GESSI, ALESSANDRA

GESSI, ALESSANDRA  

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Risultati 1 - 14 di 14 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A computational approach to identify whole genome homozygosity mapping across multiple SNP mapping experiments 1-gen-2008 A. GessiM. ProverbioE. ManganoI. CifolaC. Battaglia + Conference Object -
Congenital hyperinsulinism of infancy (CHI) : clinical and metabolic evaluation, molecular analysis and phenotype correlation : Institution of the Italian National Registry 1-mag-2008 M.C. ProverbioE. ManganoC. BattagliaA. SalvatoniG. ChiumelloA. Gessi + Conference Object -
Congenital hyperinsulinism of infancy : a dominant K-ATP channel mutation in a Italian family 1-set-2009 M.C. ProverbioA. gessiA. GabrieliC. BattagliaG. Chiumello + Article (author) -
Defect in β-oxidation SCHAD enzyme in familial congenital hyperinsulinism of infancy (CHI) 1-mag-2008 A. GessiM.C. ProverbioE. ManganoC. Battaglia + Conference Object -
Elevated serum progesterone on the day of HCG administration in IVF is associated with a higher pregnancy rate in polycystic ovary syndrome 1-mar-1999 A. GessiG. Merati + Article (author) -
The first mutation in HADHSC gene in a Italian infant with congenital hyperinsulinism 1-set-2008 M.C. ProverbioA. GessiE. ManganoC. BattagliaA. SalvatoniG. Chiumello + Conference Object -
Genetic analysis of Italian patients with congenital hyperinsulinism of infancy 13-mar-2013 M.C. ProverbioC. DiceglieA. GessiR. AsseltaC. Battaglia + Article (author) -
Genome-wide homozygosity mapping in Congenital Hyperinsulinism of Infancy (CHI) :a family based study 1-gen-2009 A. Gessi Doctoral Thesis -
Homozygousity mapping of congenital hyperinsulinism of infancy (CHI) in Italian patients 1-mag-2008 A. GessiM.C. ProverbioE . ManganoSALVATONI, ALESSANDRAG. ChiumelloC. Battaglia + Conference Object -
Homozygousity mapping of congenital hyperinsulinism of infancy (CHI) in Italian patients 1-giu-2008 A. GessiC. Battaglia + Book Part (author) -
Identification of a diffuse form of hyperinsulinemic hypoglycemia by 18-fluoro-L-3,4 dihydroxyphenylalanine positron emission tomography/CT in a patient carrying a novel mutation of the HADH gene 1-gen-2009 A. GessiE. ManganoG. ChiumelloM.C. Proverbio + Article (author) -
Iperinsulinismo congenito : mutazione dominante nel canale ATP+-dipendente in una famiglia Italiana 1-nov-2009 M.C. ProverbioA. GessiA. GabrieliC. BattagliaG. Chiumello + Conference Object -
Iperinsulinismo congenito dell'infanzia : valutazione clinica e metabolica, analisi genetica e correlazione fenotipica, creazione registro nazionale 1-ott-2007 M. C. ProverbioA. GessiC. BattagliaE. Mangano + Conference Object -
Putative identification of susceptibility genes for autism on 15q11-q13 : role of UBE3A and ATP10A 1-gen-2006 G. Guffanti MasettiA. GessiSTRIK LIEVERS, LUISAL. LarizzaF. Macciardi + Article (author) -