Kamoun P - Search Results

1

Hyperhomocysteinaemia: a significant risk factor for cardiovascular disease in renal transplant recipients.

Massy ZA, Chadefaux-Vekemans B, Chevalier A, Bader CA, Drüeke TB, Legendre C, Lacour B, Kamoun P, Kreis H. Massy ZA, et al. Among authors: kamoun p. Nephrol Dial Transplant. 1994;9(8):1103-8. doi: 10.1093/ndt/9.8.1103. Nephrol Dial Transplant. 1994. PMID: 7800208 Clinical Trial.

2

[Hyperhomocysteinemia in coronary artery diseases. Apropos of a study on 102 patients].

Blacher J, Montalescot G, Ankri A, Chadefaux-Vekemans B, Benzidia R, Grosgogeat Y, Kamoun P, Thomas D. Blacher J, et al. Among authors: kamoun p. Arch Mal Coeur Vaiss. 1996 Oct;89(10):1241-6. Arch Mal Coeur Vaiss. 1996. PMID: 8952820 French.

3

Plasma homocysteine and the extent of atherosclerosis in patients with coronary artery disease.

Montalescot G, Ankri A, Chadefaux-Vekemans B, Blacher J, Philippe F, Drobinski G, Benzidia R, Kamoun P, Thomas D. Montalescot G, et al. Among authors: kamoun p. Int J Cardiol. 1997 Aug 8;60(3):295-300. doi: 10.1016/s0167-5273(97)00099-5. Int J Cardiol. 1997. PMID: 9261641

4

Does the polymorphism 677C-T of the 5,10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?

Thuillier L, Chadefaux-Vekemans B, Bonnefont JP, Kara A, Aupetit J, Rochette C, Montalescot G, Couty MC, Kamoun P, Ankri A. Thuillier L, et al. Among authors: kamoun p. J Inherit Metab Dis. 1998 Dec;21(8):812-22. doi: 10.1023/a:1005414617390. J Inherit Metab Dis. 1998. PMID: 9870206

5

Four novel mutations at the cystathionine beta-synthase locus causing homocystinuria.

Coudé M, Aupetit J, Zabot MT, Kamoun P, Chadefaux-Vekemans B. Coudé M, et al. Among authors: kamoun p. J Inherit Metab Dis. 1998 Dec;21(8):823-8. doi: 10.1023/a:1005466601461. J Inherit Metab Dis. 1998. PMID: 9870207

6

Free amino acids in amniotic fluid and the prenatal diagnosis of homocystinuria with methylmalonic aciduria.

Parvy P, Bardet J, Chadefaux-Vekemans B, Rabier D, Gasquet M, Aupetit J, Kamoun P. Parvy P, et al. Among authors: kamoun p. Clin Chem. 1995 Nov;41(11):1663-4. Clin Chem. 1995. PMID: 7586560 No abstract available.

7

Two novel mutations (K384E and L539S) in the C-terminal moiety of the cystathionine beta-synthase protein in two French pyridoxine-responsive homocystinuria patients.

Aral B, Coudé M, London J, Aupetit J, Chassé JF, Zabot MT, Chadefaux-Vekemans B, Kamoun P. Aral B, et al. Among authors: kamoun p. Hum Mutat. 1997;9(1):81-2. doi: 10.1002/(SICI)1098-1004(1997)9:1<81::AID-HUMU18>3.0.CO;2-L. Hum Mutat. 1997. PMID: 8990018 No abstract available.

8

Improving the prenatal diagnosis of citrullinemia using citrulline/ornithine+arginine ratio in amniotic fluid.

Chadefaux-Vekemans B, Rabier D, Chabli A, Blanc A, Aupetit J, Bardet J, Kamoun P. Chadefaux-Vekemans B, et al. Among authors: kamoun p. Prenat Diagn. 2002 Jun;22(6):456-8. doi: 10.1002/pd.344. Prenat Diagn. 2002. PMID: 12116302

9

Gestational age-related reference values for amniotic fluid amino acids: a useful tool for prenatal diagnosis of aminoacidopathies.

Rabier D, Chadefaux-Vekemans B, Oury JF, Aupetit J, Bardet J, Gasquet M, Merhand E, Parvy P, Kamoun P. Rabier D, et al. Among authors: kamoun p. Prenat Diagn. 1996 Jul;16(7):623-8. doi: 10.1002/(SICI)1097-0223(199607)16:7<623::AID-PD921>3.0.CO;2-5. Prenat Diagn. 1996. PMID: 8843471

10

Methylenetetrahydrofolate reductase polymorphism in the etiology of Down syndrome.

Chadefaux-Vekemans B, Coudé M, Muller F, Oury JF, Chabli A, Jaïs J, Kamoun P. Chadefaux-Vekemans B, et al. Among authors: kamoun p. Pediatr Res. 2002 Jun;51(6):766-7. doi: 10.1203/00006450-200206000-00018. Pediatr Res. 2002. PMID: 12032275

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