Marina Rubinshtein

Cardiac failure in very long chain acyl-CoA dehydrogenase deficiency requiring extracorporeal membrane oxygenation (ECMO) treatment: A case report and review of the literature

B. Pode-Shakked, Y. Anikster, G. Paret, 2016, Molecular genetics and metabolism reports.

Transillumination of the palm for venipuncture in infants

J. Kuint, G. Paret, A. Augarten, 2001, Pediatric emergency care.

Neonatal Cervical Osteomyelitis With Bilateral Upper Limb Paresis.

Z. Feldman, I. Pessach, N. Keller, 2017, The Pediatric infectious disease journal.

Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated Cardiomyopathy.

T. Meitinger, T. Strom, H. Prokisch, 2018, American journal of human genetics.

Blood Lactate Levels Differ Significantly Between Surviving and Nonsurviving Patients Within the Same Risk-Adjusted Classification for Congenital Heart Surgery (RACHS-1) Group After Pediatric Cardiac Surgery

A. Vardi, G. Paret, I. Keidan, 2010, Pediatric Cardiology.

Point of care testing in children undergoing cardiopulmonary bypass

G. Kenet, T. Tirosh-Wagner, G. Paret, 2011, Pediatric blood & cancer.

Beneficial effects of terlipressin in prolonged pediatric cardiopulmonary resuscitation: A case series

A. Vardi, G. Paret, A. Augarten, 2007, Critical care medicine.

Terlipressin as rescue therapy for intractable hypotension during neonatal septic shock*

A. Vardi, G. Paret, Z. Barzilay, 2004, Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.

Spectral dosimetry in low light therapy

Valentin Grimblatov, Alexander Rubinshtein, Marina Rubinshtein, 2006, SPIE BiOS.

Glutaric Aciduria type I and acute renal failure — Coincidence or causality?

B. Pode-Shakked, Y. Anikster, G. Paret, 2014, Molecular genetics and metabolism reports.