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You searched for: Author/Creator Vecchio, Davide

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1. 4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterization. (July 2015)

3. Dysregulated miRNAs in bone cells of patients with Gorham‐Stout disease. Issue 3 (20th February 2021)

5. Evolocumab in the management of children <10 years of age affected by homozygous familial hypercholesterolemia. (May 2021)

6. Expanding phenotype of FAM111B‐related disease focusing on liver involvement: Literature review, report of a case with end‐stage liver disease and proposal for a new acronym. Issue 10 (23rd July 2022)

7. Expanding the novel MAPKAPK5–related developmental disorder's genotype–phenotype correlation: Patient report and 19 months of follow‐up. Issue 2 (21st May 2022)

9. MASTREE+: Time‐series of plant reproductive effort from six continents. (5th March 2022)

10. Outbreak of ST395 KPC-Producing Klebsiella pneumoniae in a Neonatal Intensive Care Unit in Palermo, Italy. (15th February 2018)