143 research outputs found

    Relationship between the social and vocational adjustment of children under the care of the Children's Aid Association

    Full text link
    Thesis (M.S.)--Boston University, 1943. This item was digitized by the Internet Archive

    A many-channel FPGA control system

    Full text link
    We describe a many-channel experiment control system based on a field-programmable gate array (FPGA). The system has 16 bit resolution on 10 analog 100 MS/s input channels, 14 analog 100 MS/s output channels, 16 slow analog input and output channels, dozens of digital inputs and outputs, and a touchscreen display for experiment control and monitoring. The system can support 10 servo loops with 155 ns latency and MHz bandwidths, in addition to as many as 30 lower bandwidth servos. We demonstrate infinite-impulse-response (IIR) proportional-integral-differential (PID) filters with 30 ns latency by using only bit-shifts and additions. These IIR filters allow timing margin at 100 MS/s and use fewer FPGA resources than straightforward multiplier-based filters, facilitating many servos on a single FPGA. We present several specific applications: H\"ansch-Couillaud laser locks with automatic lock acquisition and a slow dither correction of lock offsets, variable duty cycle temperature servos, and the generation of multiple synchronized arbitrary waveforms

    Normocalcaemic hypoparathyroidism: prevalence and effect on bone status in older women. The OPUS study.

    Get PDF
    There are no consistent data on the prevalence and bone status of normocalcaemic hypoparathyroidism (NHYPO) as defined by normal adjusted calcium and low PTH level. Our aim was to determine the prevalence and the metabolic bone profile of NHYPO in older women, assessing its evolution over time. The second objective was to evaluate the prevalence of other calcium metabolic disorders

    Multiple Endocrine Neoplasia Type 1 with Multiple Leiomyomas Linked to a Novel Mutation in the MEN1 Gene

    Get PDF
    Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominantly inherited syndrome. MEN1 is characterized by the presence of functioning and nonfunctioning tumors or hyperplasia of the pituitary gland, parathyroid glands, and pancreatic islet cells. In addition, MEN1 carriers can have adrenal or thyroid tumors and non-endocrine tumors, such as lipomas, angiofibromas, and leiomyomas. Although leiomyoma is not a major component of MEN1, it is thought to occur more frequently than expected. However, there has been no report of a case of MEN1 with leiomyoma in Korea so far. This report describes a patient with multiple leiomyomas in MEN1. A 50-year-old woman was referred for further evaluation of elevated calcium levels and osteoporosis. Biochemical abnormalities included hypercalcemia with elevated parathyroid hormone. There was hyperprolactinemia with pituitary microadenoma in sella MRI. An abdominal MRI demonstrated adrenal nodules and leiomyomas in the bladder and uterus. Endoscopic ultrasonography demonstrated esophageal leiomyoma and pancreatic islet cell tumor. A subtotal parathyroidectomy with thymectomy was performed. Sequencing of the MEN1 gene in this patient revealed a novel missense mutation (D350V, exon 7). This is the first case of MEN1 accompanied with multiple leiomyomas, parathyroid adenoma, pituitary adenoma, pancreatic tumor, and adrenal tumor

    Bilateral adrenocortical carcinoma in a patient with multiple endocrine neoplasia type 1 (MEN1) and a novel mutation in the MEN1 gene

    Get PDF
    The incidence of adrenal involvement in MEN1 syndrome has been reported between 9 and 45%, while the incidence of adrenocortical carcinoma (ACC) in MEN1 patients has been reported between 2.6 and 6%. In the literature data only unilateral development of ACCs in MEN1 patients has been reported. We report a 31 years-old female MEN1-patient, in whom hyperplasia of the parathyroid glands, prolactinoma, non functioning pancreatic endocrine carcinoma and functioning bilateral adrenal carcinomas were diagnosed. Interestingly, a not previously described in the literature data, novel germline mutation (p.E45V) in exon 2 of MEN1 gene, was detected. The association of exon 2 mutation of the MEN1 gene with bilateral adrenal carcinomas in MEN1 syndrome, should be further investigated

    A Mathematics Laboratory Without Its Own Room

    No full text

    Colección viajeros del conocimiento

    No full text
    El libro presenta la biografía de Iván P. Pavlov y la generación de teorías para el análisis de la conducta humana, partiendo del estudio de la conducta de los animales, dando un giro en el estudio de la psicología modernaDepartamento Nacional de Ciencia, Tecnología e Innovación - COLCIENCIA
    corecore