M. Rasoulpour

Mutations in Kelch-like 3 and Cullin 3 cause hypertension and electrolyte abnormalities

Jai Radhakrishnan, Murim Choi, Robert Bjornson, 2012, Nature.

Very low birth weight is a risk factor for secondary focal segmental glomerulosclerosis.

V. D’Agati, J. Hodgin, M. Rasoulpour, 2009, Clinical journal of the American Society of Nephrology : CJASN.

Hypertension in hypophosphatemic rickets—role of secondary hyperparathyroidism

M. Geffner, U. Alon, M. Rasoulpour, 2003, Pediatric Nephrology.

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

Murim Choi, R. Lifton, U. Scholl, 2015, eLife.

Increased frequency of steroid non-responsive nephrotic syndrome in Iranian children

M. Rasoulpour, G. Hashemi, S. Masood, 1985, Indian journal of pediatrics.

Hypokalemia and Nocturia in a 15-Year-Old Girl

M. Rasoulpour, M. Seifert, 2009, Clinical pediatrics.

Systemic hypertension.

M. Rasoulpour, K. Marinelli, 1992, Clinics of Perinatology.

Mutations in the vasopressin V2 receptor gene in two families with nephrogenic diabetes insipidus

L. F. Kolakowski, D. Ausiello, E. Holtzman, 1995, Pediatric Nephrology.