Publications by authors named "J Abulafia"

Data-driven models, addressing the internal motivations, pathways to offending, and supportive cognitions amongst women who have sexually offended have emerged in recent years, with significant consequences for understanding risk factors and developing treatment programmes. In the current research, recent empirically based models were explored in a national sample consisting of all women who had committed sexual offences and were assessed over a 12-year period ( = 28). The utility of the motivational and cognitive models tested was supported, although not all cases could be easily coded, and new categories are suggested in order to better characterize the unique aspects of sex offending amongst women who have sexually offended.

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Fixated pedophilic sexual attraction is considered to be a major determinant of risk among sex offenders, but there is little empirical evidence regarding its treatment. It was hypothesized that two prominent factors which have emerged in the literature as being present among some sexual offenders, namely, impersonal, narcissistic, and predatory patterns of offending against victims, and experiencing childhood sexual abuse, may be related to specifically to the strength of pedophilic interest. Such a relationship would provide a deeper understanding of the corollaries of pedophilic interest and would suggest targets for treatment.

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Background: Histopathologic studies of vitiligo have been rather limited in number, thus the microscopic features of this common disorder are not very well known.

Subjects And Methods: Skin specimens from 20 human vitiligo patients and skin specimens from five equine vitiligo patients were studied by light and transmission electron microscopy.

Results And Discussion: Absence of melanocytes, increased number of Langerhans' cells, epidermal vacuolization, thickening of the basement membrane, T-cell inflammatory infiltrate, and neural alterations were noted in the vitiligo lesions.

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Cole disease is an uncommon disorder characterized by distinctive cutaneous hypopigmentation and punctate keratosis of the palms and soles. It is a congenital skin disease with an autosomal dominant inheritance pattern. We report two patients from a family with 15 members, 5 of whom were affected.

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