Ippolita Rana

Rome, Italy

Last Updated: 09/26/2026

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Found 27 publications

Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome's clinical and molecular spectrum through NALCN in-silico structural analysis.

Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome's clinical and molecular spectrum through NALCN in-silico structural analysis.

Journal: Frontiers in genetics

Published: August 08, 2024

Analysis of circulating osteoclast and osteogenic precursors in patients with Gorham-Stout disease.

Analysis of circulating osteoclast and osteogenic precursors in patients with Gorham-Stout disease.

Journal: Journal of endocrinological investigation

Published: December 05, 2023

A pediatric case of TEK-Related malformations and marfanoid habitus: an incidental finding or a feature?

A pediatric case of TEK-Related malformations and marfanoid habitus: an incidental finding or a feature?

Journal: Lymphology

Published: July 27, 2022

Characterization of Extracellular Vesicles in Osteoporotic Patients Compared to Osteopenic and Healthy Controls.

Characterization of Extracellular Vesicles in Osteoporotic Patients Compared to Osteopenic and Healthy Controls.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Published: March 19, 2022

Expanding the novel MAPKAPK5-related developmental disorder's genotype-phenotype correlation: Patient report and 19 months of follow-up.

Expanding the novel MAPKAPK5-related developmental disorder's genotype-phenotype correlation: Patient report and 19 months of follow-up.

Journal: Clinical genetics

Published: March 08, 2022

Two new cases of nonepileptic neurodevelopmental disorder due to GRIN2B variants and detailed clinical description of the behavioral phenotype.

Two new cases of nonepileptic neurodevelopmental disorder due to GRIN2B variants and detailed clinical description of the behavioral phenotype.

Journal: Clinical dysmorphology

Published: March 03, 2022

Expanding the spectrum of Gorham Stout disease exploring a single center pediatric case series.

Expanding the spectrum of Gorham Stout disease exploring a single center pediatric case series.

Journal: Lymphology

Published: January 24, 2022

Stimulation of Treg Cells to Inhibit Osteoclastogenesis in Gorham-Stout Disease.

Stimulation of Treg Cells to Inhibit Osteoclastogenesis in Gorham-Stout Disease.

Journal: Frontiers in cell and developmental biology

Published: May 07, 2021

Evolocumab in the management of children <10 years of age affected by homozygous familial hypercholesterolemia.

Evolocumab in the management of children <10 years of age affected by homozygous familial hypercholesterolemia.

Journal: Atherosclerosis

Published: March 01, 2021

New Insights into the Role of Lipoprotein(a) as Predictor of Early Onset of Cardiovascular Disease in Pediatric Familial Hypercholesterolemia (FH).

New Insights into the Role of Lipoprotein(a) as Predictor of Early Onset of Cardiovascular Disease in Pediatric Familial Hypercholesterolemia (FH).

Journal: Pediatric cardiology

Published: May 11, 2020

Diffuse infantile hepatic hemangiomas in a patient with Beckwith-Wiedemann syndrome: A new association?

Diffuse infantile hepatic hemangiomas in a patient with Beckwith-Wiedemann syndrome: A new association?

Journal: American journal of medical genetics. Part A

Published: January 13, 2020

Dissecting the mechanisms of bone loss in Gorham-Stout disease.

Dissecting the mechanisms of bone loss in Gorham-Stout disease.

Journal: Bone

Published: July 01, 2019

Showing 1-12 of 27

Last Updated: 09/26/2026