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Salpietro V
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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..
 
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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...
 
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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...
 
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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...
 
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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..
 
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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...
 
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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...
 
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