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Francesca Del Vecchio Blanco
Francesca Del Vecchio Blanco
universitÓ degli studi della Campania
Verified email at unicampania.it
Title
Cited by
Cited by
Year
The genetic basis of undiagnosed muscular dystrophies and myopathies: results from 504 patients
M Savarese, G Di Fruscio, A Torella, C Fiorillo, F Magri, M Fanin, ...
Neurology 87 (1), 71-76, 2016
1102016
New ribosome-inactivating proteins with polynucleotide:adenosine glycosidase and antiviral activities from Basella rubra L. and Bougainvillea spectabilis Willd.
A Bolognesi, L Polito, F Olivieri, P Valbonesi, L Barbieri, MG Battelli, ...
Planta 203, 422-429, 1997
1041997
Next-generation sequencing identifies transportin 3 as the causative gene for LGMD1F
A Torella, M Fanin, M Mutarelli, E Peterle, F Del Vecchio Blanco, R Rispoli, ...
PloS one 8 (5), e63536, 2013
812013
Motor chip: a comparative genomic hybridization microarray for copy-number mutations in 245 neuromuscular disorders
G Piluso, M Dionisi, F Del Vecchio Blanco, A Torella, S Aurino, ...
Clinical chemistry 57 (11), 1584-1596, 2011
672011
Amplification and overexpression of PRUNE in human sarcomas and breast carcinomas–a possible mechanism for altering the nm23-H1 activity
A Forus, A D'angelo, J Henriksen, G Merla, GM Maelandsmo, VA Fl°renes, ...
Oncogene 20 (47), 6881-6890, 2001
662001
Ribosome‐Inactivating Proteins (RNA N‐glycosidases) from the Seeds of Saponaria ocymoides and Vaccaria pyramidata
A Bolognesi, F Olivieri, MG Battelli, L Barbieri, AI Falasca, A Parente, ...
European journal of biochemistry 228 (3), 935-940, 1995
411995
Ethanol consumption, amino acid and glutathione blood levels in patients with and without chronic liver disease
C Loguercio, F Del Vecchio Blanco, V De Girolamo, D Disalvo, G Nardi, ...
Alcoholism: Clinical and Experimental Research 23 (11), 1780-1784, 1999
401999
Clinical and genetic findings in children with neurofibromatosis type 1, Legius syndrome, and other related neurocutaneous disorders
T Giugliano, C Santoro, A Torella, F Del Vecchio Blanco, A Grandone, ...
Genes 10 (8), 580, 2019
392019
The position of nonsense mutations can predict the phenotype severity: A survey on the DMD gene
A Torella, M Zanobio, R Zeuli, F del Vecchio Blanco, M Savarese, ...
PLoS One 15 (8), e0237803, 2020
382020
Expanding the phenotype of RTTN variations: a new family with primary microcephaly, severe growth failure, brain malformations and dermatitis
A Grandone, A Torella, C Santoro, T Giugliano, F Del Vecchio Blanco, ...
Clinical Genetics 90 (5), 445-450, 2016
262016
Complete amino-acid sequence of PD-S2, a new ribosome-inactivating protein from seeds of Phytolacca dioica L.
FDV Blanco, A Bolognesi, A Malorni, MJW Sande, G Savino, A Parente
Biochimica et Biophysica Acta (BBA)-Protein Structure and Moleculará…, 1997
231997
Isolation and primary structure determination of a metallothionein from Paracentrotus lividus (Echinodermata, Echinoidea)
R Scudiero, C Capasso, F Del Vecchio-Blanco, G Savino, A Capasso, ...
Comparative Biochemistry and Physiology Part B: Biochemistry and Moleculará…, 1995
231995
One hundred twenty-one dystrophin point mutations detected from stored DNA samples by combinatorial denaturing high-performance liquid chromatography
A Torella, A Trimarco, FDV Blanco, A Cuomo, S Aurino, G Piluso, ...
The Journal of Molecular Diagnostics 12 (1), 65-73, 2010
222010
A recombinant ribosome‐inactivating protein from the plant Phytolacca dioica L. produced from a synthetic gene 1
F Del Vecchio Blanco, V Cafaro, A Di Maro, R Scognamiglio, G Siniscalco, ...
FEBS letters 437 (3), 241-245, 1998
201998
Elicitin 172 from an isolate of Phytophthora nicotianae pathogenic to tomato
R Capasso, G Cristinzio, A Evidente, C Visca, P Ferranti, FDV Blanco, ...
Phytochemistry 50 (5), 703-709, 1999
191999
BROX haploinsufficiency in familial nonmedullary thyroid cancer
D Pasquali, A Torella, G Accardo, D Esposito, F Del Vecchio Blanco, ...
Journal of Endocrinological Investigation 44, 165-171, 2021
132021
Can dietary intake influence plasma levels of amino acids in liver cirrhosis?
C Loguercio, FDV Blanco, A Nastasi, A Federico, GDV Blanco, ...
Digestive and Liver Disease 32 (7), 611-616, 2000
132000
Enhancer chip: detecting human copy number variations in regulatory elements
M Savarese, G Piluso, D Orteschi, G Di Fruscio, M Dionisi, FV Blanco, ...
PLoS One 7 (12), e52264, 2012
122012
UBE2A deficiency in two siblings: A novel splicing variant inherited from a maternal germline mosaicism
T Giugliano, C Santoro, A Torella, F Del Vecchio Blanco, P Bernardo, ...
American Journal of Medical Genetics Part A 176 (3), 722-726, 2018
112018
Urine concentrating defect as presenting sign of progressive renal failure in Bardet–Biedl syndrome patients
M Zacchia, FDV Blanco, A Torella, R Raucci, G Blasio, ME Onore, ...
Clinical Kidney Journal 14 (6), 1545-1551, 2021
102021
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Articles 1–20