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

The Lancet (British edition), 1994-04, Vol.343 (8901), p.824-827

1994

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

The Lancet (British edition), 1991-08, Vol.338 (8766), p.552-553

1991

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Copper deficiency in humans

Annual review of nutrition, 1988-01, Vol.8 (1), p.235-257

DANKS, D. M

1988

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Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease

The Lancet (British edition), 1992-11, Vol.340 (8831), p.1330-1333

1992

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

Wilderness & environmental medicine, 2004-12, Vol.15 (4), p.293-300

2004

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Hairs from Patients with Maple Syrup Urine Disease Show a Structural Defect in the Fiber Cuticle

Journal of investigative dermatology, 1996-03, Vol.106 (3), p.461-464

1996

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DNA ii. clinical applications

Australian prescriber, 1995-07, Vol.18 (3), p.76-79

1995

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DNA i. approach and techniques

Australian prescriber, 1995-04, Vol.18 (2), p.45-48

1995

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Metabolic stroke in methylmalonic acidemia

The Journal of pediatrics, 1989-09, Vol.115 (3), p.499-500

1989

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Extrahepatic biliary atresia: Comments on the frequency of potentially operable cases

The Journal of pediatrics, 1966-07, Vol.69 (1), p.21-29

1966

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A geneticist’s view of A.I.D

Pathology, 1983, Vol.15 (1), p.102-103

Danks, D.M.

1983

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Reply

The Journal of pediatrics, 1977-11, Vol.91 (5), p.852

Danks, D.M.

1977

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Copper-induced dystonia secondary to cholestatic liver disease

The Lancet (British edition), 1990-02, Vol.335 (8686), p.410-410

Danks, D.M

1990

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Current developments in the assessment of inborn errors of metabolism: a review

Pathology, 1975, Vol.7 (3), p.249-249

Danks, D.M.

1975

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Treatable complications in undiagnosed cases of autosomal dominant polycystic kidney disease

The Lancet (British edition), 1991-01, Vol.337 (8734), p.127-129

1991

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REYE'S SYNDROME AND ASPIRIN

The Lancet (British edition), 1987-10, Vol.330 (8563), p.864-864

Danks, D.M.

1987

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

Biological trace element research, 1991-04, Vol.29 (1), p.11-29

1991

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

Journal of inorganic biochemistry, 1987-10, Vol.31 (2), p.123-131

1987

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FETAL CHROMOSOME ABNORMALITIES

The Lancet (British edition), 1985-01, Vol.325 (8426), p.463-463

Danks, D.M.

1985

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INCIDENCE OF NEURAL TUBE DEFECTS IN VICTORIA, AUSTRALIA

The Lancet (British edition), 1983, Vol.321 (8314), p.65-65

1983

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DIAGNOSIS OF WILSON'S DISEASE IN CHILDREN WITH LIVER DISEASE

The Lancet (British edition), 1969-01, Vol.293 (7584), p.22-25

1969

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

Nuclear instruments & methods in physics research. Section B, Beam interactions with materials and atoms, 1991-03, Vol.54 (1), p.171-174

1991

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

The Lancet (British edition), 1984-08, Vol.324 (8398), p.349-349

1984

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MONOSACCHARIDE MALABSORPTION IN YOUNG INFANTS

The Lancet (British edition), 1966-05, Vol.287 (7448), p.1177-1180

1966

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[16] Use of a naphthoquinone adsorbent for the isolation of human dihydropteridine reductase

Methods in Enzymology, 1987, Vol.142, p.116-126

1987

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

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

Copper deficiency in humans

Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease

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

Hairs from Patients with Maple Syrup Urine Disease Show a Structural Defect in the Fiber Cuticle

DNA ii. clinical applications

DNA i. approach and techniques

Metabolic stroke in methylmalonic acidemia

Extrahepatic biliary atresia: Comments on the frequency of potentially operable cases

A geneticist’s view of A.I.D

Reply

Copper-induced dystonia secondary to cholestatic liver disease

Current developments in the assessment of inborn errors of metabolism: a review

Treatable complications in undiagnosed cases of autosomal dominant polycystic kidney disease

REYE'S SYNDROME AND ASPIRIN

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

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

FETAL CHROMOSOME ABNORMALITIES

INCIDENCE OF NEURAL TUBE DEFECTS IN VICTORIA, AUSTRALIA

DIAGNOSIS OF WILSON'S DISEASE IN CHILDREN WITH LIVER DISEASE

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

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

MONOSACCHARIDE MALABSORPTION IN YOUNG INFANTS

[16] Use of a naphthoquinone adsorbent for the isolation of human dihydropteridine reductase

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