A. M. Zalin

Human lysozyme gene mutations cause hereditary systemic amyloidosis

Mark B. Pepys, Philip N. Hawkins, David R. Booth et al. · Nature · 1993 · 655 citations

Alzheimer's Disease, Mendelian Disorder, Genetic Disorder +6

Non-DNA binding, dominant-negative, human PPARγ mutations cause lipodystrophic insulin resistance

Maura Agostini, Erik Schoenmakers, Catherine Mitchell et al. · Cell Metabolism · 2006 · 180 citations · Full text

Care of diabetic patients in hospital clinics and general practice clinics: a study in Dudley.

S. J. Parnell, A. M. Zalin, C. W. CLARKE · PubMed · 1993 · 29 citations · Full text

Family Medicine, Disease Management, Hospital Clinics +21

Primary Neuropathic Amyloidosis in Three Brothers

A. M. Zalin, A. J. Darby, Stuart L. Vaughan et al. · BMJ · 1974 · 28 citations · Full text

Alzheimer's Disease, Neurological Disorder, Pathology +9

Familial nephropathic non-neuropathic amyloidosis: clinical features, immunohistochemistry and chemistry.

A. M. Zalin, Sally Jones, N J Fitch et al. · PubMed · 1991 · 22 citations

Arg26 Variant, Alzheimer's Disease, Autoimmune Disease +12