Congenital hypophosphatasia is absence or low levels of serum alkaline phosphatase due to mutations in the gene encoding tissue-nonspecific alkaline ...
#24.
Current Research Opportunities | Greenberg Center for ...
Hypophosphatasia (HPP) is a rare inherited metabolic disorder characterized by defective bone and teeth mineralization caused by mutations of the ALPL gene, ...
#26.
Hypophosphatasia United States Molecular Research Center
Hypophosphatasia is a disease that affects the development of bones and teeth. Sometimes people appear to have hypophosphatasia, but their molecular testing ...
#28.
Efficacy and safety of asfotase alfa in patients with infantile ...
Hypophosphatasia (HPP) is a rare, inherited metabolic disease that manifests in infants and young children as impaired bone mineralization and systemic ...
Hypophosphatasia (HPP), caused by harmful genetic changes (mutations) in the ALPL gene, is an inherited disorder that disrupts the body's ability to deposit ...
#31.
A Case Report with Seven Years Follow-Up,Journal of ...
This paper reports a case with hypophosphatasia and prosthodontic rehabilitation using dental implants with 7-year follow-up. 中文翻译： ...
#32.
Prevalence of Hypophosphatasia in Patients with ...
About this study. The overall goal of this research is to identify patients in clinical practice that have unrecognized hypophosphatasia (HPP) and select ...
#33.
Hypophosphatasia Bone Disease Affecting 15,000 Spaniards ...
Hypophosphatasia is caused by one or more mutations in the gene coding for alkaline phosphatase (ALPL). It is frequently misdiagnosed.
#34.
Hypophosphatasia - NORD (National Organization for Rare ...
Hypophosphatasia (HPP) is a rare genetic disorder characterized by impaired mineralization (“calcification”) of bones and teeth. Problems occur because ...
#35.
Hypophosphatasia: Clinical updates and therapeutic advances
Most commonly utilized medications for osteoporosis may further impair skeletal mineralization and should be avoided in patients with ...
#37.
Hypophosphatasia Could Explain Some Atypical Femur ...
[1] Research in recent years suggests that low levels of an enzyme called alkaline phosphatase (ALP) can cause bone loss and stress fractures in ...
#38.
hypophosphatasia的中文解释和发音 - 欧路词典
Hypophosphatasia is a rare inherited metabolic disease of decreased tissue nonspecific alkaline phosphatase (TNSALP) and defective bone mineralization.
#39.
Pharmacotherapy of Perinatal/Infantile and Juvenile-Onset ...
Hypophosphatasia (HPP), also known as phosphoethanolaminuria, Rathbun disease, ... 注意：如果您使用繁體中文，您可以免費獲得語言援助服務。
#40.
期刊界All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息 ...
The human tissue nonspecific alkaline phosphatase (TNAP) is found in liver, kidney, and bone. Mutations in the TNAP gene can lead to Hypophosphatasia, ...
#41.
完整显示页面
Correlation of alkaline phosphatase (ALP) determination and analysis of the tissue non-specific ALP gene in prenatal diagnosis of severe hypophosphatasia.
英文: Hypophosphatasia is a rare inherited metabolic disease characterized by rickets with reduced plasma and tissue alkaline phosphatase activity. 中文: ...
Hypophosphatasia (HPP, Rathburn disease) is a rare, possibly life-threatening, genetic metabolic disease defined by low tissue-nonspecific ...
#46.
Center for Bone Health | Children's Hospital of Philadelphia
Hypophosphatasia ; Hypophosphatemia; Kidney stones; Low bone density and osteoporosis; McCune-Albright syndrome; Multiple or fragility fractures; Osteogenesis ...
#47.
Search Orphan Drug Designations and Approvals
Generic Name: Asfotase alfa. Trade Name: Strensiq. Date Designated: 09/12/2008. Orphan Designation: Treatment of hypophosphatasia. Orphan Designation Status ...
#60.
Prevention of Pressure Sores: Engineering and Clinical Aspects
clinical and genetic aspects of hypophosphatasia ... Nintendo Switch遊戲軟體《星之卡比探索發現》中文一般版[台灣公司貨].
#61.
5.01.573 Pharmacotherapy of Perinatal/Infantile and ... - LifeWise
Hypophosphatasia (HPP) ... Hypophosphatasia (HPP), also known as phosphoethanolaminuria, ... 注意：如果您使用繁體中文，您可以免費獲得語言援助服務。
#62.
Anemia 释义| 柯林斯英语词典
Source URL: https://en.wikipedia.org/wiki/Hypophosphatasia. In blood, anemia, hypoalbuminemia, and eosinophilia may be observed in all types of fasciolosis.
#63.
5.01.573 Pharmacotherapy of Perinatal/Infantile and Juvenile-Onset ...
Hypophosphatasia (HPP) ... Hypophosphatasia (HPP), also known as phosphoethanolaminuria, ... 注意：如果您使用繁體中文，您可以免費獲得語言援助服務。
#68.
WO 2018/004517 A1 - Methods for Treating ... - Patent Lens
The disclosure features methods for treating hypophosphatasia (HPP) in a patient (e.g., a child or an adolescent having HPP) exhibiting gait impairments or ...
Aetna considers asfotase alfa (Strensiq) medically necessary for the treatment of perinatal/infantile-onset and juvenile-onset hypophosphatasia (HPP) when ...
In this report, we present two cases of hypophosphatasia, one of the infantile and the other of the adult form. 我們報告了兩位不同型之先天性磷酸酶缺少癥， ...
#78.
Airiti Library華藝線上圖書館
由 S Aggarwal 著作 · 2018 · 被引用 1 次 — Language, English, 繁體中文, 简体中文, 한국어 ... Surgical management for tibial shaft fractures using flexible nailing in adult hypophosphatasia ...
#79.
血碱性磷酸酶对慢肾衰透析患者2年骨折事件的预测价值 - NCBI
10. Whyte MP. Physiological role of alkaline phosphatase explored in hypophosphatasia. http://d.old.wanfangdata.com.cn/NSTLQK/10.1111-j.1749-6632.2010.05387.x/ ...
hypophosphatasia中文 在 正常的腦回壓跡都在後腦勺的地方較為明顯，但是有些病患會在 ... 的推薦與評價
... 會有這樣現象的病患是因為顱內壓過高所導致的(小孩子)，當然其中包括了Craniosynostosis Obstructive hydrocephalus Hypophosphatasia Intracranial masses 等. ... <看更多>