensive care unit

International Journal of Contemporary Pediatrics, 2023-06, Vol.10 (7), p.1027-1032

2023

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Clinicohematological Study of Thrombocytosis in Children

ISRN hematology, 2014, Vol.2014, p.389257-4

2014

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Clinico-radiological Profile and Outcome of Children with Viral Pneumonia admitted to Paediatric Intensive Care Unit in the pre COVID 19 period

Journal of Nepal Paediatric Society, 2022-11, Vol.42 (1), p.26-32

2022

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Further evidence of affected females with a heterozygous variant in FGF13 causing X-linked developmental and epileptic encephalopathy 90

European journal of medical genetics, 2022-01, Vol.65 (1), p.104403-104403, Article 104403

2022

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An atypical giant mantoux reaction

Nasza dermatologia online, 2012-07, Vol.3 (3), p.234-234

2012

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Metabolic Bone Disease in Children With Transfusion-Dependent Thalassemia

Indian pediatrics, 2022-12, Vol.59 (12), p.920-923

2022

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Drug Induced Diabetes Mellitus in Pediatric Acute Lymphoblastic Leukemia: Approach to Diagnosis and Management

Journal of pediatric hematology/oncology, 2022-08, Vol.44 (6), p.273-279

2022

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Liver dysfunction in children with scrub typhus: association with severity of illness and outcome

Sri Lanka journal of child health, 2023-12, Vol.52 (4), p.464-469

2023

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Megalencephaly-capillary malformation syndrome: a report of two cases

Genetic and phenotypic landscape of pediatric‐onset epilepsy in 142 Indian families: Counseling and therapeutic implications

Clinical profile and role of serology in pediatric acute febrile illness: Experience from a tertiary care hospital in South India

Multilocus disease-causing genomic variations for Mendelian disorders: role of systematic phenotyping and implications on genetic counselling

Refractory microcytic hypochromic anemia with type I diabetes mellitus and reversible cardiac hemochromatosis in congenital hypotransferrinemia

Hemolytic uremic syndrome in children: Clinical characteristics and predictors of outcome

Primary chylous ascites in children: Rare cause of a common presentation

Waldmann's Disease (Primary Intestinal Lymphangiectasia) with Atrial Septal Defect

Interleukin-6 versus C-reactive Protein as Markers for Early Detection of Bacteremia in Febrile Neutropenia in Pediatric Population

Guillain-barré syndrome: a clinical study of twenty children

Colonic Arteriovenous Malformation in a Child with Klippel Trenaunay Weber Syndrome

A novel mutation (c.121‑13T>A) in the polypyrimidine tract of the splice acceptor site of intron 2 causes exon 3 skipping in mitochondrial acetoacetyl-CoA thiolase gene

Avascular Necrosis of Femoral Head in a Child with Beta Thalassaemia Major

Super-Refractory Status Epilepticus: A Therapeutic Challenge in Paediatrics

Alopecia Areata and Demyelination as Paraneoplastic Manifestation in Paediatric Hodgkin's Lymphoma

Cutaneous creeping eruption in a child

Transient cutaneous hyperpigmentation of extremities following dengue fever

Clinical profile and predictors of severity in children with scrub typhus admitted to paediatric intensive care unit

Clinicohematological Study of Thrombocytosis in Children

Clinico-radiological Profile and Outcome of Children with Viral Pneumonia admitted to Paediatric Intensive Care Unit in the pre COVID 19 period

Further evidence of affected females with a heterozygous variant in FGF13 causing X-linked developmental and epileptic encephalopathy 90

An atypical giant mantoux reaction

Metabolic Bone Disease in Children With Transfusion-Dependent Thalassemia

Drug Induced Diabetes Mellitus in Pediatric Acute Lymphoblastic Leukemia: Approach to Diagnosis and Management

Liver dysfunction in children with scrub typhus: association with severity of illness and outcome

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