NS05096/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1980	1
1981	3
1982	2
1984	2
1986	2
1987	1
1988	3
1989	1
1990	1
1991	1
1992	6
1993	1
1995	1
1996	1
1998	1
1999	1
2005	1
2024	0

1

Shih VE, Aubry RH, DeGrande G, Gursky SF, Tanaka K. Shih VE, et al. J Pediatr. 1984 Jul;105(1):77-8. doi: 10.1016/s0022-3476(84)80367-4. J Pediatr. 1984. PMID: 6547481 No abstract available.

2

Prenatal diagnosis of non-ketotic hyperglycinemia.

Applegarth DA, Levy HL, Shih VE, McGillivray B, Wong JT, Toone JR, Kirby LT. Applegarth DA, et al. Prenat Diagn. 1986 Jul-Aug;6(4):257-63. doi: 10.1002/pd.1970060405. Prenat Diagn. 1986. PMID: 3092206

3

Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiency.

Ramesh V, Gusella JF, Shih VE. Ramesh V, et al. Mol Biol Med. 1991 Feb;8(1):81-93. Mol Biol Med. 1991. PMID: 1682785 Review.

4

Use of amniotic fluid amino acids in prenatal testing for argininosuccinic aciduria and citrullinaemia.

Mandell R, Packman S, Laframboise R, Golbus MS, Schmidt K, Workman L, Saudubray JM, Shih VE. Mandell R, et al. Prenat Diagn. 1996 May;16(5):419-24. doi: 10.1002/(SICI)1097-0223(199605)16:5<419::AID-PD872>3.0.CO;2-7. Prenat Diagn. 1996. PMID: 8843999

5

Maternal phenylketonuria--results of dietary therapy.

Lenke RR, Levy HL. Lenke RR, et al. Am J Obstet Gynecol. 1982 Mar 1;142(5):548-53. doi: 10.1016/0002-9378(82)90759-1. Am J Obstet Gynecol. 1982. PMID: 7058857

6

Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferase.

Ramesh V, Shaffer MM, Allaire JM, Shih VE, Gusella JF. Ramesh V, et al. DNA. 1986 Dec;5(6):493-501. doi: 10.1089/dna.1.1986.5.493. DNA. 1986. PMID: 3816496

7

Defective lysosomal release of vitamin B12 (cb1F): a hereditary cobalamin metabolic disorder associated with sudden death.

Shih VE, Axel SM, Tewksbury JC, Watkins D, Cooper BA, Rosenblatt DS. Shih VE, et al. Am J Med Genet. 1989 Aug;33(4):555-63. doi: 10.1002/ajmg.1320330431. Am J Med Genet. 1989. PMID: 2596518

8

Glutaric acidemia: a metabolic disorder causing progressive choreoathetosis.

Leibel RL, Shih VE, Goodman SI, Bauman ML, McCabe ER, Zwerdling RG, Bergman I, Costello C. Leibel RL, et al. Neurology. 1980 Nov;30(11):1163-8. doi: 10.1212/wnl.30.11.1163. Neurology. 1980. PMID: 6775244

9

An antispasticity effect of threonine in multiple sclerosis.

Hauser SL, Doolittle TH, Lopez-Bresnahan M, Shahani B, Schoenfeld D, Shih VE, Growdon J, Lehrich JR. Hauser SL, et al. Arch Neurol. 1992 Sep;49(9):923-6. doi: 10.1001/archneur.1992.00530330045014. Arch Neurol. 1992. PMID: 1520082 Clinical Trial.

10

Molecular analysis and prenatal diagnosis of human fumarase deficiency.

Coughlin EM, Christensen E, Kunz PL, Krishnamoorthy KS, Walker V, Dennis NR, Chalmers RA, Elpeleg ON, Whelan D, Pollitt RJ, Ramesh V, Mandell R, Shih VE. Coughlin EM, et al. Mol Genet Metab. 1998 Apr;63(4):254-62. doi: 10.1006/mgme.1998.2684. Mol Genet Metab. 1998. PMID: 9635293

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

Results by year

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

29 results

Results by year

Search Page

Filters

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

29 results

Results by year