標題: Titlebook: Lectures on Nonlinear Evolution Equations; Initial Value Proble Reinhard Racke Book 2015Latest edition Springer International Publishing Sw [打印本頁] 作者: 添加劑 時間: 2025-3-21 16:32
書目名稱Lectures on Nonlinear Evolution Equations影響因子(影響力)
書目名稱Lectures on Nonlinear Evolution Equations影響因子(影響力)學科排名
書目名稱Lectures on Nonlinear Evolution Equations網(wǎng)絡(luò)公開度
書目名稱Lectures on Nonlinear Evolution Equations網(wǎng)絡(luò)公開度學科排名
書目名稱Lectures on Nonlinear Evolution Equations被引頻次
書目名稱Lectures on Nonlinear Evolution Equations被引頻次學科排名
書目名稱Lectures on Nonlinear Evolution Equations年度引用
書目名稱Lectures on Nonlinear Evolution Equations年度引用學科排名
書目名稱Lectures on Nonlinear Evolution Equations讀者反饋
書目名稱Lectures on Nonlinear Evolution Equations讀者反饋學科排名
作者: 蠟燭 時間: 2025-3-21 22:49 作者: Fraudulent 時間: 2025-3-22 01:19 作者: 偽證 時間: 2025-3-22 06:11
ons presenting details for graduate students.Giving a survey.This book mainly serves as an elementary, self-contained introduction to several important aspects of the theory of global solutions to initial value problems for nonlinear evolution equations. The book employs the classical method of cont作者: Clinch 時間: 2025-3-22 10:37 作者: 嬰兒 時間: 2025-3-22 14:43
Book 2015Latest editionlobal solutions, some blow-up results are briefly described. Moreover, the prospects for corresponding initial boundary value problems and for open questions are provided..In this second edition, initial-boundary value problems in waveguides are additionally considered..作者: 祖?zhèn)?nbsp; 時間: 2025-3-22 21:08 作者: Monotonous 時間: 2025-3-22 22:27 作者: 服從 時間: 2025-3-23 04:42
Reinhard Rackethe pancreas are involved, and a focal form, where hypersecreting β-cells are restricted to a small region of the pancreas.Focal forms can also be immediately and definitively cured by partial pancreatectomy, whereas alternative strategies for diffuse forms include subtotal pancreatectomy (leading t作者: CLEAR 時間: 2025-3-23 07:24
Reinhard Racken CRTR deficiency, creatine, arginine and glycine supplementation does not significantly improve outcome, although partial clinical improvement has been reported in single patients. Normal neurodevelopmental outcome has been reported in early treated patients with creatine synthesis defects. Seconda作者: 可商量 時間: 2025-3-23 11:04
Reinhard Rackeose and galactose carrier of hepatic, renal and pancreatic β-cells. Patients typically present with a combination of increased hepatic glycogen storage and generalised renal tubular dysfunction which includes severe glucosuria. Finally, . is an entity characterised by hyperelastic connective tissue 作者: 單調(diào)女 時間: 2025-3-23 15:38 作者: GROG 時間: 2025-3-23 19:14 作者: adumbrate 時間: 2025-3-23 23:52
Reinhard Racke. The genetic defect commonly affects the nuclear genome, and the inherited pattern is autosomal or X-linked recessive. These patterns characterize pyruvate carboxylase deficiency, pyruvate dehydrogenase deficiency, lactate dehydrogenase deficiency, fumarase deficiency, and several of the defects in作者: 起來了 時間: 2025-3-24 05:46 作者: 琺瑯 時間: 2025-3-24 10:16
Reinhard Rackedge of a large number of biochemical pathways and their interrelationships. As a matter of fact, adequate diagnostic approach can be based on the proper use of only a few screening tests. (3) The neonate has an apparently limited repertoire of responses to severe overwhelming illness and the predomi作者: CRAFT 時間: 2025-3-24 13:41
Reinhard Racke. The genetic defect commonly affects the nuclear genome, and the inherited pattern is autosomal or X-linked recessive. These patterns characterize pyruvate carboxylase deficiency, pyruvate dehydrogenase deficiency, lactate dehydrogenase deficiency, fumarase deficiency, and several of the defects in作者: commune 時間: 2025-3-24 15:26 作者: 聯(lián)想記憶 時間: 2025-3-24 21:53
Reinhard Rackece, at least subjectively..In glycolysis defects in muscles, similar muscular symptoms appear and the serum creatine kinase level increases. Myogenic hyperuricemia may occur. No beneficial effect of glucagon treatment has been reported..Mypopathy associated with increased hemolysis occurs in muscle 作者: 拱形面包 時間: 2025-3-25 02:18 作者: inscribe 時間: 2025-3-25 05:47
rial; small molecule disorders, mostly diagnosed with metabolic markers; and complex molecules disorders, mostly diagnosed with molecular techniques..Two new chapters were added, describing around 600 disorders of nucleic acid metabolism, tRNA metabolism, ribosomal biogenesis, and cellular trafficki作者: 橡子 時間: 2025-3-25 11:01
Reinhard Rackereader should first refer to Chapter 1. This chapter, which includes a number of algorithms and tables, lists the clinical findings under four main headings: the neonatal period and early infancy; acute present978-3-540-28785-8作者: 一個攪動不安 時間: 2025-3-25 12:46 作者: 專橫 時間: 2025-3-25 18:32
Introduction,Many problems arising in the applied sciences lead to nonlinear initial value problems (nonlinear Cauchy problems) of the following type 作者: Solace 時間: 2025-3-25 21:40
,Global solutions to wave equations — existence theorems,We shall start with the formulation of a global existence theorem for solutions of a class of nonlinear wave equations. The first theorem, Theorem 1.1, is typical for the kind of existence theorems that will be obtained for other evolution equations in Chapter ..作者: 細絲 時間: 2025-3-26 01:13 作者: folliculitis 時間: 2025-3-26 04:53
Linear symmetric hyperbolic systems,Let ., and let the formal linear differential operator . be defined by ..作者: 詞匯 時間: 2025-3-26 08:41 作者: Badger 時間: 2025-3-26 13:18
Local existence for quasilinear symmetric hyperbolic systems,Theorem 1.1 and Theorem 1.2 will be proved in detail for the initial value problem . with . where 作者: ALLAY 時間: 2025-3-26 17:21 作者: genesis 時間: 2025-3-26 21:39
,Global solutions to wave equations — proofs,We are now able to give a proof of Theorem 1.1, first again for the case . as discussed in the previous chapters.作者: SPALL 時間: 2025-3-27 04:08
More evolution equations,It has been anticipated in the introduction that the proof of the first global existence theorem, Theorem 1.1, follows a general principle which will lead to similar results for the systems of evolution equations in this chapter. The common structure of the proof of global existence of small, smooth solutions can be described as follows.作者: 鐵塔等 時間: 2025-3-27 05:57
Evolution equations in waveguides,Now we extend the considerations to initial-. value problems for . .. In the main part, we consider nonlinear wave equations and Schr?dinger equations as well as step . for the equations of elasticity and the Maxwell equations in . or ..作者: 忍耐 時間: 2025-3-27 10:52 作者: Infect 時間: 2025-3-27 14:00
978-3-319-34259-7Springer International Publishing Switzerland 2015作者: 罐里有戒指 時間: 2025-3-27 19:05
High energy estimates, the assumptions (5.3) – (5.6) on the nonlinearity .. Without loss of generality for further investigations we assume the constant . appearing in the local existence Theorem 5.8 to be sufficiently small as it will be needed in the proof of the next theorem.作者: 擦試不掉 時間: 2025-3-27 23:58 作者: 秘傳 時間: 2025-3-28 04:21
http://image.papertrans.cn/l/image/583548.jpg作者: Mundane 時間: 2025-3-28 08:03 作者: anus928 時間: 2025-3-28 13:02
Reinhard Rackepoint for each chapter.Reference to diagnostic options.IncluSince the publication of the first edition sixteen years ago, Inborn Metabolic Diseases – Diagnosis and Treatment has become a classic textbook, indispensable for those involved in the care of children and adults with inborn errors of metab作者: frugal 時間: 2025-3-28 18:39 作者: 自由職業(yè)者 時間: 2025-3-28 22:27 作者: Congruous 時間: 2025-3-29 02:33
Reinhard Rackedinoacetate methyltransferase (GAMT) (MIM 601240) deficiencies), and transport [the X-linked creatine transporter (CRTR)] (MIM 300036) deficiency. CDS typically present with cerebral creatine deficiency and global developmental delay/ intellectual disability along with various neurological manifesta作者: airborne 時間: 2025-3-29 06:22
Reinhard Rackeecific expression and substrate specificity of the affected transporter (Box). SGLT1 deficiency causes intestinal ., a condition that presents with severe osmotic diarrhoea and dehydration soon after birth. . mutations result in isolated . a harmless renal transport defect characterised by normal bl作者: 無王時期, 時間: 2025-3-29 08:37
Reinhard Rackes are mainly characterized by haemolytic anaemia and/or metabolic myopathy. Ten inborn errors of the glycolytic pathway are known, all inherited as an autosomal-recessive trait except the X-linked Phospho-Glycerate-Kinase and Glycerol kinase deficiencies. Hexokinase (HK), glucose-6-phosphate isomera作者: CHIDE 時間: 2025-3-29 11:59 作者: Reverie 時間: 2025-3-29 15:39 作者: 小爭吵 時間: 2025-3-29 23:02 作者: Corporeal 時間: 2025-3-30 00:28
Reinhard Racke are frequent. As a whole, they can not be recognized through systematic neonatal screening tests, which are too slow, too expensive, or unreliable. This makes it an absolute necessity to teach primary care physicians a simple method of clinical screening before deciding to initiate sophisticated bi作者: 惡意 時間: 2025-3-30 06:15
Reinhard Rackee the rule rather than the exception with these diverse syndromes. The clinical syndromes may present predominantly as encephalopathies, myopathies, or encephalomyopathies. The biochemical deficiency may be complete with no detectable cross-reacting material (CRM) by immunoblot techniques, or the de作者: 極微小 時間: 2025-3-30 12:04
Reinhard Rackescovered either through newborn screening for hypergalactosemia, or by the chance finding of reducing substance in urine, or by selective urine screening for galactose in infants or older persons examined for nuclear cataracts. In the undiagnosed newborn drinking milk, cataracts develop insidiously 作者: Constituent 時間: 2025-3-30 12:35
Reinhard Rackexercise interolerance. This is associated with muscle stiffness, weakness, and pain on exertion. Semi-ischemic forearm exercise or bicycle ergometer exercise discloses no elevation of the venous lactate level, but marked increases of serum creatine kinase, ammonia, inosine, and hypoxanthine. These p作者: 語言學 時間: 2025-3-30 19:17
Reinhard Rackety of the affected transporter. SGLT1 deficiency causes intestinal ., a condition that presents with severe osmotic diarrhoea and dehydration soon after birth. In . a harmless renal transport defect characterised by glucosuria at normal blood glucose concentrations as well as the absence of any othe
