Nicholas A. Hall

Mitochondrial ATP synthase subunit <i>c</i> storage in the ceroid‐lipofuscinoses (Batten disease)

David N. Palmer, Ian M. Fearnley, John E. Walker et al. · American Journal of Medical Genetics · 1992 · 362 citations

Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis)

Nicholas A. Hall, Brian Lake, Nazneen N. Dewji et al. · Biochemical Journal · 1991 · 162 citations · Full text

Defective Metabolism, Mitochondrial Biogenesis, Biochemistry +15

Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome.

Simon Horslen, Peter T. Clayton, Brian Harding et al. · Archives of Disease in Childhood · 1991 · 87 citations · Full text

Developmental Anomaly, Glycoprotein Metabolism, Developmental Biology +15

Plasma bile acids in patients with peroxisomal dysfunction syndromes: analysis by capillary gas chromatography — mass spectrometry

Peter T. Clayton, Brian Lake, Nicholas A. Hall et al. · European Journal of Pediatrics · 1987 · 55 citations

Plasma Bile Acids, Hepatology, Medicine +9

The substrate-specificity of human lysosomal α-<scp>d</scp>-mannosidase in relation to genetic α-mannosidosis

S al Daher, Rita De Gasperi, P Daniel et al. · Biochemical Journal · 1991 · 43 citations · Full text

Lysosomal Storage Disease, Genetics, Glycobiology +16