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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1982 1
1984 2
1985 2
1986 2
1987 2
1988 1
1989 3
1990 4
1992 4
1993 1
1994 1
1995 2
1997 1
1998 1
1999 5
2000 1
2001 2
2002 6
2003 1
2004 3
2005 3
2006 2
2008 3
2009 3
2010 3
2011 3
2012 4
2013 4
2014 6
2015 3
2016 2
2017 3
2018 3
2020 1
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83 results
Results by year
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Page 1
Phenylalanine hydroxylase deficiency: diagnosis and management guideline.
Vockley J, Andersson HC, Antshel KM, Braverman NE, Burton BK, Frazier DM, Mitchell J, Smith WE, Thompson BH, Berry SA; American College of Medical Genetics and Genomics Therapeutics Committee. Vockley J, et al. Among authors: andersson hc. Genet Med. 2014 Feb;16(2):188-200. doi: 10.1038/gim.2013.157. Epub 2013 Oct 10. Genet Med. 2014. PMID: 24385074
FGF21 underlies a hormetic response to metabolic stress in methylmalonic acidemia.
Manoli I, Sysol JR, Epping MW, Li L, Wang C, Sloan JL, Pass A, Gagné J, Ktena YP, Li L, Trivedi NS, Ouattara B, Zerfas PM, Hoffmann V, Abu-Asab M, Tsokos MG, Kleiner DE, Garone C, Cusmano-Ozog K, Enns GM, Vernon HJ, Andersson HC, Grunewald S, Elkahloun AG, Girard CL, Schnermann J, DiMauro S, Andres-Mateos E, Vandenberghe LH, Chandler RJ, Venditti CP. Manoli I, et al. Among authors: andersson hc. JCI Insight. 2018 Dec 6;3(23):e124351. doi: 10.1172/jci.insight.124351. JCI Insight. 2018. PMID: 30518688 Free PMC article.
Transformation in pretreatment manifestations of Gaucher disease type 1 during two decades of alglucerase/imiglucerase enzyme replacement therapy in the International Collaborative Gaucher Group (ICGG) Gaucher Registry.
Mistry PK, Batista JL, Andersson HC, Balwani M, Burrow TA, Charrow J, Kaplan P, Khan A, Kishnani PS, Kolodny EH, Rosenbloom B, Scott CR, Weinreb N. Mistry PK, et al. Among authors: andersson hc. Am J Hematol. 2017 Sep;92(9):929-939. doi: 10.1002/ajh.24801. Epub 2017 Jul 7. Am J Hematol. 2017. PMID: 28569047 Free PMC article. Clinical Trial.
The Baltic Sea as a time machine for the future coastal ocean.
Reusch TBH, Dierking J, Andersson HC, Bonsdorff E, Carstensen J, Casini M, Czajkowski M, Hasler B, Hinsby K, Hyytiäinen K, Johannesson K, Jomaa S, Jormalainen V, Kuosa H, Kurland S, Laikre L, MacKenzie BR, Margonski P, Melzner F, Oesterwind D, Ojaveer H, Refsgaard JC, Sandström A, Schwarz G, Tonderski K, Winder M, Zandersen M. Reusch TBH, et al. Among authors: andersson hc. Sci Adv. 2018 May 9;4(5):eaar8195. doi: 10.1126/sciadv.aar8195. eCollection 2018 May. Sci Adv. 2018. PMID: 29750199 Free PMC article. Review.
Disorders of purines and pyrimidines.
Kelley RE, Andersson HC. Kelley RE, et al. Among authors: andersson hc. Handb Clin Neurol. 2014;120:827-38. doi: 10.1016/B978-0-7020-4087-0.00055-3. Handb Clin Neurol. 2014. PMID: 24365355 Review.
Dietary guidelines for inborn errors of metabolism.
Andersson HC. Andersson HC. J Pediatr. 2017 Sep;188:1-2. doi: 10.1016/j.jpeds.2017.07.020. J Pediatr. 2017. PMID: 28843300 No abstract available.
A severity score in PGM-1 deficiency.
Andersson HC. Andersson HC. J Pediatr. 2016 Aug;175:1-4. doi: 10.1016/j.jpeds.2016.06.013. J Pediatr. 2016. PMID: 27507310 No abstract available.
Stippled Chondral Calcifications of the Patella in Zellweger Syndrome.
Rife E, Dunbar AE, Nelson SL, Andersson HC. Rife E, et al. Among authors: andersson hc. J Pediatr. 2018 Jan;192:265. doi: 10.1016/j.jpeds.2017.09.064. J Pediatr. 2018. PMID: 29246349 No abstract available.
Adamson MD, Andersson HC, Gahl WA. Adamson MD, et al. Among authors: andersson hc. Semin Nephrol. 1989 Jun;9(2):147-61. Semin Nephrol. 1989. PMID: 2672222 Review. No abstract available.
83 results
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