AVEMARIA, FRANCESCA

AVEMARIA, FRANCESCA  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype 1-apr-2014 V.A. SansoneC. TarlariniF. AvemariaG. Meola + Article (author) -
DIABETES MELLITUS: A COMPLEX METABOLIC DISORDER.EXPLORING THE DISEASE THROUGH FRUCTOSAMINE 3-KINASE GENE ANALYSIS 9-dic-2015 F. Avemaria Doctoral Thesis -
Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression 1-gen-2011 F. AvemariaC. TarlariniL. Mosca + Article (author) -
De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformations 1-gen-2012 L. MoscaS. PileggiF. AvemariaC. TarlariniCIGOLI, MARIA SOLE + Article (author) -
PDCD10 gene mutations in multiple cerebral cavernous malformations 1-giu-2014 F. AvemariaS. De BenedettiA. Mosca + Article (author) -
Phenotypic heterogeneity in a SOD1 G93D Italian ALS family : an example of human model to study a complex disease 1-gen-2011 L. MoscaF. AvemariaC. Tarlarini + Article (author) -
Possible role of fructosamine 3-kinase genotyping for the management of diabetic patients 1-ago-2015 F. AvemariaR. PaleariA. Mosca + Article (author) -
Role of fructosamine-3-kinase in protecting against the onset of microvascular and macrovascular complications in patients with T2DM 1-gen-2020 Paleari R.Mosca A.Avemaria F. + Article (author) -
Wide phenotypic spectrum of the TARDBP gene : homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject 1-gen-2012 L. MoscaC. TarlariniF. Avemaria + Article (author) -