Articles dans des revues avec comité de lecture (150)
  1. 118. De Witte, O., Noterman, J., Oulad Ben Taib, N., Abramowicz, M., Balériaux, D., Vandesteene, A., & Brotchi, J. (1997). Anévrismes multiples et "de novo" dans le syndrome d'Ehlers-Danlos. Neuro-chirurgie, 43(4), 250-254.
  2. 119. Heinrichs, C., Parma, J., Duprez, L., Bourdoux, P., Ziereisen, F., Bergmann, P., Vassart, G., & Abramowicz, M. (1997). Familial congenital hypothyroidism due to an inactivating mutation in the TSH receptor gene causing profound hypoplasia of the thyroid gland. Hormone research, 48(2), 164.
  3. 120. Abramowicz, M., Parma, J., & Cochaux, P. (1996). Slight instability of a FMR-1 allele over three generations in a family from the general population. American journal of medical genetics, 64(2), 268-269. doi:10.1002/(SICI)1096-8628(19960809)64:2<268::AID-AJMG6>3.0.CO;2-Q
  4. 121. Hollemaert, S., Wautrecht, J.-C., Capel, P., Abramowicz, M., Englert, Y., & Delbaere, A. (1996). Thrombosis associated with ovarian hyperstimulation syndrome in a carrier of the factor V Leiden mutation. Thrombosis and haemostasis, 76(2), 275-277.
  5. 122. Abramowicz, M., Dorchy, H., & Vamos, E. (1996). Neonatal diabetes mellitus. The New England journal of medicine, 334(1), 58-9; author reply 59.
  6. 123. Abramowicz, M., Cochaux, P., Cohen, L. H., & Vamos, E. (1996). Pernicious anaemia and hypoparathyroidism in a patient with Kearns-Sayre syndrome with mitochondrial DNA duplication. Journal of inherited metabolic disease, 19(2), 109-111.
  7. 124. Seneca, S., Abramowicz, M., Lissens, W., Muller, M.-F., Vamos, E., & De Meirleir, L. (1996). A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosis. Journal of inherited metabolic disease, 19(2), 115-118.
  8. 125. Corvilain, B., Abramowicz, M., Fery, F., Schoutens, A., Verlinden, M., Balasse, E., & Horowitz, M. (1995). Effect of short-term starvation on gastric emptying in humans: relationship to oral glucose tolerance. The American journal of physiology, 269(4 Pt 1), G512-G517. doi:10.1152/ajpgi.1995.269.4.g512
  9. 126. donner, C., Simon, P., Karioun, A., Delneste, D., Abramowicz, M., Cochaux, P., & Rodesch, F. (1995). Experience with 1251 transcervical chorionic villus samplings performed in the first trimester by a single team of operators. European journal of obstetrics, gynecology, and reproductive biology, 60(1), 45-51. doi:10.1016/0028-2243(95)02080-2
  10. 127. Abramowicz, M. (1995). Le diagnostic moléculaire des maladies héréditaires. Revue médicale de Bruxelles, 16(3), 113-116.
  11. 128. Abramowicz, M., Andrien, M., Dupont, E., Dorchy, H., Parma, J., Duprez, L., Ledley, F. D., Courtens, W., & Vamos, E. (1994). Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus. The Journal of clinical investigation, 94(1), 418-421. doi:10.1172/JCI117339
  12. 129. Naeije, R., Lipski, A., Abramowicz, M., Lejeune, P., Melot, C., Antoine, M., De Smet, J.-M., Leclerc, J. L., & Primo, G. (1994). Nature of pulmonary hypertension in congestive heart failure: Effects of cardiac transplantation. American journal of respiratory and critical care medicine, 149(4), 881-887.
    13. << Précédent 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 Suivant >>