Guéant JL - Search Results

1

Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant Article.

Oussalah A, Bosco P, Anello G, Spada R, Guéant-Rodriguez RM, Chery C, Rouyer P, Josse T, Romano A, Elia M, Bronowicki JP, Guéant JL. Oussalah A, et al. Among authors: gueant jl, gueant rodriguez rm. Medicine (Baltimore). 2015 Jun;94(22):e925. doi: 10.1097/MD.0000000000000925. Medicine (Baltimore). 2015. PMID: 26039129 Free PMC article.

2

Cobalamin deficiency with megaloblastic anaemia in one patient under long-term omeprazole therapy.

Bellou A, Aimone-Gastin I, De Korwin JD, Bronowicki JP, Moneret-Vautrin A, Nicolas JP, Bigard MA, Guéant JL. Bellou A, et al. Among authors: gueant jl. J Intern Med. 1996 Sep;240(3):161-4. doi: 10.1046/j.1365-2796.1996.20846000.x. J Intern Med. 1996. PMID: 8862126

3

Autoantibodies in pernicious anemia type I patients recognize sequence 251-256 in human intrinsic factor.

Guéant JL, Safi A, Aimone-Gastin I, Rabesona H, Bronowicki JP, Plénat F, Bigard MA, Haertlé T. Guéant JL, et al. Proc Assoc Am Physicians. 1997 Sep;109(5):462-9. Proc Assoc Am Physicians. 1997. PMID: 9285945

4

Prospective evaluation of protein bound vitamin B12 (cobalamin) malabsorption in the elderly using trout flesh labelled in vivo with 57Co-cobalamin.

Aimone-Gastin I, Pierson H, Jeandel C, Bronowicki JP, Plénat F, Lambert D, Nabet-Belleville F, Guéant JL. Aimone-Gastin I, et al. Among authors: gueant jl. Gut. 1997 Oct;41(4):475-9. doi: 10.1136/gut.41.4.475. Gut. 1997. PMID: 9391245 Free PMC article.

5

Allele varepsilon4 of apolipoprotein E gene is less frequent in Down syndrome patient of the Sicilian population and has no influence on the grade of mental retardation.

Anello G, Guéant J, Romano C, Barone C, Pettinato R, Pillot T, Rodriguez R, Romano A, Bosco P. Anello G, et al. Neurosci Lett. 2001 Jun 22;306(1-2):129-31. doi: 10.1016/s0304-3940(01)01851-1. Neurosci Lett. 2001. PMID: 11403974

6

Overexpression of folate binding protein alpha is one of the mechanism explaining the adaptation of HT29 cells to high concentration of methotrexate.

de Nonancourt-Didion M, Guéant JL, Adjalla C, Chéry C, Hatier R, Namour F. de Nonancourt-Didion M, et al. Among authors: gueant jl. Cancer Lett. 2001 Oct 10;171(2):139-45. doi: 10.1016/s0304-3835(01)00552-3. Cancer Lett. 2001. PMID: 11520597

7

Immediate hypersensitivity to cephalosporins.

Romano A, Torres MJ, Namour F, Mayorga C, Artesani MC, Venuti A, Guéant JL, Blanca M. Romano A, et al. Among authors: gueant jl. Allergy. 2002;57 Suppl 72:52-7. doi: 10.1034/j.1398-9995.57.s72.18.x. Allergy. 2002. PMID: 12144556 Review. No abstract available.

8

The 18 kDa peanut oleosin is a candidate allergen for IgE-mediated reactions to peanuts.

Pons L, Chery C, Romano A, Namour F, Artesani MC, Guéant JL. Pons L, et al. Among authors: gueant jl. Allergy. 2002;57 Suppl 72:88-93. doi: 10.1034/j.1398-9995.57.s72.16.x. Allergy. 2002. PMID: 12144563

9

Transcobalamin and methionine synthase reductase mutated polymorphisms aggravate the risk of neural tube defects in humans.

Guéant-Rodriguez RM, Rendeli C, Namour B, Venuti L, Romano A, Anello G, Bosco P, Debard R, Gérard P, Viola M, Salvaggio E, Guéant JL. Guéant-Rodriguez RM, et al. Among authors: gueant jl. Neurosci Lett. 2003 Jul 3;344(3):189-92. doi: 10.1016/s0304-3940(03)00468-3. Neurosci Lett. 2003. PMID: 12812837

10

Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome.

Bosco P, Guéant-Rodriguez RM, Anello G, Barone C, Namour F, Caraci F, Romano A, Romano C, Guéant JL. Bosco P, et al. Among authors: gueant jl, gueant rodriguez rm. Am J Med Genet A. 2003 Sep 1;121A(3):219-24. doi: 10.1002/ajmg.a.20234. Am J Med Genet A. 2003. PMID: 12923861

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