Henry H - Search Results

1

Congenital disorder of glycosylation type Id (CDG Id): phenotypic, biochemical and molecular characterization of a new patient.

Rimella-Le-Huu A, Henry H, Kern I, Hanquinet S, Roulet-Perez E, Newman CJ, Superti-Furga A, Bonafé L, Ballhausen D. Rimella-Le-Huu A, et al. Among authors: henry h. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S381-6. doi: 10.1007/s10545-008-0959-x. Epub 2008 Aug 9. J Inherit Metab Dis. 2008. PMID: 18679822

2

Brain damage in methylmalonic aciduria: 2-methylcitrate induces cerebral ammonium accumulation and apoptosis in 3D organotypic brain cell cultures.

Jafari P, Braissant O, Zavadakova P, Henry H, Bonafé L, Ballhausen D. Jafari P, et al. Among authors: henry h. Orphanet J Rare Dis. 2013 Jan 8;8:4. doi: 10.1186/1750-1172-8-4. Orphanet J Rare Dis. 2013. PMID: 23298464 Free PMC article.

3

Ammonium accumulation and cell death in a rat 3D brain cell model of glutaric aciduria type I.

Jafari P, Braissant O, Zavadakova P, Henry H, Bonafé L, Ballhausen D. Jafari P, et al. Among authors: henry h. PLoS One. 2013;8(1):e53735. doi: 10.1371/journal.pone.0053735. Epub 2013 Jan 10. PLoS One. 2013. PMID: 23326493 Free PMC article.

4

Ammonium accumulation and chemokine decrease in culture media of Gcdh^-/- 3D reaggregated brain cell cultures.

Cudré-Cung HP, Remacle N, do Vale-Pereira S, Gonzalez M, Henry H, Ivanisevic J, Schmiesing J, Mühlhausen C, Braissant O, Ballhausen D. Cudré-Cung HP, et al. Among authors: henry h. Mol Genet Metab. 2019 Apr;126(4):416-428. doi: 10.1016/j.ymgme.2019.01.009. Epub 2019 Jan 18. Mol Genet Metab. 2019. PMID: 30686684

5

Ammonium accumulation is a primary effect of 2-methylcitrate exposure in an in vitro model for brain damage in methylmalonic aciduria.

Cudré-Cung HP, Zavadakova P, do Vale-Pereira S, Remacle N, Henry H, Ivanisevic J, Tavel D, Braissant O, Ballhausen D. Cudré-Cung HP, et al. Among authors: henry h. Mol Genet Metab. 2016 Sep;119(1-2):57-67. doi: 10.1016/j.ymgme.2016.07.013. Epub 2016 Jul 30. Mol Genet Metab. 2016. PMID: 27599447 Free article.

6

New in vitro model derived from brain-specific Mut-/- mice confirms cerebral ammonium accumulation in methylmalonic aciduria.

Remacle N, Forny P, Cudré-Cung HP, Gonzalez-Melo M, do Vale-Pereira S, Henry H, Teav T, Gallart-Ayala H, Braissant O, Baumgartner M, Ballhausen D. Remacle N, et al. Among authors: henry h. Mol Genet Metab. 2018 Aug;124(4):266-277. doi: 10.1016/j.ymgme.2018.06.008. Epub 2018 Jun 18. Mol Genet Metab. 2018. PMID: 29934063

7

AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: a review.

Braissant O, Henry H. Braissant O, et al. Among authors: henry h. J Inherit Metab Dis. 2008 Apr;31(2):230-9. doi: 10.1007/s10545-008-0826-9. Epub 2008 Apr 4. J Inherit Metab Dis. 2008. PMID: 18392746 Free article. Review.

8

Congenital cataract and familial brachydactyly in carbohydrate-deficient glycoprotein syndrome.

Skladal D, Sperl W, Henry H, Bachmann C. Skladal D, et al. Among authors: henry h. J Inherit Metab Dis. 1996;19(2):251-2. doi: 10.1007/BF01799442. J Inherit Metab Dis. 1996. PMID: 8739978 No abstract available.

9

Argininosuccinate neurotoxicity and prevention by creatine in argininosuccinate lyase deficiency: An in vitro study in rat three-dimensional organotypic brain cell cultures.

Diez-Fernandez C, Hertig D, Loup M, Diserens G, Henry H, Vermathen P, Nuoffer JM, Häberle J, Braissant O. Diez-Fernandez C, et al. Among authors: henry h. J Inherit Metab Dis. 2019 Nov;42(6):1077-1087. doi: 10.1002/jimd.12090. Epub 2019 Apr 14. J Inherit Metab Dis. 2019. PMID: 30907007 Free article. Review.

10

Microheterogeneity of serum glycoproteins and their liver precursors in patients with carbohydrate-deficient glycoprotein syndrome type I: apparent deficiencies in clusterin and serum amyloid P.

Henry H, Tissot JD, Messerli B, Markert M, Muntau A, Skladal D, Sperl W, Jaeken J, Weidinger S, Heyne K, Bachmann C. Henry H, et al. J Lab Clin Med. 1997 Apr;129(4):412-21. doi: 10.1016/s0022-2143(97)90074-3. J Lab Clin Med. 1997. PMID: 9104884

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