ライフサイエンスコーパス: Fanconi syndrome

コーパス検索結果 (１語後でソート)

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 tations include mental retardation and renal Fanconi syndrome.

2 is the most common inherited cause of renal Fanconi syndrome.

3 tal cataracts, mental retardation, and renal Fanconi syndrome.

4 Biopsy indications included Fanconi syndrome (38%; all with crystalline LCPT), renal

5 They are all forms of the renal Fanconi syndrome and are associated with tubular protein

6 idence linking cellular stress and injury to Fanconi syndrome and progressive renal injury in nephrop

7 ystinosis, which may contribute to the renal Fanconi syndrome and progressive renal injury.

8 zed by bilateral congenital cataracts, renal Fanconi syndrome, and mental retardation.

9 ting apical dedifferentiation accounting for Fanconi syndrome before atrophy.

10 d proximal tubular dysfunction indicative of Fanconi syndrome, characterized by glycosuria, aminoacid

11 ial deafness, sideroblastic anemia and renal Fanconi syndrome, dying at 21 months.

12 Adult-acquired Fanconi syndrome (FS) is a rare complication of monoclon

13 - mice have type 2 diabetes, dwarfism, renal Fanconi syndrome, hepatic dysfunction and hypercholestro

14 is the most common inherited cause of renal Fanconi syndrome in children.

15 provide an explanation for the appearance of Fanconi syndrome in cystinosis.

16 ropathic cystinosis, we defined the onset of Fanconi syndrome in KO mice between 3 and 6 months of ag

17 Autosomal dominant renal Fanconi syndrome is a genetic model for the study of pro

18 Cystinosis, a main cause of Fanconi syndrome, is reproduced in congenic C57BL/6 cyst

19 he family with autosomal dominant idiopathic Fanconi syndrome (n = 2) exhibited megalin levels within

20 not develop the congenital cataracts, renal Fanconi syndrome, or neurological abnormalities seen in

21 The Acadian variant of Fanconi Syndrome refers to a specific condition characte

22 ults demonstrate that the Acadian variant of Fanconi Syndrome results from mitochondrial respiratory

23 g proximal tubule (PT) dysfunction and renal Fanconi syndrome (RFS).

24 eralized proximal tubular dysfunction (renal Fanconi syndrome), then the disease rapidly affects glom

25 s syndrome, or autosomal dominant idiopathic Fanconi syndrome was explored.

26 t all complications of cystinosis, including Fanconi syndrome, we hypothesized that cystinosin could

27 product altered in autosomal dominant renal Fanconi syndrome will allow the study of the physiology

28 pha homozygous knockout mice exhibit a renal Fanconi syndrome with glucosuria and generalized aminoac

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。