尿崩症

Objective To approach the observation and nursing of high cervical spinal cord injury paraplegic with diabetes insipidus.

目的 探讨对颈髓损伤高位截瘫患者并发尿崩症的观察与护理。

Objective To elucidate the molecular mechanism of autosomal dominant neurohypophyseal diabetes insipidus in Chinese.

目的 探讨中国人的常染色体显性遗传垂体性尿崩症的分子发病机制。

When MR imaging shows thickening and enhancement of the pituitary stalk and associated leptomeningeal disease as in this case, sarcoidosis is a very strong possibility, along with meningitis, particularly fungal.

结节病为一种不明原因的炎性病变，可以影像多个系统，包括中枢神经系统，女性多见，大于10：1，黑人比白人更多见，15%病人累及中枢神经系统，5%有神经症状，脑神经功能障碍和尿崩症是最常见的神经系统结节病的临床表现，MR改变包括脑膜增厚及强化，孤立性肿块或多发性小，散在的脑膜或实质病变，此例病例中MR图像出现增厚强化的垂体蒂伴有软脑膜病变，强烈提示结节病，伴随脑膜炎尤其是真菌性，通常T2表现为低信号，虽然这些也能够在霉菌病/淋巴瘤/脑膜瘤中看到。

Clinical symptoms appear mild because of part of secretion of thyroid hormone,but followed by other signs of pituitary hormone deficiency ,for example ,hypoglycemia,micropenis diabetics insipidus.

TSH和TRH分泌不足的患儿常保留部分甲状腺激素分泌功能，因此临床症状较轻，但常有其他其他多种垂体激素缺乏的症状如低血糖小阴茎或尿崩症等。

Diabetes insipidus in dogs and cats can be central, caused by a lack of antidiuretic hormone, or nephrogenic, caused by a lack of response of the kidneys to ADH.

尿崩症在犬猫中可能是中枢性的，由抗利尿激素缺乏，或肾脏对抗利尿激素的不应答所引起的疾病。

Congenital nephrogenic diabetes insipidus is a rare inherited disease in which infants suffer serious dehydration as the result of an inability of their kidneys to produce a concentrated urine.

先天性肾源性尿崩症是一种罕见的遗传性疾病，由于患病的婴儿的肾脏缺乏产生终尿的能力，他们会遭受严重的脱水。

Nephrogenic diabetes insipidus can be primary or secondary (caused by a variety of metabolic and renal diseases, including Cushing's syndrome and pyometra).

肾性尿崩症可能是原发性的或继发性的(由一系列代谢疾病和肾脏疾病引起，如库欣综合征和子宫蓄脓)。

Diabetes insipidus is a clinical syndrome characterized by excretion of large volumes of dilute urine due to deficiency and reduction of AVP secretion (central diabetes insipidus, CDI) or renal insensitive to AVP (nephrogenic diabetes insipidus, NDI).

尿崩症是由于抗利尿激素的产生不足或作用障碍使肾脏不能将原尿浓缩而排出大量低渗尿的一组临床综合征。

So far transgenic knockout models of AQP1, AQP3, AQP4 and AQP5, and a knock-in model introducing a point mutation (T126M) that causes autosomal recessive nephrogenic diabetes insipidus in human have been successfully established. Significant progresses have been made in characterizing the physiological functions of these AQPs by systematic mouse phenotype studies.

目前AQP1、3、4、5基因敲除和AQP2基因点突变的基因敲入小鼠模型（模拟人类常染色体隐性遗传尿崩症）已成功建立并广泛用于表型研究，在AQP水通道蛋白生理功能方面获得许多重要进展。

Changes in Red Cell Enzyme Activity in Relation to Red Cell Survival in Infancy Antibody Deficiency Syndrome with Increased Gamma1 M(B2M) Globulins and Absent Gamma1 A(B2A) Globulins and Gamma2 Globulins. Needle Biopsy of the Liver in Various Forms of Childhood Tuberculosis Jaundice Associated with Severe Bacterial Infection in Young Infants Effectt of Hypoxia on Newborn Animals Renal Amyloidosis Resulting From a Chronically Infected Burn. Skin Testing of Allergic and Normal Children with Purified Milk Proteins. Pericarditis in Juvenile Rheumatoid Arthritis Cardiac Complication of Diphtheria Adenovirus Complement-fixing Titers from Birth through First Year Congenital Coronary A-V Fistula Narcotic and Methamphetamine Use During Pregnancy Purulent Pericarditis Transfer of Bilirubin-C^4 Across Monkey Placenta Plasma Antidiuretic Hormone in Nephrogenic Diabetes Insipidus Studies of Anabolic Steroids:Ⅰ.

红血球酵素活性度之变化与婴儿红血球生存期之关系 Gamma1 M(B2M)球蛋白增加而无Gamma1 A(B2A)球蛋白与Gamma2球蛋白之抗体缺乏症候羣儿童期各型结核病之肝藏针管活体切片检查幼儿细菌严重感染并发之黄疸缺氧对於新生动物之影响及其与肺玻璃膜病之关系烧伤处慢性感染引起之肾性淀粉样变性以精制奶粉蛋白对过敏症与正常小儿作皮肤试验年幼性类风湿性关节为合并的心包炎白喉之心脏合并症自出生至一岁之腺病毒补体结合滴定度先天性冠状动静脉瘻管怀孕时使用麻醉剂与Methamphetamine之结果化脓性心囊炎胆红素C^14标猴子胎盘之转送肾因性尿崩症患儿之血清抗利尿荷尔蒙之证明同化类固醇之研究Ⅰ。

For a big chunk of credit-card losses; the number of filings (and thus charge-off rates) would be rising again, whether

年美国个人破产法的一个改动使得破产登记急速下降，而后引起了信用卡大规模的亏损。

Eph. 4:23 And that you be renewed in the spirit of your mind

弗四23 而在你们心思的灵里得以更新