Enns GM - Search Results

1

Postpartum "psychosis" in mild argininosuccinate synthetase deficiency.

Enns GM, O'Brien WE, Kobayashi K, Shinzawa H, Pellegrino JE. Enns GM, et al. Obstet Gynecol. 2005 May;105(5 Pt 2):1244-6. doi: 10.1097/01.AOG.0000157769.90230.24. Obstet Gynecol. 2005. PMID: 15863597

2

Neurologic damage and neurocognitive dysfunction in urea cycle disorders.

Enns GM. Enns GM. Semin Pediatr Neurol. 2008 Sep;15(3):132-9. doi: 10.1016/j.spen.2008.05.007. Semin Pediatr Neurol. 2008. PMID: 18708004 Review.

3

Prenatal treatment of ornithine transcarbamylase deficiency.

Wilnai Y, Blumenfeld YJ, Cusmano K, Hintz SR, Alcorn D, Benitz WE, Berquist WE, Bernstein JA, Castillo RO, Concepcion W, Cowan TM, Cox KL, Lyell DJ, Esquivel CO, Homeyer M, Hudgins L, Hurwitz M, Palma JP, Schelley S, Akula VP, Summar ML, Enns GM. Wilnai Y, et al. Among authors: enns gm. Mol Genet Metab. 2018 Mar;123(3):297-300. doi: 10.1016/j.ymgme.2018.01.004. Epub 2018 Jan 16. Mol Genet Metab. 2018. PMID: 29396029

4

Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.

Enns GM, Bennett MJ, Hoppel CL, Goodman SI, Weisiger K, Ohnstad C, Golabi M, Packman S. Enns GM, et al. J Pediatr. 2000 Feb;136(2):251-4. doi: 10.1016/s0022-3476(00)70111-9. J Pediatr. 2000. PMID: 10657835

5

Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins.

Enns GM, Steiner RD, Buist N, Cowan C, Leppig KA, McCracken MF, Westphal V, Freeze HH, O'brien JF, Jaeken J, Matthijs G, Behera S, Hudgins L. Enns GM, et al. J Pediatr. 2002 Nov;141(5):695-700. doi: 10.1067/mpd.2002.128658. J Pediatr. 2002. PMID: 12410200

6

Head imaging abnormalities in dihydropyrimidine dehydrogenase deficiency.

Enns GM, Barkovich AJ, van Kuilenburg AB, Manning M, Sanger T, Witt DR, van Gennip AH. Enns GM, et al. J Inherit Metab Dis. 2004;27(4):513-22. doi: 10.1023/B:BOLI.0000037350.24142.d5. J Inherit Metab Dis. 2004. PMID: 15303009

7

Systemic hyalinosis: a distinctive early childhood-onset disorder characterized by mutations in the anthrax toxin receptor 2 gene (ANTRX2).

Shieh JT, Swidler P, Martignetti JA, Ramirez MC, Balboni I, Kaplan J, Kennedy J, Abdul-Rahman O, Enns GM, Sandborg C, Slavotinek A, Hoyme HE. Shieh JT, et al. Among authors: enns gm. Pediatrics. 2006 Nov;118(5):e1485-92. doi: 10.1542/peds.2006-0824. Epub 2006 Oct 16. Pediatrics. 2006. PMID: 17043134

8

Survival after treatment with phenylacetate and benzoate for urea-cycle disorders.

Enns GM, Berry SA, Berry GT, Rhead WJ, Brusilow SW, Hamosh A. Enns GM, et al. N Engl J Med. 2007 May 31;356(22):2282-92. doi: 10.1056/NEJMoa066596. N Engl J Med. 2007. PMID: 17538087 Free article. Clinical Trial.

9

Glutaric acidemia type I: a neurosurgical perspective. Report of two cases.

Hou LC, Veeravagu A, Hsu AR, Enns GM, Huhn SL. Hou LC, et al. Among authors: enns gm. J Neurosurg. 2007 Aug;107(2 Suppl):167-72. doi: 10.3171/PED-07/08/167. J Neurosurg. 2007. PMID: 18459892

10

Cell-based therapies for metabolic liver disease.

Enns GM, Millan MT. Enns GM, et al. Mol Genet Metab. 2008 Sep-Oct;95(1-2):3-10. doi: 10.1016/j.ymgme.2008.06.001. Epub 2008 Jul 18. Mol Genet Metab. 2008. PMID: 18640065 Review.

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