Search Results - "POSTERARO, P"
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1
Off-site versus on-site clinical microbiology laboratory: a 2-year comparison study of blood culture result reporting
Published in Clinical microbiology and infection (01-11-2019)Get full text
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2
Epidermodysplasia verruciformis with multiple mucosal carcinomas treated with pegylated interferon alfa and acitretin
Published in The Journal of dermatological treatment (01-09-2003)“…Epidermodysplasia verruciformis (EV) is characterized by abnormal genetically-determined susceptibility to widespread and persistent infection of the skin with…”
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3
Pretibial dystrophic epidermolysis bullosa: a recessively inherited COL7A1 splice site mutation affecting procollagen VII processing
Published in British journal of dermatology (1951) (01-11-1999)“…Pretibial epidermolysis bullosa (PEB) is a rare form of localized epidermolysis bullosa dystrophica (EBD), a heterogeneous group of inherited, blistering…”
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4
Detection of human papillomavirus DNA in laryngeal squamous cell carcinoma by polymerase chain reaction
Published in European journal of cancer (1990) (01-05-1996)“…Although human papillomaviruses (HPVs) have been found in many, but not all, tumours of the oral cavity, nose, pharynx and larynx, the true role of HPV in…”
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5
Compound Heterozygosity for an Out-of-Frame Deletion and a Splice Site Mutation in the LAMB3 Gene Causes Nonlethal Junctional Epidermolysis Bullosa
Published in Biochemical and biophysical research communications (24-02-1998)“…Laminin-5 is the major adhesion ligand of epithelial cells. Mutations in the genes encoding laminin-5 cause junctional epidermolysis bullosa (JEB), a…”
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6
Chronic staphylococcal osteomyelitis: a new experimental rat model
Published in Infection and Immunity (01-12-1993)“…A rat model of chronic staphylococcal osteomyelitis was developed. Fibrin glue (5 microliters) and Staphylococcus aureus [2x10(6) CFU/5 microliters] were…”
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7
180-kDa bullous pemphigoid antigen defective generalized atrophic benign epidermolysis bullosa: report of four cases with an unusually mild phenotype
Published in British journal of dermatology (1951) (01-05-1998)“…Generalized atrophic benign epidermolysis bullosa (GABEB) is a rare variant of non‐lethal junctional epidermolysis bullosa characterized by generalized skin…”
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8
Genotype–Phenotype Correlation in Italian Patients with Dystrophic Epidermolysis Bullosa
Published in Journal of investigative dermatology (01-12-2002)“…Dystrophic epidermolysis bullosa (DEB) is a rare skin disorder that is clinically heterogeneous and is transmitted either in dominant (DDEB) or recessive…”
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9
Denaturing HPLC-based approach for detection of COL7A1 gene mutations causing dystrophic epidermolysis bullosa
Published in Biochemical and biophysical research communications (23-12-2005)“…Dystrophic epidermolysis bullosa (DEB) is a rare clinically heterogeneous genodermatosis due to genetic defects in type VII collagen gene ( COL7A1)…”
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10
Laminin-5 Mutational Analysis in an Italian Cohort of Patients with Junctional Epidermolysis Bullosa
Published in Journal of investigative dermatology (01-10-2004)“…Junctional epidermolysis bullosa (JEB) is a rare genodermatosis characterized by dermal–epidermal separation that is caused by mutations in the genes encoding…”
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11
Rapid detection of clarithromycin resistance in Helicobacter pylori using a PCR-based denaturing HPLC assay
Published in Journal of antimicrobial chemotherapy (01-01-2006)“…Objectives: We evaluated a new approach for the rapid detection of clarithromycin resistance in Helicobacter pylori, based on PCR and denaturing HPLC (DHPLC)…”
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12
Novel Mutations in the LAMC2 Gene in Non-Herlitz Junctional Epidermolysis Bullosa: Effects on Laminin-5 Assembly, Secretion, and Deposition
Published in Journal of investigative dermatology (01-09-2001)“…Laminin-5 is the major adhesion ligand of epithelial cells. Mutations in the three genes (LAMA3, LAMB3, LAMC2) encoding the laminin-5 chains cause junctional…”
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Journal Article Conference Proceeding -
13
A missense mutation (G1506E) in the adhesion G domain of laminin-5 causes mild junctional epidermolysis bullosa
Published in Biochemical and biophysical research communications (12-09-2003)“…Laminin-5 is the major adhesion ligand for epithelial cells. Mutations in the genes encoding laminin-5 cause junctional epidermolysis bullosa (JEB), a…”
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14
A Homozygous Nonsense Mutation in Type XVII Collagen Gene (COL17A1) Uncovers an Alternatively Spliced mRNA Accounting for an Unusually Mild Form of Non-Herlitz Junctional Epidermolysis Bullosa
Published in Journal of investigative dermatology (01-01-2001)“…In this study we describe six Italian patients presenting an unusually mild variant of non-Herlitz junctional epidermolysis bullosa associated with a reduced…”
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15
Uv mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patients
Published in Oncogene (20-01-2000)“…Molecular analysis of p53 and patched (PTCH), two candidate tumor suppressor genes for non-melanocytic skin cancer, was performed in skin tumors from six…”
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16
Persistent subcutaneous Scedosporium apiospermum infection
Published in EJD. European journal of dermatology (01-11-2003)“…We report the case of a 52-year-old male heart transplant recipient with a persistent localized subcutaneous infection by Scedosporium apiospermum. This form…”
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17
Compound Heterozygosity for a Recessive Glycine Substitution and a Splice Site Mutation in the COL7A1 Gene Causes an Unusually Mild Form of Localized Recessive Dystrophic Epidermolysis Bullosa
Published in Journal of investigative dermatology (01-11-1998)“…Type VII collagen is the major component of anchoring fibrils, adhesion structures of stratified epithelia that span the basement membrane region and papillary…”
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18
Idiopathic CD4+ T Lymphocytopenia Associated with Disseminated Flat Warts and Alopecia Areata
Published in Journal of dermatology (01-10-2002)“…Idiopathic CD4+ T lymphocytopenia is a very rare condition characterized by persistent depletion of circulating CD4+ T lymphocytes, without evidence of HIV or…”
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19
Non-Herlitz junctional epidermolysis bullosa without hair involvement associated with BP180 deficiency
Published in Dermatology (Basel) (2001)“…Junctional epidermolysis bullosa (JEB) is a clinically and genetically heterogeneous recessively inherited blistering disease of the skin and mucous membranes…”
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20
LAMB3 gene mutations in a patient with herlitz junctional epidermolysis bullosa displaying immunoreactivity to laminin-5
Published in Journal of dermatological science (01-03-1998)Get full text
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