Associate Professor Padraic Grattan-Smith

Clinical Associate Professor
Paediatrics & Child Health, Children's Hospital, Westmead

Telephone 93110740

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Clinical Specialty

Paediatrics

Selected publications

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Journals

  • Zhang, Y., Burgess, R., Malone, J., Glubb, G., Helbig, K., Vadlamudi, L., Kivity, S., Afawi, Z., Bleasel, A., Grattan-Smith, P., et al (2017). Genetic epilepsy with febrile seizures plus Refining the spectrum. Neurology, 89(12), 1210-1219. [More Information]
  • Chang, F., Westenberger, A., Dale, R., Smith, M., Pall, H., Perez-Duenas, B., Grattan-Smith, P., Ouvrier, R., Mahant, N., Hanna, B., Fung, V., et al (2016). Phenotypic insights into ADCY5-associated disease. Movement Disorders, 31(7), 1033-1040. [More Information]
  • Mohammad, S., Nosadini, M., Grattan-Smith, P., Dale, R. (2015). Intravenous immunoglobulin in acute Sydenham's chorea: A systematic review. Journal of Paediatrics and Child Health, 51(12), 1235-1238. [More Information]
  • Mohammad, S., Fung, V., Grattan-Smith, P., Gill, D., Pillai, S., Ramanathan, S., Brilot-Turville, F., Dale, R. (2014). Movement disorders in children with anti-NMDAR encephalitis and other autoimmune encephalopathies. Movement Disorders, 29(12), 1539-1542. [More Information]
  • Willemsen, M., Verbeek, M., Kamsteeg, E., de Rijk-van Andel, J., Aeby, A., Blau, N., Burlina, A., Donati, M., Geurtz, B., Grattan-Smith, P., Wilcken, B., et al (2010). Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis. Brain, 133(6), 1810-1822. [More Information]
  • Farrar, M., Johnston, H., Grattan-Smith, P., Turner, A., Kiernan, M. (2009). Spinal muscular atrophy: molecular mechanisms. Current Molecular Medicine, 9(7), 851-862. [More Information]
  • Kipps, C., Fung, V., Grattan-Smith, P., De Moore, G., Morris, J. (2005). Movement disorder emergencies. Movement Disorders, 20(3), 322-334. [More Information]
  • Kyriagis, M., Grattan-Smith, P., Scheinberg, A., Teo, C., Nakaji, N., Waugh, M. (2004). Status Dystonicus And Hallervorden-Spatz Disease: Treatment With Intrathecal Baclofen And Pallidotomy. Journal of Paediatrics and Child Health, 40(5-6), 322-325. [More Information]
  • Field, M., Grattan-Smith, P., Piper, S., Thompson, E., Haan, E., Edwards, M., James, S., Wilkinson,, I., Ades, L. (2003). PEHO and PEHO-like syndromes. Report of five Australian cases. American Journal of Medical Genetics, Part A, 122A (1), 6-12.
  • Morris, J., Jankelowitz, S., Fung, V., Clouston, P., Hayes, M., Grattan-Smith, P. (2002). Athetosis I: historical considerations. Movement Disorders, 17(6), 1278-1280. [More Information]
  • Morris, J., Grattan-Smith, P., Jankelowitz, S., Fung, V., Clouston, P., Hayes, M. (2002). Athetosis II: the syndrome of mild athetoid cerebral palsy. Movement Disorders, 17(6), 1281-1287. [More Information]
  • Grattan-Smith, P., Wevers, R., Steenbergen-Spanjers, G., Fung, V., Earl, J., Wilcken, B. (2002). Tyrosine hydroxylase deficiency: Clinical manifestations of catecholamine insufficiency in infancy. Movement Disorders, 17(2), 354-359. [More Information]

2017

  • Zhang, Y., Burgess, R., Malone, J., Glubb, G., Helbig, K., Vadlamudi, L., Kivity, S., Afawi, Z., Bleasel, A., Grattan-Smith, P., et al (2017). Genetic epilepsy with febrile seizures plus Refining the spectrum. Neurology, 89(12), 1210-1219. [More Information]

2016

  • Chang, F., Westenberger, A., Dale, R., Smith, M., Pall, H., Perez-Duenas, B., Grattan-Smith, P., Ouvrier, R., Mahant, N., Hanna, B., Fung, V., et al (2016). Phenotypic insights into ADCY5-associated disease. Movement Disorders, 31(7), 1033-1040. [More Information]

2015

  • Mohammad, S., Nosadini, M., Grattan-Smith, P., Dale, R. (2015). Intravenous immunoglobulin in acute Sydenham's chorea: A systematic review. Journal of Paediatrics and Child Health, 51(12), 1235-1238. [More Information]

2014

  • Mohammad, S., Fung, V., Grattan-Smith, P., Gill, D., Pillai, S., Ramanathan, S., Brilot-Turville, F., Dale, R. (2014). Movement disorders in children with anti-NMDAR encephalitis and other autoimmune encephalopathies. Movement Disorders, 29(12), 1539-1542. [More Information]

2010

  • Willemsen, M., Verbeek, M., Kamsteeg, E., de Rijk-van Andel, J., Aeby, A., Blau, N., Burlina, A., Donati, M., Geurtz, B., Grattan-Smith, P., Wilcken, B., et al (2010). Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis. Brain, 133(6), 1810-1822. [More Information]

2009

  • Farrar, M., Johnston, H., Grattan-Smith, P., Turner, A., Kiernan, M. (2009). Spinal muscular atrophy: molecular mechanisms. Current Molecular Medicine, 9(7), 851-862. [More Information]

2005

  • Kipps, C., Fung, V., Grattan-Smith, P., De Moore, G., Morris, J. (2005). Movement disorder emergencies. Movement Disorders, 20(3), 322-334. [More Information]

2004

  • Kyriagis, M., Grattan-Smith, P., Scheinberg, A., Teo, C., Nakaji, N., Waugh, M. (2004). Status Dystonicus And Hallervorden-Spatz Disease: Treatment With Intrathecal Baclofen And Pallidotomy. Journal of Paediatrics and Child Health, 40(5-6), 322-325. [More Information]

2003

  • Field, M., Grattan-Smith, P., Piper, S., Thompson, E., Haan, E., Edwards, M., James, S., Wilkinson,, I., Ades, L. (2003). PEHO and PEHO-like syndromes. Report of five Australian cases. American Journal of Medical Genetics, Part A, 122A (1), 6-12.

2002

  • Morris, J., Jankelowitz, S., Fung, V., Clouston, P., Hayes, M., Grattan-Smith, P. (2002). Athetosis I: historical considerations. Movement Disorders, 17(6), 1278-1280. [More Information]
  • Morris, J., Grattan-Smith, P., Jankelowitz, S., Fung, V., Clouston, P., Hayes, M. (2002). Athetosis II: the syndrome of mild athetoid cerebral palsy. Movement Disorders, 17(6), 1281-1287. [More Information]
  • Grattan-Smith, P., Wevers, R., Steenbergen-Spanjers, G., Fung, V., Earl, J., Wilcken, B. (2002). Tyrosine hydroxylase deficiency: Clinical manifestations of catecholamine insufficiency in infancy. Movement Disorders, 17(2), 354-359. [More Information]

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