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Rosti, Giulia
51
results:
Search for persons
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Format
Online (51)
Mediatypes
Articles (Online) (19)
OpenAccess-fulltext (32)
Sorted by: Relevance
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?
1
Truncating variants in PAPSS2 gene: A cause of early prenat..:
Biancotto, Giulia
;
Rosti, Giulia
;
Madia, Francesca
...
Prenatal Diagnosis. , 2024
Link:
https://doi.org/10.1002/..
?
2
Abnormalities of pubertal development and gonadal function ..:
Patti, Giuseppa
;
Scaglione, Marco
;
Maiorano, Nadia Gabriella
...
Frontiers in Endocrinology. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
3
A case of Huntington disease‐like 2 in a patient of African..:
Ruscitti, Federica
;
Origone, Paola
;
Rosti, Giulia
...
Clinical Case Reports. 10 (2022) 10 - p. , 2022
Link:
https://doi.org/10.1002/..
?
4
Neurodevelopmental Disorders in Patients With Complex Pheno..:
Servetti, Martina
;
Pisciotta, Livia
;
Tassano, Elisa
...
Frontiers in Genetics. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
5
A novel mutation in COL3A1 associates to vascular Ehlers–Da..:
Ruscitti, Federica
;
Trevisan, Lucia
;
Rosti, Giulia
...
Molecular Genetics & Genomic Medicine. 9 (2021) 9 - p. , 2021
Link:
https://doi.org/10.1002/..
?
6
Intragenic duplication of KCNQ5 gene results in aberrant sp..:
Rosti, Giulia
;
Tassano, Elisa
;
Bossi, Simone
...
European Journal of Medical Genetics. 62 (2019) 9 - p. 103555 , 2019
Link:
https://doi.org/10.1016/..
?
7
Liver chemistry in new-onset Henoch-Schönlein syndrome:
Rosti, Giulia
;
Milani, Gregorio P.
;
Laicini, Emanuela A.
..
Italian Journal of Pediatrics. 43 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
?
8
Abnormalities of pubertal development and gonadal function ..:
Patti, Giuseppa
;
Scaglione, Marco
;
Maiorano, Nadia Gabriella
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422880/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
9
A case of Huntington disease‐like 2 in a patient of African..:
Ruscitti, Federica
;
Origone, Paola
;
Rosti, Giulia
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9536496/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
10
A novel mutation in COL3A1 associates to vascular Ehlers–Da..:
Ruscitti, Federica
;
Trevisan, Lucia
;
Rosti, Giulia
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457703/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
11
Neurodevelopmental Disorders in Patients With Complex Pheno..:
Servetti, Martina
;
Pisciotta, Livia
;
Tassano, Elisa
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8490884/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
12
Abnormalities of pubertal development and gonadal function ..:
Giuseppa Patti
;
Marco Scaglione
;
Nadia Gabriella Maiorano
...
https://www.frontiersin.org/articles/10.3389/fendo.2023.1213098/full. , 2023
Link:
https://doi.org/10.3389/..
?
13
A case of Huntington disease‐like 2 in a patient of African..:
Federica Ruscitti
;
Paola Origone
;
Giulia Rosti
...
https://doi.org/10.1002/ccr3.6308. , 2022
Link:
https://doi.org/10.1002/..
?
14
Table1_Neurodevelopmental Disorders in Patients With Comple..:
Martina Servetti
;
Livia Pisciotta
;
Elisa Tassano
...
doi:10.3389/fgene.2021.732002.s002. , 2021
Link:
https://doi.org/10.3389/..
?
15
DataSheet1_Neurodevelopmental Disorders in Patients With Co..:
Martina Servetti
;
Livia Pisciotta
;
Elisa Tassano
...
doi:10.3389/fgene.2021.732002.s001. , 2021
Link:
https://doi.org/10.3389/..
1-15