skip to main content
Show Results with:

Results 1 - 10 of 35  for Explore Further

results 1 2 3 4 next page
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Material Type:
Article
Add to My workspace

High-dose cysteine administration does not increase synthesis of the antioxidant glutathione preterm infants.

Pediatrics, November 2009, Vol.124(5), pp.e978-e984 [Peer Reviewed Journal]

No full-text

View all versions
2
Material Type:
Article
Add to My workspace

Premature aging in mice deficient in DNA repair and transcription

Science, May 17, 2002, Vol.296(5571), pp.1276-9 [Peer Reviewed Journal]

No full-text

3
Material Type:
Article
Add to My workspace

Rapid Ultraperformance Liquid Chromatography- Tandem Mass Spectrometry Assay for a Characteristic Glycogen-Derived Tetrasaccharide in Pompe Disease and Other Glycogen Storage Diseases

Clinical Chemistry, Jul 2012, Vol.58(7), pp.1139-47 [Peer Reviewed Journal]

No full-text

4
Material Type:
Article
Add to My workspace

Rapid ultraperformance liquid chromatography-tandem mass spectrometry assay for a characteristic glycogen-derived tetrasaccharide in Pompe disease and other glycogen storage diseases.

Clinical chemistry, July 2012, Vol.58(7), pp.1139-1147 [Peer Reviewed Journal]

No full-text

View all versions
5
Material Type:
Article
Add to My workspace

Black discolouration of urine in two young sisters.

Journal of paediatrics and child health, June 2016, Vol.52(6), pp.680-681 [Peer Reviewed Journal]

No full-text

View all versions
6
Material Type:
Article
Add to My workspace

Premature aging in mice deficient in DNA repair and transcription.

Science (New York, N.Y.), May 17, 2002, Vol.296(5571), pp.1276-1279 [Peer Reviewed Journal]

No full-text

View all versions
7
Material Type:
Article
Add to My workspace

The gut takes nearly all: threonine kinetics in infants1,2,3

The American Journal of Clinical Nutrition, Oct 1, 2007, Vol.86(4), p.1132 [Peer Reviewed Journal]

No full-text

8
Material Type:
Article
Add to My workspace

Quantification of free sialic acid in urine by HPLC-electrospray tandem mass spectrometry: a tool for the diagnosis of sialic acid storage disease.

Clinical chemistry, February 2004, Vol.50(2), pp.403-409 [Peer Reviewed Journal]

No full-text

View all versions
9
Material Type:
Article
Add to My workspace

Prenatal screening of sialic acid storage disease and confirmation in cultured fibroblasts by LC-MS/MS

Journal of Inherited Metabolic Disease, 2011, Vol.34(5), pp.1069-1073 [Peer Reviewed Journal]

Full text available

View all versions
10
Material Type:
Article
Add to My workspace

Incidental finding of alpha-methylacyl-CoA racemase deficiency in a patient with oculocutaneous albinism type 4

American Journal of Medical Genetics. Part A, Nov 2012, Vol.158A(11), pp.2931-2934 [Peer Reviewed Journal]

No full-text

View all versions

Results 1 - 10 of 35  for Explore Further

results 1 2 3 4 next page

Refine Search Results

Creation date 

From To
  1. Before1995  (4)
  2. 1995To2001  (6)
  3. 2002To2005  (9)
  4. 2006To2011  (8)
  5. After 2011  (8)
  6. Refine further open sub menu

Try a new search

Ignore my search and look for everything

by this Author/Contributor:

  1. Huijmans, Jan
  2. Huijmans, J.G.M.
  3. Huijmans, Jgm
  4. Huijmans, Jan G. M.
  5. Huijmans, Jan G M

on this subject:

  1. Humans
  2. Medicine
  3. Female
  4. Child
  5. Infant

Searching Remote Databases, Please Wait