J. Connelly

发表

T. Brown, J. Tibballs, M. E. Dunlop, 1980, Australian paediatric journal.

Newborn Screening for Congenital Hypothyroidism, Victoria, Australia, 1977-1997. Part 1: The Screening Programme, Demography, Baseline Perinatal Data and Diagnostic Classification

A. Rickards, J. Coakley, I. Francis, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

PLASMA C19 STEROID SULPHATE LEVELS AND INDICES OF ANDROGEN BIOAVAILABILITY IN FEMALE PATTERN ANDROGENIC ALOPECIA

J. Funder, C. Whorwood, J. Montalto, 1990, Clinical endocrinology.

A fatty acid characteristic of a deficiency of linoleic acid in a case of hepatoma.

J. Connelly, F. D. Collins, 1965, Lancet.

HYPOTHALAMIC HYPOPITUITARISM FOLLOWING EXTERNAL RADIOTHERAPY FOR TUMOURS DISTANT FROM THE ADENOHYPOPHYSIS

F. Martin, D. Perry-Keene, J. Connelly, 1976, Clinical endocrinology.

An unusual case of variegate porphyria with possible homozygous inheritance.

Y. Nordmann, J. Coakley, N. Crinis, 1990, Australian and New Zealand journal of medicine.

AN AETIOLOGICAL STUDY OF NEONATAL JAUNDICE IN A CHILDREN'S HOSPITAL *

P. Campbell, D. Danks, J. Connelly, 1965 .

A review of therapeutic monitoring of chloramphenicol in patients with Haemophilus influenzae meningitis

F. Shann, J. Coakley, I. Hudson, 1992, Journal of paediatrics and child health.

Diagnosis of 21‐hydroxylase deficiency in newborn infants by GC‐MS of urinary steroids

J. Pitt, G. Warne, J. Montalto, 1988, Australian paediatric journal.

An analysis of the variation of incidence of congenital dysgenetic hypothyroidism in various countries.

J. Morissette, M. Irie, P. Walfish, 1984, Endocrinologia japonica.

Newborn screening for metabolic disorders in Australia and New Zealand: results for 1983: HumanGenetics Society of Australasia Newborn Screening Committee

B. Wilcken, E. Robertson, I. Lyon, 1985, The Medical journal of Australia.

Hyperammonaemia Due to Ornithine Transcarbamylase Deficiency

I. Hopkins, F. Hird, A. G. Dawson, 1969, Archives of disease in childhood.

GENETIC SCREENING OF THE NEWBORN IN AUSTRALIA

D. Pitt, B. Wilcken, J. Raby, 1977, Australian paediatric journal.

Newborn Screening for Congenital Hypothyroidism, Victoria, Australia, 1977-1997. Part 2: Treatment, Progress and Outcome

A. Rickards, J. Coakley, I. Francis, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

GENETIC SCREENING OF NEWBORN IN AUSTRALIA: RESULTS FOR 1979

D. Pitt, J. Raby, R. Tucker, 1981, The Medical journal of Australia.

GENETIC SCREENING OF THE NEWBORN IN AUSTRALIA: RESULTS FOR 1978

D. Pitt, J. Raby, R. Tucker, 1979, The Medical journal of Australia.

Measurement of TSH receptor blocking immunoglobulins using 3H‐adenine incorporation into FRTL‐5 and JPO9 cells: use in a child with neonatal hypothyroidism

P. Colman, A. Frauman, J. Connelly, 1995, Clinical endocrinology.

The Role of Serum 17 Alpha‐Hydroxy Progesterone in the Diagnosis of Virilizing Congenital Adrenal Hyperplasia

J. Montalto, H. Davies, J. Connelly, 1977, Australian paediatric journal.

Transient primary hypothyroidism in the newborn: Experience of the Victorian Neonatal Thyroid Screening Programme

J. Coakley, I. Francis, H. Gold, 1989, Australian paediatric journal.

THE INVESTIGATION AND TREATMENT OF PITUITARY DWARFISM: PRELIMINARY EXPERIENCE WITH HUMAN GROWTH HORMONE

H. Burger, K. Catt, F. Martin, 1967, The Medical journal of Australia.

Urinary 5-ene-steroid excretion in non-classical congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency (NC-3BHSD).

C. Whorwood, J. Montalto, J. Connelly, 1990, Journal of steroid biochemistry.

Serum levels of 5-androstene-3β, 7β-DIOL sulphate, 5α-androstane-3α,17β-DIOL sulphate and glucuronide, in late onset 21-hydroxylase deficiency

J. Funder, C. Whorwood, J. Montalto, 1990, The Journal of Steroid Biochemistry and Molecular Biology.

Serum 5-androstene-3β,17β-diol sulphate, sex hormone binding globulin and free androgen index in girls with premature adrenarche

J. Funder, J. Montalto, J. Connelly, 1989 .

Application of a non-chromatographic radio-immunoassay to the measurement of plasma 5 alpha-dihydrotestosterone in females with idiopathic hirsutism.

J. Funder, J. Montalto, J. Connelly, 1989, Scandinavian Journal of Clinical and Laboratory Investigation.

Serum C-19 steroid sulphates in females with clinical hyperandrogenism.

J. Funder, H. Davies, J. Connelly, 1989, Journal of steroid biochemistry.

Serum 5-androstene-3β,17β-DIOL sulphate and 5α-androstane-3α,17β-DIOL sulphate in hirsute females with polycystic ovarian disease

J. Funder, J. Montalto, H. Davies, 1990 .

X-linked recessive hypopituitarism.

F. Martin, P. Phelan, J. Connelly, 1971, Birth defects original article series.

Serum 5-androstene-3 beta,17 beta-diol sulphate and 5 alpha-androstane-3 alpha,17 beta-diol sulphate in hirsute females with polycystic ovarian disease.

J. Funder, J. Montalto, H. Davies, 1990, Journal of Steroid Biochemistry.