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/vufind/Search/Results?lookfor=%22McGown%2C+Ivan%22&type=Person&page=2
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PubPharm (29)
11
Is it time to commence newborn screening for congenital adrenal hyperplasia in Australia?
enthalten in:
The Medical journal of Australia
| 2011
von
Wu, J.
|
Sudeep
|
Cowley, D.
| +3
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12
Is it time to commence newborn screening for congenital adrenal hyperplasia in Australia?
enthalten in:
The medical journal of Australia
| 2011
von
Wu, J.
|
Sudeep
|
Cowley, D.
| +3
Wird geladen...
13
Adenylosuccinate lyase deficiency in a Malaysian patient, with novel adenylosuccinate lyase gene mutations
enthalten in:
Journal of inherited metabolic disease
| 2010
von
Chen, B.
|
McGown, I.
|
Thong, M.
| +5
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14
Adenylosuccinate lyase deficiency in a Malaysian patient, with novel adenylosuccinate lyase gene mutations
enthalten in:
Journal of inherited metabolic disease
| 2010
von
Chen, B.
|
McGown, I.
|
Thong, M.
| +5
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15
Adenylosuccinate lyase deficiency in a Malaysian patient, with novel adenylosuccinate lyase gene mutations
enthalten in:
Journal of inherited metabolic disease
| 2010
von
Chen, B.
|
McGown, I.
|
Thong, M.
| +5
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16
Adenylosuccinate lyase deficiency in a Malaysian patient, with novel adenylosuccinate lyase gene mutations
enthalten in:
Journal of inherited metabolic disease
| 2010
von
Chen, B.
|
McGown, I.
|
Thong, M.
| +5
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17
Investigating maturity onset diabetes of the young
enthalten in:
The Clinical biochemist. Reviews
| 2009
von
Nyunt, O.
|
Wu, J.
|
McGown, I.
| +5
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18
The clinical and biochemical spectrum of congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency
enthalten in:
The Clinical biochemist. Reviews
| 2009
von
Huynh, T.
|
McGown, I.
|
Cowley, D.
| +4
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19
A Novel V185DfsX4 Mutation of the AAAS Gene in a 2-year-old Boy with Triple A Syndrome
enthalten in:
Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
| 2009
von
Huynh, T.
|
McGown, I.
|
Nyunt, O.
| +4
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20
Utility of AVP gene testing in familial neurohypophyseal diabetes insipidus
enthalten in:
Clinical endocrinology
| 2008
von
Chitturi, S.
|
Harris, M.
|
Thomsett, M.
| +6
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Journal of inherited metabolic disease
3
Pediatric and developmental pathology
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Clinical endocrinology <Oxford>
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International journal of pediatric endocrinology
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Thema
12
Journal Article
7
Case Reports
5
Research Support, Non-U.S. Gov't
3
21-hydroxylase deficiency
3
AICAR
3
Adenylosuccinate Lyase
3
EC 4.3.2.2
3
High Performance Liquid Chromatography
3
Myoclonic Jerk
3
Plasma Amino Acid
3
Severe Psychomotor Retardation
3
congenital adrenal hyperplasia
3
neonatal screening
3
sudden infant death syndrome
2
19240-42-7
2
415SHH325A
2
4542-23-8
2
7LP2MPO46S
2
Adenosine
2
Adenosine Monophosphate
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Erscheinungszeitraum
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2000-
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1900-1999
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