VALENTE, ENZA MARIA
 Distribuzione geografica
Continente #
EU - Europa 14
NA - Nord America 4
Totale 18
Nazione #
IT - Italia 14
US - Stati Uniti d'America 3
CA - Canada 1
Totale 18
Città #
Pavia 9
Fleming Island 2
Brooklyn 1
Calgary 1
Pognana Lario 1
Sassari 1
Verbania 1
Totale 16
Nome #
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutation, file e1f104fc-377d-8c6e-e053-1005fe0aa0dd 3
Guidelines for the use and interpretation of assays for monitoring autophagy, file e1f104fa-0fa1-8c6e-e053-1005fe0aa0dd 2
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutation, file e1f104fc-2b7d-8c6e-e053-1005fe0aa0dd 2
Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder population, file e1f104fc-3e0f-8c6e-e053-1005fe0aa0dd 2
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)., file e1f104fc-b0c9-8c6e-e053-1005fe0aa0dd 2
KCTD17-related myoclonus-dystonia syndrome: clinical and electrophysiological findings of a patient with atypical late onset, file 2e23408b-c398-4ec2-b914-5a31aac16a88 1
Paroxysmal Dystonic Posturing Mimicking Nocturnal Leg Cramps as a Presenting Sign in an Infant with DCC Mutation, Callosal Agenesis and Mirror Movements, file ae2c6227-e347-45c3-b85a-5d79222870d1 1
Simultaneous Labeling of Adipogenic and Osteogenic Differentiating Stem Cells for Live Confocal Analysis, file b4c0840c-4cc4-4a3d-9794-775e27675307 1
A novel variant in NEUROD2 in a patient with Rett-like phenotype points to Glu130 codon as a mutational hotspot, file b91d0cc5-6ca5-40a2-936b-36ab1df75b5c 1
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene, file e1f104fc-38b5-8c6e-e053-1005fe0aa0dd 1
Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal Defects, file e1f104fc-8543-8c6e-e053-1005fe0aa0dd 1
Between SCA5 and SCAR14: delineation of the SPTBN2 p.R480W-associated phenotype, file e1f104fc-8545-8c6e-e053-1005fe0aa0dd 1
Totale 18
Categoria #
all - tutte 79
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 79


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20206 5 0 0 1 0 0 0 0 0 0 0 0
2020/20213 0 0 0 0 0 1 2 0 0 0 0 0
2022/20237 0 0 0 0 1 1 3 0 0 2 0 0
2023/20241 0 0 0 0 0 0 0 0 1 0 0 0
Totale 18