E.I. Schwartz

Paraoxonase 1 Met–Leu 54 polymorphism is associated with Parkinson’s disease

S N Akhmedova, Andrey K Yakimovsky, E.I. Schwartz · Journal of the Neurological Sciences · 2001 · 96 citations

Neurodegenerative Diseases, Neurological Disorder, Parkinson Disease +9

The Effect of HLA-B Allele on the IDDM Risk Defined by DRB1*04 Subtypes and DQB1*0302

Sergei Nejentsev, Helena Reijonen, Bela Adojaan et al. · Diabetes · 1997 · 69 citations

CONGENITAL ABSENCE OF THE PARATHYROID AND THYMUS GLANDS IN AN INFANT

L S Taitz, Concepcion Zarate-Salvador, E.I. Schwartz · PEDIATRICS · 1966 · 56 citations

Urology, Congenital Absence, Parathyroid Hormone +11

Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans.

Randy C. Eisensmith, Alexei A. Goltsov, C. O’Neill et al. · PubMed · 1995 · 50 citations

Congenital absence of the parathyroid and thymus glands in an infant. (3 and 4 pharyngeal pouch syndrome).

L S Taitz, Concepcion Zarate-Salvador, E.I. Schwartz · PubMed · 1966 · 50 citations

Urology, Congenital Absence, Pharyngeal Pouch Syndrome +11