Wessel AE - Search Results

1

Rhabdomyolysis, acute renal failure, and cardiac arrest secondary to status dystonicus in a child with glutaric aciduria type I.

Jamuar SS, Newton SA, Prabhu SP, Hecht L, Costas KC, Wessel AE, Harris DJ, Anselm I, Berry GT. Jamuar SS, et al. Among authors: wessel ae. Mol Genet Metab. 2012 Aug;106(4):488-90. doi: 10.1016/j.ymgme.2012.05.018. Epub 2012 May 30. Mol Genet Metab. 2012. PMID: 22771013

2

The adult galactosemic phenotype.

Waisbren SE, Potter NL, Gordon CM, Green RC, Greenstein P, Gubbels CS, Rubio-Gozalbo E, Schomer D, Welt C, Anastasoaie V, D'Anna K, Gentile J, Guo CY, Hecht L, Jackson R, Jansma BM, Li Y, Lip V, Miller DT, Murray M, Power L, Quinn N, Rohr F, Shen Y, Skinder-Meredith A, Timmers I, Tunick R, Wessel A, Wu BL, Levy H, Elsas L, Berry GT. Waisbren SE, et al. J Inherit Metab Dis. 2012 Mar;35(2):279-86. doi: 10.1007/s10545-011-9372-y. Epub 2011 Jul 21. J Inherit Metab Dis. 2012. PMID: 21779791 Free PMC article.

3

Skeletal health in adult patients with classic galactosemia.

Batey LA, Welt CK, Rohr F, Wessel A, Anastasoaie V, Feldman HA, Guo CY, Rubio-Gozalbo E, Berry G, Gordon CM. Batey LA, et al. Osteoporos Int. 2013 Feb;24(2):501-9. doi: 10.1007/s00198-012-1983-0. Epub 2012 Apr 19. Osteoporos Int. 2013. PMID: 22525982

4

Management of a Woman With Maple Syrup Urine Disease During Pregnancy, Delivery, and Lactation.

Wessel AE, Mogensen KM, Rohr F, Erick M, Neilan EG, Chopra S, Levy HL, Gray KJ, Wilkins-Haug L, Berry GT. Wessel AE, et al. JPEN J Parenter Enteral Nutr. 2015 Sep;39(7):875-9. doi: 10.1177/0148607114526451. Epub 2014 Mar 11. JPEN J Parenter Enteral Nutr. 2015. PMID: 24618664

5

The complexity of newborn screening follow-up in phenylketonuria.

Hecht LE, Wessel AE, Levy HL, Berry GT. Hecht LE, et al. Among authors: wessel ae. JIMD Rep. 2014;17:37-9. doi: 10.1007/8904_2014_329. Epub 2014 Aug 26. JIMD Rep. 2014. PMID: 25155776 Free PMC article.

6

Adherence to tetrahydrobiopterin therapy in patients with phenylketonuria.

Rohr F, Wessel A, Brown M, Charette K, Levy HL. Rohr F, et al. Mol Genet Metab. 2015 Jan;114(1):25-8. doi: 10.1016/j.ymgme.2014.10.013. Epub 2014 Oct 31. Mol Genet Metab. 2015. PMID: 25467057

7

Maternal Phenylketonuria: Long-term Outcomes in Offspring and Post-pregnancy Maternal Characteristics.

Waisbren SE, Rohr F, Anastasoaie V, Brown M, Harris D, Ozonoff A, Petrides S, Wessel A, Levy HL. Waisbren SE, et al. JIMD Rep. 2015;21:23-33. doi: 10.1007/8904_2014_365. Epub 2015 Feb 25. JIMD Rep. 2015. PMID: 25712380 Free PMC article.

8

Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach.

Singh RH, Cunningham AC, Mofidi S, Douglas TD, Frazier DM, Hook DG, Jeffers L, McCune H, Moseley KD, Ogata B, Pendyal S, Skrabal J, Splett PL, Stembridge A, Wessel A, Rohr F. Singh RH, et al. Mol Genet Metab. 2016 Jun;118(2):72-83. doi: 10.1016/j.ymgme.2016.04.008. Epub 2016 Apr 17. Mol Genet Metab. 2016. PMID: 27211276 Review.

9

Liver Failure as the Presentation of Ornithine Transcarbamylase Deficiency in a 13-Month-Old Female.

Rajabi F, Rodan LH, Jonas MM, Soul JS, Ullrich NJ, Wessel A, Waisbren SE, Tan WH, Berry GT. Rajabi F, et al. JIMD Rep. 2018;40:17-22. doi: 10.1007/8904_2017_55. Epub 2017 Sep 9. JIMD Rep. 2018. PMID: 28887792 Free PMC article.

10

Phenylalanine hydroxylase genotype-phenotype associations in the United States: A single center study.

Rajabi F, Rohr F, Wessel A, Martell L, Dobrowolski SF, Guldberg P, Güttler F, Levy HL. Rajabi F, et al. Mol Genet Metab. 2019 Dec;128(4):415-421. doi: 10.1016/j.ymgme.2019.09.004. Epub 2019 Sep 14. Mol Genet Metab. 2019. PMID: 31623983

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

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

23 results

Search Page

Filters