2002 Research Publications

Baker, E., Hinton, L., Callen, D.F., Altree, M., Dobbie, A., Eyre, H.J., Sutherland, G.R., Thompson, E., Thompson, P., Woollatt, E. & Haan, E. (2002). Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies. American Journal of Medical Genetics 107, 285-293

Baker, E., Hinton, L., Callen, D.F., Haan, E.A., Dobbie, A. & Sutherland, G.R. (2002). A familial cryptic subtelomeric deletion 12p with variable phenotypic effect. Clinical Genetics 61, 198-201

Berg, T. & Hopwood, J.J. (2002). alpha-mannosidosis in the guinea pig: cloning of the lysosomal alpha-mannosidase cDNA and identification of a missense mutation causing alpha-mannosidosis. Biochimica et Biophysica Acta-Molecular Basis of Disease 1586, 169-176

Bertrand, D., Picard, F., Le Hellard, S., Weiland, S., Favre, I., Phillips, H., Bertrand, S., Berkovic, S.F., Malafosse, A. & Mulley, J. (2002). How mutations in the nAChRs can cause ADNFLE epilepsy. Epilepsia 43 (Suppl 5), 112-122

Bienvenu, T., Poirier, K., Friocourt, G., Bahi, N., Beaumont, D., Fauchereau, F., Ben Jeema, L., Zemni, R., Vinet, M.C., Francis, F., Couvert, P., Gomot, M., Moraine, C., van Bokhoven, H., Kalscheuer, V., Frints, S., Gecz, J., Ohzaki, K., Chaabouni, H., Fryns, J.P., Desportes, V., Beldjord, C. & Chelly, J. (2002). ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation. Human Molecular Genetics 11, 981-91.

Blank, C., Neumann, M.A., Makrides, M. & Gibson, R.A. (2002). Optimizing DHA levels in piglets by lowering the linoleic acid to alpha-linolenic acid ratio. Journal of Lipid Research 43, 1537-1543

Bowser, D.N., Wagner, D.A., Czajkowski, C., Cromer, B.A., Parker, M.W., Wallace, R.H., Harkin, L.A., Mulley, J.C., Marini, C., Berkovic, S.F., Williams, D.A., Jones, M.V. & Petrou, S. (2002). Altered kinetics and benzodiazepine sensitivity of a GABA(A) receptor subunit mutation [gamma(2)(R43Q)] found in human epilepsy. Proceedings of the National Academy of Sciences of the United States of America 99, 15170-15175

Bradford, T.M., Litjens, T., Parkinson, E.J., Hopwood, J.J. & Brooks, D.A. (2002). Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): A Y210C mutation causes either altered protein handling or altered protein function of N-acetylgalactosamine 4-sulfatase at multiple points in the vacuolar network. Biochemistry 41, 4962-4971

Brennan, P.W., Everest, E.R., Griggs, W.M., Slater, A., Carter, L., Lee, C., Semmens, J.K., Wood, D.J., Nguyen, A.M.T., Owen, D.L., Pilkington, P., Roder, D.M. & Somers, R.L. (2002). Risk of death among cases attending South Australian major trauma services after severe trauma: The first 4 years of operation of a state trauma system. Journal of Trauma-Injury Infection and Critical Care 53, 333-339

Brooks, D.A. (2002). alpha-L-Iduronidase and enzyme replacement therapy for mucopolysaccharidosis I. Expert Opinion on Biological Therapy 2, 967-76.

Buller, H., Chin, S., Kirschner, B., Kohn, J., Markowitz, J., Moore, D., Murch, S. & Taminiau, J. (2002). Inflammatory bowel disease in children and adolescents: Working group report of the First World Congress of Pediatric Gastroenterology, Hepatology, and Nutrition. Journal of Pediatric Gastroenterology and Nutrition 35, S151-S158

Burnell, R.H. & Byard, R.W. (2002). Are these really SIDS deaths? Not by definition (Letter). Journal of Paediatrics and Child Health 38, 623-624

Burnet, S.P., Duncan, E.M., Lloyd, J.V. & Han, P. (2002). Treatment of acquired haemophilia - Reply. Internal Medicine Journal 32, 626-627

Callen, D.F., Crawford, J., Derwas, C., Cleton-Jansen, A.M., Cornelisse, C.J. & Baker, E. (2002). Defining regions of loss of heterozygosity of 16q in breast cancer cell lines. Cancer Genetics and Cytogenetics 133, 76-82

Callen, D.F., Eyre, H., McDonnell, S., Schuffenhauer, S. & Bhalla, K. (2002). A complex rearrangement involving simultaneous translocation and inversion is associated with a change in chromatin compaction. Chromosoma 111, 170-175

Chang, M.H.Y., Karageorgos, L.E. & Meikle, P. (2002). CD107a (LAMP-1) and CD107b (LAMP-2). Journal of Biological Regulators and Homeostatic Agents 16, 147-151

Clarke, J., Butler, R., Howarth, G., Read, L. & Regester, G. (2002). Exposure of oral mucosa to bioactive milk factors reduces severity of chemotherapy-induced mucositis in the hamster. Oral Oncology 38, 478-485

Conover, C.A., Johnstone, E.W., Turner, R.T., Evans, G.L., Ballard, F.J., Doran, P.M. & Khosla, S. (2002). Subcutaneous administration of insulin-like growth factor (IGF)-II/IGF binding protein-2 complex stimulates bone formation and prevents loss of bone mineral density in a rat model of disuse osteoporosis. Growth Hormone & IGF Research 12, 178-183

Corbould, A.M., Bawden, M.J., Lavranos, T.C., Rodgers, R.J. & Judd, S.J. (2002). The effect of obesity on the ratio of type 3 17 beta-hydroxysteroid dehydrogenase mRNA to cytochrome P450 aromatase mRNA in subcutaneous abdominal and intra-abdominal adipose tissue of women. International Journal of Obesity 26, 165-175

Couper, J.J. (2002). Children with type 1 diabetes: where are we at? Medical Journal of Australia 177, 228-229

Couper, R. (2002). Re: Phytoestrogens: The pediatric perspective (Letter). Journal of Pediatric Gastroenterology and Nutrition 34, 569-569

Couper, R., Belli, D., Durie, P., Gaskin, K., Sarles, J. & Werlin, S. (2002). Pancreatic disorders and cystic fibrosis: Working group report of the First World Congress of Pediatric Gastroenterology, Hepatology, and Nutrition. Journal of Pediatric Gastroenterology and Nutrition 35, S213-S223

Couper, R.L. (2002). Re: Hepatocyte growth factor and inflammatory bowel disease (Letter). Journal of Pediatric Gastroenterology and Nutrition 35, 231-231

Couper, R.T.L. (2002). Complementary therapies and children (Editorial). Journal of Paediatrics and Child Health 38, 339-340

Couper, R.T.L. (2002). Near-death experiences (Letter). Lancet 359, 2116-2116

Couper, R.T.L. (2002). Variant cystic fibrosis phenotypes in the absence of CFTR mutations (Letter). New England Journal of Medicine 347, 1892-1892

Couper, R.T.L. & Huynh, H. (2002). Female masturbation masquerading as abdominal pain (Case Report). Journal of Paediatrics and Child Health 38, 199-200

Couper, R.T.L., McPhee, A. & Morris, L. (2001). Indomethacin treatment of infantile cortical periostosis in twins (Case Report). Journal of Paediatrics and Child Health 37, 305-308

Crawford, J., Zielinski, M.A., Fisher, L.J., Sutherland, G.R. & Goldney, R.D. (2002). Is there a relationship between Wolfram syndrome carrier status and suicide? American Journal of Medical Genetics 114, 343-346

Cundy, T., Hegde, M., Naot, D., Chong, B., King, A., Wallace, R., Love, D.R., Seidel, J., Fawkner, M., Banovic, T., Callon, K.E., Grey, A.B., Reid, I.R., Middleton-Hardie, C.A. & Cornish, J. (2002). A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype. Human Molecular Genetics 11, 2119-2127

Davidson, G., Barnes, G., Bass, D., Cohen, M., Fasano, A., Fontaine, O. & Guandalini, S. (2002). Infectious diarrhea in children: Working group report of the First World Congress of Pediatric Gastroenterology, Hepatology, and Nutrition. Journal of Pediatric Gastroenterology and Nutrition 35, S143-S150

Dunaiski, V. & Belford, D.A. (2002). Contribution of circulating IGF-I to wound repair in GH-treated rats. Growth Hormone and IGF Research 12, 381-387

Dunaiski, V., Dunshea, F.R., Walton, P.E. & Goddard, C. (2002). Short-term infusion of LongR(3) insulin-like growth factor (IGF)-I decreases hepatic IGF-I mRNA but not IGF binding protein-3 mRNA expression in pigs. General and Comparative Endocrinology 126, 221-228

Dwivedi, P.P., Hii, C.S.T., Ferrante, A., Tan, J., Der, C.J., Omdahl, J.L., Morris, H.A. & May, B.K. (2002). Role of MAP kinases in the 1,25-dihydroxyvitamin D-3-induced transactivation of the rat cytochrome P450C24 (CYP24) promoter - Specific functions for ERK1/ERK2 and ERK5. Journal of Biological Chemistry 277, 29643-29653

Easton, C.J., Ferrante, A., Robertson, T.A. & Xia, L. (2002). Antioxidant behaviour of thia fatty acids. Australian Journal of Chemistry 55, 647-653

Emre, S., Terzioglu, M., Coskun, T., Tokath, A., Ozalp, I., Muller, V. & Hopwood, J. (2002). Biochemical and molecular analysis of mucopolysaccharidoses in Turkey. Turkish Journal of Pediatrics 44, 13-7.

Emre, S., Terzioglu, M., Tokatli, A., Coskun, T., Ozalp, I., Weber, B. & Hopwood, J.J. (2002). Sanfilippo syndrome in Turkey: Identification of novel mutations in subtypes A and B. Human Mutation 19, 184-5.

Ford, W., Furness, M., Morris, D., Kirby, C. & Wilkinson, C. (2002). Early Antenatal Betamethasone for the Treatment of Poor Prognosis congenital diaphragmatic hernia (Abstract). Australian and New Zealand Journal of Surgery 72, 733-4.

Ford, W.D.A., Kirby, C.P., Wilkinson, C.S., Furness, V.E. & Slater, A.J. (2002). Antenatal betamethasone and favourable outcomes in fetuses with 'poor prognosis' diaphragmatic hernia. Pediatric Surgery International 18, 244-246

Gardner, R.J.M., Savarirayan, R., Coleman, L.T., Suthers, G.K. & Sheffield, L.J. (2002). Response to Ten Berg and Lindhout. Clinical Dysmorphology 11, 229-230

Garnaut, S.M., Howarth, G.S. & Read, L.C. (2002). Effects of insulin-like growth factor-I and its analogue, long-R-3-IGF-I, on intestinal absorption of 3-O-methyl-D-glucose are less pronounced than gut mucosal growth responses. Growth Factors 20, 17-25

Gaustadnes, M., Wilcken, B., Oliveriusova, J., McGill, J., Fletcher, J., Kraus, J.P. & Wilcken, D.E. (2002). The molecular basis of cystathionine beta-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment. Human Mutation 20, 117-126

Gecz, J. & Fish, G. (2003). FRAXE fragile site associated non-specific mental retardation and the FMR2 gene. in Genetics of Neurobehavioral Disorders (ed. Fish, G.) Humana Press, pp?

Gecz, J. & Gedeon, A.K. (2002). SEDL. in Encyclopedia of Molecular Medicine (ed. Creighton, T.E.) Wiley, pp 2875-2876

Gibson, R.A. (2002). Essential role of fats throughout the lifecycle (Guest Editor). Medical Journal of Australia 176 (Suppl), S105

Gibson, R.A., Makrides, M. & Colyer, C. (2002). Summary and recommendations. Medical Journal of Australia 176 (Suppl), S107-S109

Glaros, E.N., Turner, C.T., Parkinson, E.J., Hopwood, J.J. & Brooks, D.A. (2002). Immune response to enzyme replacement therapy: single epitope control of antigen distribution from circulation. Molecular Genetics and Metabolism 77, 127-135

Gold, M.S. (2002). Hypotonic-hyporesponsive episodes following pertussis vaccination - A cause for concern? Drug Safety 25, 85-90

Goldwater, P.N. & Bettelheim, K.A. (2002). Curliated Escherichia coli, soluble curlin and the sudden infant death syndrome (SIDS). Journal of Medical Microbiology 51, 1009-1012

Goldwater, P.N. & Bettelheim, K.A. (2002). Role of non-O157 : H7 Escherichia coli in hemolytic uremic syndrome. Clinical Infectious Diseases 35, 346-347

Goldwater, P.N. & Bettelheim, K.A. (2002). Verocytotoxigenic Escherichia coli serologic responses in patients with hemolytic uremic syndrome. Journal of Infectious Diseases 186, 582-582

Han, P., Guo, X.H. & Story, C.J. (2002). Enhanced expansion and maturation of megakaryocytic progenitors by fibronectin. Cytotherapy 4, 277-283

Han, P., Story, C., McDonald, T., Mrozik, K. & Snell, L. (2002). Immune escape mechanisms of childhood ALL and a potential countering role for DC-like leukemia cells. Cytotherapy 4, 165-175

Harkin, L.A., Bowser, D.N., Dibbens, L.M., Singh, R., Phillips, F., Wallace, R.H., Richards, M.C., Williams, D.A., Mulley, J.C., Berkovic, S.F., Scheffer, I.E. & Petrou, S. (2002). Truncation of the GABA(A)-receptor gamma 2 subunit in a family with generalized epilepsy with febrile seizures plus. American Journal of Human Genetics 70, 530-536

Hassan, B.B., Butler, R., Davidson, G.P., Benninga, M., Haslam, R., Barnett, C., Dent, J. & Omari, T.I. (2002). Patterns of antropyloric motility in fed healthy preterm infants. Archives of Disease in Childhood 87, F95-F99

Hawkes, J.S., Bryan, D.L. & Gibson, R.A. (2002). Cytokine production by human milk cells and peripheral blood mononuclear cells from the same mothers. Journal of Clinical Immunology 22, 338-344

Hawkes, J.S., Bryan, D.L. & Gibson, R.A. (2002). Variations in transforming growth factor beta in human milk are not related to levels in plasma. Cytokine 17, 182-186

Hawkes, J.S., Bryan, D.L., Makrides, M., Neumann, M.A. & Gibson, R.A. (2002). The effect of dietary DHA supplementation on human milk cytokines. Advances in  Experimental Medicine and Biology 503, 265-66

Hawkes, J.S., Bryan, L., Makrides, M., Neumann, M.A. & Gibson, R.A. (2002). A randomized trial of supplementation with docosahexaenoic acid-rich tuna oil and its effects on the human milk cytokines interleukin 1 beta, interleukin 6, and tumor necrosis factor alpha(1-3). American Journal of Clinical Nutrition 75, 754-760

Ho, T.T., Maguire, A.M., Aguirre, G.D., Surace, E.M., Anand, V., Zeng, Y., Salvetti, A., Hopwood, J.J., Haskins, M.E. & Bennett, J. (2002). Phenotypic rescue after adeno-associated virus-mediated detivery of 4-sutfatase to the retinal pigment epithetium of fetine mucopolysaccharidosis VI. Journal of Gene Medicine 4, 613-621

Hodge, G., Hodge, S. & Han, P. (2002). Allium sativum (garlic) suppresses leukocyte inflammatory cytokine production in vitro: Potential therapeutic use in the treatment of inflammatory bowel disease. Cytometry 48, 209-215

Holbrook, F.L., Nicholson, I.C. & Zola, H. (2002). Tolerization as a tool for generating novel monoclonal antibodies. Immunology and Cell Biology 80, 319-322

Hughes, R.J., Tivey, D.R. & Butler, R.N. (2002). Breath tests for estimating digesta transit time in chickens. Australian Poultry Science Symposium 14, 108-111

Jeffrey, B.G., Mitchell, D.C., Gibson, R.A. & Neuringer, M. (2002). n-3 Fatty acid deficiency alters recovery of the rod photoresponse in rhesus monkeys. Investigative Ophthalmology & Visual Science 43, 2806-2814

Jeffrey, B.G., Mitchell, D.C., Hibbeln, J.R., Gibson, R.A., Chedester, A.L. & Salem, N. (2002). Visual acuity and retinal function in infant monkeys fed long-chain PUFA. Lipids 37, 839-848

Johnstone, E.W., McArthur, M., Solly, P.B., Higginson, K., Byers, S. & Foster, B.K. (2002). The effect of osteogenic protein-1 in an in vivo physeal injury model. Clinical Orthopaedics and Related Research 395, 234-240

Kochetkova, M., McKenzie, O.L., Bais, A.J., Martin, J.M., Secker, G.A., Seshadri, R., Powell, J.A., Hinze, S.J., Gardner, A.E., Spendlove, H.E., O'Callaghan, N.J., Cleton-Jansen, A.M., Cornelisse, C., Whitmore, S.A., Crawford, J., Kremmidiotis, G., Sutherland, G.R. & Callen, D.F. (2002). CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3. Cancer Research 62, 4599-4604

Kulkarni, H., Goldwater, P.N., Martin, A. & Bettelheim, K.A. (2002). Escherichia coli 'O' group serological responses and clinical correlations in epidemic HUS patients. Comp Immunol Microbiol Infect Dis 25, 249-68.

Li, L., Xian, C.J., Zhong, J.H. & Zhou, X.F. (2002). Effect of lumbar 5 ventral root transection on pain behaviors: A novel rat model for neuropathic pain without axotomy of primary sensory neurons. Experimental Neurology 175, 23-34

Limberis, M., Anson, D.S., Fuller, M. & Parsons, D.W. (2002). Recovery of airway cystic fibrosis transmembrane conductance regulator function in mice with cystic fibrosis after single-dose lentivirus-mediated gene transfer. Human Gene Therapy 13, 1961-70.

Lobb, E., Butow, P., Meiser, B., Barratt, A., Kirk, J., Gattas, M., Haan, E. & Tucker, K. (2002). The use of audiotapes in consultations with women from high risk breast cancer families: a randomised trial. Journal of Medical Genetics 39, 697-703

Lobb, E.A., Butow, P.N., Meiser, B., Barratt, A., Gaff, C., Young, M.A., Kirk, J., Suthers, G.K. & Tucker, K. (2002). Tailoring communication in consultations with women from high risk breast cancer families. British Journal of Cancer 87, 502-508

Lossi, A.M., Laugier-Anfossi, F., Depetris, D., Gecz, J., Gedeon, A., Kooy, F., Schwartz, C., Mattei, M.G., Croquette, M.F. & Villard, L. (2002). Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation. Journal of Medical Genetics 39, 113-117

Lower, K., Mangelsdorf, M. & Gecz, J. (2001). Molecular genetics of X-linked mental retardation: a complex picture emerging. Expert Review of Molecular Diagnosis 1, 220-5.

Lower, K.M., Turner, G., Kerr, B.A., Mathews, K.D., Shaw, M.A., Gedeon, A.K., Schelley, S., Hoyme, H.E., White, S.M., Delatycki, M.B., Lampe, A.K., Clayton-Smith, J., Stewart, H., van Ravenswaay, C.M.A., de Vries, B.B.A., Cox, B., Grompe, M., Ross, S., Thomas, P., Mulley, J.C. & Gecz, J. (2002). Mutations in PHF6 are associated with Borjeson-Forssman-Lehmann syndrome. Nature Genetics 32, 661-665

Macardle, P.J., Mardell, C., Bailey, S., Wheatland, L., Ho, A., Jessup, C., Roberton, D.M. & Zola, H. (2002). Fc gamma Rllb expression on human germinal center B lymphocytes. European Journal of Immunology 32, 3736-3744

Maguire, A.M., Vowels, M.R., Russell, S., Cohn, R.J., Cole, C., Saxon, B., Alvaro, F. & Marshall, G.M. (2002). Allogeneic bone marrow transplant improves outcome for juvenile myelomonocytic leukaemia. Journal of Paediatrics and Child Health 38, 166-169

Makrides, M. & Gibson, R.A. (2002). The role of fats in the lifecycle stages: pregnancy and the first year of life. Medical Journal of Australia 176 (Suppl), S111-S112

Makrides, M., Hawkes, J.S., Neumann, M.A. & Gibson, R.A. (2002). Nutritional effect of including egg yolk in the weaning diet of breast-fed and formula-fed infants: a randomized controlled trial. American Journal of Clinical Nutrition 75, 1084-1092

Marini, C., Harkin, L.A., Wallace, R.H., Mulley, J.C., Scheffer, I.E. & Berkovic, S.F. (2003). Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation. Brain 126, 230-240

Martin, A.J., Pratt, N., Kennedy, J.D., Ryan, P., Ruffin, R.E., Miles, H. & Marley, J. (2002). Natural history and familial relationships of infant spilling to 9 years of age. Pediatrics 109, 1061-1067

Mason, D., Andre, P., Bensussan, A., Buckley, C., Civin, C., Clark, E., de Haas, M., Goyert, S., Hadam, M., Hart, D., Horejsi, V., Meuer, S., Morrissey, J., Schwartz-Albiez, R., Shaw, S., Simmons, D., Uguccioni, M., van der Schoot, E., Vivier, E. & Zola, H. (2002). CD antigens 2001. Modern Pathology 15, 71-76

Mason, D., Andre, P., Bensussan, A., Buckley, C., Civin, C., Clark, E., de Haas, M., Goyert, S., Hadam, M., Hart, D., Horejsi, V., Meuer, S., Morrissey, J., Schwartz-Albiez, R., Shaw, S., Simmons, D., Uguccioni, M., van der Schoot, E., Vivier, E. & Zola, H. (2002). CD antigens 2002. Journal of Immunology 168, 2083-2086

Mason, D., Andre, P., Bensussan, A., Buckley, C., Civin, C., Clark, E., de Haas, M., Goyert, S., Hadam, M., Hart, D., Horejsi, V., Meuer, S., Morrissey, J., Schwartz-Albiez, R., Shaw, S., Simmons, D., Uguccioni, M., van der Schoot, E., Vivier, E. & Zola, H. (2002). To the editor: CD antigens 2002 (Letter). Blood 99, 3877-3880

Maxwell, M.A., Allen, T., Solly, P.B., Svingen, T., Paton, B.C. & Crane, D.I. (2002). Novel PEX1 mutations and genotype-phenotype correlations in Australasian peroxisome biogenesis disorder patients. Human Mutation 20, 342-351

McRae, J.L., Murphy, B.F., Eyre, H.J., Sutherland, G.R., Crawford, J. & Cowan, P.J. (2002). Location and structure of the human FHR-5 gene. Genetica 114, 157-161

Meertens, L., Zhao, Y.J., Rosic-Kablar, S., Li, L.H., Chan, K., Dobson, H., Gartley, C., Lutzko, C., Hopwood, J., Kohn, D., Kruth, S., Hough, M.R. & Dube, I.D. (2002). In utero injection of alpha-L-iduronidase-carrying retrovirus in canine mucopolysaccharidosis type I: Infection of multiple tissues and neonatal gene expression. Human Gene Therapy 13, 1809-1820

Meikle, P.J. & Hopwood, J.J. (2002). Newborn screening for lysosomal storage disorders: issues and strategies. Current Medical Literature: Lysosomal Storage Diseases with focus on Fabry disease 2, 1-7

Nguyen, N.L., Gun, R.T., Sparnon, A.L. & Ryan, P. (2002). The importance of immediate cooling - a case series of childhood burns in Vietnam. Burns 28, 173-176

Nguyen, N.L., Gun, R.T., Sparnon, A.L. & Ryan, P. (2002). The importance of initial management: a case series of childhood burns in Vietnam. Burns 28, 167-172

Nolan, T., McIntyre, P., Roberton, D. & Descamps, D. (2002). Reactogenicity and immunogenicity of a live attenuated tetravalent measles-mumps-rubella-varicella (MMRV) vaccine. Vaccine 21, 281-289

O'Brien, T.A., Russell, S.J., Vowels, M.R., Oswald, C.M., Tiedemann, K., Shaw, P.J., Lockwood, L., Teague, L., Rice, M. & Marshall, G.M. (2002). Results of consecutive trials for children newly diagnosed with acute myeloid leukemia from the Australian and New Zealand Children's Cancer Study Group. Blood 100, 2708-2716

Omari, T.I., Barnett, C.P., Benninga, M.A., Lontis, R., Goodchild, L., Haslam, R.R., Dent, J. & Davidson, G.P. (2002). Mechanisms of gastro-oesophageal reflux in preterm and term infants with reflux disease. Gut 51, 475-479

Paton, B.C., Solly, P.B., Nelson, P.V., Pollard, A.N., Sharp, P.C. & Fietz, M.J. (2002). Molecular analysis of genomic DNA allows rapid, and accurate, prenatal diagnosis of peroxisomal D-bifunctional protein deficiency. Prenatal Diagnosis 22, 38-41

Philip, I., Ford, A. & Haslam, R. (2002). Congenital bowel perforation in twin-to-twin transfusion syndrome. Pediatric Surgery International 18, 733-4.

Pontifex, E., Williams, M.T., Lunn, R. & Parsons, D. (2002). The effect of huffing and directed coughing on energy expenditure in young asymptomatic subjects. Australian Journal of Physiotherapy 48, 209-13.

Poplawski, N.K., Harrison, J.R., Norton, W., Wiltshire, E. & Fletcher, J.M. (2002). Urine amino and organic acids analysis in developmental delay or intellectual disability. Journal of Paediatrics and Child Health 38, 475-480

Powell, J.A., Gardner, A.E., Bais, A.J., Hinze, S.J., Baker, E., Whitmore, S., Crawford, J., Kochetkova, M., Spendlove, H.E., Doggett, N.A., Sutherland, G.R., Callen, D.F. & Kremmidiotis, G. (2002). Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genes. Genomics 80, 303-310

Rey, J.M., Sawyer, M.G., Raphael, B., Patton, G.C. & Lynskey, M. (2002). Mental health of teenagers who use cannabis - Results of an Australian survey. British Journal of Psychiatry 180, 216-221

Rozaklis, T., Ramsay, S.L., Whitfield, P.D., Ranieri, E., Hopwood, J.J. & Meikle, P.J. (2002). Determination of oligosaccharides in Pompe disease by electrospray ionization tandem mass spectrometry. Clinical Chemistry 48, 131-139

Russell, F.E., van der Walt, J.H., Jacob, J., Slater, A.J. & Baghurst, P. (2002). Pulmonary volume recruitment manoeuvre restores pulmonary compliance and resistance after apnoea in anaesthetized lambs. Paediatric Anaesthesia 12, 499-506

Ruszkiewicz, A., Bennett, G., Moore, J., Manavis, J., Rudzki, B., Shen, L. & Suthers, G. (2002). Correlation of mismatch repair genes immunohistochemistry and microsatellite instability status in HNPCC-associated tumours. Pathology 34, 541-547

Sawyer, M. (2002). The mental health of young people in Australia: Report by the National Mental Health Strategy - Reply (Letter). Australian and New Zealand Journal of Psychiatry 36, 141-141

Sawyer, M., Graetz, B. & Baghurst, P. (2002). Determining child mental health. Australian and New Zealand Journal of Psychiatry 36, 483-485

Sawyer, M.G., Rey, J.M., Graetz, B.W., Clark, J.J. & Baghurst, P.A. (2002). Use of medication by young people with attention-deficit/hyperactivity disorder. Medical Journal of Australia 177, 21-25

Sawyer, M.G., Whaites, L., Rey, J.M., Hazell, P.L., Graetz, B.W. & Baghurst, P. (2002). Health-related quality of life of children and adolescents with mental disorders. Journal of the American Academy of Child and Adolescent Psychiatry 41, 530-7.

Scheffer, I.E., Wallace, R.H., Phillips, F.L., Hewson, P., Reardon, K., Parasivam, G., Stromme, P., Berkovic, S.F., Gecz, J. & Mulley, J.C. (2002). X-linked myoclonic epilepsy with spasticity and intellectual disability - Mutation in the homeobox gene ARX. Neurology 59, 348-356

Scher, A.I., Petterson, B., Blair, E., Ellenberg, J.H., Grether, J.K., Haan, E., Reddihough, D.S., Yeargin-Allsopp, M. & Nelson, K.B. (2002). The risk of mortality or cerebral palsy in twins: A collaborative population-based study. Pediatric Research 52, 671-681

Shaw, M.A., Chiurazzi, P., Romain, D.R., Neri, G. & Gecz, J. (2002). A novel gene, FAM11A, associated with the FRAXF CpG island is transcriptionally silent in FRAXF full mutation. European Journal of Human Genetics 10, 767-772

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