Search Results - "Giustini, S."
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Ocular surface involvement in patients with neurofibromatosis type 1 syndrome
Published in Graefe's archive for clinical and experimental ophthalmology (01-08-2020)“…Purpose The aim of this study is to evaluate ocular surface morphological and functional changes in patients with neurofibromatosis type 1 (NF1). Methods…”
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Mite bites, comet signs and possible mammary prosthesis rejection after returning to a vacation home: a diagnostic challenge
Published in Travel medicine and infectious disease (01-07-2021)“…Pyemotes ventricosus is a free-living mite feeding on larvae or nymphs of insects, including moths, beetles, wasps and bees, that are usually found in grain,…”
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Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasia
Published in Journal of the European Academy of Dermatology and Venereology (01-02-2017)“…Background Ectodermal dysplasia is a clinically and genetically heterogeneous group of inherited disorders characterized by abnormal development of two or more…”
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Madelung's disease. Two case reports with pseudoathletic appearance
Published in Clinica terapeutica (05-05-2021)“…Madelung's disease is a rare syndrome characterized by the pre-sence of multiple masses of unencapsulated adipose tissue, symme-trically distributed throughout…”
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Enlightening chronic obstructive pulmonary disease through patients' and caregivers' narratives
Published in International journal of chronic obstructive pulmonary disease (01-01-2018)“…The primary aim of this research was to raise awareness for COPD through real narratives of patients, caregivers, and pulmonologists. The second objective…”
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Deletions of NF1 gene and exons detected by multiplex ligation-dependent probe amplification
Published in Journal of medical genetics (01-12-2007)“…To estimate the contribution of single and multi-exon NF1 gene copy-number changes to the NF1 mutation spectrum, we analysed a series of 201 Italian patients…”
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Chiari type 1 malformation in Neurofibromatosis type 1: experience of a center and review of the literature
Published in Clinica terapeutica (2016)“…To evaluate the possible correlation and the true incidence between Neurofibromatosis type 1 and Arnold-Chiari malformation type I. We reviewed all clinical…”
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Multiple painful papulo-nodular lesions: clinical pitfall
Published in Clinica terapeutica (2014)“…A 43-year-old male presented with multiple (>10) painful, papulo-nodular lesions, associated with paresthesia, over the face, neck and trunk, appeared 15 years…”
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Basal cell carcinomas in a young woman with Steinert's disease
Published in Dermatology online journal (17-08-2014)“…Steinert's disease or Myotonic dystrophy type I (DM1) is an autosomal dominant disease characterized by myotonia, muscular dystrophy, cataracts, hypogonadism,…”
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Retrocaval mass in patient with von Recklinghausen disease: case report
Published in Il Giornale di chirurgia (01-01-2012)“…Type I Neurofibromatosis (NF1) is an autosomal-dominant inheritable disorder, with an incidence of 1:3,000, and a prevalence of 1:4,000 to 5,000. Pathogenesis…”
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Vacuum-assisted closure treatment of leg skin necrosis after angiographic embolization of a giant plexiform neurofibroma
Published in Il Giornale di chirurgia (01-06-2012)“…Type 1 neurofibromatosis is a relatively common inherited disease of the nervous system, with a frequency of almost 1 in 3000. It is associated with…”
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Treatment of cutaneous and pulmonary sarcoidosis with thalidomide
Published in Journal of the American Academy of Dermatology (01-05-1995)“…Many therapeutic agents have been proposed for treatment of steroid-resistant sarcoidosis. Because administration of low doses of thalidomide has been…”
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13
Lisch nodules of the iris in neurofibromatosis type 1
Published in Journal of the European Academy of Dermatology and Venereology (01-05-2004)“…ABSTRACT Neurofibromatosis type 1 (NF1) is a common autosomal dominant disease. The Lisch nodule represents one of the most common NF1 ocular manifestations…”
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Leopard syndrome
Published in Dermatology online journal (15-03-2008)“…The L.E.O.P.A.R.D. syndrome is an autosomal, dominant disorder with characteristic features that include: multiple lentigines, café au lait spots,…”
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Parenteral Antibiotic Therapy in General Practice in Italy: A Direct Observational Study
Published in Journal of chemotherapy (Florence) (01-02-2007)“…The aim of this study was to determine the characteristics of parenteral antimicrobial therapy (PAT) in the general practice setting in Italy, the…”
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Haemorrhagic gastritis and bleeding following rofecoxib administration
Published in Clinical and experimental rheumatology (01-09-2005)Get full text
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A study of 17 patients affected with plexiform neurofibromas in upper and lower extremities: comparison between different surgical techniques
Published in Acta chirurgiae plasticae (Anglická verze) (2009)“…Plexiform neurofibromas (PN) are one of the most common and severe types of neurofibroma that occur in neurofibromatosis type I. These tumours affect long…”
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Adrenal pheochromocytoma and jejunal neurofibroma in type 1 neurofibromatosis: report of a case
Published in Il Giornale di chirurgia (01-05-2007)“…Neurofibromatosis type 1 (NF1), known as von Recklinghausen's disease, is characterized by presence of café au lait spots, and neurofibromas in the skin or…”
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What's new in trichothiodystrophy
Published in Journal of the European Academy of Dermatology and Venereology (01-01-2001)Get full text
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A rare association between neurofibromatosis type 1 and vulvar sarcoma
Published in Giornale italiano di dermatologia e venereologia (01-06-2014)Get more information
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