» Authors » M Di Rocco

M Di Rocco

Explore the profile of M Di Rocco including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 114
Citations 874
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
Tolomeo D, Rubegni A, Severino M, Pochiero F, Bruno C, Cassandrini D, et al.
J Neurol Sci . 2019 Feb; 399:69-75. PMID: 30776730
Complex I (CI) is the largest component of the mitochondrial respiratory chain (MRC) and it is made up of 7 mitochondrial DNA (mtDNA)-encoded and at least 38 nuclear DNA-encoded subunits....
2.
Di Rocco M, Rusmini M, Caroli F, Madeo A, Bertamino M, Marre-Brunenghi G, et al.
Clin Genet . 2017 Sep; 93(3):671-674. PMID: 28892125
Beukes hip dysplasia is an autosomal dominant disease which has to date been described only in a large South African family of Dutch origin. The patients presented with progressive epiphyseal...
3.
Di Rocco M, Moloney M, OBeirne T, Earley S, Berendsen B, Furey A, et al.
J Chromatogr A . 2017 Apr; 1500:121-135. PMID: 28449875
A method was developed for the confirmatory and quantitative analysis of 30 β-lactam antibiotic residues in bovine muscle. The method includes 12 penicillins (amoxicillin, ampicillin, cloxacillin, dicloxacillin, mecillinam, methicillin, nafcillin,...
4.
Biegstraaten M, Cox T, Belmatoug N, Berger M, Collin-Histed T, Vom Dahl S, et al.
Blood Cells Mol Dis . 2017 Mar; 68:203-208. PMID: 28274788
Gaucher Disease type 1 (GD1) is a lysosomal disorder that affects many systems. Therapy improves the principal manifestations of the condition and, as a consequence, many patients show a modified...
5.
Aureli A, Oumhani K, Del Beato T, Di Rocco M, Tessitore A, El Aouad R, et al.
Int J Immunogenet . 2015 Jun; 42(4):287-91. PMID: 26041373
Two novel CD1D alleles were identified in unrelated individuals from Morocco. They differ each from the common CD1D*01 allele by one nucleotide substitution in exon 2 resulting in one amino...
6.
Barone R, Carrozzi M, Parini R, Battini R, Martinelli D, Elia M, et al.
J Neurol . 2014 Oct; 262(1):154-64. PMID: 25355454
PMM2-CDG (PMM2 gene mutations) is the most common congenital disorder of N-glycosylation. We conducted a nationwide survey to characterize the frequency, clinical features, glycosylation and genetic correlates in Italian patients...
7.
Toffan A, Brutti A, De Pasquale A, Cappellozza E, Pascoli F, Cigarini M, et al.
J Appl Microbiol . 2013 Oct; 116(1):191-8. PMID: 24102847
Aim: The aim of this work was to evaluate the efficacy of domestic cooking in inactivating Manila clams experimentally infected with murine norovirus (MNV). Methods And Results: A cooking pan...
8.
Assereto S, Robbiano A, Di Rocco M, Rossi A, Cassandrini D, Panicucci C, et al.
Clin Genet . 2013 Sep; 86(1):99-101. PMID: 24020637
No abstract available.
9.
Tassano E, Di Rocco M, Signa S, Gimelli G
Am J Med Genet A . 2013 Mar; 161A(4):894-6. PMID: 23495052
No abstract available.
10.
Feraco P, Mirabelli-Badenier M, Severino M, Alpigiani M, Di Rocco M, Biancheri R, et al.
AJNR Am J Neuroradiol . 2012 Jun; 33(11):2062-7. PMID: 22723063
CDG-1a is an early-onset neurodegenerative disease with selective hindbrain involvement and highly variable clinical presentation. We retrospectively reviewed the clinical records and MR imaging studies of 5 children (3 boys...