Vamos E - Search Results

1

A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosis.

Seneca S, Abramowicz M, Lissens W, Muller MF, Vamos E, de Meirleir L. Seneca S, et al. Among authors: vamos e. J Inherit Metab Dis. 1996;19(2):115-8. doi: 10.1007/BF01799407. J Inherit Metab Dis. 1996. PMID: 8739943 No abstract available.

2

Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunit.

de Meirleir LJ, Lissens W, Vamos E, Liebaers I. de Meirleir LJ, et al. Among authors: vamos e. J Inherit Metab Dis. 1991;14(3):301-4. doi: 10.1007/BF01811687. J Inherit Metab Dis. 1991. PMID: 1770778 No abstract available.

3

Pernicious anaemia and hypoparathyroidism in a patient with Kearns-Sayre syndrome with mitochondrial DNA duplication.

Abramowicz MJ, Cochaux P, Cohen LH, Vamos E. Abramowicz MJ, et al. Among authors: vamos e. J Inherit Metab Dis. 1996;19(2):109-11. doi: 10.1007/BF01799405. J Inherit Metab Dis. 1996. PMID: 8739941 No abstract available.

4

Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts.

Telerman-Toppet N, Biarent D, Bouton JM, de Meirleir L, Elmer C, Noel S, Vamos E, DiMauro S. Telerman-Toppet N, et al. Among authors: vamos e. J Inherit Metab Dis. 1992;15(3):323-6. doi: 10.1007/BF02435967. J Inherit Metab Dis. 1992. PMID: 1383604 No abstract available.

5

Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1 alpha subunit.

De Meirleir L, Lissens W, Vamos E, Liebaers I. De Meirleir L, et al. Among authors: vamos e. Hum Genet. 1992 Mar;88(6):649-52. doi: 10.1007/BF02265291. Hum Genet. 1992. PMID: 1551669

6

Pyruvate dehydrogenase deficiency: clinical and biochemical diagnosis.

De Meirleir L, Lissens W, Denis R, Wayenberg JL, Michotte A, Brucher JM, Vamos E, Gerlo E, Liebaers I. De Meirleir L, et al. Among authors: vamos e. Pediatr Neurol. 1993 May-Jun;9(3):216-20. doi: 10.1016/0887-8994(93)90088-t. Pediatr Neurol. 1993. PMID: 8352855

7

Assessment of an electron-impact GC-MS method for organic acids and glycine conjugates in amniotic fluid.

Kumps A, Vamos E, Mardens Y, Abramowicz M, Genin J, Duez P. Kumps A, et al. Among authors: vamos e. J Inherit Metab Dis. 2004;27(5):567-79. doi: 10.1023/b:boli.0000042981.52186.a9. J Inherit Metab Dis. 2004. PMID: 15669672

8

Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus.

Abramowicz MJ, Andrien M, Dupont E, Dorchy H, Parma J, Duprez L, Ledley FD, Courtens W, Vamos E. Abramowicz MJ, et al. Among authors: vamos e. J Clin Invest. 1994 Jul;94(1):418-21. doi: 10.1172/JCI117339. J Clin Invest. 1994. PMID: 7913714 Free PMC article.

9

Preimplantation genetic diagnosis for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.

Sermon K, Henderix P, Lissens W, De Vos A, Vandervorst M, Vanderfaeillie A, Vamos E, Van Steirteghem A, Liebaers I. Sermon K, et al. Among authors: vamos e. Mol Hum Reprod. 2000 Dec;6(12):1165-8. doi: 10.1093/molehr/6.12.1165. Mol Hum Reprod. 2000. PMID: 11101700

10

Frequent deletion of chromosome 19 and a rare rearrangement of 19p13.3 involving the insulin receptor gene in human ovarian cancer.

Amfo K, Neyns B, Teugels E, Lissens W, Bourgain C, De Sutter P, Vandamme B, Vamos E, De Grève J. Amfo K, et al. Among authors: vamos e. Oncogene. 1995 Jul 20;11(2):351-8. Oncogene. 1995. PMID: 7624149

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