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121.
In a patient with primary hyperparathyroidism an attempt was made to ablate a middle mediastinal parathyroid gland by forceful staining with radiographic contrast material. The gland was stained on two separate occasions, two weeks apart. Both times the serum calcium level temporarily fell to the normal range but reverted to abnormal levels. The patient ultimately required surgery for correction of hypercalcemia. The mechanism of staining and possible reasons for failure as well as potential complications are discussed. 相似文献
122.
Juvenile gastrointestinal polyposis 总被引:2,自引:0,他引:2
123.
Annette?AM?GerritsenEmail author Inge?Bramsen Walter?Devillé Loes?HM?van Willigen Johannes?E?Hovens Henk?M?van der Ploeg 《BMC public health》2004,4(1):7
Background
This article discusses the design of a study on the prevalence of health problems (both physical and mental) and the utilisation of health care services among asylum seekers and refugees in the Netherlands, including factors that may be related to their health and their utilisation of these services. 相似文献124.
125.
126.
Autologous hemopoietic stem-cell transplantation for children with refractory autoimmune disease 总被引:5,自引:0,他引:5
Autologous stem cell transplantation (ASCT) has been proposed as a possible treatment for severe autoimmune diseases such
as rheumatoid arthritis (RA), multiple sclerosis (MS), systemic sclerosis, and systemic lupus erythematosus (SLE). To date,
more than 250 patients with various autoimmune disorders have undergone an ASCT since 1996. Among them, there is a very limited
number of children. This review summarizes the experience with ASCT for pediatric rheumatic diseases. Most reported cases
concern juvenile idiopathic arthritis (JIA). Experience with ASCT for childhood SLE, Scleroderma, or Dermatomyositis is very
limited. To date, 12 children with severe systemic or polyarticular JIA, all with progressive disease activity despite the
use of corticosteroids, MTX, CsA, or Cyclophosphamide were treated in our center with ASCT. Rheumatologic follow-up at 3-month
intervals up to 36 months showed a marked decrease in arthritis severity as expressed by the core-set criteria for juvenile
chronic arthritis (JCA) activity. However, these children remain at risk for severe viral infections due to the prolonged
lymfopenia. ASCT in this severely ill patient group induces a very significant and drug-free remission of the disease, but
carries a significantly risk of developing fatal MAS. 相似文献
127.
目的:测定NT-3cDNA/CHO细胞表达的基因重组NT-3的生物学活性。方法:体外培养8日龄鸡胚背根神经节(DRG),加入条件培养基,测量背根节神经突起生长的长度。结果:NT-3cDNA/CHO细胞培养48h后的无血清条件培养基1:24稀释后即能促进DRG神经突破的生长;随着其中NT-3浓度增加,神经突破长度也逐渐延长,有明显的量效关系;DRG培养48h长出的神经突破与24h相比,明显长而致密; 相似文献
128.
129.
V Kannan CE Deopujari BK Misra PG Shetty MM Shroff AM Pendse 《Journal of Medical Imaging and Radiation Oncology》1999,43(3):339-341
Gamma knife was installed at the PD Hinduja National Hospital and Medical Research Centre, Mumbai, India, in January 1997. In the first year of gamma-knife radiosurgery to January 1998, we treated 110 patients, of whom six had medically refractory trigeminal neuralgia. Seven treatments were administered to this group of six patients (one had bilateral neuralgia). This report evaluates the effectiveness of radiosurgery treatment in these patients. The median age of the patients was 56 years and there were five males and one female. Following Leksell stereotactic frame fixation, a magnetic resonance imaging scan was done in all. The Leksell gamma plan was used for planning. A radiosurgery dose of 70–80 Gy was delivered to the trigeminal root entry zone, 2–4 mm anterior to the junction of the pons and trigeminal nerve with a single 4 mm collimator helmet. Complete pain relief was achieved in four patients. Two had partial relief. No patient developed any radiosurgery related morbidity during the follow-up period of 5–16 months. Radiosurgery seems to be an effective approach for medically or surgically refractory trigeminal neuralgia. 相似文献
130.
AM Pierides HA Ellis H Dellagrammatikas JE Scott AW Norman 《Archives of disease in childhood》1977,52(6):464-472
Three children with azotaemic renal osteodystrophy were treated with 1,25-dihydroxycholecalciferol (1,25(OH)2D3). All showed clinical, biochemical, and radiological improvement within 6 months of starting treatment. There were no complications. The dose of 1,25(OH)2D3 required was 0-5 microgram per day for 2 children aged 22 and 30 months, and 2 microgram per day for a 15-year-old boy. 2 of the patients were receiving phenobarbitone and phenytoin and in one of them prior treatment with dihydrotachysterol 0-5 mg daily and 6 microgram 1alpha-hydroxycholecalciferol (1alphaOHD3) daily had failed to induce improvement. In one patient, in whom serial iliac bone samples were available, 2 microgram 1,25(OH)2D3 resulted in histological improvement in previously severe osteomalacia. 1,25(OH)2D3 appears to be an effective and safe drug in the treatment of uraemic osteodystrophy. 相似文献