Hoffmann GF - Search Results

1

Living with an inborn error of metabolism detected by newborn screening-parents' perspectives on child development and impact on family life.

Gramer G, Haege G, Glahn EM, Hoffmann GF, Lindner M, Burgard P. Gramer G, et al. Among authors: hoffmann gf. J Inherit Metab Dis. 2014 Mar;37(2):189-95. doi: 10.1007/s10545-013-9639-6. Epub 2013 Aug 16. J Inherit Metab Dis. 2014. PMID: 23949009

2

Newborn screening for disorders of fatty-acid oxidation: experience and recommendations from an expert meeting.

Lindner M, Hoffmann GF, Matern D. Lindner M, et al. Among authors: hoffmann gf. J Inherit Metab Dis. 2010 Oct;33(5):521-6. doi: 10.1007/s10545-010-9076-8. Epub 2010 Apr 7. J Inherit Metab Dis. 2010. PMID: 20373143 Review.

3

Efficacy and outcome of expanded newborn screening for metabolic diseases--report of 10 years from South-West Germany.

Lindner M, Gramer G, Haege G, Fang-Hoffmann J, Schwab KO, Tacke U, Trefz FK, Mengel E, Wendel U, Leichsenring M, Burgard P, Hoffmann GF. Lindner M, et al. Among authors: hoffmann gf. Orphanet J Rare Dis. 2011 Jun 20;6:44. doi: 10.1186/1750-1172-6-44. Orphanet J Rare Dis. 2011. PMID: 21689452 Free PMC article.

4

Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 2. From screening laboratory results to treatment, follow-up and quality assurance.

Burgard P, Rupp K, Lindner M, Haege G, Rigter T, Weinreich SS, Loeber JG, Taruscio D, Vittozzi L, Cornel MC, Hoffmann GF. Burgard P, et al. Among authors: hoffmann gf. J Inherit Metab Dis. 2012 Jul;35(4):613-25. doi: 10.1007/s10545-012-9484-z. Epub 2012 Apr 28. J Inherit Metab Dis. 2012. PMID: 22544437

5

Low lysine diet in glutaric aciduria type I--effect on anthropometric and biochemical follow-up parameters.

Boy N, Haege G, Heringer J, Assmann B, Mühlhausen C, Ensenauer R, Maier EM, Lücke T, Hoffmann GF, Müller E, Burgard P, Kölker S. Boy N, et al. Among authors: hoffmann gf. J Inherit Metab Dis. 2013 May;36(3):525-33. doi: 10.1007/s10545-012-9517-7. Epub 2012 Sep 13. J Inherit Metab Dis. 2013. PMID: 22971958 Clinical Trial.

6

50 years of newborn screening.

Hoffmann GF, Lindner M, Loeber JG. Hoffmann GF, et al. J Inherit Metab Dis. 2014 Mar;37(2):163-4. doi: 10.1007/s10545-014-9688-5. J Inherit Metab Dis. 2014. PMID: 24526389 No abstract available.

7

Neonatal mortality and outcome at the end of the first year of life in early onset urea cycle disorders--review and meta-analysis of observational studies published over more than 35 years.

Burgard P, Kölker S, Haege G, Lindner M, Hoffmann GF. Burgard P, et al. Among authors: hoffmann gf. J Inherit Metab Dis. 2016 Mar;39(2):219-29. doi: 10.1007/s10545-015-9901-1. Epub 2015 Dec 3. J Inherit Metab Dis. 2016. PMID: 26634836

8

Long-term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening.

Mütze U, Garbade SF, Gleich F, Lindner M, Freisinger P, Hennermann JB, Thimm E, Gramer G, Posset R, Krämer J, Grünert SC, Hoffmann GF, Kölker S. Mütze U, et al. Among authors: hoffmann gf. J Inherit Metab Dis. 2023 Jan;46(1):15-27. doi: 10.1002/jimd.12563. Epub 2022 Oct 4. J Inherit Metab Dis. 2023. PMID: 36134599

9

Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry: results, outcome, and implications.

Schulze A, Lindner M, Kohlmüller D, Olgemöller K, Mayatepek E, Hoffmann GF. Schulze A, et al. Among authors: hoffmann gf. Pediatrics. 2003 Jun;111(6 Pt 1):1399-406. doi: 10.1542/peds.111.6.1399. Pediatrics. 2003. PMID: 12777559

10

Phenylalanine loading in pediatric patients with dopa-responsive dystonia: revised test protocol and pediatric cutoff values.

Opladen T, Okun JG, Burgard P, Blau N, Hoffmann GF. Opladen T, et al. Among authors: hoffmann gf. J Inherit Metab Dis. 2010 Dec;33(6):697-703. doi: 10.1007/s10545-010-9164-9. Epub 2010 Jul 29. J Inherit Metab Dis. 2010. PMID: 20668943 Clinical Trial.

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