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81.
82.
A Hofer AS Hassan FJ Legat H Kerl P Wolf 《Journal of the European Academy of Dermatology and Venereology》2006,20(5):558-564
BACKGROUND: The treatment with XeCl-excimer laser generated 308-nm UVB radiation has shown promising results in patients with vitiligo. OBJECTIVE: In this controlled, prospective trial we studied the primary efficacy (start and grade of repigmentation) and patient's satisfaction of XeCl-excimer laser for treatment of vitiligo patches at different body sites and re-evaluated the achieved repigmentation 12 months after the end of therapy. METHODS: Twenty-five patients with generalized or localized vitiligo with a total of 85 lesions at different body sites were enrolled in this study. Vitiligo patches were treated with 308-nm XeCl-excimer laser 3 times a week for 6 to 10 weeks. The overall repigmentation grade of each treated lesion was evaluated once a week on a 5 point scale rating from 0 (no repigmentation), 1 (1-5%), 2 (6-25%), 3 (26-50%), 4 (51-75%), to 5 (76-100%). RESULTS: Twenty-four patients completed the study. Within 6 to 10 weeks of treatment 67% of the patients (16/24) developed follicular repigmentation of at least one of their vitiligo lesions. Lesion repigmentation started after a mean of 13 treatments in lesions located on the face, trunk, arm, and/or leg (high-responder location), and after a mean of 22 treatments in lesions located on the elbow, wrist, dorsum of the hand, knee, and/or dorsum of the foot (low-responder location). Untreated control lesions and lesions located on the fingers did not achieve any repigmentation. After 10 weeks of treatment repigmentation of more than 75% was found in 25% (7/28) of lesions of the high-responder location group versus 2% (1/43) of lesions of the low-responder location group. In most cases, laser-induced repigmentation was persistent, as determined 12 months after the end of treatment. CONCLUSIONS: 308-nm excimer laser is an effective modality for the treatment of vitiligo. However, similar to other non-surgical treatment modalities, the therapeutic effect is mainly dependent on the location of vitiligo lesions. 相似文献
83.
Pulkkinen L; Smith FJ; Shimizu H; Murata S; Yaoita H; Hachisuka H; Nishikawa T; McLean WH; Uitto J 《Human molecular genetics》1996,5(10):1539-1546
In a distinct autosomal recessive variant of epidermolysis bullosa, EB- MD,
life-long skin blistering is associated with late-onset muscular dystrophy
of unknown etiology. Electron microscopy of these patients' skin suggests
that tissue separation occurs intracellularly at the level of the
hemidesmosomal inner plaque, which contains plectin, a high molecular
weight cytoskeletal associated protein, also expressed in the sarcolemma of
the muscle. In this study, we report two patients with EB-MD, each with a
homozygous deletion mutation in the plectin gene, PLEC1. In the first case,
the proband and her similarly affected sister had a homozygous 9 bp
deletion mutation, designated as 2719de19, which resulted in elimination of
three amino acids, QEA, in a sequence of 23 amino acids entirely conserved
between the mouse and human sequences. The proband in the second family
demonstrated a single nucleotide deletion at position 5866, designated as
5866delC, which resulted in frameshift and a premature termination codon
for translation 16 bp downstream from the site of deletion. The absence of
plectin in the hemidesmosomes, as reflected by negative immunofluorescence
with an anti-plectin antibody (HD-1), associated with fragility of basal
keratinocytes, implicates plectin as critical for binding of intermediate
keratin filament network to hemidesmosomal complexes. The function of
plectin as a putative attachment protein also in the muscle would explain
the clinical phenotype consisting of cutaneous fragility and muscular
dystrophy in EB-MD.
相似文献
84.
The polymerase chain reaction (PCR) technique has become an important, widely employed method for the detection and quantitation of the nucleic acid sequences used in the diagnosis and monitoring of genetic and infectious diseases. Much attention has been directed at the problem of false-positive PCR results, which are generally attributed to low-level laboratory contamination of amplified sequences ("carryover"). In contrast, few investigators have commented on the somewhat less frequent, but equally problematic, false-negative PCR results. Investigation of the source of sporadic false-negative PCR reactions found that glove powder, inadvertently introduced into tubes when gloves are changed in an effort to reduce false-positive results, can nonspecifically inhibit each of the major steps in the PCR detection process. Methodologic precautions are recommended to minimize this problem. 相似文献
85.
86.
David Antón-MartínezFrancisco-Javier Polo-Romero M. Paz Atienza-MoralesMaría Esteso-Perona 《Inmunología》2011,30(3):90
Q fever is a worldwide infection caused by Coxiella burnetti. The acute form of this condition usually produces pneumonia and hepatitis through the direct effect of Coxiella burnetti on the involved organs. Here we describe the presence of autoimmune hepatitis and antiphospholipid antibodies as a transitory complication of this infection. These manifestations are probably more frequent than thought and they maybe underdiagnosed; so this report could be important for a deeper knowledge about Q fever and its complications. 相似文献
87.
88.
SUMMARY The trend towards day-case procedures is growing, as a consequence not only of improved medical care but the increasing importance of economic considerations in today's healthcare environment. In the largest worldwide study to date to assess the safety of day-case adenotonsillectomy, we reviewed the records of 4386 patients at the otolaryngology department of the Bradford Royal Infirmary. We found a reactionary haemorrhage rate of 0.57%. All patients who underwent surgery in the morning session had presented with haemorrhage and returned to the operating theatre before the end of the afternoon session. We discuss the implications of these findings, and consider that with careful monitoring day-case tonsillectomy and/or adenoidectomy may safely be introduced. 相似文献
89.
The platelet membrane glycoprotein (Gp) Ib complex consists of four polypeptides: the disulfide-linked GpIb alpha and GpIb beta subunits; GpIX, tightly, but noncovalently associated with GpIb alpha-beta; and the more weakly associated GpV. It is not certain whether the association of GpIX to Gplb alpha-beta is via GpIB alpha, GpIb beta, or both subunits, although recently published evidence implicates an interaction with GpIb beta. We have investigated the interaction of GpIX with GpIb alpha-beta using polyclonal rabbit antibodies to GpIb alpha and GpIb beta raised by immunization with purified glycocalicin and with synthetic peptide sequences from GpIb beta, respectively, as well as monoclonal antibodies directed against GpIX (FMC-25) and against GpIb alpha (AP-1). We performed two types of experiments, using either purified GpIb complex or platelets. (1) When wells were coated with nonreduced GpIb complex, the binding of FMC-25 was inhibited 73% by GpIb alpha antibody, but only 30% by the GpIb beta antibody; when wells were coated with reduced complex, FMC-25 binding was inhibited by the same two antibodies by 86% and 13%, respectively. When wells were coated with polyclonal GpIb alpha or GpIb beta antibodies and then incubated with reduced GpIb complex, only wells coated with GpIb alpha antibodies captured GpIX reactivity. When wells were coated with FMC-25 and then incubated with nonreduced GpIb complex, both the GpIb alpha and GpIb beta polyclonal antibodies reacted strongly; in contrast, only GpIb alpha reactivity was retained when wells coated with FMC-25 were incubated with reduced GpIb complex. In the reciprocal experiment, AP-1- coated wells incubated with either nonreduced or reduced GpIb complex bound radiolabeled FMC-25. (2) The ability of polyclonal GpIb alpha and GpIb beta antibodies to inhibit binding of FMC-25 to platelets was studied by ELISA and by flow cytometry. In both systems, FMC-25 binding was inhibited by the GpIb alpha antibody, but not significantly by the GpIb beta antibody. We conclude that GpIX is strongly associated with GpIb alpha in the purified platelet GpIb complex and in the platelet membrane. 相似文献
90.