Mandell R - Search Results

1

Low vitamin B6 but not homocyst(e)ine is associated with increased risk of stroke and transient ischemic attack in the era of folic acid grain fortification.

Kelly PJ, Shih VE, Kistler JP, Barron M, Lee H, Mandell R, Furie KL. Kelly PJ, et al. Among authors: mandell r. Stroke. 2003 Jun;34(6):e51-4. doi: 10.1161/01.STR.0000071109.23410.AB. Epub 2003 May 8. Stroke. 2003. PMID: 12738890

2

Inflammation, homocysteine, and vitamin B6 status after ischemic stroke.

Kelly PJ, Kistler JP, Shih VE, Mandell R, Atassi N, Barron M, Lee H, Silveira S, Furie KL. Kelly PJ, et al. Among authors: mandell r. Stroke. 2004 Jan;35(1):12-5. doi: 10.1161/01.STR.0000106481.59944.2F. Epub 2003 Dec 4. Stroke. 2004. PMID: 14657454

3

Stroke in young patients with hyperhomocysteinemia due to cystathionine beta-synthase deficiency.

Kelly PJ, Furie KL, Kistler JP, Barron M, Picard EH, Mandell R, Shih VE. Kelly PJ, et al. Among authors: mandell r. Neurology. 2003 Jan 28;60(2):275-9. doi: 10.1212/01.wnl.0000042479.55406.b3. Neurology. 2003. PMID: 12552044

4

Neonatal form of the hyperornithinaemia, hyperammonaemia, and homocitrullinuria (HHH) syndrome and prenatal diagnosis.

Shih VE, Laframboise R, Mandell R, Pichette J. Shih VE, et al. Among authors: mandell r. Prenat Diagn. 1992 Sep;12(9):717-23. doi: 10.1002/pd.1970120905. Prenat Diagn. 1992. PMID: 1438066 No abstract available.

5

Pyridoxine effects on ornithine ketoacid transaminase activity in fibroblasts from carriers of two forms of gyrate atrophy of the choroid and retina.

Shih VE, Mandell R, Berson EL. Shih VE, et al. Among authors: mandell r. Am J Hum Genet. 1988 Dec;43(6):929-33. Am J Hum Genet. 1988. PMID: 3195590 Free PMC article.

6

Argininosuccinate lyase deficiency: longterm outcome of 13 patients detected by newborn screening.

Ficicioglu C, Mandell R, Shih VE. Ficicioglu C, et al. Among authors: mandell r. Mol Genet Metab. 2009 Nov;98(3):273-7. doi: 10.1016/j.ymgme.2009.06.011. Epub 2009 Jun 25. Mol Genet Metab. 2009. PMID: 19635676 Free PMC article.

7

A missense mutation (I278T) in the cystathionine beta-synthase gene prevalent in pyridoxine-responsive homocystinuria and associated with mild clinical phenotype.

Shih VE, Fringer JM, Mandell R, Kraus JP, Berry GT, Heidenreich RA, Korson MS, Levy HL, Ramesh V. Shih VE, et al. Among authors: mandell r. Am J Hum Genet. 1995 Jul;57(1):34-9. Am J Hum Genet. 1995. PMID: 7611293 Free PMC article.

8

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

9

A simple screening test for sulfite oxidase deficiency: detection of urinary thiosulfate by a modification of Sörbo's method.

Shih VE, Carney MM, Mandell R. Shih VE, et al. Among authors: mandell r. Clin Chim Acta. 1979 Jul 2;95(1):143-5. doi: 10.1016/0009-8981(79)90348-6. Clin Chim Acta. 1979. PMID: 509724 No abstract available.

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. Among authors: mandell r. Mol Genet Metab. 1998 Apr;63(4):254-62. doi: 10.1006/mgme.1998.2684. Mol Genet Metab. 1998. PMID: 9635293

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