Müller T - Search Results

1

Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson's disease.

Wijmenga C, Müller T, Murli IS, Brunt T, Feichtinger H, Schönitzer D, Houwen RH, Müller W, Sandkuijl LA, Pearson PL. Wijmenga C, et al. Among authors: muller w, muller t. Eur J Hum Genet. 1998 Nov-Dec;6(6):624-8. doi: 10.1038/sj.ejhg.5200235. Eur J Hum Genet. 1998. PMID: 9887382

2

Endemic Tyrolean infantile cirrhosis: an ecogenetic disorder.

Muller T, Feichtinger H, Berger H, Muller W. Muller T, et al. Among authors: muller w. Lancet. 1996 Mar 30;347(9005):877-80. doi: 10.1016/s0140-6736(96)91351-3. Lancet. 1996. PMID: 8622397

3

Idiopathic copper toxicosis.

Müller T, Müller W, Feichtinger H. Müller T, et al. Among authors: muller w. Am J Clin Nutr. 1998 May;67(5 Suppl):1082S-1086S. doi: 10.1093/ajcn/67.5.1082S. Am J Clin Nutr. 1998. PMID: 9587156 Review.

4

Non-Indian childhood cirrhosis.

Müller T, van de Sluis B, Müller W, Pearson P, Wijmenga C. Müller T, et al. Among authors: muller w. Eur J Med Res. 1999 Jul 28;4(7):293-7. Eur J Med Res. 1999. PMID: 10425268 Review.

5

Familial clustering of infantile cirrhosis in Northern Germany: A clue to the etiology of idiopathic copper toxicosis.

Müller T, Schäfer H, Rodeck B, Haupt G, Koch H, Bosse H, Welling P, Lange H, Krech R, Feist D, Mühlendahl KE, Brämswig J, Feichtinger H, Müller W. Müller T, et al. Among authors: muller w. J Pediatr. 1999 Aug;135(2 Pt 1):189-96. doi: 10.1016/s0022-3476(99)70021-1. J Pediatr. 1999. PMID: 10431113

6

Reply.

Muller T, Muller W. Muller T, et al. Among authors: muller w. J Pediatr. 2000 Sep;137(3):440. doi: 10.1067/mpd.2000.106442. J Pediatr. 2000. PMID: 10969281 No abstract available.

7

Congenital sodium diarrhea is an autosomal recessive disorder of sodium/proton exchange but unrelated to known candidate genes.

Müller T, Wijmenga C, Phillips AD, Janecke A, Houwen RH, Fischer H, Ellemunter H, Frühwirth M, Offner F, Hofer S, Müller W, Booth IW, Heinz-Erian P. Müller T, et al. Among authors: muller w. Gastroenterology. 2000 Dec;119(6):1506-13. doi: 10.1053/gast.2000.20514. Gastroenterology. 2000. PMID: 11113072

8

Copper-associated liver disease in North Ronaldsay sheep: a possible animal model for non-Wilsonian hepatic copper toxicosis of infancy and childhood.

Haywood S, Müller T, Müller W, Heinz-Erian P, Tanner MS, Ross G. Haywood S, et al. Among authors: muller w, muller t. J Pathol. 2001 Sep;195(2):264-9. doi: 10.1002/path.930. J Pathol. 2001. PMID: 11592108

9

The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis.

Müller T, van de Sluis B, Zhernakova A, van Binsbergen E, Janecke AR, Bavdekar A, Pandit A, Weirich-Schwaiger H, Witt H, Ellemunter H, Deutsch J, Denk H, Müller W, Sternlieb I, Tanner MS, Wijmenga C. Müller T, et al. Among authors: muller w. J Hepatol. 2003 Feb;38(2):164-8. doi: 10.1016/s0168-8278(02)00356-2. J Hepatol. 2003. PMID: 12547404

10

Immunohistochemical analysis of Mallory bodies in Wilsonian and non-Wilsonian hepatic copper toxicosis.

Müller T, Langner C, Fuchsbichler A, Heinz-Erian P, Ellemunter H, Schlenck B, Bavdekar AR, Pradhan AM, Pandit A, Müller-Höcker J, Melter M, Kobayashi K, Nagasaka H, Kikuta H, Müller W, Tanner MS, Sternlieb I, Zatloukal K, Denk H. Müller T, et al. Among authors: muller w, muller hocker j. Hepatology. 2004 Apr;39(4):963-9. doi: 10.1002/hep.20108. Hepatology. 2004. PMID: 15057900

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