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A sensitive noninvasive method for monitoring successful liver-directed gene transfer of the low-density lipoprotein receptor in Watanabe hyperlipidemic rabbits in vivo.
Published in:
Gene Therapy, 2004, v. 11, n. 7, p. 574, doi. 10.1038/sj.gt.3302206
By:
- Tietge, U.J.F.;
- Cichon, G.;
- Büttner, C.;
- Genschel, J.;
- Heeren, J.;
- Gielow, P.;
- Grewe, N.;
- Dogar, M.;
- Beisiegel, U.;
- Manns, M.P.;
- Lochs, H.;
- Burchert, W.;
- Schmidt, H.H.-J.
Publication type:
Article
Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease.
Published in:
Clinical Genetics, 2005, v. 68, n. 6, p. 524, doi. 10.1111/j.1399-0004.2005.00528.x
By:
- Gromadzka, G.;
- Schmidt, H. H.-J.;
- Genschel, J.;
- Bochow, B.;
- Rodo, M.;
- Tarnacka, B.;
- Litwin, T.;
- Chabik, G.;
- Członkowska, A.
Publication type:
Article
Long-term treatment experience in a subject with Dunnigan-type familial partial lipodystrophy: efficacy of rosiglitazone.
Published in:
Diabetic Medicine, 2005, v. 22, n. 11, p. 1611, doi. 10.1111/j.1464-5491.2005.01757.x
By:
- Lüdtke, A.;
- Heck, K.;
- Genschel, J.;
- Mehnert, H.;
- Spuler, S.;
- Worman, H. J.;
- Schmidt, H. H.-J.
Publication type:
Article
A Q136Stop mutation in the ARH gene causing autosomal recessive hypercholesterolaemia with severely delayed LDL catabolism.
Published in:
2003
By:
- Tietge, U. J. F.;
- Genschel, J.;
- Schmidt, H. H.-J.
Publication type:
Letter
Wilson Disease: High Prevalence in a Mountaineous Area of Crete.
Published in:
Annals of Human Genetics, 2005, v. 69, n. 3, p. 268, doi. 10.1046/J.1469-1809.2005.00171.x
By:
- Dedoussis, G. V. Z.;
- Genschel, J.;
- Sialvera, T.-E.;
- Bochow, B.;
- Manolaki, N.;
- Manios, Y.;
- Tsafantakis, E.;
- Schmidt, H.
Publication type:
Article
FH clinical phenotype in Greek patients with LDL-R defective vs. negative mutations.
Published in:
European Journal of Clinical Investigation, 2004, v. 34, n. 6, p. 402, doi. 10.1111/j.1365-2362.2004.01351.x
By:
- Dedoussis, G. V. Z.;
- Skoumas, J.;
- Pitsavos, C.;
- Choumerianou, D. M.;
- Genschel, J.;
- Schmidt, H.;
- Stefanadis, C.
Publication type:
Article
P0184 ATP7B MUTATIONS IN POLISH PEDIATRIC AND ADULT PATIENTS WITH WILSON’S DISEASE.
Published in:
Journal of Pediatric Gastroenterology & Nutrition, 2004, v. 39, p. S128, doi. 10.1097/00005176-200406001-00308
By:
- Socha, P.;
- Czlonkowska, A.;
- Schmidt, H.;
- Dadalski, M.;
- Tarnacka, B.;
- Oracz, G.;
- Genschel, J.;
- Lebensztejn, D. M.;
- Socha, J.
Publication type:
Article
Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperation.
Published in:
Alimentary Pharmacology & Therapeutics, 2004, v. 19, n. 10, p. 1073, doi. 10.1111/j.1365-2036.2004.01967.x
By:
- Büning, C.;
- Genschel, J.;
- Bühner, S.;
- Krüger, S.;
- Kling, K.;
- Dignass, A.;
- Baier, P.;
- Bochow, B.;
- Ockenga, J.;
- Schmidt, H. H.‐J.;
- Lochs, H.
Publication type:
Article

Found: 8