Zschiesche M - Search Results

1

Carrier detection of Hunter syndrome (MPS II) by biochemical and DNA techniques in families at risk.

Schröder W, Petruschka L, Wehnert M, Zschiesche M, Seidlitz G, Hopwood JJ, Herrmann FH. Schröder W, et al. Among authors: zschiesche m. J Med Genet. 1993 Mar;30(3):210-3. doi: 10.1136/jmg.30.3.210. J Med Genet. 1993. PMID: 8097259 Free PMC article.

2

Mucopolysaccharidosis type II (Hunter syndrome): characterization of the iduronate-2-sulphatase in MPS II skin fibroblasts.

Petruschka L, Zschiesche M, Bielicki J, Seidlitz G, Machill G, Hopwood JJ, Herrmann FH. Petruschka L, et al. Among authors: zschiesche m. J Inherit Metab Dis. 1994;17(1):89-92. doi: 10.1007/BF00735402. J Inherit Metab Dis. 1994. PMID: 8051941 No abstract available.

3

[Prenatal biochemical diagnosis in genetically-induced metabolic diseases].

Machill G, Seidlitz G, Grimm U, Zschiesche M, Petruschka L, Wehnert M, Knoll W, Schütz M, Knapp A, Herrmann FH. Machill G, et al. Among authors: zschiesche m. Z Arztl Fortbild (Jena). 1988;82(22):1133-7. Z Arztl Fortbild (Jena). 1988. PMID: 3150192 German. No abstract available.

4

Severe clinical expression in X-linked Emery-Dreifuss muscular dystrophy.

Hoeltzenbein M, Karow T, Zeller JA, Warzok R, Wulff K, Zschiesche M, Herrmann FH, Grosse-Heitmeyer W, Wehnert MS. Hoeltzenbein M, et al. Among authors: zschiesche m. Neuromuscul Disord. 1999 May;9(3):166-70. doi: 10.1016/s0960-8966(98)00120-5. Neuromuscul Disord. 1999. PMID: 10382910

5

Use of a fluorogenic substrate, 6-hexadecanoylamino-4-methylumbelliferyl-beta-D-galactopyranoside, in the diagnosis of Krabbe disease.

Grimm U, Zschiesche M, Widerschain G, Seidlitz G, Machill G. Grimm U, et al. Among authors: zschiesche m. J Inherit Metab Dis. 1991;14(6):940-1. doi: 10.1007/BF01800479. J Inherit Metab Dis. 1991. PMID: 1779655 No abstract available.

6

[Identification of Krabbe disease in 2 brothers from East Germany using a new fluorogenic substrate for galactocerebrosidase].

Vidershaĭn GIa, Zschiesche M, Seidlitz G. Vidershaĭn GIa, et al. Among authors: zschiesche m. Vopr Med Khim. 1988 Jan-Feb;34(1):87-9. Vopr Med Khim. 1988. PMID: 3369131 Russian.

7

[Diagnosis of lysosomal storage diseases. Pathomorphologic and biochemical possibilities].

August CH, Holzhausen HJ, Schmidt H, Stiller D, Seidlitz G, Zschiesche M. August CH, et al. Among authors: zschiesche m. Zentralbl Allg Pathol. 1990;136(5):443-53. Zentralbl Allg Pathol. 1990. PMID: 2122616 German.

8

In vivo evidence for compromised phenylalanine metabolism in vitiligo.

Schallreuter KU, Zschiesche M, Moore J, Panske A, Hibberts NA, Herrmann FH, Metelmann HR, Sawatzki J. Schallreuter KU, et al. Among authors: zschiesche m. Biochem Biophys Res Commun. 1998 Feb 13;243(2):395-9. doi: 10.1006/bbrc.1997.8107. Biochem Biophys Res Commun. 1998. PMID: 9480820

9

[Studies on tryptophan metabolism in calcium oxalate urolithiasis].

Grimm U, Steinhauser I, Wulff K, Knapp A, Zschiesche M. Grimm U, et al. Among authors: zschiesche m. Z Urol Nephrol. 1988 May;81(5):299-303. Z Urol Nephrol. 1988. PMID: 3407338 German.

10

A new fluorimetric enzyme assay for the diagnosis of Niemann-Pick A/B, with specificity of natural sphingomyelinase substrate.

van Diggelen OP, Voznyi YV, Keulemans JL, Schoonderwoerd K, Ledvinova J, Mengel E, Zschiesche M, Santer R, Harzer K. van Diggelen OP, et al. Among authors: zschiesche m. J Inherit Metab Dis. 2005;28(5):733-41. doi: 10.1007/s10545-005-0105-y. J Inherit Metab Dis. 2005. PMID: 16151905

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