Gray RG - Search Results

1

The usefulness of bone marrow aspiration in the diagnosis of Niemann-Pick disease type C in infantile liver disease.

Rodrigues AF, Gray RG, Preece MA, Brown R, Hill FG, Baumann U, McKiernan PJ. Rodrigues AF, et al. Among authors: gray rg. Arch Dis Child. 2006 Oct;91(10):841-4. doi: 10.1136/adc.2005.088013. Epub 2006 May 31. Arch Dis Child. 2006. PMID: 16737996 Free PMC article.

2

Inborn errors of metabolism as a cause of neurological disease in adults: an approach to investigation.

Gray RG, Preece MA, Green SH, Whitehouse W, Winer J, Green A. Gray RG, et al. J Neurol Neurosurg Psychiatry. 2000 Jul;69(1):5-12. doi: 10.1136/jnnp.69.1.5. J Neurol Neurosurg Psychiatry. 2000. PMID: 10864596 Free PMC article. Review. No abstract available.

3

Mutation screening for tyrosinaemia type I.

Heath SK, Gray RG, McKiernan P, Au KM, Walker E, Green A. Heath SK, et al. Among authors: gray rg. J Inherit Metab Dis. 2002 Oct;25(6):523-4. doi: 10.1023/a:1021275923668. J Inherit Metab Dis. 2002. PMID: 12555948

4

Mitochondrial DNA depletion syndrome is expressed in amniotic fluid cell cultures.

Blake JC, Taanman JW, Morris AM, Gray RG, Cooper JM, McKiernan PJ, Leonard JV, Schapira AH. Blake JC, et al. Among authors: gray rg. Am J Pathol. 1999 Jul;155(1):67-70. doi: 10.1016/S0002-9440(10)65100-0. Am J Pathol. 1999. PMID: 10393838 Free PMC article.

5

Ethylmalonic adipic aciduria--a treatable hepatomuscular disorder in two adult brothers.

Elias E, Gray RG, Poulton K, Green A. Elias E, et al. Among authors: gray rg. J Hepatol. 1997 Feb;26(2):433-6. doi: 10.1016/s0168-8278(97)80063-3. J Hepatol. 1997. PMID: 9059968

6

The cryopreservation of skin biopsies--a technique for reducing workload in a cell culture laboratory.

Gray RG, Ryan D, Green A. Gray RG, et al. Ann Clin Biochem. 1995 Mar;32 ( Pt 2):190-2. doi: 10.1177/000456329503200210. Ann Clin Biochem. 1995. PMID: 7785948

7

Tyrosinaemia type 1 and glutathione synthetase deficiency: two disorders with reduced hepatic thiol group concentrations and a liver 4-fumarylacetoacetate hydrolase deficiency.

Lloyd AJ, Gray RG, Green A. Lloyd AJ, et al. Among authors: gray rg. J Inherit Metab Dis. 1995;18(1):48-55. doi: 10.1007/BF00711372. J Inherit Metab Dis. 1995. PMID: 7623442

8

The Leber hereditary optic neuropathy 14,484 mutation and X-linked adrenoleukodystrophy: a possible modifier of phenotypic expression?

Gray RG, Green SH, Davies P, Alger S, Green A. Gray RG, et al. J Inherit Metab Dis. 1999 Aug;22(6):760-1. doi: 10.1023/a:1005520922737. J Inherit Metab Dis. 1999. PMID: 10472539 No abstract available.

9

Rhizomelic chondrodysplasia punctata--a new clinical variant.

Gray RG, Green A, Chapman S, McKeown C, Schutgens RB, Wanders RJ. Gray RG, et al. J Inherit Metab Dis. 1992;15(6):931-2. doi: 10.1007/BF01800236. J Inherit Metab Dis. 1992. PMID: 1293391 No abstract available.

10

Antenatal diagnosis of rhizomelic chondrodysplasia punctata in the second trimester.

Gray RG, Green A, Schutgens RB, Wanders RJ, Farndon PA, Kennedy CR. Gray RG, et al. J Inherit Metab Dis. 1990;13(3):380-2. doi: 10.1007/BF01799400. J Inherit Metab Dis. 1990. PMID: 2122105 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

145 results

Search Page

Filters