15 results
Galactosemia
- from Part Two - Neonatal Conditions and Diseases
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- Neonatology
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- 05 November 2011
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- 04 August 2008, pp 157-157
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Glycogen Storage Disease Type II (Pompe’s Disease)
- from Part Two - Neonatal Conditions and Diseases
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- Neonatology
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- 05 November 2011
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- 04 August 2008, pp 165-165
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Phenylketonuria, Maternal
- from Part One - Maternal Conditions and Diseases
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- Neonatology
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- 05 November 2011
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- 04 August 2008, pp 49-49
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Ornithine Transcarbamylase Deficiency/Urea Cycle Disorders
- from Part Two - Neonatal Conditions and Diseases
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- 05 November 2011
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- 04 August 2008, pp 239-240
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Biotinidase Deficiency
- from Part Two - Neonatal Conditions and Diseases
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- 05 November 2011
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- 04 August 2008, pp 85-85
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Lysosomal Storage Disorders
- from Part Two - Neonatal Conditions and Diseases
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- Neonatology
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- 05 November 2011
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- 04 August 2008, pp 207-208
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Lactic Acidemias
- from Part Two - Neonatal Conditions and Diseases
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- Neonatology
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- 05 November 2011
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- 04 August 2008, pp 203-204
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Phenylketonuria, Neonatal
- from Part Two - Neonatal Conditions and Diseases
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- Neonatology
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- 05 November 2011
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- 04 August 2008, pp 257-257
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Glycogen Storage Disease Type 1A (Von Gierke’s Disease)
- from Part Two - Neonatal Conditions and Diseases
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- 04 August 2008, pp 163-164
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Fatty Acid Oxidation Disorders
- from Part Two - Neonatal Conditions and Diseases
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- 04 August 2008, pp 150-152
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Propionic Acidemia
- from Part Two - Neonatal Conditions and Diseases
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- 05 November 2011
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- 04 August 2008, pp 267-267
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Nonketotic Hyperglycinemia
- from Part Two - Neonatal Conditions and Diseases
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- 05 November 2011
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- 04 August 2008, pp 236-237
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Tyrosinemia Type I
- from Part Two - Neonatal Conditions and Diseases
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- 05 November 2011
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- 04 August 2008, pp 345-346
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Medium-Chain Acyl CoA Dehydrogenase Deficiency (MCAD)
- from Part Two - Neonatal Conditions and Diseases
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- 04 August 2008, pp 217-217
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Maple Syrup Urine Disease
- from Part Two - Neonatal Conditions and Diseases
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- Neonatology
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- 05 November 2011
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- 04 August 2008, pp 210-210
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