Experimental Assessment of Linear Sampling and Factorization Methods for Microwave Imaging of Concealed Targets

Shape reconstruction methods are particularly well suited for imaging of concealed targets. Yet, these methods are rarely employed in real nondestructive testing applications, since they generally require the electrical parameters of outer object as a priori knowledge. In this regard, we propose an approach to relieve two well known shape reconstruction algorithms, which are the linear sampling and the factorization methods, from the requirement of the a priori knowledge on electrical parameters of the surrounding medium. The idea behind this paper is that if a measurement of the reference medium (a medium which can approximate the material, except the inclusion) can be supplied to these methods, reconstructions with very high qualities can be obtained even when there is no information about the electrical parameters of the surrounding medium. Taking the advantage of this idea, we consider that it is possible to use shape reconstruction methods in buried object detection. To this end, we perform several experiments inside an anechoic chamber to verify the approach against real measurements. Accuracy and stability of the obtained results show that both the linear sampling and the factorization methods can be quite useful for various buried obstacle imaging problems

Turner syndrome and associated problems in turkish children: A multicenter study

Objective: Turner syndrome (TS) is a chromosomal disorder caused by complete or partial X chromosome monosomy that manifests various clinical features depending on the karyotype and on the genetic background of affected girls. This study aimed to systematically investigate the key clinical features of TS in relationship to karyotype in a large pediatric Turkish patient population. Methods: Our retrospective study included 842 karyotype-proven TS patients aged 0-18 years who were evaluated in 35 different centers in Turkey in the years 2013-2014. Results: The most common karyotype was 45,X (50.7%), followed by 45,X/46,XX (10.8%), 46,X,i(Xq) (10.1%) and 45,X/46,X,i(Xq) (9.5%). Mean age at diagnosis was 10.2±4.4 years. The most common presenting complaints were short stature and delayed puberty. Among patients diagnosed before age one year, the ratio of karyotype 45,X was significantly higher than that of other karyotype groups. Cardiac defects (bicuspid aortic valve, coarctation of the aorta and aortic stenosi) were the most common congenital anomalies, occurring in 25% of the TS cases. This was followed by urinary system anomalies (horseshoe kidney, double collector duct system and renal rotation) detected in 16.3%. Hashimoto’s thyroiditis was found in 11.1% of patients, gastrointestinal abnormalities in 8.9%, ear nose and throat problems in 22.6%, dermatologic problems in 21.8% and osteoporosis in 15.3%. Learning difficulties and/or psychosocial problems were encountered in 39.1%. Insulin resistance and impaired fasting glucose were detected in 3.4% and 2.2%, respectively. Dyslipidemia prevalence was 11.4%. Conclusion: This comprehensive study systematically evaluated the largest group of karyotype-proven TS girls to date. The karyotype distribution, congenital anomaly and comorbidity profile closely parallel that from other countries and support the need for close medical surveillance of these complex patients throughout their lifespan. © Journal of Clinical Research in Pediatric Endocrinology

Does the unification of health financing affect the distribution pattern of out‐of‐pocket health expenses in Turkey?

Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/149529/1/ijsw12389_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/149529/2/ijsw12389.pd

Diagnosis and treatment approach in newborn infants with ambiguous genitalia with sex development disorder: Turkish neonatal and pediatric endocrinology and diabetes societies consensus report [Cinsiyet gelişim bozukluğu olan ambiguous genitalyalı yenidoğan bebeklerde tanı ve tedavi yaklaşımı: Türk neonatoloji ve çocuk endokrinoloji ve diyabet dernekleri uzlaşı raporu]

Disorders of sex development are defined as conditions in which the chromosomal, gonadal, and anatomic sex is discordant. Patients usually present with atypical appearing genitals. In the assessment of neonates with disorders of sex development, first, it is important to determine whether this situation requires prompt evaluation, and then the karyotype, hormone levels, and underlying etiology should be determined as soon as possible. All these procedures should be performed in the guidance of a multidisciplinary team in reference centers. The physician should suspect and then perform a detailed history and physical examination because the physical examination of the infant is very important, and lastly plan the required laboratory and imaging procedures for the exact diagnosis. It is important not to be hurried in the choice of sex. The aim of this article, which includes the diagnostic and therapeutic approaches in infants with ambiguous genitalia, was to provide a common practice for all pediatricians. © Copyright 2018 by Turkish Pediatric Association