Annapia P. Verri
Pavia, Italy
Last Updated: 09/26/2026
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Found 12 publications
Antidepressant effect of vagal nerve stimulation in epilepsy patients: a systematic review.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: March 19, 2020
Food-related problems in Klinefelter Syndrome? A probable case of Pica.
Journal: Minerva pediatrica
Published: May 28, 2019
Molecular cytogenetics characterization of seven small supernumerary marker chromosomes derived from chromosome 19: Genotype-phenotype correlation and review of the literature.
Journal: European journal of medical genetics
Published: August 07, 2017
Early/late-life adversities and behavioural phenotypes: insight into metabolomics, genomics and connectomics.
Journal: Journal of intellectual disability research : JIDR
Published: August 17, 2016
Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature.
Journal: Molecular cytogenetics
Published: August 09, 2015
A precocious cerebellar ataxia and frequent Fever episodes in a 16-month-old infant revealing ataxia-telangiectasia syndrome.
Journal: Case reports in immunology
Published: January 01, 2013
Novel automated system for magnetic resonance imaging quantification of the inflamed synovial membrane volume in patients with juvenile idiopathic arthritis.
Journal: Arthritis care & research
Published: May 25, 2012
Conceiving a hematopoietic stem cell donor: twenty-five years after our decision to save a child.
Journal: Haematologica
Published: April 12, 2012
Klinefelter's syndrome and psychoneurologic function.
Journal: Molecular human reproduction
Published: March 04, 2010
Psychotic disorder and focal epilepsy in a left-handed patient with chromosome XYY abnormality.
Journal: Genetic counseling (Geneva, Switzerland)
Published: February 26, 2009
Late diagnosis in severe and mild intellectual disability in adulthood.
Journal: Journal of intellectual disability research : JIDR
Published: September 11, 2004
Chromosome 10p deletion in a patient with hypoparathyroidism, severe mental retardation, autism and basal ganglia calcifications.
Journal: Annales de genetique
Published: October 30, 2003
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Last Updated: 09/26/2026