Batshaw ML - Search Results

1

A longitudinal study of urea cycle disorders.

Batshaw ML, Tuchman M, Summar M, Seminara J; Members of the Urea Cycle Disorders Consortium. Batshaw ML, et al. Mol Genet Metab. 2014 Sep-Oct;113(1-2):127-30. doi: 10.1016/j.ymgme.2014.08.001. Epub 2014 Aug 10. Mol Genet Metab. 2014. PMID: 25135652 Free PMC article. Review.

2

Clinical outcomes of neonatal onset proximal versus distal urea cycle disorders do not differ.

Ah Mew N, Krivitzky L, McCarter R, Batshaw M, Tuchman M; Urea Cycle Disorders Consortium of the Rare Diseases Clinical Research Network. Ah Mew N, et al. J Pediatr. 2013 Feb;162(2):324-9.e1. doi: 10.1016/j.jpeds.2012.06.065. Epub 2012 Aug 15. J Pediatr. 2013. PMID: 22901741 Free PMC article.

3

1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency.

Gropman AL, Fricke ST, Seltzer RR, Hailu A, Adeyemo A, Sawyer A, van Meter J, Gaillard WD, McCarter R, Tuchman M, Batshaw M; Urea Cycle Disorders Consortium. Gropman AL, et al. Mol Genet Metab. 2008 Sep-Oct;95(1-2):21-30. doi: 10.1016/j.ymgme.2008.06.003. Epub 2008 Jul 26. Mol Genet Metab. 2008. PMID: 18662894 Free PMC article.

4

Alternative pathway therapy for urea cycle disorders: twenty years later.

Batshaw ML, MacArthur RB, Tuchman M. Batshaw ML, et al. J Pediatr. 2001 Jan;138(1 Suppl):S46-54; discussion S54-5. doi: 10.1067/mpd.2001.111836. J Pediatr. 2001. PMID: 11148549 Review.

5

Cognitive outcome in urea cycle disorders.

Gropman AL, Batshaw ML. Gropman AL, et al. Among authors: batshaw ml. Mol Genet Metab. 2004 Apr;81 Suppl 1:S58-62. doi: 10.1016/j.ymgme.2003.11.016. Mol Genet Metab. 2004. PMID: 15050975 Review.

6

Genotype spectrum of ornithine transcarbamylase deficiency: correlation with the clinical and biochemical phenotype.

McCullough BA, Yudkoff M, Batshaw ML, Wilson JM, Raper SE, Tuchman M. McCullough BA, et al. Among authors: batshaw ml. Am J Med Genet. 2000 Aug 14;93(4):313-9. doi: 10.1002/1096-8628(20000814)93:4<313::aid-ajmg11>3.0.co;2-m. Am J Med Genet. 2000. PMID: 10946359

7

The Clinical and Translational Science Institute at Children's National: improving health through pediatric research.

Joseph J, Purucker M, Eskandanian K, Batshaw M, Tuchman M. Joseph J, et al. Clin Transl Sci. 2012 Feb;5(1):5-7. doi: 10.1111/j.1752-8062.2011.00368.x. Epub 2011 Dec 13. Clin Transl Sci. 2012. PMID: 22376250 Free PMC article. No abstract available.

8

In vivo measurement of ureagenesis with stable isotopes.

Yudkoff M, Daikhin Y, Ye X, Wilson JM, Batshaw ML. Yudkoff M, et al. Among authors: batshaw ml. J Inherit Metab Dis. 1998;21 Suppl 1:21-9. doi: 10.1023/a:1005345205403. J Inherit Metab Dis. 1998. PMID: 9686342

9

Evidence of excitotoxicity in the brain of the ornithine carbamoyltransferase deficient sparse fur mouse.

Robinson MB, Hopkins K, Batshaw ML, McLaughlin BA, Heyes MP, Oster-Granite ML. Robinson MB, et al. Among authors: batshaw ml. Brain Res Dev Brain Res. 1995 Dec 21;90(1-2):35-44. doi: 10.1016/0165-3806(96)83484-5. Brain Res Dev Brain Res. 1995. PMID: 8777776 Free article.

10

Correction of ureagenesis after gene transfer in an animal model and after liver transplantation in humans with ornithine transcarbamylase deficiency.

Batshaw ML, Robinson MB, Ye X, Pabin C, Daikhin Y, Burton BK, Wilson JM, Yudkoff M. Batshaw ML, et al. Pediatr Res. 1999 Nov;46(5):588-93. doi: 10.1203/00006450-199911000-00016. Pediatr Res. 1999. PMID: 10541323

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