Rosa M. Alfano
Milan, 20122, Italy
Last Updated: 09/26/2026
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Found 11 publications
STAG1: Bridging the Gap Between Cohesin Complex and Epigenetic Machinery.
Journal: Genes
Published: February 20, 2026
Natural history of adults with KBG syndrome: A physician-reported experience.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 31, 2024
Targeted Genomic Sequencing of TSC1 and TSC2 Reveals Causal Variants in Individuals for Whom Previous Genetic Testing for Tuberous Sclerosis Complex Was Normal.
Journal: Human mutation
Published: November 15, 2022
Novel Variant in Exon 3 of the BMP4 Gene Resulted in Ectopic Posterior Pituitary, Craniocervical Junction Dysmorphism and Limb Anomaly.
Journal: Case reports in pediatrics
Published: February 11, 2022
p53, p16 and ki67 as immunohistochemical prognostic markers in uterine smooth muscle tumors of uncertain malignant potential (STUMP).
Journal: Pathology, research and practice
Published: June 11, 2021
Tuberous sclerosis complex: new insights into clinical and therapeutic approach.
Journal: Journal of nephrology
Published: April 24, 2018
Deep phenotyping of patients with Tuberous Sclerosis Complex and no mutation identified in TSC1 and TSC2.
Journal: European journal of medical genetics
Published: November 14, 2017
Women with TSC: Relationship between Clinical, Lung Function and Radiological Features in a Genotyped Population Investigated for Lymphangioleiomyomatosis.
Journal: PloS one
Published: December 04, 2015
Glioblastoma multiforme in a child with tuberous sclerosis complex.
Journal: American journal of medical genetics. Part A
Published: January 20, 2015
A novel TSC2 mutation causing tuberless tuberous sclerosis.
Journal: Seizure
Published: January 22, 2014
Epilepsy in TSC: certain etiology does not mean certain prognosis.
Journal: Epilepsia
Published: September 20, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026