Puthenpurackal M. Mathew

Mutations in the Sulfonylurea Receptor Gene in Familial Persistent Hyperinsulinemic Hypoglycemia of Infancy

Pamela M. Thomas, Gilbert J. Cote, Nelson Wohllk et al. · Science · 1995 · 815 citations

Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

Su'e Chang, Stefan Gründer, Aaron Hanukoglu et al. · Nature Genetics · 1996 · 812 citations

Hyperkalaemic Acidosis, Electrolyte Disorder, Molecular Physiology +8

Persistent Neonatal Hyperinsulinism

Puthenpurackal M. Mathew, Janet M. Young, Yousef K. Abu‐Osba et al. · Clinical Pediatrics · 1988 · 127 citations

Molecular Neuroscience, Neonatology, Saudi Arabian Origin +11

Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy.

Pamela M. Thomas, Gilbert J. Cote, David Hallman et al. · PubMed · 1995 · 82 citations

Complications of diazoxide treatment in persistent neonatal hyperinsulinism.

Yousef K. Abu‐Osba, Khader Manasra, Puthenpurackal M. Mathew · Archives of Disease in Childhood · 1989 · 40 citations · Full text

Diazoxide Toxicity, Heart Failure, Neonatology +13