Search Results - "Amantea, Ada"
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The HtrA1 serine protease is down-regulated during human melanoma progression and represses growth of metastatic melanoma cells
Published in Oncogene (26-09-2002)“…Differential gene expression of cell lines derived from a malignant melanoma or its autologous lymph node metastasis using cDNA arrays indicated…”
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Epithelioma of Malherbe: new ultrasound patterns
Published in Journal of experimental & clinical cancer research (06-05-2010)“…Calcifying epithelioma of Malherbe, or Pilomatricoma, is considered an uncommon cutaneous neoplasia, normally occurring in children as a solitary, firm,…”
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Merkel cell polyomavirus in Merkel cell carcinoma of Italian patients
Published in Virology journal (07-03-2011)“…Merkel cell carcinoma (MCC) is a rare but very aggressive human malignancy of elderly or immunosuppressed patients. Clonal integration of a new human…”
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Lichenoid keratosis-like melanomas
Published in Journal of the American Academy of Dermatology (01-09-2011)Get full text
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Eccrine Poroma : A Clinical-Dermoscopic Study of Seven Cases
Published in Acta dermato-venereologica (01-01-2009)“…Eccrine poroma can mimic benign and malignant melanocytic and non-melanocytic lesions. To date, little is known about the dermoscopic features of this…”
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Mucosal Alpha-Papillomavirus (HPV89) in a rare skin lesion
Published in Virology journal (07-07-2015)“…Apocrine acrosyringeal keratosis is a rare skin lesion showing a unique benign keratotic lesion associated with syringocystoadenoma papilliferum. It is…”
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Recurrent verruciform xanthoma on a skin autograft of the penis
Published in EJD. European journal of dermatology (01-11-2013)Get full text
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High β-HPV DNA Loads and Strong Seroreactivity Are Present in Epidermodysplasia Verruciformis
Published in Journal of investigative dermatology (01-04-2009)“…Epidermodysplasia verruciformis (EV) is a rare disease, characterized by cutaneous warts and associated with a strong predisposition to β-genus human…”
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Eccrine Syringofibroadenoma and Clear Cell Acanthoma: An Association by Chance?
Published in The American journal of dermatopathology (01-04-2011)“…A 58-year-old white woman with stasis dermatitis developed a solitary, slowly growing keratotic nodule of the dorsum of the foot. The excision biopsy specimen…”
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Obesity-associated lymphoedematous mucinosis
Published in Journal of cutaneous pathology (01-10-2009)“…Background: Mucin deposition on the shins is considered as an indicator of pretibial myxoedema, which is typically seen in patients with Graves’ disease…”
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Prurigo Pigmentosa Associated with an Atopic Diathesis in a 13‐Year‐Old Girl
Published in Pediatric dermatology (01-05-2007)“…: We report an Italian prepubescent girl with the typical clinical and histologic features of prurigo pigmentosa associated with an atopic diathesis. The…”
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Detection of HPV-15 in painful subungual tumors of incontinentia pigmenti : successful topical therapy with retinoic acid
Published in EJD. European journal of dermatology (01-05-2009)“…Incontinentia pigmenti (IP) is an X-linked dominant disorder, which occurs in female patients. We present a typical case of IP with subungual tumors (STIP)…”
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Milia En Plaque: Three New Pediatric Cases
Published in Pediatric dermatology (01-11-2009)“…: Milia en plaque (MEP) is an unusual and extremely rare clinical variant of milia, characterized by multiple milia‐like lesions overlying an erythematous…”
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Sclerosing nevus with pseudomelanomatous features and regressing melanoma with nevoid features
Published in Journal of cutaneous pathology (01-08-2009)Get full text
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A kindred with familial progressive hyperpigmentation-like disorder: implication of fibroblast-derived growth factors in pigmentation
Published in EJD. European journal of dermatology (01-09-2009)“…Two patients with a generalized, progressive dyschromatosis disorder are described and investigated as a model to study the role of fibroblast-derived…”
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Challenging the schemes: acantholytic (Darier's disease-like) Kyrle's disease
Published in Journal of cutaneous pathology (01-10-2009)Get full text
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AXIN2 germline mutations are rare in familial melanoma
Published in Genes chromosomes & cancer (01-05-2011)Get full text
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