Study of transition temperatures in superconductors Quarterly progress report, 11 Jun. - 10 Sep. 1968

Superconducting properties of niobium-tin alloy and large single crystal growt

Do adults with high functioning autism or Asperger Syndrome differ in empathy and emotion recognition?

The present study examined whether adults with high functioning autism (HFA) showed greater difficulties in (i) their self-reported ability to empathise with others and/or (ii) their ability to read mental states in others’ eyes than adults with Asperger syndrome (AS). The Empathy Quotient (EQ) and ‘Reading the Mind in the Eyes’ Test (Eyes Test) were compared in 43 adults with AS and 43 adults with HFA. No significant difference was observed on EQ score between groups, while adults with AS performed significantly better on the Eyes Test than those with HFA. This suggests that adults with HFA may need more support, particularly in mentalizing and complex emotion recognition, and raises questions about the existence of subgroups within autism spectrum conditions

Quartic Parameters for Acoustic Applications of Lattice Boltzmann Scheme

Using the Taylor expansion method, we show that it is possible to improve the lattice Boltzmann method for acoustic applications. We derive a formal expansion of the eigenvalues of the discrete approximation and fit the parameters of the scheme to enforce fourth order accuracy. The corresponding discrete equations are solved with the help of symbolic manipulation. The solutions are explicited in the case of D3Q27 lattice Boltzmann scheme. Various numerical tests support the coherence of this approach.Comment: 23 page

The power of propagation:when GAC is enough

Considerable effort in constraint programming has focused on the development of efficient propagators for individual constraints. In this paper, we consider the combined power of such propagators when applied to collections of more than one constraint. In particular we identify classes of constraint problems where such propagators can decide the existence of a solution on their own, without the need for any additional search. Sporadic examples of such classes have previously been identified, including classes based on restricting the structure of the problem, restricting the constraint types, and some hybrid examples. However, there has previously been no unifying approach which characterises all of these classes: structural, language-based and hybrid. In this paper we develop such a unifying approach and embed all the known classes into a common framework. We then use this framework to identify a further class of problems that can be solved by propagation alone

The prenatal ultrasonographic detection of myelomeningocele in patients referred to Children's Hospital Medical Center: a cross sectional study

BACKGROUND: To find out about the prenatal diagnosis rate of myelomeningocele (MMC) by ultrasound scan in patients referred to the Children's Hospital Medical Center in Tehran, Iran from July 2004 to July 2005. METHODS: We included 140 children born with MMC and who were referred for management, surgery and treatment of complications associated with it. The ultrasound reports were examined. Data on sex, age, location of MMC, time of prenatal ultrasound and the trimester in which the diagnosis was made along with the results of the diagnosis (MMC, hydrocephalus, or both), were collected. RESULTS: Among the studied patients, 136 (97.1%) cases had prenatal ultrasound, amongst those, 58 (42.6%) sonographic evaluations were diagnostic for hydrocephalus and/or MMC. The prenatal ultrasound was positive for MMC in 16 (11.8%), hydrocephalus in 25 (18.4%) and both MMC and hydrocephalus in 17 (12.5%) cases. Among all cases with prenatal diagnosis of MMC, 3.4% were detected in the first, 31% in the second and 65.5% in the third trimester. Thoracic/thoracolumbar lesions were found prenatally in 40% of cases, which is significantly higher than the detection rate of other locations including cervical/cervicothoracic and lumbar/lumbosacral/sacral regions diagnosed only in 0% and 21% of cases respectively. CONCLUSION: There is a large difference between the detection rate of our population (24.3%) compared to others (68%). Pregnant women should have an ultrasound at 20–22 week for detection of congenital anomalies including MMC

On the electroweak phase transition in the Minimal Supersymmetric Standard Model

We study the finite-temperature effective potential of the Minimal Supersymmetric Standard Model, in the limit of only one light Higgs boson. Because of the large top Yukawa coupling, there can be significant differences with respect to the Standard Model case: for given values of the Higgs and top masses, little supersymmetry breaking in the stop sector can make the phase transition more strongly first-order. After including the full structure of the stop mass matrix, the most important experimental constraints and the leading plasma effects, we find that the present limits on Higgs and squark masses are still compatible with the scenario of electroweak baryogenesis, in a small region of parameter space corresponding to m_h \simlt 70 \gev and \msba \simlt 105 \gev.Comment: 10 A4 pages, 7 figures available upon request, CERN-TH.6833/93, IEM-FT-69/93 (one paragraph expanded for clarity

Deletion 22q13.3 syndrome

The deletion 22q13.3 syndrome (deletion 22q13 syndrome or Phelan-McDermid syndrome) is a chromosome microdeletion syndrome characterized by neonatal hypotonia, global developmental delay, normal to accelerated growth, absent to severely delayed speech, and minor dysmorphic features. The deletion occurs with equal frequency in males and females and has been reported in mosaic and non-mosaic forms. Due to lack of clinical recognition and often insufficient laboratory testing, the syndrome is under-diagnosed and its true incidence remains unknown. Common physical traits include long eye lashes, large or unusual ears, relatively large hands, dysplastic toenails, full brow, dolicocephaly, full cheeks, bulbous nose, and pointed chin. Behavior is autistic-like with decreased perception of pain and habitual chewing or mouthing. The loss of 22q13.3 can result from simple deletion, translocation, ring chromosome formation and less common structural changes affecting the long arm of chromosome 22, specifically the region containing the SHANK3 gene. The diagnosis of deletion 22q13 syndrome should be considered in all cases of hypotonia of unknown etiology and in individuals with absent speech. Although the deletion can sometimes be detected by high resolution chromosome analysis, fluorescence in situ hybridization (FISH) or array comparative genomic hybridization (CGH) is recommended for confirmation. Differential diagnosis includes syndromes associated with hypotonia, developmental delay, speech delay and/or autistic-like affect (Prader-Willi, Angelman, Williams, Smith-Magenis, Fragile X, Sotos, FG, trichorhinophalangeal and velocardiofacial syndromes, autism spectrum disorders, cerebral palsy). Genetic counseling is recommended and parental laboratory studies should be considered to identify cryptic rearrangements and detect parental mosaicism. Prenatal diagnosis should be offered for future pregnancies in those families with inherited rearrangements. Individuals with deletion 22q13 should have routine examinations by the primary care physician as well as genetic evaluations with referral to specialists if neurological, gastrointestinal, renal, or other systemic problems are suspected. Affected individuals benefit from early intervention programs, intense occupational and communication therapies, adaptive exercise and sport programs, and other therapies to strengthen their muscles and increase their communication skills. No apparent life-threatening organic abnormalities accompany the diagnosis of deletion 22q13