Search results for "35"

showing 10 items of 2413 documents

Leishmaniosi Cutanea

2008

Settore MED/35 - Malattie Cutanee E VenereeLeishmaniosi Cutanea
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Aspetti Clinici, Classificazione, Varianti Cliniche

2008

Settore MED/35 - Malattie Cutanee E VenereeMELANOMA
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La Malattia Di Anderson –Fabry

2008

Settore MED/35 - Malattie Cutanee E VenereeMalattia Di Anderson –Fabry
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Terapia Enzimatica Sostitutiva Della Malattia Di Fabry:Due Anni Di Esperienza

2004

Settore MED/35 - Malattie Cutanee E VenereeMalattia Di Fabry
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Matrix metalloproteinases 2 and 9 in lentigo maligna melanoma

2009

Settore MED/35 - Malattie Cutanee E VenereeMatrix metalloproteinases lentigo maligna melanoma
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Metabolic abnormalities associated with initiation of systemic treatment for psoriasis: evidence from the Italian Psocare Registry

2013

Objective To evaluate variations in laboratory parameters and diagnoses of selected clinical conditions up to 16 weeks after starting a new systemic psoriasis treatment for Psocare Registry enrollees. Design Prospective cohort study. Setting Italian public referral centres for psoriasis treatment. Patients First-time recipients (n = 10,539) of continuous systemic psoriasis treatment for at least 16 weeks. Main outcome measure Mean variations in (weeks 8 and 16) and proportions of patients reaching a clinically meaningful increase in serum levels (week 16) of total and low-density lipoprotein cholesterol, triglycerides, aspartate amino transferase, alanine amino transferase and creatinine, a…

Settore MED/35 - Malattie Cutanee E VenereePSORIASISTHERAPY
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Panniculiti

2009

Settore MED/35 - Malattie Cutanee E VenereePanniculiti
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Reflectance mode confocal microscopy and digital image analysis in naevus of Hori and pathogenetic evaluation

2012

Settore MED/35 - Malattie Cutanee E VenereeReflectance mode confocal microscopy
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Mucosal Neuroma Syndrome without mutations of the RET-protooncogene: A histologic study on a case, supported by molecular genetic analysis.

2010

Mucosal neuromas are nerve hamartomas of the digestive tract and larynx, usually observed in the setting of Multiple Endocrine Neoplasia type 2B (MEN2B), i.e. in the presence of typical mutations and in association with medullary thyroid carcinoma, pheochromocytoma and marfanoid habitus. Exceptionally, they arise without the accompanying mutations and endocrine tumors, and in this paper we are reporting a histologic study on a case lacking the specific mutations. The patient was an adolescent girl with marfanoid habitus, with a left-sided epidermal nevus of the neck, and a bulging left upper lip and cheek. The left side of her tongue was considerably enlarged and studded with multiple protr…

Settore MED/35 - Malattie Cutanee E VenereeSettore MED/08 - Anatomia Patologicamucosal neuroma histopathology DNA sequencing MEN2B syndrome
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Neurofibromatosis of the nipple-areolar area : nine case reports

2010

Introduction: Neurofibromatosis type 1 is an autosomal dominant disorder that occurs across all ethnic groups and affects approximately one in 4000 individuals. One of the most noticeable characteristics of the disease is the development of neurofibromas. Case presentation: A total of 258 patients (131 women, 127 men) with neurofibromatosis type 1 were evaluated between 1994 and 2004 in our hospital's dermatology department. Nine patients (3.45%, 95% confidence limits 1.22 to 5.68) had neurofibromas of the breast. One of these nine patients presented with an extensive congenital plexiform neurofibroma in the outer quadrants of her right breast, extending to the nipple-areolar complex. Meanw…

Settore MED/35 - Malattie Cutanee E Venereebreast nipple-areolar areaplexiform neurofibromaneurofibromatosis type 1neurofibroma
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