Mild osteitis fibrosa and osteitis fibrosa, the most frequent forms of renal osteodystrophy, were observed in 13.(22.8%) and 14 patients (24.6%), respectively. Mixed uremic osteodystrophy was found in 7 patients (12.3%), adynamic renal bone disease in 3 patients (5.3%), and osteomalacia in 2 patients (3.5%).

輕度纖維性骨炎和纖維性骨炎是腎病性骨營養(yǎng)不良最常見的形式九色最新地址，分別有13名患者（22.8%）和14名患者（24.6%）出現(xiàn)以上兩種疾病可以进的黄网站。7名患者（12.3%）為混合性腎病性骨營養(yǎng)不良癥，3名患者（5.3%）為骨再生不良三级特级婬国产高清，2名患者（3.5%）為骨軟化国产美女呻吟免费网站999。

To prevent adynamic bone disease, the administration of high concentration of dialysate calcium and the overzealous use of oral calcium and calcitriol supplement should be avoided. In patients with hypoparathyroidism, low calcium dialysate could be tried in order to stimulate the parathyroid gland.

至於再生不良型骨病變之預防，則需避免過度使用高鈣透析男人的天堂网在线，避免過度服用含鈣磷結合劑或維生素D制劑而造成過度抑制副甲狀腺91精品视频自拍偷拍第4页，并可使用低鈣透析來刺激副甲狀腺。

Renal osteodystrophy is a common complication in patients with chronic renal failure. According to difference in bone turnover rates, it is classified into high turnover renal osteodystrophy, and low turnover renal osteodystrophy (including mixed uremic osteodystrophy, aluminum-induced osteomalacia and adynamic bone disease).

腎骨病變?yōu)槁阅I衰竭病患常見之并發(fā)癥国产精品178页，其傳統(tǒng)之分類根據(jù)骨周轉速率之不同分為高周轉型骨病變国产一级不卡性爱av黄片在线免费观看，及低周轉型骨病變（包括混合型腎骨病變，鋁中毒引起之骨軟化癥一级伦奷视频A片一女，及再生不良型骨病變）AA级女人大片免费观看视频。

Just like hungry humans, underfed plants grow more slowly, are more susceptible[3] to disease and pests, and reproduce less often than healthy plants.

與人類營養(yǎng)不良類似，營養(yǎng)不良的植物生長變得遲緩一级欧洲免费视频在线观看，越來越容易受到疾病和有害物的侵擾玖玖色综合国产，再生的速度遠不如健康的植物。

Loss-of-function mutations in telomerase complex genes can cause bone marrow failure, dyskeratosis congenita, and acquired aplastic anemia, both diseases that predispose to acute myeloid leukemia.

端粒末端轉移酶的復雜基因喪失功能性突變可導致骨髓衰竭黄色网站久、先天性角化不良及獲得性再生障礙性貧血三级在线理论国产精品第一页，這些疾病都可以誘發(fā)急性髓樣白血病。

Germ-line mutations in the genes hTERT and hTR, encoding telomerase reverse transcriptase and telomerase RNA, respectively, cause autosomal dominant dyskeratosis congenita, a rare hereditary disorder associated with premature death from aplastic anemia and pulmonary fibrosis.

分別編碼端粒末端轉移酶反轉錄酶和端粒酶RNA的hTERT和hTR基因的種系突變導致常染色體顯性先天性角化不良www.欧美色图，它是一種罕見的因為再生障礙性貧血和肺纖維化而早亡的遺傳性疾病亚洲白浆一区二区三区四区。

Germ-line mutations in the genes hTERT and hTR, encoding telomerase reverse transcriptase and telomerase RNA, respectively, cause autosomal dominant dyskeratosis congenita, a rare hereditary disorder associated with premature death from aplastic anemia and pulmonary fibrosis.

端粒酶逆轉錄酶的編碼基因hTERT和端粒酶RNA的編碼基因hTR發(fā)生種系突變時黄色免费cnm，可引起常染色體顯性先天性角化不良，這是一種罕見的遺傳性疾病日本h纯肉无遮掩3d动漫，它與再生障礙性貧血和肺纖維變性所致的早產(chǎn)兒死亡具有相關性一级女人18片毛片免费视频辶。

Genes related to myogenesis, stem cells and apoptosis were detected at high levels in normal human EOMs, suggesting that efficient and continuous regeneration and/or myogenesis may be a mechanism by which the EOMs remain clinically and pathologically spared in diseases such as DMD.

與肌肉形成、干細胞和凋亡有關的基因在正常眼外肌中有較高表達在线一级毛片免费视频，提示眼外肌中有充分的肌肉再生或形成国产A级强奸黄片，可能可以解釋為何在杜興型肌營養(yǎng)不良癥中為何不受累。

Genes related to myogenesis, stem cells and apoptosis were detected at high leels in normal human EOMs, suggesting that efficient and continuous regeneration and/or myogenesis may be a mechanism by which the EOMs remain clinically and pathologically spared in diseases such as DMD.

與肌肉形成狠狠亚洲婷婷综合色香五月加勒比、干細胞和凋亡有關的基因在正常眼外肌中有較高表達亚洲综合偷拍一区二区三区，提示眼外肌中有充分的肌肉再生或形成，可能可以解釋為何在杜興型肌營養(yǎng)不良癥中為何不受累欧美一级aa看片免费。

Methods The skeletal muscle specimens with obviously regenerating muscle fibers were obtained from 9 patients with pseudohypertrophic muscular dystrophy and 5 patients with polymyositis. Then frozen serial sections were made and the sections were treated with HE stain, immunohistochemistry stains including antiEzrin and antiNeural cell adhesion molecule monoclonal antibodies. The pathological changes and the expression of Ezrin were observed.

取肌纖維再生活躍的假肥大型肌營養(yǎng)不良（DMD欧美性交黄色视频，9例）和多發(fā)性肌炎（PM，5例）患者的骨骼肌標本性色在线播放免费人成片，冰凍連續(xù)切片久久毛片免费全部播放无码，進行HE染色及抗Ezrin、抗神經(jīng)細胞黏附分子單克隆抗體免疫組化染色无翼乌邪恶全彩女教师，觀察被檢肌的病理改變和Ezrin蛋白的表達婷婷激情永久就去吻亚洲综合。

atresia：閉鎖, 不通

idiosyncratic特(異反)應性的,特異體質的 | atresia閉鎖; 不通 | hypoplasia發(fā)育不全,再生不良,低常增生

race track：賽馬現(xiàn)象

17Regrinding粉碎再生 | 18Race Track賽馬現(xiàn)象 | 19Hesitation遲滯現(xiàn)象 (因排氣不良,模垢,防鏽油)

hypotrophy：營養(yǎng)不良

hypotony 張力減退 | hypotrophy 營養(yǎng)不良 | hypotypic regeneration 過少再生

hypotypic regeneration：過少再生

hypotrophy 營養(yǎng)不良 | hypotypic regeneration 過少再生 | hypoxanthine 次黃質

muscular neurotization：神經(jīng)再生

強直性肌營養(yǎng)不良:Myotonic dystrophy | 神經(jīng)再生:muscular neurotization | 肌肉病理:muscular pathology

regrinding：粉碎再生

17Regrinding粉碎再生 | 18Race Track賽馬現(xiàn)象 | 19Hesitation遲滯現(xiàn)象 (因排氣不良,模垢,防鏽油)