ライフサイエンスコーパス: Albright

コーパス検索結果 (left1)

通し番号をクリックするとPubMedの該当ページを表示します

1 Albright hereditary osteodystrophy (AHO), a disorder cha

2 Albright hereditary osteodystrophy (AHO), an autosomal d

3 Albright's Hereditary Osteodystrophy (AHO) was the first

4 den Dystonia Rating Scale-Motor Scale, Barry Albright Dystonia Scale), disability (Burke Fahn Marsden

5 d hyperphosphatemia but without evidence for Albright hereditary osteodystrophy who has paternal unip

6 n the 1940s with the demonstration by Fuller Albright that treatment with oestrogen could reverse the

7 ings potentially have implications for human Albright hereditary osteodystrophy, a condition caused b

8 In Albright Hereditary Osteodystrophy (AHO) heterozygous lo

9 ha-inactivating mutations lead to obesity in Albright hereditary osteodystrophy (AHO) patients, but o

10 reports of mild heterotopic ossification in Albright's hereditary osteodystrophy (AHO) and a recent

11 e resistance that is limited to PTH and lack Albright hereditary osteodystrophy.

12 McCune-Albright syndrome (MAS), a mosaic condition associated w

13 ently, IPMNs have been described as a McCune-Albright syndrome-associated tumor, present in about 15%

14 of polyostotic fibrous dysplasia and McCune-Albright syndrome among patients operated on for presump

15 ts with fibrous dysplasia of bone and McCune-Albright syndrome generated more basal cAMP accumulation

16 use of fibrous dysplasia of bone (FD)/McCune-Albright syndrome (MAS).

17 utations) and hormone hypersecretion (McCune-Albright syndrome caused by gain-of-function mutations).

18 ary mucinous neoplasms (IPMNs) and in McCune-Albright syndrome, characterized by fibrous dysplasia, p

19 trimeric G-protein disorders, joining McCune-Albright and Sturge-Weber syndromes.

20 predisposing to pituitary neoplasias: McCune-Albright syndrome, multiple endocrine neoplasia type 1,

21 e of a syndromic IPMN as a feature of McCune-Albright syndrome, this observation is further evidence

22 on clinical examination suggestive of McCune-Albright syndrome.

23 Because of its similarities to the McCune-Albright syndrome and other features, such as paradoxica

24 tic fibrous dysplasia, and 26 had the McCune-Albright syndrome.

25 sia of bone is a major finding in the McCune-Albright syndrome.

26 nd bone age advancement in girls with McCune-Albright syndrome (MAS), despite ovarian enlargement.

27 raphy was performed on a patient with McCune-Albright syndrome and acromegaly.

28 have been identified in patients with McCune-Albright syndrome, but the mechanism leading to the spec

29 H) resistance, but lack physical features of Albright hereditary osteodystrophy.

30 denylyl cyclase plus somatic features termed Albright hereditary osteodystrophy.

31 PHP), a disease which shares features of the Albright hereditary osteodystrophy (AHO) phenotype.

32 ygous Gsalpha inactivating mutations lead to Albright hereditary osteodystrophy.

33 is mutation was identified in a patient with Albright hereditary osteodystrophy.

34 Studies in patients with Albright hereditary osteodystrophy suggest a similar G(s

35 an homologue GNAS1, mutated in patients with Albright hereditary osteodystrophy, is also imprinted.

WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。