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Items: 1 to 50 of 100

1.

Controversies and Variation in Diagnosing and Treating Children With Wilson Disease: Results of an International Survey.

Sturm E, Piersma FE, Tanner MS, Socha P, Roberts EA, Shneider BL.

J Pediatr Gastroenterol Nutr. 2016 Jul;63(1):82-7. doi: 10.1097/MPG.0000000000001102.

PMID:
26720766
2.

Plasma treatment of PDMS for applications of in vitro motility assays.

Lycans RM, Higgins CB, Tanner MS, Blough ER, Day BS.

Colloids Surf B Biointerfaces. 2014 Apr 1;116:687-94. doi: 10.1016/j.colsurfb.2013.11.007. Epub 2013 Nov 15.

PMID:
24309136
3.

Neonatal haemochromatosis associated with gastroschisis.

Thornton MP, Marven SS, Tanner MS, Gürtl-Lackner B.

Pediatr Surg Int. 2008 May;24(5):637-9. doi: 10.1007/s00383-008-2129-5. Epub 2008 Mar 13.

PMID:
18338135
4.

High frequency of missense mutations in glycogen storage disease type VI.

Beauchamp NJ, Taybert J, Champion MP, Layet V, Heinz-Erian P, Dalton A, Tanner MS, Pronicka E, Sharrard MJ.

J Inherit Metab Dis. 2007 Oct;30(5):722-34. Epub 2007 Aug 21.

PMID:
17705025
5.

Changes in liver volume from birth to adulthood: a meta-analysis.

Johnson TN, Tucker GT, Tanner MS, Rostami-Hodjegan A.

Liver Transpl. 2005 Dec;11(12):1481-93.

6.

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.

Hepatology. 2004 Apr;39(4):963-9.

PMID:
15057900
7.

Copper-induced hepatotoxicosis with hepatic stellate cell activation and severe fibrosis in North Ronaldsay lambs: a model for non-Wilsonian hepatic copper toxicosis of infants.

Haywood S, Müller T, Mackenzie AM, Müller W, Tanner MS, Heinz-Erian P, Williams CL, Loughran MJ.

J Comp Pathol. 2004 May;130(4):266-77.

PMID:
15053929
8.

Severe iodine deficiency in southern Albania.

Zimmermann MB, Bridson J, Bozo M, Grimci L, Selimaj V, Tanner MS.

Int J Vitam Nutr Res. 2003 Oct;73(5):347-50.

PMID:
14639798
9.

Use of basiliximab in pediatric liver transplantation for Langerhans cell histiocytosis.

Rajwal SR, Stringer MD, Davison SM, Gerrard M, Glaser A, Tanner MS, McClean P.

Pediatr Transplant. 2003 Jun;7(3):247-51. Review.

PMID:
12756053
10.

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.

J Hepatol. 2003 Feb;38(2):164-8.

PMID:
12547404
11.

Contribution of midazolam and its 1-hydroxy metabolite to preoperative sedation in children: a pharmacokinetic-pharmacodynamic analysis.

Johnson TN, Rostami-Hodjegan A, Goddard JM, Tanner MS, Tucker GT.

Br J Anaesth. 2002 Sep;89(3):428-37.

12.

Neonatal liver transplantation for fulminant hepatitis caused by herpes simplex virus type 2.

Lee WS, Kelly DA, Tanner MS, Ramani P, de Ville de Goyet J, McKiernan PJ.

J Pediatr Gastroenterol Nutr. 2002 Aug;35(2):220-3. No abstract available.

PMID:
12187302
13.

Developmental changes in the expression of enterocytic and hepatic cytochromes P4501A in rat.

Johnson TN, Tanner MS, Tucker GT.

Xenobiotica. 2002 Jul;32(7):595-604.

PMID:
12162855
14.
15.

Mechanisms of liver injury relevant to pediatric hepatology.

Tanner MS.

Crit Rev Clin Lab Sci. 2002 Feb;39(1):1-61. Review.

PMID:
11890207
16.

Successful treatment of refractory ascites in a child with transjugular intrahepatic portosystemic shunt.

Lee WS, McKiernan PJ, de Ville de Goyet JV, Tanner MS, John PR.

Acta Paediatr. 2001 Nov;90(11):1352-5.

PMID:
11808914
17.

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.

J Pathol. 2001 Sep;195(2):264-9.

PMID:
11592108
18.
19.

Alpha-1 antitrypsin deficiency.

Primhak RA, Tanner MS.

Arch Dis Child. 2001 Jul;85(1):2-5. Review. No abstract available.

20.

Features of carnitine palmitoyltransferase type I deficiency.

Olpin SE, Allen J, Bonham JR, Clark S, Clayton PT, Calvin J, Downing M, Ives K, Jones S, Manning NJ, Pollitt RJ, Standing SJ, Tanner MS.

J Inherit Metab Dis. 2001 Feb;24(1):35-42.

PMID:
11286380
21.

A comparison of the ontogeny of enterocytic and hepatic cytochromes P450 3A in the rat.

Johnson TN, Tanner MS, Tucker GT.

Biochem Pharmacol. 2000 Dec 1;60(11):1601-10.

PMID:
11077042
22.

Copper toxicity affects proliferation and viability of human hepatoma cells (HepG2 line).

Aston NS, Watt N, Morton IE, Tanner MS, Evans GS.

Hum Exp Toxicol. 2000 Jun;19(6):367-76.

PMID:
10962511
23.
24.

Assessment of stool colour in community management of prolonged jaundice in infancy.

Crofts DJ, Michel VJ, Rigby AS, Tanner MS, Hall DM, Bonham JR.

Acta Paediatr. 1999 Sep;88(9):969-74.

PMID:
10519339
25.

Recommended approaches for the laboratory measurement of homocysteine in the diagnosis and monitoring of patients with hyperhomocysteinaemia.

Moat SJ, Bonham JR, Tanner MS, Allen JC, Powers HJ.

Ann Clin Biochem. 1999 May;36 ( Pt 3):372-9.

PMID:
10376081
26.

The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial disease.

Bonham JR, Guthrie P, Downing M, Allen JC, Tanner MS, Sharrard M, Rittey C, Land JM, Fensom A, O'Neill D, Duley JA, Fairbanks LD.

J Inherit Metab Dis. 1999 Apr;22(2):174-84.

PMID:
10234613
27.

Indian childhood cirrhosis and Tyrolean childhood cirrhosis. Disorders of a copper transport gene?

Tanner MS.

Adv Exp Med Biol. 1999;448:127-37. Review. No abstract available.

PMID:
10079821
28.

Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type II.

Manning NJ, Bonham JR, Downing M, Edwards RG, Olpin SE, Pollitt RJ, Pourfarzam M, Sharrard MJ, Tanner MS.

J Inherit Metab Dis. 1999 Feb;22(1):88-9. No abstract available.

PMID:
10070625
29.

An animal model for copper-associated cirrhosis in infancy.

Aston NS, Morris PA, Tanner MS, Variend S.

J Pathol. 1998 Oct;186(2):215-21.

PMID:
9924439
30.

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis.

Strautnieks SS, Bull LN, Knisely AS, Kocoshis SA, Dahl N, Arnell H, Sokal E, Dahan K, Childs S, Ling V, Tanner MS, Kagalwalla AF, Németh A, Pawlowska J, Baker A, Mieli-Vergani G, Freimer NB, Gardiner RM, Thompson RJ.

Nat Genet. 1998 Nov;20(3):233-8.

PMID:
9806540
31.

Role of copper in Indian childhood cirrhosis.

Tanner MS.

Am J Clin Nutr. 1998 May;67(5 Suppl):1074S-1081S. doi: 10.1093/ajcn/67.5.1074S. Review.

PMID:
9587155
32.

Genetic hemochromatosis in alpha1-antitrypsin-deficient liver disease.

Sharrard MJ, Durkie M, Tanner MS.

Hepatology. 1997 Nov;26(5):1366. No abstract available.

PMID:
9362386
33.

Carnitine-acylcarnitine translocase deficiency--a mild phenotype.

Olpin SE, Bonham JR, Downing M, Manning NJ, Pollitt RJ, Sharrard MJ, Tanner MS.

J Inherit Metab Dis. 1997 Sep;20(5):714-5. No abstract available.

PMID:
9323572
34.

Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on chromosome 2q24.

Strautnieks SS, Kagalwalla AF, Tanner MS, Knisely AS, Bull L, Freimer N, Kocoshis SA, Gardiner RM, Thompson RJ.

Am J Hum Genet. 1997 Sep;61(3):630-3.

35.

Gene polymorphisms and the use of the bonferroni correction factor: when and when not to apply?

Tanner MS, Sharrard MJ, Rigby AS.

Arch Dis Child. 1997 Apr;76(4):386. No abstract available.

36.

Locus heterogeneity in progressive familial intrahepatic cholestasis.

Strautnieks SS, Kagalwalla AF, Tanner MS, Gardiner RM, Thompson RJ.

J Med Genet. 1996 Oct;33(10):833-6.

37.

Long term survival in Indian childhood cirrhosis treated with D-penicillamine.

Bavdekar AR, Bhave SA, Pradhan AM, Pandit AN, Tanner MS.

Arch Dis Child. 1996 Jan;74(1):32-5.

38.

The major histocompatibility complex influences the development of chronic liver disease in male children and young adults with cystic fibrosis.

Duthie A, Doherty DG, Donaldson PT, Scott-Jupp R, Tanner MS, Eddleston AL, Mowat AP.

J Hepatol. 1995 Nov;23(5):532-7.

PMID:
8583140
39.
40.

Liver disease in cystic fibrosis.

Tanner MS, Taylor CJ.

Arch Dis Child. 1995 Apr;72(4):281-4. Review. No abstract available.

41.

Reversal of Indian childhood cirrhosis by D-penicillamine therapy.

Pradhan AM, Bhave SA, Joshi VV, Bavdekar AR, Pandit AN, Tanner MS.

J Pediatr Gastroenterol Nutr. 1995 Jan;20(1):28-35.

PMID:
7884615
42.

Copper associated childhood cirrhosis.

Horslen SP, Tanner MS, Lyon TD, Fell GS, Lowry MF.

Gut. 1994 Oct;35(10):1497-500.

43.
45.

Pneumococcal infection in the newborn.

Primhak RA, Tanner MS, Spencer RC.

Arch Dis Child. 1993 Sep;69(3 Spec No):317-8.

46.

Three-base pair resolution of DNA fragments on agarose: application to delta F508 analysis in cystic fibrosis.

Plaha DS, Linforth GH, Duckett DP, Scott-Jupp R, Tanner MS, Jeffreys AJ.

Biotechniques. 1993 Apr;14(4):566-7. No abstract available.

PMID:
8476599
47.

Lafora disease: a progressive myoclonus epilepsy.

Elliott EJ, Talbot IC, Pye IF, Hodges S, Swift PG, Tanner MS.

J Paediatr Child Health. 1992 Dec;28(6):455-8.

PMID:
1466943
48.
49.

Liver and biliary problems in cystic fibrosis.

Williams SG, Westaby D, Tanner MS, Mowat AP.

Br Med Bull. 1992 Oct;48(4):877-92. Review.

PMID:
1458306
50.

Genotype analysis for delta F508, G551D and R553X mutations in children and young adults with cystic fibrosis with and without chronic liver disease.

Duthie A, Doherty DG, Williams C, Scott-Jupp R, Warner JO, Tanner MS, Williamson R, Mowat AP.

Hepatology. 1992 Apr;15(4):660-4.

PMID:
1551644

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