Komal A. Vora

Newcastle, NSW, Australia

Last Updated: 09/26/2026

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Found 8 publications

Daytime sleepiness and emotional and behavioral disturbances in Prader-Willi syndrome.

Daytime sleepiness and emotional and behavioral disturbances in Prader-Willi syndrome.

Journal: European journal of pediatrics

Published: November 07, 2021

Associations Between Hyperphagia, Symptoms of Sleep Breathing Disorder, Behaviour Difficulties and Caregiver Well-Being in Prader-Willi Syndrome: A Preliminary Study.

Associations Between Hyperphagia, Symptoms of Sleep Breathing Disorder, Behaviour Difficulties and Caregiver Well-Being in Prader-Willi Syndrome: A Preliminary Study.

Journal: Journal of autism and developmental disorders

Published: August 28, 2021

Childhood type 1 diabetes is associated with abnormal bone development.

Childhood type 1 diabetes is associated with abnormal bone development.

Journal: Pediatric diabetes

Published: August 15, 2021

Sleep-disordered breathing in Australian children with Prader-Willi syndrome following initiation of growth hormone therapy.

Sleep-disordered breathing in Australian children with Prader-Willi syndrome following initiation of growth hormone therapy.

Journal: Journal of paediatrics and child health

Published: September 06, 2020

Role of cross-campus multidisciplinary team meetings in decision-making for children and adolescents with differences of sex development/intersex.

Role of cross-campus multidisciplinary team meetings in decision-making for children and adolescents with differences of sex development/intersex.

Journal: Journal of paediatrics and child health

Published: August 13, 2020

A guide to differences/disorders of sex development/intersex in children and adolescents.

A guide to differences/disorders of sex development/intersex in children and adolescents.

Journal: Australian journal of general practice

Published: July 01, 2020

Requirements for improving health and well-being of children with Prader-Willi syndrome and their families.

Requirements for improving health and well-being of children with Prader-Willi syndrome and their families.

Journal: Journal of paediatrics and child health

Published: February 25, 2019

Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variants.

Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variants.

Journal: Atherosclerosis

Published: May 25, 2017

Showing 1-8 of 8

Last Updated: 09/26/2026