نتایج جستجو برای: 13 families
تعداد نتایج: 449872 فیلتر نتایج به سال:
This article presents the description of internal spaces fermion and boson fields in d-dimensional spaces, with odd even “basis vectors” which are superposition products operators γa. While Clifford manifest properties fields, appearing families, demonstrate corresponding gauge fields. In d≥(13+1) creation d=(3+1) all observed quarks leptons, families included, their scalar making several predi...
Purpose To illuminate children with cancer and their families' experiences and wishes regarding CAM, and to develop a model for data collection, which may be internationally useful. Methods An exploratory approach using mixed methods was done in two phases. Phase One: Focus group consisting of families of children with cancer. Exchange of experiences based on 7 questions regarding traditional /...
In this paper we study the topological class of universal covering maps from the plane to the sphere with two removed points; we call the elements topological transcendental maps with two asymptotic values and we denote the space byAV2. We prove that an element f ∈ AV2 with finite post-singular set is combinatorially equivalent to a meromorphic transcendental map g with constant Schwarzian deri...
White sponge nevus (WSN) is an autosomal dominant hereditary disease. Keratin 4 (KRT4) and Keratin 13 (KRT13) gene mutations were involved in the WSN. We recruited two WSN Chinese families, and oral lesion biopsy with hematoxylin and eosin staining showed that patients had significant pathological characteristics. The mutations of KRT4 and KRT13 gene were detected by PCR and direct sequencing. ...
For decades, it has been recognised that cases of pulmonary fibrosis cluster in families. While previous studies have implicated mutations in several surfactant-related proteins [1–3] and telomere-related genes [4–12], in most families the genetic basis of their disease has remained uncertain [13]. In this issue of the European Respiratory Journal, KANNENGIESSER et al. [14] report that rare gen...
This article focuses on the views and experiences of professionals providing specialised services to disabled children their families. It is part a larger research project that investigates gap between policy ideals service provision for young families in Iceland. Contrary official policies, earlier findings based families’ perspectives reported strain stress from fragmented inflexible services...
, I≤k (n, t) = I (n, t) ∩ 2 ( [n] ≤k ) . After the maximal families in I (n, t) [13] and in Ik (n, t) [1, 9] are known we study now maximal families in I≤k (n, t). We present a conjecture about the maximal cardinalities and prove it in several cases. More generally cardinalities are replaced by weights and asymptotic estimates are given. Analogous investigations are made for I (n, t) ∩ C(n, s),...
توسعه وسایل تشخیصی در پزشکی هسته ای از جمله سیستم توموگرافی گسیل پوزیترون (pet) سهم به سزایی در تشخیص و درمان بسیاری از بیماری ها ی صعب العلاج داشته است. ولیکن با وجود پیشرفت های چشمگیر در زمینه ی توسعه ی سیستم های تصویر برداری، این روش بدلیل عدم توسعه ای هم پا در زمینه تولید رادیوایزوتوپ های کوتاه عمر مورد استفاده در pet به طور گسترده مورد استفاده ی بیمارستانی قرار نگرفته است. پیچیده و پرهزینه...
To clarify the possible environmental mediation of familial aggregation of blood pressure (BP), we examined whether the behavior of family members differed between families with a hypertensive (n = 16) or a normotensive (n = 15) father. Three-member families consisting of a father, mother, and a boy or girl aged 8-13 years were videotaped as they interacted under standard conditions calling for...
Hemophilia A (HA) is an inherited X-linked bleeding disorder caused by mutations in the factor VIII gene. Prenatal detection in female carriers from families with HA is important to reduce the number of HA patients. The purpose of this study was to detect carriers in families with HA from Sichuan, China, using linkage analysis and a direct genotyping method. A total of 18 HA families were studi...
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