I. B. Sardharwalla

Detection of heterozygotes for homocystinuria: Study of sulphur-containing amino acids in plasma and urine after L-methionine loading

I. B. Sardharwalla, Brian Fowler, A. J. Robins et al. · Archives of Disease in Childhood · 1974 · 91 citations · Full text

Standard L-methionine Loads, Urology, L-methionine Loading Test +11

Management of maternal phenylketonuria: an emerging clinical problem.

G. M. Komrower, I. B. Sardharwalla, Jennifer M. J. Coutts et al. · BMJ · 1979 · 58 citations · Full text

Complete Genomic Structure and Mutational Spectrum of PHKA2 in Patients with X-Linked Liver Glycogenosis Type I and II

Jan Hendrickx, Philip Lee, James Keating et al. · The American Journal of Human Genetics · 1999 · 54 citations · Full text

Somatic Variant, Hepatology, Genetic Disorder +10

Human β‐mannosidase deficiency: Biochemical findings in plasma, fibroblasts, white cells and urine

Alan Cooper, C. E. Hatton, Margaret J. Thornley et al. · Journal of Inherited Metabolic Disease · 1987 · 52 citations

A patient with severe type of epimerase deficiency galactosaemia

I. B. Sardharwalla, J. E. Wraith, Christine Bridge et al. · Journal of Inherited Metabolic Disease · 1988 · 45 citations

Diabetes, Pathology, Epimerase Deficiency Galactosaemia +2