Bachmann C - Search Results

1

Microheterogeneity of serum glycoproteins in patients with chronic alcohol abuse compared with carbohydrate-deficient glycoprotein syndrome type I.

Henry H, Froehlich F, Perret R, Tissot JD, Eilers-Messerli B, Lavanchy D, Dionisi-Vici C, Gonvers JJ, Bachmann C. Henry H, et al. Among authors: bachmann c. Clin Chem. 1999 Sep;45(9):1408-13. Clin Chem. 1999. PMID: 10471642

2

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. Among authors: bachmann c. 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

3

Determination of medium chain fatty acids in serum.

Dionisi Vici C, Bachmann C, Gradwoht M, Colombo JP. Dionisi Vici C, et al. Among authors: bachmann c. Clin Chim Acta. 1988 Mar 15;172(2-3):233-8. doi: 10.1016/0009-8981(88)90328-2. Clin Chim Acta. 1988. PMID: 3370837

4

Apolipoprotein J deficiency in types I and IV carbohydrate-deficient glycoprotein syndrome (glycanosis CDG).

Heyne K, Henry H, Messerli B, Bachmann C, Stephani U, Tissot JD, Weidinger S. Heyne K, et al. Among authors: bachmann c. Eur J Pediatr. 1997 Mar;156(3):247-8. Eur J Pediatr. 1997. PMID: 9083771 No abstract available.

5

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

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

6

Expression and function of AGAT, GAMT and CT1 in the mammalian brain.

Braissant O, Bachmann C, Henry H. Braissant O, et al. Among authors: bachmann c. Subcell Biochem. 2007;46:67-81. doi: 10.1007/978-1-4020-6486-9_4. Subcell Biochem. 2007. PMID: 18652072 Review.

7

Amyloid and non-amyloid forms of 5q31-linked corneal dystrophy resulting from kerato-epithelin mutations at Arg-124 are associated with abnormal turnover of the protein.

Korvatska E, Henry H, Mashima Y, Yamada M, Bachmann C, Munier FL, Schorderet DF. Korvatska E, et al. Among authors: bachmann c. J Biol Chem. 2000 Apr 14;275(15):11465-9. doi: 10.1074/jbc.275.15.11465. J Biol Chem. 2000. PMID: 10753964 Free article.

8

Evaluation of an intrathecal immune response in amyotrophic lateral sclerosis patients implanted with encapsulated genetically engineered xenogeneic cells.

Zurn AD, Henry H, Schluep M, Aubert V, Winkel L, Eilers B, Bachmann C, Aebischer P. Zurn AD, et al. Among authors: bachmann c. Cell Transplant. 2000 Jul-Aug;9(4):471-84. doi: 10.1177/096368970000900404. Cell Transplant. 2000. PMID: 11038064 Free article. Clinical Trial.

9

Endogenous synthesis and transport of creatine in the rat brain: an in situ hybridization study.

Braissant O, Henry H, Loup M, Eilers B, Bachmann C. Braissant O, et al. Among authors: bachmann c. Brain Res Mol Brain Res. 2001 Jan 31;86(1-2):193-201. doi: 10.1016/s0169-328x(00)00269-2. Brain Res Mol Brain Res. 2001. PMID: 11165387 Free article.

10

Ammonia toxicity to the brain and creatine.

Bachmann C, Braissant O, Villard AM, Boulat O, Henry H. Bachmann C, et al. Mol Genet Metab. 2004 Apr;81 Suppl 1:S52-7. doi: 10.1016/j.ymgme.2003.10.014. Mol Genet Metab. 2004. PMID: 15050974 Free article. Review.

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