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2. Delayed appearance of 3‐methylglutaconic aciduria in neonates with early onset metabolic cardiomyopathies: A potential pitfall for the diagnosis. Issue 1 (15th November 2019)

3. Delineating the neurological phenotype in children with defects in the ECHS1 or HIBCH gene. Issue 2 (16th August 2020)

4. Differential effects of extracellular vesicles secreted by mesenchymal stem cells from different sources on glioblastoma cells. (April 2015)

5. Differential effects of extracellular vesicles secreted by mesenchymal stem cells from different sources on glioblastoma cells. (April 2015)

6. Expanding the molecular diversity and phenotypic spectrum of glycerol 3‐phosphate dehydrogenase 1 deficiency. Issue 5 (1st July 2016)

7. Plasma methylcitric acid and its correlations with other disease biomarkers: The impact in the follow up of patients with propionic and methylmalonic acidemia. Issue 6 (23rd August 2020)

8. Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutations. Issue 2 (14th December 2012)

9. Thiamine Deficiency in a Developed Country: Acute Lactic Acidosis in Two Neonates Due to Unsupplemented Parenteral Nutrition. (15th January 2015)

10. Thiamine Deficiency in a Developed Country: Acute Lactic Acidosis in Two Neonates Due to Unsupplemented Parenteral Nutrition. (August 2016)