Agostina De Crescenzo

Naples, Italy

Last Updated: 09/26/2026

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Found 12 publications

Fetal growth patterns in Beckwith-Wiedemann syndrome.

Fetal growth patterns in Beckwith-Wiedemann syndrome.

Journal: Clinical genetics

Published: December 01, 2015

Whole-body MRI with diffusion-weighted imaging: a valuable alternative to contrast-enhanced CT for initial staging of aggressive lymphoma.

Whole-body MRI with diffusion-weighted imaging: a valuable alternative to contrast-enhanced CT for initial staging of aggressive lymphoma.

Journal: Clinical radiology

Published: March 16, 2015

(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome.

(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome.

Journal: European journal of human genetics : EJHG

Published: October 27, 2014

A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype.

A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype.

Journal: Journal of human genetics

Published: October 24, 2014

A new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: a twelve-year follow-up and literature review.

A new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: a twelve-year follow-up and literature review.

Journal: BMC medical genetics

Published: June 24, 2014

Looking for CDKN1C enhancers.

Looking for CDKN1C enhancers.

Journal: European journal of human genetics : EJHG

Published: October 17, 2013

Silver-Russell syndrome due to paternal H19/IGF2 hypomethylation in a twin girl born after in vitro fertilization.

Silver-Russell syndrome due to paternal H19/IGF2 hypomethylation in a twin girl born after in vitro fertilization.

Journal: American journal of medical genetics. Part A

Published: May 06, 2013

Giant breast tumors in a patient with Beckwith-Wiedemann syndrome.

Giant breast tumors in a patient with Beckwith-Wiedemann syndrome.

Journal: American journal of medical genetics. Part A

Published: March 22, 2013

Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction.

Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction.

Journal: Journal of medical genetics

Published: December 18, 2012

Prevalence of Beckwith-Wiedemann syndrome in North West of Italy.

Prevalence of Beckwith-Wiedemann syndrome in North West of Italy.

Journal: American journal of medical genetics. Part A

Published: November 06, 2012

The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites.

The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites.

Journal: Human molecular genetics

Published: November 03, 2012

22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review.

22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review.

Journal: Molecular syndromology

Published: September 27, 2011

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Last Updated: 09/26/2026