D. Danks

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Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1

R. G. Walker, R. Gibson, D. Ravine, 1994, The Lancet.

Congenital hypothyroidism and neonatal jaundice.

D. Danks, A. Weldon, 1972, Archives of disease in childhood.

D. Danks, J. Colebatch, H. Ekert, 1968 .

Copper metabolism in mottled mouse mutants. The effect of copper therapy on lysyl oxidase activity in brindled (Mobr) mice.

D. Danks, J. Mann, J. Camakaris, 1982, The Biochemical journal.

Journal of Inherited Metabolic Disease

Heidelberg, Padova, C., 1991, Springer Netherlands.

International Nosology of Heritable Disorders of Connective Tissue, Berlin, 1986.

D. Sillence, J. Opitz, P. Beighton, 1988, American journal of medical genetics.

Studies of the aetiology of neonatal hepatitis and biliary atresia.

A L Smith, P E Campbell, I Jack, 1977, Archives of disease in childhood.

Copper and liver disease

D. Danks, 2005, European Journal of Pediatrics.

Long term prognosis for babies with neonatal liver disease.

D. Danks, A. Smith, P. Campbell, 1985, Archives of disease in childhood.

Management of Neonatal Obstructive Jaundice

D. Danks, 1977, Australian paediatric journal.

Prognosis of babies with neonatal hepatitis.

D. Danks, A. Smith, J. Rogers, 1977, Archives of disease in childhood.

A Genetic Study of Neonatal Obstructive Jaundice

D. Danks, M. Bodian, 1963, Archives of disease in childhood.

Extrahepatic biliary atresia: the frequency of potentially operable cases.

D. Danks, A. Clarke, P. Campbell, 1974, American journal of diseases of children.

Management of newborn babies in whom serious metabolic illness is anticipated.

D. Danks, 1974, Archives of disease in childhood.

Copper deficiency in humans.

D. Danks, 1980, Ciba Foundation symposium.

Treatable complications in undiagnosed cases of autosomal dominant polycystic kidney disease

D. Ravine, L. Sheffield, D. Danks, 1991, The Lancet.

Mutations affecting trace elements in humans and animals. A genetic approach to an understanding of trace elements.

D. Danks, J. Camakaris, 1983, Advances in human genetics.

LINKAGE ANALYSIS OF X-LINKED MENTAL RETARDATION WITH AND WITHOUT FRAGILE-X USING FACTOR IX GENE PROBE

M. Leversha, D. Danks, J. Halliday, 1984, The Lancet.

Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: Plasma changes and skin fibroblast phytanic acid oxidase

D. Danks, A. Fellenberg, A. Poulos, 1985, Human Genetics.

Letter: Patient with defect in leucine metabolism.

S. Wysocki, R. Hähnel, D. Danks, 1976, The New England journal of medicine.

Neuropathology in glutaric acidaemia type 1

D. Danks, B. Kleinschmidt-DeMasters, Anderson Rm, 2004, Acta Neuropathologica.

PENICILLAMINE IN WILSON'S DISEASE

D. Danks, 1982, The Lancet.

SERUM LIPOPROTEINS IN INFANTS WITH LIVER DISEASE

D. Danks, R. F. Leonard, J. Court, 1971, Australian paediatric journal.

Menkes' kinky-hair syndrome.

B. J. Stevens, D. Danks, J. Gillespie, 1972, Lancet.

A NEW FORM OF PROLONGED TRANSIENT TYROSINEMIA PRESENTING WITH SEVERE METABOLIC ACIDOSIS

D. Danks, J. Rogers, D. Danks, 1975, Acta paediatrica Scandinavica.

Studies on the mechanism of zinc uptake by human fibroblasts

D. Danks, H. Mcardle, M. Ackland, 1988, Journal of cellular physiology.

Stability of protein and mRNA in human postmortem liver--analysis by two-dimensional gel electrophoresis.

R. Cotton, D. Danks, J. Mercer, 1987, Clinica chimica acta; international journal of clinical chemistry.

Application of DNA-DNA hybridization of dual labeled probes to the detection of trisomy 21, monosomy 21, and sex determination.

D. Danks, H. Dahl, K. H. Choo, 1988, American journal of human genetics.

Identification of the mutations in the T-protein gene causing typical and atypical nonketotic hyperglycinemia

E. R. Baumgartner, D. Danks, K. Okamura-Ikeda, 1994, Human Genetics.

New estimates of down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined population

D. Danks, L. Watson, J. Halliday, 1995, Prenatal diagnosis.

ANTICONVULSANTS AND CONGENITAL ABNORMALITIES

D. Danks, J. Barry, 1974 .

DNA repair characteristics and mutations in the ERCC2 DNA repair and transcription gene in a trichothiodystrophy patient

D. Danks, K. Takayama, J. Cleaver, 1997, Human mutation.

TETRAHYDROBIOPTERIN TREATMENT OF VARIANT FORM OF PHENYLKETONURIA

R. Cotton, D. Danks, P. Schlesinger, 1975, The Lancet.

Letter: Tetrahydrobiopterin treatment of variant form of phenylketonuria.

R. Cotton, D. Danks, P. Schlesinger, 1975, Lancet.

Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication.

J. Cashman, D. Danks, S. Forrest, 1998, Human molecular genetics.

Medium-chain triglyceride diet: its use in treatment of liver disease.

D. Danks, V. Burke, 1966, British medical journal.

Clinical variability in osteogenesis imperfecta-variable expressivity or genetic heterogeneity.

D. Sillence, D. Rimoin, D. Danks, 1979, Birth defects original article series.

X-linked pyruvate dehydrogenase E1α subunit deficiency in heterozygous females: Variable manifestation of the same mutation

G. Brown, D. Danks, H. Dahl, 1992, Journal of Inherited Metabolic Disease.

Hypohidrotic ectodermal dysplasia. A study of sweat pores in the X-linked form and in a family with probable autosomal recessive inheritance.

D. Danks, I. A. Crump, 1971, The Journal of pediatrics.

Malignant hyperphenylalaninaemia—Current status (June 1977)

D. Danks, W. Pfleiderer, B. Clayton, 1978, Journal of Inherited Metabolic Disease.

FETAL CHROMOSOME ABNORMALITIES

D. Danks, 1985, The Lancet.

DIHYDROPTERIDINE REDUCTASE DEFICIENCY DIAGNOSIS BY ASSAYS ON PERIPHERAL BLOOD CELLS

D. Danks, R. Cotton, F. Firgaira, 1979, The Lancet.

Human dihydropteridine reductase: a method for the measurement of activity in cultured cells, and its application to malignant hyperphenylalaninemia.

R. Cotton, D. Danks, F. Firgaira, 1979, Clinica chimica acta; international journal of clinical chemistry.

VARIANT FORMS OF PHENYLKETONURIA

R. Cotton, D. Danks, 1976, The Lancet.

VARIANT FORMS OF PHENYLKETONURIA

R. Cotton, D. Danks, P. Schlesinger, 1976, The Lancet.

HEREDITARY FRUCTOSE INTOLERANCE: REPORT OF A CASE AND COMMENTS ON THE HAZARDS OF FRUCTOSE INFUSION

D. Danks, J. Solomon, D. Danks, 1972, Australian paediatric journal.

Diagnosis of Wilson's disease in children with liver disease. A report of two families.

B. J. Stevens, D. Danks, 1969, Lancet.

Menkes' Kinky Hair Disease: Further Definition of the Defect in Copper Transport

B. J. Stevens, D. Danks, R. Townley, 1973, Science.

Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuria.

R. Cotton, D. Danks, I. Jennings, 1979, The Biochemical journal.

Developmental variation in copper, zinc and metallothionein mRNA in brindled mutant and nutritionally copper deficient mice.

D. Danks, J. Camakaris, J. Mercer, 1991, Biochimica et biophysica acta.

Homocystinuria, addisonian pernicious anaemia, and partial deletion of a G chromosome.

D. Danks, R. Townley, R. Shipman, 1969, Lancet.

The natural history of untreated phenylketonuria over 20 years

D. Danks, D. Pitt, 1991, Journal of paediatrics and child health.

Screening for cystic fibrosis: use of ΔF508 mutation

D. Danks, R. Shepherd, F. Bowling, 1990, The Lancet.

Phenylalanine hydroxylation and tyrosine requirement of cultured cells. Evidence of phenylalanine hydroxylation in mastocytoma cells in culture.

R. Cotton, D. Danks, K. H. Choo, 1976, Experimental cell research.

Ketotic hypoglycaemia presenting as a life-threatening situation in a child with amelia

D. Danks, E. Treacy, 2005, European Journal of Pediatrics.

The importance of further cytogenetic and molecular investigation of acrocentric variants: justification by presentation of a case [t(8;14)(q24;p11)]

M. Leversha, D. Danks, L. Voullaire, 1991, Human Genetics.

Of mice and men, metals and mutations.

D. Danks, 1986, Journal of medical genetics.

Demonstration of two forms of phenylalanine hydroxylase in human liver obtained at autopsy.

D. Danks, J. Connellan, 1973, Biochimica et biophysica acta.

A comparison of phenotype and copper distribution in blotchy and brindled mutant mice and in nutritionally copper deficient controls

D. Danks, J. Camakaris, M. Phillips, 1991, Biological Trace Element Research.

Failure to confirm abnormal copper utilization in crinkler (cr) mice

D. Danks, J. Mann, J. Camakaris, 1981, Biological Trace Element Research.

Altered copper metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutants

R. Cotton, D. Danks, J. Camakaris, 1980, Biochemical Genetics.

Distribution of trace elements in normal and diseased mouse ileum and kidney tissues

D. Danks, B. Kirby, H. Mcardle, 1991 .

The mild form of Menkes disease: progress report on the original case.

D. Danks, 1988, American journal of medical genetics.

Copper Metabolism in Menkes’ Syndrome and Mottled Mouse Mutants

D. Danks, J. Mann, J. Camakaris, 1982 .

Copper Dependent Enzymes in Mottled Mouse Mutants

D. Danks, J. Mann, J. Camakaris, 1981 .

Steely Hair, Mottled Mice and Copper Metabolism

D. Danks, 1975 .

Is Menkes' syndrome a heritable disorder of connective tissue?

D. Danks, P. Campbell, D. Danks, 1971, Lancet.

“Cerebral” lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis

G. Brown, D. Danks, D. Kirby, 2004, European Journal of Pediatrics.

X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia.

D. Danks, J. Halliday, C. W. Chow, 1986, Journal of medical genetics.

Chondrodysplasia punctata-23 cases of a mild and relatively common variety.

D. Danks, L. Sheffield, V. Mayne, 1976, The Journal of pediatrics.

Digital hypoplasia and anticonvulsants during pregnancy

D. Danks, L. Sheffield, J. Barry, 1974 .

Copper metabolism in mottled mouse mutants: distribution of 64Cu in brindled (Mobr) mice.

D. Danks, J. Mann, J. Camakaris, 1979, The Biochemical journal.

The effect of D-penicillamine on metallothionein mRNA levels and copper distribution in mouse hepatocytes.

D. Danks, H. Mcardle, P. Kyriakou, 1990, Chemico-biological interactions.

Studies oftheaetiology ofneonatal hepatitis andbiliary atresia

D. Danks, A. Smith, J. Rogers, 1977 .

IS DEATH THE END?

D. Danks, J. Rogers, 1981, Medical Journal of Australia.

Achondroplasia and hypochondroplasia. Comments on frequency, mutation rate, and radiological features in skull and spine.

D. Danks, L. Stace, F. Jensen, 1979, Journal of medical genetics.

Genetic heterogeneity in osteogenesis imperfecta.

D. Sillence, D. Danks, D M Danks, 1979, Journal of medical genetics.

Achondroplasia and hypochondroplasia Comments on frequency, mutation rate, and radiological features in skull and spine

D. Danks, L. Stace, F. Jensen, 2022 .

Zinc, Copper and Metallothionein mRNA in Sheep Liver during Development

D. Danks, A. Grimes, J. Mercer, 1988 .

MENKES'S KINKY HAIR SYNDROME

P E Campbell, B. J. Stevens, D. Danks, 1972, Pediatrics.

Early treatment of Menkes disease with parenteral copper-histidine: long-term follow-up of four treated patients.

Z. Tümer, J. Christodoulou, D. Danks, 1998, American journal of medical genetics.

Albumin has no role in the uptake of copper by human fibroblasts.

D. Danks, H. Mcardle, M. Ackland, 1987, Journal of inorganic biochemistry.

Copper metabolism in mottled mouse mutants: copper therapy of brindled (Mobr) mice.

D. Danks, J. Mann, J. Camakaris, 1979, The Biochemical journal.

Leigh syndrome: Clinical features and biochemical and DNA abnormalities

J. Christodoulou, D. Danks, H. Dahl, 1996, Annals of neurology.

SCREENING FOR AMINOACIDURIA: A CRITICAL EVALUATION OF FOUR TECHNIQUES AND A SURVEY OF A MENTALLY RETARDED POPULATION *

D. Danks, P. Tippett, L. Dimech, 1972, Australian paediatric journal.

NEONATAL JAUNDICE IN DOWN'S SYNDROME

D. Danks, 1965 .

New metabolites in isovaleric acidemia.

W. Nyhan, D. Danks, J. Hammond, 1981, Clinica chimica acta; international journal of clinical chemistry.

The urinary organic acid profile associated with 3-hydroxy-3-methylglutaric aciduria.

D. Danks, J. Hammond, K. Faull, 1976, Clinica chimica acta; international journal of clinical chemistry.

Hereditary Hyperammonaemic Syndromes — A Six Year Experience

D. Danks, J. Rogers, E. Haan, 1979, Australian paediatric journal.

The identification of 3-keto-2-methylvaleric acid and 3-hydroxy-2-methylvaleric acid in a patient with propionic acidemia.

J Hammond, D. Danks, J. Hammond, 1979, Biomedical mass spectrometry.

Asphyxiating thoracic dysplasia. Clinical, radiological, and pathological information on 10 patients.

D. Danks, P. Campbell, V. Mayne, 1977, Archives of disease in childhood.

Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiency.

R. Cotton, D. Danks, R. Cotton, 1977, The Journal of pediatrics.

A mild form of Menkes steely hair syndrome.

D. Danks, J. Camakaris, P. Procopis, 1981, The Journal of pediatrics.

Congenital cutis laxa

D. Danks, J. Rogers, 1986, Clinical genetics.

Effects of cellular copper content on copper uptake and metallothionein and ceruloplasmin mRNA levels in mouse hepatocytes.

D. Danks, H. Mcardle, J. Mercer, 1990, The Journal of nutrition.

Menkes' steely-hair (kinky-hair) disease.

B. J. Stevens, D. Danks, E. Cartwright, 1973, Lancet.

Cytomegalovirus in human milk.

D. Danks, H. Gibas, I. Jack, 1972, The New England journal of medicine.

CYTOMEGALOVIRUS INFECTION IN MELBOURNE CHILDREN *

D. Danks, E. K. Turner, J. Colebatch, 1967 .

Peroxisomal L-Pipecolic Acid Oxidation Is Deficient in Liver from Zellweger Syndrome Patients

H. Moser, D. Danks, A. Poulos, 1989, Pediatric Research.

Abnormal deoxyribose metabolites in the urine of a child with a possible new inborn error of metabolism.

J Hammond, R. Cotton, D. Danks, 1979, Biomedical mass spectrometry.

Tertiary lactic acidosis.

D. Danks, J. Rogers, R. Wilkinson, 1981, The Journal of pediatrics.

Heterogeneity of the molecular defect in human dihydropteridine reductase deficiency.

R. Cotton, D. Danks, K. H. Choo, 1981, Biochemical Journal.

Two new sulphur-containing amino acids in man.

R. Cotton, D. Danks, J. Hammond, 1981, Biomedical mass spectrometry.

Isolation and characterization of dihydropteridine reductase from human liver.

R. Cotton, D. Danks, F. Firgaira, 1981, The Biochemical journal.

Profound neurological illness, relieved by protein restriction, in a baby with a transient disturbance in the metabolism of ingested isoleucine

G. Brown, D. Danks, S. Hunt, 1987, European Journal of Pediatrics.

Urinary dihydroxanthopterin in the diagnosis of malignant hyperphenylalaninemia and phenylketonuria.

R. Cotton, D. Danks, P. Schlesinger, 1979, Clinica chimica acta; international journal of clinical chemistry.

Malignant Hyperphenylalaninemia—Clinical Features, Biochemical Findings, and Experience with Administration of Biopterins

R. Cotton, D. Danks, F. Firgaira, 1979, Pediatric Research.

The use of restriction fragment length polymorphisms in prenatal diagnosis of dihydropteridine reductase deficiency.

R. Cotton, D. Danks, H. Dahl, 1988, Journal of medical genetics.

Use of naphthoquinone adsorbent for the isolation of human dihydropteridine reductase.

R. Cotton, D. Danks, I. Jennings, 1987, Methods in enzymology.

Prenatal determination of dihydropteridine reductase in a normal fetus at risk for malignant hyperphenylalaninemia

D. Danks, K. Fowler, A. Lipson, 1983, Prenatal diagnosis.

Normal metallothionein synthesis in fibroblasts obtained from children with Indian childhood cirrhosis or copper-associated childhood cirrhosis.

W. Gahl, D. Danks, S. Hahn, 1995, Biochemical and molecular medicine.

Genetics of the mammalian phenylalanine hydroxylase system. IV. Evidence of phenylalanine hydroxylase in a cultured human hepatoma cell line

R. Cotton, D. Danks, I. Jennings, 1980, Biochemical Genetics.

Observations indicating the nature of the mutation in phenylketonuria

R. Cotton, D. Danks, I. Jennings, 1979, Journal of Inherited Metabolic Disease.

Purification of inactive phenylalanine hydroxylase protein from liver in classical phenylketonuria

D. Danks, R. Cotton, 1976, Nature.

EPIDEMIOLOGY OF HEPATITIS

D. Danks, R. Cole, 1966 .

PROLONGED NEONATAL OBSTRUCTIVE JAUNDICE. A SURVEY OF MODERN CONCEPTS.

D. Danks, 1965, Clinical pediatrics.

HEPATITIS VIRUS IN NEONATAL LIVER DISEASE

D. Danks, P. Campbell, R. Cole, 1965 .

Phenylalanine hydroxylase activity in human foetal fibroblastic cells in culture.

D. Danks, E. Cartwright, 1972, Biochimica et biophysica acta.

Isolation of phenylalanine hydroxylase-stimulating monoclonal antibody by rat-myeloma--rat-spleen-cell fusion.

R. Cotton, D. Danks, J. Camakaris, 1980, The Biochemical journal.

Familial occurrence of meconium ileus

D. Danks, P. Phelan, M. Robbie, 1981, European Journal of Pediatrics.

Cerebro-hepato-renal syndrome of Zellweger. A report of eight cases with comments upon the incidence, the liver lesion, and a fault in pipecolic acid metabolism.

D. Danks, C. Adams, P. Campbell, 1975, The Journal of pediatrics.

Autopsy findings in two siblings with infantile Refsum disease

J. Christodoulou, D. Danks, A. Fellenberg, 2004, Acta Neuropathologica.

Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophy

H. Moser, D. Danks, A. Poulos, 1988, Journal of Inherited Metabolic Disease.

A new disorder of leucine metabolism

S. Wysocki, R. Hähnel, D. Danks, 1977 .

Hypohidrotic ectodermal dysplasia A study of sweat pores in the X-linked form and in a family with

D. Danks, I. A. Crump, 1971 .

Genetic counselling.

D. Danks, 1967, Scottish medical journal.

Mental retardation, unusual face, and intrauterine growth retardation: a new recessive syndrome?

D. Danks, D. Pitt, J. Rogers, 1984, American journal of medical genetics.

beta-hydroxyisobutyryl coenzyme A deacylase deficiency: a defect in valine metabolism associated with physical malformations.

G. Brown, R. Cotton, D. Danks, 1982, Pediatrics.

Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome)

G. Brown, D. Danks, B. Kadenbach, 1989, Journal of Inherited Metabolic Disease.

The Opitz trigonocephaly syndrome. A case report.

D. Danks, F. Oberklaid, 1975, American journal of diseases of children.

DNA diagnostic tests: expanding role and evolving techniques.

D. Danks, 1991, The Medical journal of Australia.

A study of the inheritance of duplication of the kidneys and ureters.

D. Danks, J. Whitaker, 1966, The Journal of urology.

Extrahepatic biliary atresia: comments on the frequency of potentially operable cases.

D. Danks, P. Campbell, 1966, The Journal of pediatrics.

Properties of succinic semialdehyde dehydrogenase in cultured human lymphoblasts.

G. Brown, K. Gibson, W. Nyhan, 1985, Journal of neurogenetics.

Two-dimensional polyacrylamide gel analysis of fibroblast polypeptides: Discussion of its Relevance for inherited diseases

R. Cotton, D. Danks, K. Choo, 1981, Journal of Inherited Metabolic Disease.

Problems encountered in the diagnosis of galactosaemia

D. Danks, F. Oberklaid, H. Davies, 1976, Australian paediatric journal.

Copper metabolism in mottled mouse mutants: copper concentrations in tissues during development.

D. Danks, J. Mann, J. Camakaris, 1979, The Biochemical journal.

Human copper deficiency: ultrastructural studies of the aorta and skin in a child with Menkes' syndrome.

D. Danks, B. Oakes, P. Campbell, 1976, Experimental and molecular pathology.

MONOSACCHARIDE MALABSORPTION IN YOUNG INFANTS

D. Danks, V. Burke, 1966 .

The mucopolysaccharidoses

D. Danks, J. Wraith, J. Rogers, 1987, Australian paediatric journal.

Jaundice associated with bacterial infection in the newborn.

D. Danks, D. J. Hill, J. Rooney, 1971, American journal of diseases of children.

A NEW SYNDROME OF BROAD TERMINAL PHALANGES AND FACIAL ABNORMALITIES

D. Danks, M. G. Fitzgerald, J. Keipert, 1973, Australian paediatric journal.

NEONATAL RESPIRATORY DISTRESS ASSOCIATED WITH A HIGH HAEMATOCRIT READING.

D. Danks, L. Stevens, 1964, The Lancet.

Letter: Anticonvulsants and congenital abnormalities.

D. Danks, J. Barry, 1974, Lancet.

Neonatal hepatic necrosis.

B. Ruebner, D. Danks, A. Greenfield, 1969, Pediatrics.

Further delineation of the C (trigonocephaly) syndrome.

J. Opitz, R. Gorlin, E. McPherson, 1981, American journal of medical genetics.

Familial occurrence of congenital laryngeal clefts.

D. Danks, P. Phelan, H. Williams, 1973, Archives of disease in childhood.

Massive pulmonary hemorrhage as a presenting feature in congenital hyperammonemia.

D. Danks, J. Hammond, L. Sheffield, 1976, The Journal of pediatrics.

Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22.

A. Donnelly, J. Mulley, D. Danks, 1994, American journal of medical genetics.

Renal ultrasound examination of parents in dominantly inherited renal adysplasia--a note of caution.

D. Danks, A. Bankier, L. Sheffield, 1988, American journal of medical genetics.

Metaphyseal chondrodysplasia, neutropenia, and pancreatic insufficiency presenting with respiratory distress in the neonatal period.

R. Haslam, D. Danks, P. Holtzapple, 1976, Archives of disease in childhood.

Familial occurrence of congenital laryngeal clefts

D. Danks, P. Phelan, H. Williams, 1973, Archives of disease in childhood.

Carrier testing for cystic fibrosis

D. Danks, 1993, The Medical journal of Australia.

Geleophysic dysplasia.

D. Danks, A. Bankier, J. E. Wraith, 2020, American journal of medical genetics.

Trimethylaminuria, fish odour syndrome: a new method of detection and response to treatment with metronidazole

D. Danks, J. Pitt, E. Treacy, 1995, Journal of Inherited Metabolic Disease.

4 Inborn errors of trace element metabolism

D. Danks, 1985 .

Reduced lysyl oxidase activity in skin fibroblasts from patients with Menkes' syndrome.

D. Danks, J. Camakaris, P. Royce, 1980, The Biochemical journal.

The glucagonoma syndrome (necrolytic migratory erythema) and zinc

D. Danks, J. Hammond, K. Faull, 1976 .

Comments upon the classification of infantile polycystic diseases of the liver and kidney, based upon three-dimensional reconstruction of the liver

D. Danks, C. Adams, P. Campbell, 1974, Journal of medical genetics.

Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome

M. Leversha, D. Danks, K. Fowler, 1990, Human Genetics.

Genetic aspects of respiratory disease.

V. McKusick, Richard M. Goodman, D. Danks, 1963, Archives of environmental health.

Succinic semialdehyde dehydrogenase deficiency—A further case

G. Brown, D. Danks, E. Haan, 1985, Journal of Inherited Metabolic Disease.

Excerpts from: Heat Illness in Infants and Young Children a Study of 47 Cases

D. Danks, D. Webb, Jeannie Allen, 2004 .

Heat Illness in Infants and Young Children

D. Danks, D. Webb, J. Allen, 1962, British medical journal.

Uptake of copper by mouse hepatocytes

D. Danks, H. Mcardle, S. Gross, 1988, Journal of cellular physiology.

Metachromatic fibroblasts in pseudoxanthoma elasticum and Marfan's syndrome.

D. Danks, I. Jack, E. Cartwright, 1969, Lancet.

THE SANFILIPPO SYNDROME: CLINICAL, BIOCHEMICAL, RADIOLOGICAL, HAEMATOLOGICAL AND PATHOLOGICAL FEATURES OF NINE CASES

D. Danks, P. Campbell, E. Cartwright, 1972, Australian paediatric journal.

Bacterial antibodies in liver disease.

D. Danks, R. Bishop, 1972, The Lancet.

Thoracic-pelvic dysostosis: a 'new' autosomal dominant form.

D. Danks, A. Bankier, 1983, Journal of medical genetics.

Dihydrofolate reductase deficiency causing megaloblastic anemia in two families.

D. Danks, M. Schwarz, P. B. Rowe, 1976, The New England journal of medicine.

DNA and clinical medicine.

D. Danks, 1988, Australian and New Zealand journal of medicine.

Australia . of a 20 year period in Victoria , X linked hydrocephalus : a survey

D. Danks, J. Halliday, C. W. CHOWt, 2022 .

Simple method for cutting transverse sections of hair. Comments on shape of hair in Hurler and Sanfilippo syndromes.

D. Danks, I. A. Crump, 1971, Archives of disease in childhood.

The Frequency of Potentially Operable Cases

D. Danks, A. Clarke, P. Campbell, 2017 .

Nonketotic hyperglycinemia: analyses of glycine cleavage system in typical and atypical cases.

S. Packman, W. Nyhan, D. Danks, 1987, The Journal of pediatrics.

CURRENT PRACTICE Current Status of PKU Diagnosis and Treatment

D. Danks, 1979 .

Maternal phenylketonuria: successful outcome in four pregnancies treated prior to conception

D. Danks, D. Pitt, J. E. Wraith, 1988, European Journal of Pediatrics.

Difficulties in assessing the effect of strychnine on the outcome of non-ketotic hyperglycinaemia. Observations on sisters with a mild T-protein defect

D. Danks, K. Hayasaka, K. Tada, 1986, European Journal of Pediatrics.

Metabolic Causes of Mental Retardation an Appreciation of the Contribution of the Late Dr. Brian Turner

D. Danks, 1976 .

A case of craniomandibular dermatodysostosis associated with focal glomerulosclerosis

G. Becker, D. Danks, R. Walker, 1995, Pediatric Nephrology.

Early diagnosis of hyperphenylalaninemia due to tetrahydrobiopterin deficiency (malignant hyperphenylalaninemia).

R. Cotton, D. Danks, 1980, The Journal of pediatrics.

Profiles of urinary volatiles from metabolic disorders characterized by unusual odors.

D. Danks, B. Wilken, B. Halpern, 1983, Clinical chemistry.

Cloning and sequencing of a sheep metallothionein cDNA.

D. Danks, J. Mercer, I. Lazdins, 1984, European journal of biochemistry.

Spurenelemente - Analytik, Umsatz, Bedarf Mangel und Toxikologie - Symposium in Bad Kissingen 1977

J. M. Munoz, H. Bremer, G. Pahlke, 1979 .

Prevalence of K329E mutation in the medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards.

E. McCabe, D. Danks, Y. Matsubara, 1992, Progress in clinical and biological research.

Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards

D. Danks, Y. Matsubara, K. Narisawa, 1991, The Lancet.

Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease

R. Richards, D. Ravine, L. Sheffield, 1992, The Lancet.

MENKES'S KINKY HAIR SYNDROME

D. Danks, B. Stevens, P. Campbell, 1972, Pediatrics.

Difficulty in showing mosaicism in the mother of three mongols.

G. Sutherland, D. Danks, M. G. Fitzgerald, 1972, Archives of disease in childhood.

INCIDENCE OF NEURAL TUBE DEFECTS IN VICTORIA, AUSTRALIA

D. Danks, J. Halliday, 1983, The Lancet.

Gene therapy and related novel forms of treatment

D. Danks, 1993, The Medical journal of Australia.

Complete follow-up in assessing fetal losses after chorion villus sampling

D. Danks, J. Lumley, J. Halliday, 1990, The Lancet.

Extrahepatic biliary atresia. Further comments on potentially operable cases.

D. Danks, A. Clarke, P. Campbell, 1968, Journal of pediatric surgery.

The incidence and presentation of cystic fibrosis in Victoria 1955–1978

D. Danks, P. Phelan, M. Robbie, 1980, Australian paediatric journal.

Uptake and efflux of copper-64 in Menkes'-disease and normal continuous lymphoid cell lines.

D. Danks, J. Camakaris, P. Wookey, 1987, The Biochemical journal.

Malonyl coenzyme a decarboxylase deficiency

G. Brown, D. Danks, A. Bankier, 1984, Journal of Inherited Metabolic Disease.

Hairs from patients with maple syrup urine disease show a structural defect in the fiber cuticle.

D. Peet, D. Danks, A. Negri, 1996, The Journal of investigative dermatology.

A new sulfur amino acid, named hawkinsin, identified in a baby with transient tyrosinemia and her mother.

D. Danks, A. Niederwieser, A. Matasović, 1977, Clinica chimica acta; international journal of clinical chemistry.

Hepatic ceruloplasmin gene expression is unaltered in the toxic milk mouse.

D. Danks, A. Grimes, J. Mercer, 1991, The Journal of nutrition.

PALMOPLANTAR KERATODERMA WITH NORMAL INTELLIGENCE IN TYROSINAEMIA II

D. Danks, Noel J. Callan, 1988, The Australasian journal of dermatology.

Congenital absence of pyramids and its significance in genetic diseases

D. Danks, D. Fortune, J. Halliday, 2004, Acta Neuropathologica.

Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuria.

D. Danks, F. Endo, I. Matsuda, 2000, Molecular genetics and metabolism.

Craniomandibular dermatodysostosis.

D. Danks, V. Mayne, R. K. Hall, 1974, Birth defects original article series.

Frontometaphyseal dysplasia: a progressive disease of bone and connective tissue.

D. Danks, V. Mayne, 1974, Birth defects original article series.

Fronto-metaphyseal dysplasia. A progressive disease of bone and connective tissue.

D. Danks, V. Mayne, R. K. Hall, 1972, American journal of diseases of children.

Striatal degeneration in glutaric acidaemia type II

G. Brown, D. Danks, J. Pitt, 2004, Acta Neuropathologica.

Germ-line gene therapy: no place in treatment of genetic disease.

D. Danks, 1994, Human gene therapy.

PAEDIATRICIANS' REPORTS TO GENERAL PRACTITIONERS: SHOULD PARENTS RECEIVE COPIES?

D. Danks, 1994, Journal of paediatrics and child health.

Precocious Type of Osteodysplasia

D. Danks, K. Kozłowski, V. Mayne, 1973, Acta radiologica: diagnosis.

Deoxyribose-5-phosphate aldolase deficiency — A harmless inborn error of metabolism

G. Brown, R. Cotton, D. Danks, 1983, Journal of Inherited Metabolic Disease.

X linked hydrocephalus: a surveyofa20yearperiod inVictoria, Australia

D. Danks, J. Halliday, C. W. CHOWt, 1986 .

Menkes kinky-hair syndrome. An inherited defect in the intestinal absorption of copper with widespread effects.

B. J. Stevens, D. Danks, J. Gillespie, 1974, Birth defects original article series.

Wilson's disease in adults with cirrhosis but no neurological abnormalities.

D. Danks, E. Prewett, R. Sewell, 1990, BMJ.

Excretion of cis- and trans-4-hydroxycyclohexylacetic acid in addition to hawkinsin in a family with a postulated defect of 4-hydroxyphenylpyruvate dioxygenase.

S. K. Wadman, D. Danks, A. Niederwieser, 1978, Clinica chimica acta; international journal of clinical chemistry.

Prenatal diagnosis of sex-linked hydrocephalus.

D. Danks, J. Rogers, 1983, Prenatal diagnosis.

Copper-induced dystonia secondary to cholestatic liver disease

D. Danks, 1990, The Lancet.

Copper induction of translatable metallothionein messenger RNA

D. Danks, J. Camakaris, J. Mercer, 1981, Bioscience reports.

Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypes.

D. Danks, F. Endo, A. Kitano, 1990, The Journal of clinical investigation.

Comment on the Diagnosis of Inborn Errors of Metabolism in Australia

D. Danks, 1976, Australian paediatric journal.

Genetic Disorders of Copper Transport: Menkes’ Disease, Occipital Horn Syndrome, and Wilson’s Disease

D. Danks, 1990 .

Comparisons of copper deficiency states in the murine mutants blotchy and brindled. Changes in copper-dependent enzyme activity in 13-day-old mice.

D. Danks, J. Camakaris, M. Phillips, 1986, The Biochemical journal.

MEDICAL GENETICS 1962.

V. McKusick, E. Murphy, W. M. Ginn, 1963, Journal of chronic diseases.

Double-labeling and high precision comparison of complex protein patterns on two-dimensional polyacrylamide gels.

R. Cotton, D. Danks, K. H. Choo, 1980, Analytical biochemistry.

Pseudoprecocity in an Infant due to a Luteoma of the Ovary

D. Danks, P. Campbell, 1963, Archives of disease in childhood.

Liver enzyme activities in hyperphenylalaninaemia due to a defective synthesis of tetrahydrobiopterin

D. Danks, R. Cotton, J. Dhondt, 1985, Journal of Inherited Metabolic Disease.

Normal hydroxylation of proline in collagen synthesized by skin fibroblasts from a patient with prolidase deficiency

D. Danks, Dr P. M. Royce, 1982, Journal of Inherited Metabolic Disease.

Cutis laxa with delayed development

D. Danks, J. Rogers, 1985, Australian paediatric journal.

Observations on the Menkes' and brindled mouse phenotypes in cell hybrids

D. Danks, J. Camakaris, Ruth M. Brown, 1984, Somatic cell and molecular genetics.

Mutations in humans and animals which affect copper metabolism

D. Danks, J. Camakaris, T. Stevenson, 1983, Journal of Inherited Metabolic Disease.

Retraction: No evidence for more than one locus in cystic fibrosis .

D. Danks, P. Phelan, C. Chapman, 1984, American Journal of Human Genetics.

Mutations at more than one locus may be involved in cystic fibrosis--evidence based on first-cousin data and direct counting of cases.

D. Danks, P. Phelan, C. Chapman, 1983, American Journal of Human Genetics.

Whither genetic services?

D. Danks, 1993, The Medical journal of Australia.

Postoperative ascending cholangitis following portoenterostomy for biliary atresia: measures and control. Invited commentary.

D. Danks, A. Smith, 1978, World Journal of Surgery.

Molecular biology of phenylalanine hydroxylase

R. Cotton, D. Danks, I. Jennings, 1986, Journal of Inherited Metabolic Disease.

Non-specific elevation of immunoreactive trypsinogen in sick infants

D. Ravine, D. Danks, R. Francis, 1993, European Journal of Pediatrics.

Trimethylaminuria: diet does not always control the fishy odor.

D. Danks, J. Hammond, K. Faull, 1976, The New England journal of medicine.

Metabolic Studies on Two Patients with Nonhepatic Tyrosinemia Using Deuterated Tyrosine Loads

D. Danks, R. Cotton, I. Gan, 1977, Pediatric Research.

Profiles of urinary volatiles from metabolic disorders characterized by unusual odors.

D. Danks, B. Wilken, B. Halpern, 1983, Clinical chemistry.

A screening test for urinary purines and pyrimidines and related compounds using auxotrophic mutants of Escherichia coli K12.

R. Cotton, D. Danks, J. Camakaris, 1970, Biochemical medicine.

Failure to Confirm Copper Deficiency in Crinkled Mice

D. Danks, J. Mann, J. Camakaris, 1981 .

PROSPECTS FOR THE PREVENTION OF GENETIC DISEASE

D. Danks, 1973, The Medical journal of Australia.

Difficulties in assessing the effect of strychnine on the outcome of non-ketotic hyperglycinaemia. Observations on sisters with a mild T-protein defect

D. Danks, K. Hayasaka, D. Kirby, 1986, European Journal of Pediatrics.

Blame, compensation and birth defects

D. Danks, 1985, The Medical journal of Australia.

Trimethylaminuria or fish odour syndrome in a child

D. Danks, M. Greaves, R. Marks, 1976, The British journal of dermatology.