17 research outputs found
Photodynamic therapy: A promising new modality for the treatment of cancer
The first reports on photodynamic therapy (PDT) date back to the 1970s. Since then, several thousands of patients, both with early stage and advanced stage solid tumours, have been treated with PDT and many claims have been made regarding its efficacy. Nevertheless, the therapy has not yet found general acceptance by oncologists. Therefore it seems legitimate to ask whether PDT can still be described as "a promising new therapy in the treatment of cancer". Clinically, PDT has been mainly used for bladder cancer, lung cancer and in malignant diseases of the skin and upper aerodigestive tract. The sensitizer used in the photodynamic treatment of most patients is Photofrin, (Photofrin, the commercial name of dihematoporphyrin ether/ester, containing > 80% of the active porphyrin dimers/oligomers (A.M.R. Fisher, A.L. Murphee and C.J. Gomer, Clinical and preclinical photodynamictherapy, Review Series Article, Lasers Surg. Med., 17 (1995) 2-31). It is a complex mixture of porphyrins derived from hematoporphyrin. Although this sensitizer is effective, it is not the most suitable photosensitizer for PDT. Prolonged skin photosensitivity and the relatively low absorbance at 630 nm, a wavelength where tissue penetration of light is not optimal, have been frequently cited as negative aspects hindering general acceptance. A multitude of new sensitizers is currently under evaluation. Most of these "second generation photosensitizers" are chemically pure, absorb light at around 650 nm or greater and induce no or less general skin photosensitivity. Another novel approach is the photosensitization of neoplasms by the induction of endogenous photosensitizers through the application of 5-aminolevulinic acid (ALA). This article addresses the use of PDT in the disciplines mentioned above and attempts to indicate developments of PDT which could be necessary for this therapy to gain a wider acceptance in the various field
Performance of a light applicator for photodynamic therapy in the oral cavity: calculations and measurements
Planning of syllables in children with developmental apraxia of speech
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Coarticulation patterns in children with developmental apraxia of speech.
Item does not contain fulltextThe aim of this study was to enhance our insight into the underlying deficit in developmental apraxia of speech (DAS). In particular, the involvement of planning and/or programming of speech movements in context was tested by analysing coarticulatory cohesion. For this purpose, second formant frequency measurements were conducted in repetitions of nonsense utterances ([[symbol: see text]] C = /s,x,b,d/; V = /i.a.u/), and compared across nine children with DAS, six normally speaking (NS) children and six adult women. The results showed both intra- and intersyllabic anticipatory coarticulation in NS children and adult women, in which the intersyllabic coarticulation was stronger in NS children than in adult women. The children with DAS showed more variability as compared to NS children, made, on average, less distinction between the vowels, and showed individually idiosyncratic coarticulation patterns. These results are discussed in the light of a delay as well as a deviance of speech development in children with DAS
The role of bone centers in the pathogenesis of craniosynostosis
This paper describes the role of the displacement of bone centers, i.e., the
tubers, in the pathogenesis of craniosynostosis. This displacement was studied in
54 patients with isolated or syndromic craniosynostosis in the form of CT scans
as well as in two dry neonate skulls with Apert syndrome. For comparison, 49
fetal and 8 normal infant dry skulls were studied. Our investigation was
restricted to the coronal and metopic sutures.
The results showed a significantly
more occipital localization of the frontal bone center and a more frontal
localization of the parietal bone center at the side of a synostotic coronal
suture in the isolated form as well as in Apert syndrome. In contrast, this was
not the case in Crouzon syndrome, thus showing that these two syndromes have a
different pathogenesis. For trigonocephaly, a more anteromedial localization of
the frontal bone centers was found