2024

• Billich, N., Sowerby, B., Farrar, M., Menezes, M., Holland, S., Lindeback, R., Cairns, A., Davidson, Z., Bray, P., Truby, H., et al (2024). Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy. Muscle and Nerve, 69(4), 448-458. [More Information]
• Riley, L., Smith, J., Wong, R., Menezes, M., Gupta, S., Cooper, S., Balasubramaniam, S., Sabui, S., Said, H., Niaz, A., et al (2024). Genome sequencing enables diagnosis and treatment of SLC5A6 neuropathy. European Journal of Human Genetics. [More Information]
• Li, L., Menezes, M., Smith, M., Forbes, R., Zuchner, S., Burgess, A., Woodcock, I., Delatycki, M., Yiu, E. (2024). Rare homozygous disease-associated sequence variants in children with spinal muscular atrophy: a phenotypic description and review of the literature. Neuromuscular Disorders, 37, 29-35. [More Information]

2023

• Dale, R., Thomas, T., Patel, S., Han, V., Kothur, K., Troedson, C., Gupta, S., Gill, D., Subramanian, G., Andrews, P., Menezes, M., Ardern-Holmes, S., Mohammad, S., Bandodkar, S., Yan, J., et al (2023). CSF neopterin and quinolinic acid are biomarkers of neuroinflammation and neurotoxicity in FIRES and other infection-triggered encephalopathy syndromes. Annals of Clinical and Translational Neurology, 10(8), 1417-1432. [More Information]
• Yan, J., Kothur, K., Mohammad, S., Chung, J., Patel, S., Jones, H., Keating, B., Han, V., Webster, R., Ardern-Holmes, S., Antony, J., Menezes, M., Tantsis, E., Gill, D., Gupta, S., Troedson, C., Bandodkar, S., Dale, R., et al (2023). CSF neopterin, quinolinic acid and kynurenine/tryptophan ratio are biomarkers of active neuroinflammation. EBioMedicine, 91. [More Information]
• Dwan, L., Gibbons, P., Jamil, K., Little, D., Birke, O., Menezes, M., Burns, J. (2023). Reliability and sensitivity of radiographic measures of hip dysplasia in childhood Charcot-Marie-Tooth disease. Hip International, 33(2), 323-331. [More Information]
• Vetro, A., Pelorosso, C., Balestrini, S., Masi, A., Hambleton, S., Argilli, E., Conti, V., Giubbolini, S., Barrick, R., Bergant, G., Menezes, M., et al (2023). Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration. American Journal of Human Genetics, 110(8), 1356-1376. [More Information]

2022

• Wong, W., Bryen, S., Bournazos, A., Yasa, J., Lemckert, F., Bommireddipalli, S., Waddell, L., Menezes, M., Webster, R., Davis, M., Cooper, S., Jones, K., et al (2022). A genetic basis is identified in 74% cases of paediatric hyperCKaemia without weakness presenting to a tertiary paediatric neuromuscular centre. Neuromuscular Disorders, 32(9), 707-717. [More Information]
• Yiu, E., Bray, P., Baets, J., Baker, S., Barisic, N., De Valle, K., Estilow, T., Farrar, M., Finkel, R., Haberlová, J., Rose, K., Menezes, M., Burns, J., et al (2022). Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth disease. Journal of Neurology, Neurosurgery and Psychiatry. [More Information]
• Yan, J., Kothur, K., Innes, E., Han, V., Jones, H., Patel, S., Tsang, E., Webster, R., Gupta, S., Troedson, C., Menezes, M., Antony, J., Ardern-Holmes, S., Tantsis, E., Mohammad, S., Gill, D., Bandodkar, S., Dale, R., et al (2022). Decreased cerebrospinal fluid kynurenic acid in epileptic spasms: A biomarker of response to corticosteroids. EBioMedicine, 84. [More Information]
• Babu, I., Howard-Jones, A., Goetti, R., Menezes, M., Arbuckle, S., Britton, P. (2022). Paediatric neurocysticercosis in high income countries: Neurocysticercosis in high income countries. European Journal of Paediatric Neurology, 39, 88-95. [More Information]
• Wojciechowski, E., Cheng, T., Hogan, S., Mudge, A., Balassone, D., Menezes, M., Little, D., Dwan, L., Burns, J. (2022). Replicating and redesigning ankle-foot orthoses with 3D printing for children with Charcot-Marie-Tooth disease. Gait and Posture, 96, 73-80. [More Information]
• Wong, W., Troedson, C., Peacock, K., Brilot-Turville, F., Menezes, M., Dale, R., Webster, R. (2022). Steroid-responsive aseptic meningitis with raised intracranial pressure syndrome associated with myelin oligodendrocyte glycoprotein autoantibodies. Journal of Paediatrics and Child Health, 58(12), 2322-2326. [More Information]

2021

• Donlevy, G., Garnett, S., Cornett, K., Baldwin, J., Shy, R., Yum, S., Estilow, T., Moroni, I., Foscan, M., Pagliano, E., Burns, J., Menezes, M., et al (2021). Association Between Body Mass Index and Disability in Children With Charcot-Marie-Tooth Disease. Neurology, 97(17), e1727-e1736. [More Information]
• Argente-Escrig, H., Burns, J., Donlevy, G., Frasquet, M., Cornett, K., Sevilla, T., Menezes, M. (2021). Clinical, Genetic, and Disability Profile of Pediatric Distal Hereditary Motor Neuropathy. Neurology, 96(3), e423-e432. [More Information]
• Lorentzos, M., Heyman, I., Baig, B., Coughtrey, A., Mcwilliams, A., Dossetor, D., Waugh, M., Evans, R., Hollywood, J., Burns, J., Grattan-Smith, P., Dale, R., et al (2021). Psychiatric comorbidity is common in dystonia and other movement disorders. Archives of Disease in Childhood, 106(1), 62-67. [More Information]

2020

• Chambers, G., Settumba, S., Carey, K., Cairns, A., Menezes, M., Ryan, M., Farrar, M. (2020). Prenusinersen economic and health-related quality of life burden of spinal muscular atrophy. Neurology, 95(1), 1-10. [More Information]
• Cornett, K., Menezes, M., Bray, P., Shy, R., Moroni, I., Pagliano, E., Pareyson, D., Estilow, T., Yum, S., Bhandari, T., Burns, J., et al (2020). Refining clinical trial inclusion criteria to optimize the standardized response mean of the CMTPedS. Annals of Clinical and Translational Neurology, 7(9), 1713-1715. [More Information]

2019

• Estilow, T., Glanzman, A., Burns, J., Harrington, A., Cornett, K., Menezes, M., Shy, R., Moroni, I., Pagliano, E., Pareyson, D., Bray, P., et al (2019). Balance Impairment in Pediatric Charcot-Marie-Tooth Disease. Muscle and Nerve, 60(3), 242-249. [More Information]
• Wojciechowski, E., Chang, A., Balassone, D., Ford, J., Cheng, T., Little, D., Menezes, M., Hogan, S., Burns, J. (2019). Feasibility of designing, manufacturing and delivering 3D printed ankle-foot orthoses: a systematic review. Journal of Foot and Ankle Research, 12(1), 1-12. [More Information]
• Cornett, K., Wojciechowski, E., Sman, A., Walker, T., Menezes, M., Bray, P., Halaki, M., Burns, J. (2019). Magnetic Resonance Imaging of the anterior compartment of the lower leg is a biomarker for weakness, disability and impaired gait in childhood Charcot-Marie-Tooth disease. Muscle and Nerve, 59(2), 213-217. [More Information]
• Lin, T., Gibbons, P., Mudge, A., Cornett, K., Menezes, M., Burns, J. (2019). Surgical outcomes of cavovarus foot deformity in children with Charcot-Marie-Tooth disease. Neuromuscular Disorders, 29(6), 427-436. [More Information]
• Misra, S., Peters, G., Barnes, E., Ardern-Holmes, S., Webster, R., Troedson, C., Mohammad, S., Gill, D., Menezes, M., Gupta, S., Dale, R., et al (2019). Yield of comparative genomic hybridization microarray in pediatric neurology practice. Neurology: Genetics, 5(6), 1-9. [More Information]

2018

• Mandarakas, M., Menezes, M., Rose, K., Shy, R., Eichinger, K., Foscan, M., Estilow, T., Kennedy, R., Herbert, K., Bray, P., Refshauge, K., Burns, J., et al (2018). Development and validation of the Charcot-Marie-Tooth Disease Infant Scale. Brain, 141(12), 3319-3330. [More Information]
• Kothur, K., Holman, K., Farnsworth, E., Ho, G., Lorentzos, M., Troedson, C., Gupta, S., Webster, R., Procopis, P., Menezes, M., Ardern-Holmes, S., Dale, R., Gill, D., Bennetts, B., et al (2018). Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy. Seizure: European Journal of Epilepsy, 59, 132-140. [More Information]
• Cornett, K., Menezes, M., Bray, P., Halaki, M., Burns, J. (2018). Established and novel measures of upper limb impairment in children with Charcot-Marie-Tooth disease type 1A and Riboflavin Transporter Deficiency type 2. Journal of the Peripheral Nervous System, 23(1), 29-35. [More Information]
• Mandarakas, M., Rose, K., Sanmaneechai, O., Menezes, M., Refshauge, K., Burns, J. (2018). Functional outcome measures for infantile Charcot-Marie-Tooth disease: a systematic review. Journal of the Peripheral Nervous System, 23(2), 99-107. [More Information]
• Woodcock, I., Menezes, M., Coleman, L., Yaplito-Lee, J., Peters, H., White, S., Stapleton, R., Phelan, D., Chong, B., Lunke, S., et al (2018). Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome. Seminars in Pediatric Neurology, 26, 2-9. [More Information]
• Farrar, M., Teoh, H., Carey, K., Cairns, A., Forbes, R., Herbert, K., Holland, S., Jones, K., Menezes, M., Morrison, M., Webster, R., et al (2018). Nusinersen for SMA: expanded access programme. Journal of Neurology, Neurosurgery and Psychiatry, 89(9), 937-942. [More Information]
• Chaya, S., Zampoli, M., Gray, D., Booth, J., Riordan, G., Ndondo, A., Fieggen, K., Rusch, J., van der Watt, G., Pillay, K., Menezes, M., et al (2018). The First Case of Riboflavin Transporter Deficiency in sub-Saharan Africa. Seminars in Pediatric Neurology, 26, 10-14. [More Information]
• Kanhangad, M., Cornett, K., Brewer, M., Nicholson, G., Ryan, M., Smith, R., Subramanian, G., Young, H., Zuchner, S., Kennerson, M., Burns, J., Menezes, M. (2018). Unique clinical and neurophysiologic profile of a cohort of children with CMTX3. Neurology, 90(19), e1706-e1710. [More Information]

2017

• Yiu, E., Burns, J., Menezes, M., Ryan, M. (2017). Development of best practice guidelines for paediatric Charcot-Marie-Tooth disease. 6th International Charcot-Marie-Tooth and Related Neuropathy Consortium (CMTR) Meeting, Minneapolis, MN, USA: Peripheral Nerve Society.
• Dwan, L., Wojciechowski, E., Gibbons, P., Jamil, K., Menezes, M., Burns, J. (2017). Functional Consequences of Hip Dysplasia in Paediatric Charcot-Marie-Tooth Disease. Peripheral Nerve Society Meeting, Australia: Journal of the Peripheral Nervous System. [More Information]
• Wojciechowski, E., Sman, A., Cornett, K., Raymond, J., Refshauge, K., Menezes, M., Burns, J. (2017). Gait patterns of children and adolescents with Charcot-Marie-Tooth disease. Gait and Posture, 56, 89-94. [More Information]
• Cornett, K., Menezes, M., Shy, R., Moroni, I., Pagliano, E., Pareyson, D., Estilow, T., Yum, S., Bhandari, T., Muntoni, F., Bray, P., Halaki, M., Burns, J., et al (2017). Natural history of Charcot-Marie-Tooth disease during childhood. Annals of Neurology, 82(3), 353-359. [More Information]
• Burns, J., Sman, A., Cornett, K., Wojciechowski, E., Walker, T., Menezes, M., Mandarakas, M., Rose, K., Bray, P., Sampaio, H., Refshauge, K., Raymond, J., et al (2017). Safety and efficacy of progressive resistance exercise for Charcot-Marie-Tooth disease in children: a randomised, double-blind, sham-controlled trial. The Lancet Child and Adolescent Health, 1(2), 106-113. [More Information]

2016

• Menezes, M., O'Brien, K., Hill, M., Webster, R., Antony, J., Ouvrier, R., Birman, C., Gardner-Berry, K. (2016). Auditory neuropathy in Brown-Vialetto-Van Laere syndrome dueto riboflavin transporter RFVT2 deficiency. Developmental Medicine and Child Neurology, 58(8), 848-854. [More Information]
• Tantsis, E., Gill, D., Griffiths, L., Gupta, S., Lawson, J., Maksemous, N., Ouvrier, R., Riant, F., Smith, R., Troedson, C., et al (2016). Eye movement disorders are an early manifestation of CACNA1A mutations in children. Developmental Medicine and Child Neurology, 58(6), 639-644. [More Information]
• Menezes, M., Rahman, S., Bhattacharya, K., Clark, D., Christodoulou, J., Ellaway, C., Farrar, M., Pitt, M., Sampaio, H., Ware, T., Ouvrier, R., et al (2016). Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease. Mitochondrion, 30, 162-167. [More Information]
• Menezes, M., Farrar, M., Webster, R., Antony, J., O'Brien, K., Ouvrier, R., Kiernan, M., Burns, J., Vucic, S. (2016). Pathophysiology of motor dysfunction in a childhood motor neuron disease caused by mutations in the riboflavin transporter. Clinical Neurophysiology, 127(1), 911-918. [More Information]
• Cornett, K., Menezes, M., Bray, P., Halaki, M., Shy, R., Yum, S., Estilow, T., Moroni, I., Foscan, M., Pagliano, E., Burns, J., et al (2016). Phenotypic variability of childhood Charcot-Marie-Tooth disease. JAMA Neurology, 73(6), 645-651. [More Information]
• O'Grady, G., Ma, A., Sival, D., Wong, M., Peduto, A., Menezes, M., Young, H., Waddell, L., Ghaoui, R., Needham, M., Lek, M., Clarke, N., et al (2016). Prominent scapulae mimicking an inherited myopathy expands the phenotype of CHD7-related disease. European Journal of Human Genetics, 24(8), 1216-1219. [More Information]
• O'Grady, G., Verschuuren, C., Yuen, M., Webster, R., Menezes, M., Fock, J., Pride, N., Best, H., Benavides Damm, T., Turner, C., North, K., Clarke, N., Cooper, S., et al (2016). Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome. Neurology, 87(14), 1442-1448. [More Information]
• Brewer, M., Chaudhry, R., Qi, J., Kidambi, A., Drew, A., Menezes, M., Ryan, M., Farrar, M., Mowat, D., Subramanian, G., Young, H., Nicholson, G., Kennerson, M., et al (2016). Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3. PLoS Genetics, 12(7), 1-16. [More Information]

2015

• Guo, Y., Menezes, M., Menezes, M., Liang, J., Li, D., Riley, L., Clarke, N., Andrews, P., Tian, L., Webster, R., Christodoulou, J., et al (2015). Delayed diagnosis of congenital myasthenia due to associated mitochondrial enzyme defect. Neuromuscular Disorders, 25, 257-261. [More Information]
• Pillai, S., Hacohen, Y., Tantsis, E., Prelog, K., Merheb, V., Kesson, A., Barnes, E., Gill, D., Webster, R., Menezes, M., Brilot-Turville, F., Dale, R., et al (2015). Infectious and Autoantibody-Associated Encephalitis: Clinical Features and Long-term Outcome. Pediatrics, 135(4), e974-e984. [More Information]
• Rossor, A., Oates, E., Salter, H., Liu, Y., Murphy, S., Schule, R., Gonzalez, M., Scoto, M., Phadke, R., Sewry, C., Rodriguez, M., Menezes, M., Clarke, N., North, K., et al (2015). Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2. Brain, 138(2), 293-310. [More Information]
• Rossor, A., Oates, E., Slater, H., Liu, Y., Murphy, S., Schule, R., Gonzales, M., Scoto, M., Phadke, R., Sewry, C., Rodriguez, M., Menezes, M., Clarke, N., North, K., et al (2015). Reply: The p.Ser107Leu in BICD2 is a mutation 'hot spot' causing distal spinal muscular atrophy. Brain, 138(11), 1-2. [More Information]
• Menezes, M., Waddell, L., Lenk, G., Kaur, S., Macarthur, D., Meisler, M., Clarke, N. (2015). Response. Neuromuscular Disorders, 25(4), 360-360. [More Information]
• Sman, A., Hackett, D., Fiatarone Singh, M., Fornusek, C., Menezes, M., Burns, J. (2015). Systematic review of exercise for Charcot-Marie-Tooth disease. Journal of the Peripheral Nervous System, 20(4), 347-362. [More Information]

2014

• Rice, G., del Toro Duany, Y., Jenkinson, E., Forte, G., Anderson, B., Ariaudo, G., Bader-Meunier, B., Baildam, E., Battini, R., Beresford, M., Dale, R., Menezes, M., et al (2014). Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling. Nature Genetics, 46(5), 503-509. [More Information]
• Ouvrier, R., Menezes, M. (2014). Giant axonal neuropathy. In Jean-Michel Vallat, Joachim Weis (Eds.), Peripheral nerve disorders: pathology and genetics, (pp. 142-145). Oxford, UK: Wiley-Blackwell Publishing. [More Information]
• Ouvrier, R., Menezes, M. (2014). Neuroaxonal dystrophy. In Jean-Michel Vallat, Joachim Weis (Eds.), Peripheral nerve disorders: pathology and genetics, (pp. 146-148). Oxford, UK: Wiley-Blackwell Publishing. [More Information]
• Ouvrier, R., Menezes, M. (2014). Peripheral nerve involvement in neurolipidoses. In Jean-Michel Vallat, Joachim Weis (Eds.), Peripheral nerve disorders: pathology and genetics, (pp. 149-157). Oxford, UK: Wiley-Blackwell Publishing. [More Information]
• Sman, A., Raymond, J., Refshauge, K., Menezes, M., Walker, T., Ouvrier, R., Burns, J. (2014). Randomised controlled trial protocol of foot and ankle exercise for children with Charcot-Marie-Tooth disease. Journal of Physiotherapy, 60(1), 55-55. [More Information]
• Foley, A., Menezes, M., Pandraud, A., Gonzalez, M., Al-Odaib, A., Abrams, A., Sugano, K., Yonezawa, A., Manzur, A., Burns, J., Wang, M., Carpenter, K., Lek, M., Gold, W., Ouvrier, R., Christodoulou, J., et al (2014). Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2. Brain, 137(Pt 1), 44-56. [More Information]
• Menezes, M., Waddell, L., Lenk, G., Kaur, S., MacArthur, D., Meisler, M., Clarke, N. (2014). Whole exome sequencing identifies three recessive FIG4 mutations in an apparently dominant pedigree with Charcot-Marie-Tooth disease. Neuromuscular Disorders, 24(8), 666-670. [More Information]

2013

• Burns, J., Menezes, M., Shy, R., Sanmaneechai, O., Laura, M., Muntoni, F., Estilow, T., Yum, S., Finkel, R., Herrmann, D., et al (2013). Determinants of balance deficit in children with Charcot-Marie-Tooth Disease. 2013 Meeting of the Peripheral Nerve Society, USA: Wiley-Blackwell Publishing, Inc.
• Menezes, M., Nowland, T., Onikul, E. (2013). Diffusion-Weighted Imaging Changes Caused by Acute Hypoglycemia and Prolonged Febrile Convulsion in Childhood. American Journal Of Neuroradiology, 34(4), E43-E44. [More Information]
• Oates, E., Rossor, A., Hafezparast, M., Gonzalez, M., Speziani, F., MacArthur, D., Lek, M., Cottenie, E., Scoto, M., Foley, A., Menezes, M., Clarke, N., et al (2013). Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia. American Journal of Human Genetics, 92(6), 965-973. [More Information]
• Menezes, M., Farrar, M., Burns, J., Menon, P., Webster, R., Antony, J., Kiernan, M., Vucic, S. (2013). Peripheral motor contributions to the pathophysiology of BVVL-related mutations in riboflavin transporter 3: Pathophysiological insights from nerve excitability testing. 2013 Meeting of the Peripheral Nerve Society, USA: Wiley-Blackwell Publishing, Inc.
• Sman, A., Raymond, J., Refshauge, K., Menezes, M., Walker, T., Ouvrier, R., Burns, J. (2013). Randomised controlled trial protocol of progressive resistance strength training for children with Charcot-Marie-Tooth Disease. 2013 Meeting of the Peripheral Nerve Society, USA: Wiley-Blackwell Publishing, Inc.
• Cottenie, E., Menezes, M., Rossor, A., Morrow, J., Yousry, T., Dick, D., Anderson, J., Jaunmuktane, Z., Brandner, S., Blake, J., et al (2013). Rapidly progressive asymmetrical weakness in Charcot-Marie-Tooth disease type 4J resembles chronic inflammatory demyelinating polyneuropathy. Neuromuscular Disorders, 23(5), 399-403. [More Information]
• Burns, J., Menezes, M., Finkel, R., Estilow, T., Moroni, I., Pagliano, E., Laura, M., Muntoni, F., Herrmann, D., Eichinger, K., et al (2013). Transitioning outcome measures: relationship between the CMTPedS and CMTNSv2 in children, adolescents, and young adults with Charcot-Marie-Tooth disease. Journal of the Peripheral Nervous System, 18(2), 177-180. [More Information]
• Burns, J., Menezes, M., Shy, R., Sanmaneechai, O., Laura, M., Muntoni, F., Estilow, T., Yum, S., Finkel, R., Herrmann, D., et al (2013). Two year natural history of disease progression in childhood Charcot-Marie-Tooth Disease. 2013 Meeting of the Peripheral Nerve Society, USA: Wiley-Blackwell Publishing, Inc.

2012

• Cederquist, G., Luchniak, A., Tischfield, M., Peeva, M., Song, Y., Menezes, M., Chan, W., Andrews, C., Chew, S., Jamieson, R., Gomes, L., et al (2012). An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation. Human Molecular Genetics, 21(26), 5484-5499. [More Information]
• Menezes, M., Waddell, L., Evesson, F., Cooper, S., Webster, R., Jones, K., Mowat, D., Kiernan, M., Johnston, H., Corbett, A., North, K., Clarke, N., et al (2012). Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy. Neurology, 78(16), 1258-1263. [More Information]
• Menezes, M., North, K. (2012). Inherited neuromuscular disorders: Pathway to diagnosis. Journal of Paediatrics and Child Health, 48(6), 458-465. [More Information]
• Johnson, S., Menezes, M. (2012). Motor and coordination problems. In Sandra Johnson (Eds.), A Clinical Handbook on Child Development Paediatrics, (pp. 40-49). Sydney: Churchill Livingstone.
• Wan, J., Yourshaw, M., Mamsa, H., Rudnik-Schöneborn, S., Menezes, M., Hong, J., Leong, D., Senderek, J., Salman, M., Chitayat, D., et al (2012). Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration. Nature Genetics, 44(6), 704-708. [More Information]
• Menezes, M., Ouvrier, R. (2012). Peripheral neuropathy associated with mitochondrial disease in children. Developmental Medicine and Child Neurology, 54(5), 407-414. [More Information]

2009

• Nagesh, K., Menezes, M. (2009). Birth Trauma. In Unknown (Eds.), Achar's Textbook of Pediatrics (Fourth Edition), (pp. 172-177). India: Universities Press (India) Private Limited.