Woontner M - Search Results

1

REVIEW: Practical strategies to maintain anabolism by intravenous nutritional management in children with inborn metabolic diseases.

Kripps KA, Baker PR 2nd, Thomas JA, Skillman HE, Bernstein L, Gaughan S, Burns C, Coughlin CR 2nd, McCandless SE, Larson AA, Kochar A, Stillman CF, Wymore EM, Hendricks EG, Woontner M, Van Hove JLK. Kripps KA, et al. Among authors: woontner m. Mol Genet Metab. 2021 Jul;133(3):231-241. doi: 10.1016/j.ymgme.2021.04.007. Epub 2021 May 7. Mol Genet Metab. 2021. PMID: 33985889 Free article. Review.

2

Management of a patient with holocarboxylase synthetase deficiency.

Van Hove JL, Josefsberg S, Freehauf C, Thomas JA, Thuy le P, Barshop BA, Woontner M, Mock DM, Chiang PW, Spector E, Meneses-Morales I, Cervantes-Roldán R, León-Del-Río A. Van Hove JL, et al. Among authors: woontner m. Mol Genet Metab. 2008 Dec;95(4):201-5. doi: 10.1016/j.ymgme.2008.09.006. Epub 2008 Oct 29. Mol Genet Metab. 2008. PMID: 18974016 Free PMC article.

3

[No title available]

[No authors listed] [No authors listed] PMID: 33354834

4

The M405V allele of the glutaryl-CoA dehydrogenase gene is an important marker for glutaric aciduria type I (GA-I) low excretors.

Schillaci LA, Greene CL, Strovel E, Rispoli-Joines J, Spector E, Woontner M, Scharer G, Enns GM, Gallagher R, Zinn AB, McCandless SE, Hoppel CL, Goodman SI, Bedoyan JK. Schillaci LA, et al. Among authors: woontner m. Mol Genet Metab. 2016 Sep;119(1-2):50-6. doi: 10.1016/j.ymgme.2016.06.012. Epub 2016 Jul 1. Mol Genet Metab. 2016. PMID: 27397597

5

Maternal obesity and increased neonatal adiposity correspond with altered infant mesenchymal stem cell metabolism.

Baker PR 2nd, Patinkin Z, Shapiro AL, De La Houssaye BA, Woontner M, Boyle KE, Vanderlinden L, Dabelea D, Friedman JE. Baker PR 2nd, et al. Among authors: woontner m. JCI Insight. 2017 Nov 2;2(21):e94200. doi: 10.1172/jci.insight.94200. JCI Insight. 2017. PMID: 29093265 Free PMC article.

6

An explanation for metabolite excretion in high- and low-excretor patients with glutaric acidemia type 1.

Goodman SI, Woontner M. Goodman SI, et al. Among authors: woontner m. Mol Genet Metab. 2019 Aug;127(4):325-326. doi: 10.1016/j.ymgme.2019.07.005. Epub 2019 Jul 11. Mol Genet Metab. 2019. PMID: 31324527 No abstract available.

7

Chromatographic analysis of amino and organic acids in physiological fluids to detect inborn errors of metabolism.

Woontner M, Goodman SI. Woontner M, et al. Curr Protoc Hum Genet. 2006 Nov;Chapter 17:Unit 17.2. doi: 10.1002/0471142905.hg1702s51. Curr Protoc Hum Genet. 2006. PMID: 18428392 Review.

8

Glutaric acidemia type II: gene structure and mutations of the electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) gene.

Goodman SI, Binard RJ, Woontner MR, Frerman FE. Goodman SI, et al. Mol Genet Metab. 2002 Sep-Oct;77(1-2):86-90. doi: 10.1016/s1096-7192(02)00138-5. Mol Genet Metab. 2002. PMID: 12359134

9

Striatal neuronal death mediated by astrocytes from the Gcdh-/- mouse model of glutaric acidemia type I.

Olivera-Bravo S, Ribeiro CA, Isasi E, Trías E, Leipnitz G, Díaz-Amarilla P, Woontner M, Beck C, Goodman SI, Souza D, Wajner M, Barbeito L. Olivera-Bravo S, et al. Among authors: woontner m. Hum Mol Genet. 2015 Aug 15;24(16):4504-15. doi: 10.1093/hmg/ddv175. Epub 2015 May 12. Hum Mol Genet. 2015. PMID: 25968119

10

Analysis of the expression of murine glutaryl-CoA dehydrogenase: in vitro and in vivo studies.

Woontner M, Crnic LS, Koeller DM. Woontner M, et al. Mol Genet Metab. 2000 Feb;69(2):116-22. doi: 10.1006/mgme.2000.2962. Mol Genet Metab. 2000. PMID: 10720438

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

38 results

Search Page