ライフサイエンスコーパス: exocrine pancreatic insufficiency

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1 s primarily characterized by neutropenia and exocrine pancreatic insufficiency.

2 and led to progressive diabetes mellitus and exocrine pancreatic insufficiency.

3 essively inherited disorder characterized by exocrine pancreatic insufficiency and bone marrow failur

4 utosomal-recessive disorder characterized by exocrine pancreatic insufficiency and hematopoietic dysf

5 No patients had endocrine or exocrine pancreatic insufficiency, and none required chr

6 rine congenital onset with sequelae of early exocrine pancreatic insufficiency as in the diseases of

7 a rare multisystem disorder characterized by exocrine pancreatic insufficiency, bone marrow dysfuncti

8 ve ribosome assembly and are associated with exocrine pancreatic insufficiency, chronic neutropenia a

9 icroscopic colitis, steatorrhea secondary to exocrine pancreatic insufficiency, dietary lactose or fr

10 pitfalls in the use of diagnostic tests for exocrine pancreatic insufficiency (EPI) confound interpr

11 Treatment of human exocrine pancreatic insufficiency is suboptimal.

12 a rare multisystem disorder characterized by exocrine pancreatic insufficiency, multilineage hematopo

13 s with insulin-treated neonatal diabetes and exocrine pancreatic insufficiency requiring enzyme repla

14 Two of the four patients had exocrine pancreatic insufficiency requiring replacement

15 % of Alagille syndrome patients also display exocrine pancreatic insufficiency, the pathobiology of w

16 25-hydroxyvitamin D in 10 adults with CF and exocrine pancreatic insufficiency was compared with that

17 We observed endocrine/exocrine pancreatic insufficiency, which had not previou

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