M L Wilkinson|P T Clayton - JoVE Visualize

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Neurology|April 14, 2004

Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosisR Pons, B Ford, C A Chiriboga, et al.

Hepatology (Baltimore, Md.)|January 1, 1991

Dual association of HLA DR2 and DR3 with primary sclerosing cholangitisP T Donaldson, J M Farrant, M L Wilkinson, et al.

Acta Endocrinologica|April 1, 1987

Foetal steroid binding protein in British and Japanese womenJ M Iqbal, A Forbes, M L Wilkinson, et al.

Human Molecular Genetics|June 1, 1997

Molecular mechanisms in mitochondrial DNA depletion syndromeJ W Taanman, A G Bodnar, J M Cooper, et al.

Gut|May 1, 1994

Measurement of androgen receptor expression in adult liver, fetal liver, and Hep-G2 cells by the polymerase chain reactionA P Stubbs, J L Engelman, J I Walker, et al.

Archives of Disease in Childhood. Fetal and Neonatal Edition|February 12, 1998

Neonatal presentation of Caroli's diseaseF Keane, N Hadzić, M L Wilkinson, et al.

Endoscopy|June 15, 2012

What predicts failed cannulation and therapy at ERCP? Results of a large-scale multicenter analysisE J Williams, R Ogollah, P Thomas, et al.

Hepatology (Baltimore, Md.)|November 1, 1994

Hereditary tyrosinemia type I: a new clinical classification with difference in prognosis on dietary treatmentF J van Spronsen, Y Thomasse, G P Smit, et al.

Gastroenterology|June 1, 1991

Natural history and prognostic variables in primary sclerosing cholangitisJ M Farrant, K M Hayllar, M L Wilkinson, et al.

European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 21, 2004

Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathyM Kinali, S E Olpin, P T Clayton, et al.

Pageof 13

Showing results (101-110 of 128) with videos related to

Sort By:

Pageof 13

Neurology|April 14, 2004

Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosisR Pons, B Ford, C A Chiriboga, et al.

Hepatology (Baltimore, Md.)|January 1, 1991

Dual association of HLA DR2 and DR3 with primary sclerosing cholangitisP T Donaldson, J M Farrant, M L Wilkinson, et al.

Acta Endocrinologica|April 1, 1987

Foetal steroid binding protein in British and Japanese womenJ M Iqbal, A Forbes, M L Wilkinson, et al.

Human Molecular Genetics|June 1, 1997

Molecular mechanisms in mitochondrial DNA depletion syndromeJ W Taanman, A G Bodnar, J M Cooper, et al.

Gut|May 1, 1994

Measurement of androgen receptor expression in adult liver, fetal liver, and Hep-G2 cells by the polymerase chain reactionA P Stubbs, J L Engelman, J I Walker, et al.

Archives of Disease in Childhood. Fetal and Neonatal Edition|February 12, 1998

Neonatal presentation of Caroli's diseaseF Keane, N Hadzić, M L Wilkinson, et al.

Endoscopy|June 15, 2012

What predicts failed cannulation and therapy at ERCP? Results of a large-scale multicenter analysisE J Williams, R Ogollah, P Thomas, et al.

Hepatology (Baltimore, Md.)|November 1, 1994

Hereditary tyrosinemia type I: a new clinical classification with difference in prognosis on dietary treatmentF J van Spronsen, Y Thomasse, G P Smit, et al.

Gastroenterology|June 1, 1991

Natural history and prognostic variables in primary sclerosing cholangitisJ M Farrant, K M Hayllar, M L Wilkinson, et al.

European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 21, 2004

Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathyM Kinali, S E Olpin, P T Clayton, et al.

Pageof 13