Detalhe da pesquisa
1.
Bifidobacteriumbreve Bif195 Protects Against Small-Intestinal Damage Caused by Acetylsalicylic Acid in Healthy Volunteers.
Gastroenterology
; 157(3): 637-646.e4, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31095949
2.
Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-Ic.
Hum Mutat
; 22(5): 420-1, 2003 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-14517965
3.
[Time limits for gastrointestinal decontamination in poisoning]. / Tidsgraenser for gastrointestinal dekontaminering ved forgiftning.
Ugeskr Laeger
; 171(9): 718, 2009 Feb 23.
Artigo
em Dinamarquês
| MEDLINE | ID: mdl-19258001
4.
Ablation of mouse phosphomannose isomerase (Mpi) causes mannose 6-phosphate accumulation, toxicity, and embryonic lethality.
J Biol Chem
; 281(9): 5916-27, 2006 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-16339137
5.
Congenital disorder of glycosylation (CDG)-Ih patient with a severe hepato-intestinal phenotype and evolving central nervous system pathology.
J Pediatr
; 147(6): 847-50, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16356445
6.
A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency.
Hum Mol Genet
; 11(5): 599-604, 2002 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11875054
7.
Molecular cloning, gene organization, and expression of mouse Mpi encoding phosphomannose isomerase.
Glycobiology
; 12(7): 435-42, 2002 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12122025
8.
Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins.
J Pediatr
; 141(5): 695-700, 2002 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-12410200