Andersson H - Search Results

1

False-Positive Newborn Screen Using the Beutler Spot Assay for Galactosemia in Glucose-6-Phosphate Dehydrogenase Deficiency.

Stuhrman G, Perez Juanazo SJ, Crivelly K, Smith J, Andersson H, Morava E. Stuhrman G, et al. Among authors: andersson h. JIMD Rep. 2017;36:1-5. doi: 10.1007/8904_2016_34. Epub 2017 Jan 12. JIMD Rep. 2017. PMID: 28078493 Free PMC article.

2

Autism in patients with propionic acidemia.

Witters P, Debbold E, Crivelly K, Vande Kerckhove K, Corthouts K, Debbold B, Andersson H, Vannieuwenborg L, Geuens S, Baumgartner M, Kozicz T, Settles L, Morava E. Witters P, et al. Among authors: andersson h. Mol Genet Metab. 2016 Dec;119(4):317-321. doi: 10.1016/j.ymgme.2016.10.009. Epub 2016 Oct 31. Mol Genet Metab. 2016. PMID: 27825584

3

Focal skin defect, limb anomalies and microphthalmia.

Morava É, Jackson KE, Andersson HC. Morava É, et al. Clin Dysmorphol. 2004 Apr;13(2):113-115. Clin Dysmorphol. 2004. PMID: 15057130

4

Management dilemmas in patients with hereditary renal adysplasia.

Morava E, Smith C, Pierce M, Andersson HC. Morava E, et al. Among authors: andersson hc. J La State Med Soc. 2001 Jan;153(1):27-30. J La State Med Soc. 2001. PMID: 11272448

5

D-galactose supplementation in individuals with PMM2-CDG: results of a multicenter, open label, prospective pilot clinical trial.

Witters P, Andersson H, Jaeken J, Tseng L, van Karnebeek CDM, Lefeber DJ, Cassiman D, Morava E. Witters P, et al. Among authors: andersson h. Orphanet J Rare Dis. 2021 Mar 20;16(1):138. doi: 10.1186/s13023-020-01609-z. Orphanet J Rare Dis. 2021. PMID: 33743737 Free PMC article. Clinical Trial.

6

Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics.

Adams D, Andersson HC, Bausell H, Crivelly K, Eggerding C, Lah M, Lilienstein J, Lindstrom K, McNutt M, Ray JW, Saavedra H, Sacharow S, Starin D, Tiffany-Amaro J, Thomas J, Vucko E, Wessenberg LB, Whitehall K. Adams D, et al. Among authors: andersson hc. Mol Genet Metab Rep. 2021 Aug 14;28:100790. doi: 10.1016/j.ymgmr.2021.100790. eCollection 2021 Sep. Mol Genet Metab Rep. 2021. PMID: 34430209 Free PMC article.

7

HSD10 disease in a female: A case report and review of literature.

Upadia J, Walano N, Noh GS, Liu J, Li Y, Deputy S, Elliott LT, Wong J, Lee JA, Caylor RC, Andersson HC. Upadia J, et al. JIMD Rep. 2021 Sep 15;62(1):35-43. doi: 10.1002/jmd2.12250. eCollection 2021 Nov. JIMD Rep. 2021. PMID: 34765396 Free PMC article.

8

A SUCLG1 mutation in a patient with mitochondrial DNA depletion and congenital anomalies.

Landsverk ML, Zhang VW, Wong LC, Andersson HC. Landsverk ML, et al. Mol Genet Metab Rep. 2014 Oct 14;1:451-454. doi: 10.1016/j.ymgmr.2014.09.007. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896121 Free PMC article.

9

High protein diet mimics hypertyrosinemia in newborn infants.

Techakittiroj C, Cunningham A, Hooper PF, Andersson HC, Thoene J. Techakittiroj C, et al. J Pediatr. 2005 Feb;146(2):281-2. doi: 10.1016/j.jpeds.2004.10.013. J Pediatr. 2005. PMID: 15689925

10

Newborn screening: a national snapshot with implications for emergency preparedness.

Floyd-Browning P, Perry W, Andersson HC; Southeast Regional Collaborative Emergency Preparedness Workgroup. Floyd-Browning P, et al. J Pediatr. 2013 May;162(5):955-7.e1-2. doi: 10.1016/j.jpeds.2012.10.058. Epub 2012 Dec 11. J Pediatr. 2013. PMID: 23245195

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