Mark Sharrard

Phosphoserine Aminotransferase Deficiency: A Novel Disorder of the Serine Biosynthesis Pathway

Claire Hart, Valérie Race, Younès Achouri et al. · The American Journal of Human Genetics · 2007 · 132 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +14

Glycogen storage disease type IX: High variability in clinical phenotype

Nicholas Beauchamp, Ann Dalton, Uma Ramaswami et al. · Molecular Genetics and Metabolism · 2007 · 125 citations

Life Sciences, Genetics, Molecular Genetics +12

Monocarboxylate Transporter 1 Deficiency and Ketone Utilization

Peter M. van Hasselt, Sacha Ferdinandusse, Glen R. Monroe et al. · New England Journal of Medicine · 2014 · 120 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency

S. E. Olpin, S. Clark, Brage Storstein Andresen et al. · Journal of Inherited Metabolic Disease · 2004 · 74 citations

Life Sciences, Biochemistry, Molecular Biology +14

Massive subdural haematomas in Menkes disease mimicking shaken baby syndrome

Mark Sharrard, Lucie Hertz‐Pannier, D Armengaud et al. · Child s Nervous System · 2002 · 69 citations

Medicine, Neurology, Pathology +9