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Salpietro, V
297
results:
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Online (297)
Mediatypes
Articles (Online) (45)
OpenAccess-fulltext (252)
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english (290)
italian (2)
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1
Genetic investigation of inherited neuropathy in families f..:
Khan, A.M.
;
Sultan, T.
;
Kriouile, Y.
...
Neuromuscular Disorders. 28 (2018) - p. S22 , 2018
Link:
https://doi.org/10.1016/..
?
2
Inflammatory biomarkers and intellectual disability in pati..:
Manti, S.
;
Cutrupi, M. C.
;
Cuppari, C.
...
Journal of Intellectual Disability Research. 62 (2018) 5 - p. 382-390 , 2018
Link:
https://doi.org/10.1111/..
?
3
Association between maternal serum high mobility group box ..:
Giacobbe, A.
;
Granese, R.
;
Grasso, R.
...
Nutrition, Metabolism and Cardiovascular Diseases. 26 (2016) 5 - p. 414-418 , 2016
Link:
https://doi.org/10.1016/..
?
4
PP02.3 – 2478: Hyperhomocysteinemia and MTHFR polymorphisms..:
Marseglia, L.M.
;
Nicotera, A.
;
Salpietro, V.
...
European Journal of Paediatric Neurology. 19 (2015) - p. S33 , 2015
Link:
https://doi.org/10.1016/..
?
5
The natural history of spinal neurofibromatosis: a critical..:
Ruggieri, M.
;
Polizzi, A.
;
Spalice, A.
...
Clinical Genetics. 87 (2014) 5 - p. 401-410 , 2014
Link:
https://doi.org/10.1111/..
?
6
LMNA gene mutation as a model of cardiometabolic dysfunctio..:
Chirico, V.
;
Ferraù, V.
;
Loddo, I.
...
Diabetes & Metabolism. 40 (2014) 3 - p. 224-228 , 2014
Link:
https://doi.org/10.1016/..
?
7
Upper Respiratory Tract Infection and Torticollis in Childr..:
Salpietro, V.
;
Polizzi, A.
;
Granata, F.
...
Clinical Neuroradiology. 22 (2012) 4 - p. 351-353 , 2012
Link:
https://doi.org/10.1007/..
?
8
5-51-03 Cerebral blood flow changes in simulated microgravi..:
Bramanti, P.
;
Malara, A.
;
Salpietro, V.
...
Journal of the Neurological Sciences. 150 (1997) - p. S338 , 1997
Link:
https://doi.org/10.1016/..
?
9
Bi-allelic genetic variants in the translational GTPases GT..:
Salpietro V
;
Maroofian R
;
Zaki M. S
...
info:eu-repo/semantics/altIdentifier/pmid/38118446. , 2024
Link:
https://hdl.handle.net/1..
?
10
Biallelic MED27 variants lead to variable ponto-cerebello-l..:
Maroofian, R
;
Kaiyrzhanov, R
;
Cali, E
...
https://openaccess.sgul.ac.uk/id/eprint/116030/1/awad257.pdf. , 2023
Link:
https://openaccess.sgul...
?
11
Lunapark deficiency leads to an autosomal recessive neurode..:
Accogli, A
;
Zaki, MS
;
Al-Owain, M
...
https://openaccess.sgul.ac.uk/id/eprint/115885/1/fcad222.pdf. , 2023
Link:
https://openaccess.sgul...
?
12
Biallelic PRMT7 pathogenic variants are associated with a r..:
Cali, E
;
Suri, M
;
Scala, M
...
https://openaccess.sgul.ac.uk/id/eprint/115315/1/1-s2.0-S1098360022009546-main.pdf. , 2023
Link:
https://openaccess.sgul...
?
13
Bi-allelic genetic variants in the translational GTPases GT..:
Salpietro, V
;
Maroofian, R
;
Zaki, MS
...
https://discovery.ucl.ac.uk/id/eprint/10184635/1/1-s2.0-S0002929723004305-main.pdf. , 2023
Link:
https://discovery.ucl.ac..
?
14
Bi-allelic ACBD6 variants lead to a neurodevelopmental synd..:
Kaiyrzhanov, R
;
Rad, A
;
Lin, S-J
...
https://openaccess.sgul.ac.uk/id/eprint/115881/1/awad380.pdf. , 2023
Link:
https://openaccess.sgul...
?
15
The clinical and genetic spectrum of autosomal-recessive TO..:
Saffari, A
;
Lau, T
;
Tajsharghi, H
...
https://openaccess.sgul.ac.uk/id/eprint/115591/1/awad039.pdf. , 2023
Link:
https://openaccess.sgul...
1-15