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Philip Lee

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Radha Ramachandran; Fiona Walker; Yehani Wedatilake; Caroline Coats; Perry Elliott; Robin H Lachmann; Philip J Lee; Elaine Murphy
Pregnancy and its management in women with GSD type III - a single centre experience.
E Martín-Hernández; Philip J Lee; A Micciche; S Grunewald; R H Lachmann
Long-term needs of adult patients with organic acidaemias: outcome and prognostic factors.
Philip J Lee; Robin H Lachmann
Acute presentations of inherited metabolic disease in adulthood.

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All Publications

2012: Radha Ramachandran; Fiona Walker; Yehani Wedatilake; Caroline Coats; Perry Elliott; Robin H Lachmann; Philip J Lee; Elaine Murphy
Pregnancy and its management in women with GSD type III - a single centre experience.
Journal of inherited metabolic disease 2012;35(2):245-51.
2009: E Martín-Hernández; Philip J Lee; A Micciche; S Grunewald; R H Lachmann
Long-term needs of adult patients with organic acidaemias: outcome and prognostic factors.
Journal of inherited metabolic disease 2009;32(4):523-33.
2008: Philip J Lee; Robin H Lachmann
Acute presentations of inherited metabolic disease in adulthood.
Clinical medicine (London, England) 2008;8(6):621-4.
2008: François Maillot; Maggie Lilburn; Jenny Baudin; David W Morley; Philip J Lee
Factors influencing outcomes in the offspring of mothers with phenylketonuria during pregnancy: the importance of variation in maternal blood phenylalanine.
The American journal of clinical nutrition 2008;88(3):700-5.
2008: R Ramachandran; Philip J Lee
Pancreatic calcification in a patient with homocystinuria.
Journal of inherited metabolic disease 2008;31(1):124-6.
2008: Francois Maillot; Jan P Kraus; Philip J Lee
Environmental influences on familial discordance of phenotype in people with homocystinuria: a case report.
Journal of medical case reports 2008;2():113.
2007: K Bhattacharya; R C Orton; X Qi; Helen Mundy; D W Morley; Michael Champion; S Eaton; R F Tester; Philip J Lee
A novel starch for the treatment of glycogen storage diseases.
Journal of inherited metabolic disease 2007;30(3):350-7.
2007: F Maillot; P Cook; Maggie Lilburn; Philip J Lee
A practical approach to maternal phenylketonuria management.
Journal of inherited metabolic disease 2007;30(2):198-201.
2007: Philip J Lee; A Briddon
A rationale for cystine supplementation in severe homocystinuria.
Journal of inherited metabolic disease 2007;30(1):35-8.
2006: Philip J Lee; P Cook
Frequency of metabolic disorders: more than one needle in the haystack.
Archives of disease in childhood 2006;91(11):879-80.
2006: Philip J Lee
Pregnancy issues in inherited metabolic disorders.
Journal of inherited metabolic disease 2006;29(2-3):311-6.
2006: Helen Mundy; J E Williams; AJ Cousins; Philip J Lee
The effect of L-alanine therapy in a patient with adult onset glycogen storage disease type II.
Journal of inherited metabolic disease 2006;29(1):226-9.
2006: Carel le Roux; Elaine Murphy; Maggie Lilburn; Philip J Lee
The longest-surviving patient with classical maple syrup urine disease.
Journal of inherited metabolic disease 2006;29(1):190-4.
2005: Helen Mundy; Panagiota Georgiadou; Ceri Davies; AJ Cousins; James V Leonard; Philip J Lee
Exercise capacity and biochemical profile during exercise in patients with glycogen storage disease type I.
The Journal of clinical endocrinology and metabolism 2005;90(5):2675-80.
2005: Philip J Lee; D Ridout; J H Walter; F Cockburn
Maternal phenylketonuria: report from the United Kingdom Registry 1978-97.
Archives of disease in childhood 2005;90(2):143-6.
2005: P Hallam; Maggie Lilburn; Philip J Lee
A new protein substitute for adolescents and adults with maple syrup urine disease (MSUD).
Journal of inherited metabolic disease 2005;28(5):665-72.
2004: D J Cartwright; A L Cole; AJ Cousins; Philip J Lee
Raised HDL cholesterol in Fabry disease: response to enzyme replacement therapy.
Journal of inherited metabolic disease 2004;27(6):791-3.
2004: Philip J Lee; P Muiesan; N Heaton
Successful pregnancy after combined renal-hepatic transplantation in glycogen storage disease type Ia.
Journal of inherited metabolic disease 2004;27(4):537-8.
2003: Philip J Lee; Maggie Lilburn; Jenny Baudin
Maternal phenylketonuria: experiences from the United Kingdom.
Pediatrics 2003;112(6 Pt 2):1553-6.
2003: Helen Mundy; S J Jones; Jeremy C Hobart; M G Hanna; Philip J Lee
A randomized controlled study of modified cobratoxin in adrenomyeloneuropathy.
Neurology 2003;61(4):528-30.
2003: Philip J Lee; Maggie Lilburn; Udo Wendel; Peter Schadewaldt
A woman with untreated galactosaemia.
Lancet 2003;362(9382):446.
2003: Helen Mundy; Peter C Hindmarsh; David R Matthews; James V Leonard; Philip J Lee
The regulation of growth in glycogen storage disease type 1.
Clinical endocrinology 2003;58(3):332-9.
2002: Philip J Lee
Glycogen storage disease type I: pathophysiology of liver adenomas.
European journal of pediatrics 2002;161 Suppl 1():S46-9.
2002: Helen Mundy; Philip J Lee
Glycogenosis type I and diabetes mellitus: a common mechanism for renal dysfunction?
Medical hypotheses 2002;59(1):110-4.
2002: Philip J Lee
Growing older: the adult metabolic clinic.
Journal of inherited metabolic disease 2002;25(3):252-60.
2001: C J Ellaway; Helen Mundy; Philip J Lee
Successful pregnancy outcome in atypical hyperglycinaemia.
Journal of inherited metabolic disease 2001;24(5):599-600.
1999: E Hershkovitz; Ann Donald; Michael J Mullen; Philip J Lee; James V Leonard
Blood lipids and endothelial function in glycogen storage disease type III.
Journal of inherited metabolic disease 1999;22(8):891-8.
1997: Philip J Lee; John E Deanfield; M Burch; K Baig; W J McKenna; James V Leonard
Comparison of the functional significance of left ventricular hypertrophy in hypertrophic cardiomyopathy and glycogenosis type III.
The American journal of cardiology 1997;79(6):834-8.
1996: Philip J Lee; M A Dixon; James V Leonard
Uncooked cornstarch--efficacy in type I glycogenosis.
Archives of disease in childhood 1996;74(6):546-7.
1996: Philip J Lee; C Chatterton; James V Leonard
Urinary lactate excretion in type 1 glycogenosis--a marker of metabolic control or renal tubular dysfunction?
Journal of inherited metabolic disease 1996;19(2):201-4.
1995: Philip J Lee; R N Dalton; Vanita Shah; Peter C Hindmarsh; James V Leonard
Glomerular and tubular function in glycogen storage disease.
Pediatric nephrology (Berlin, Germany) 1995;9(6):705-10.
1995: Philip J Lee; A Patel; Peter C Hindmarsh; A P Mowat; James V Leonard
The prevalence of polycystic ovaries in the hepatic glycogen storage diseases: its association with hyperinsulinism.
Clinical endocrinology 1995;42(6):601-6.
1995: Philip J Lee; J S Patel; Mary S Fewtrell; James V Leonard; NJ Bishop
Bone mineralisation in type 1 glycogen storage disease.
European journal of pediatrics 1995;154(6):483-7.
1995: Philip J Lee; W G Van't Hoff; James V Leonard
Catch-up growth in Fanconi-Bickel syndrome with uncooked cornstarch.
Journal of inherited metabolic disease 1995;18(2):153-6.
1995: Philip J Lee; James V Leonard
The hepatic glycogen storage diseases--problems beyond childhood.
Journal of inherited metabolic disease 1995;18(4):462-72.
1994: Philip J Lee; David S Celermajer; J Robinson; S N McCarthy; D John Betteridge; James V Leonard
Hyperlipidaemia does not impair vascular endothelial function in glycogen storage disease type 1a.
Atherosclerosis 1994;110(1):95-100.