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Vitiello, Giuseppina
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1

Comprehensive Molecular Analysis of Disease-Related Genes a..:

Fioretti, Tiziana ; Martora, Fabrizio ; De Maggio, Ilaria...
Biomedicines.  12 (2024)  5 - p. 1112 , 2024
Link: https://doi.org/10.3390/..
 
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2

Paroxysmal Dystonic Posturing Mimicking Nocturnal Leg Cramp..:

Prato, Adriana ; Cirnigliaro, Lara ; Maugeri, Federica...
Journal of Clinical Medicine.  13 (2024)  4 - p. 1109 , 2024
Link: https://doi.org/10.3390/..
 
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3

CHAMP1-related disorders: pathomechanisms triggered by diff..:

Amenta, Simona ; Marangi, Giuseppe ; Orteschi, Daniela...
European Journal of Human Genetics.  31 (2023)  6 - p. 648-653 , 2023
Link: https://doi.org/10.1038/..
 
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4

A Case Report of a Feto-Placental Mosaicism Involving a Seg..:

De Falco, Luigia ; Vitiello, Giuseppina ; Savarese, Giovanni...
Genes.  14 (2023)  3 - p. 668 , 2023
Link: https://doi.org/10.3390/..
 
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5

SLITRK2 variants associated with neurodevelopmental disorde..:

El Chehadeh, Salima ; Han, Kyung Ah ; Kim, Dongwook...
Nature Communications.  13 (2022)  1 - p. , 2022
Link: https://doi.org/10.1038/..
 
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6

Different Mechanisms Cause Hypomethylation of Both H19 and ..:

Passaretti, Francesco ; Pignata, Laura ; Vitiello, Giuseppina...
Genes.  13 (2022)  10 - p. 1875 , 2022
Link: https://doi.org/10.3390/..
 
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7

Electroencephalographic findings in ATRX syndrome: A new ca..:

Aiello, Salvatore ; Mancardi, Maria Margherita ; Romano, Alfonso...
European Journal of Paediatric Neurology.  40 (2022)  - p. 69-72 , 2022
Link: https://doi.org/10.1016/..
 
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8

Milder presentation of TELO2-related syndrome in two sister..:

Ciaccio, Claudia ; Duga, Valentina ; Pantaleoni, Chiara...
European Journal of Medical Genetics.  64 (2021)  1 - p. 104116 , 2021
Link: https://doi.org/10.1016/..
 
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9

The frameshift Leu220Phefs*2 variant in KRIT1 accounts for ..:

Buonagura, Autilia Tommasina ; Somma, Teresa ; Vitulli, Francesca...
Interdisciplinary Neurosurgery.  26 (2021)  - p. 101367 , 2021
Link: https://doi.org/10.1016/..
 
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10

M170. GENETIC CHARACTERIZATION OF A COHORT OF PATIENTS AFFE..:

de Bartolomeis, Andrea ; Iolascon, Achille ; Nitsch, Lucio...
Schizophrenia Bulletin.  46 (2020)  Supplement_1 - p. S201-S201 , 2020
Link: https://doi.org/10.1093/..
 
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11

Multi-Gene Next-Generation Sequencing for Molecular Diagnos..:

Fioretti, Tiziana ; Auricchio, Luigi ; Piccirillo, Angelo...
Diagnostics.  10 (2020)  12 - p. 995 , 2020
Link: https://doi.org/10.3390/..
 
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12

De novo heterozygous missense and loss‐of‐function variants..:

Chilton, Ilana ; Okur, Volkan ; Vitiello, Giuseppina...
American Journal of Medical Genetics Part A.  182 (2020)  5 - p. 962-973 , 2020
Link: https://doi.org/10.1002/..
 
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13

Three de novo DDX3X variants associated with distinctive br..:

TUDP consortium ; Scala, Marcello ; Torella, Annalaura...
European Journal of Human Genetics.  27 (2019)  8 - p. 1254-1259 , 2019
Link: https://doi.org/10.1038/..
 
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14

Exploring by whole exome sequencing patients with initial d..:

Negri, Gloria ; Magini, Pamela ; Milani, Donatella...
Human Genetics.  138 (2019)  3 - p. 257-269 , 2019
Link: https://doi.org/10.1007/..
 
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15

Reply to letter: "Brain MRI abnormalities resembling uniden..:

Terrone, Gaetano ; Vitiello, Giuseppina ; Del Giudice, Ennio
European Journal of Paediatric Neurology.  22 (2018)  3 - p. 570 , 2018
Link: https://doi.org/10.1016/..
 
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