AAAAAA

   
Results: 1-12 |
Results: 12
Familial juvenile hyperuricemic nephropathy and autosomal dominant medullary cystic kidney disease type 2: Two facets of the same disease?
Authors: Dahan, K Fuchshuber, A Adamis, S Smaers, M Kroiss, S Loute, G Cosyns, JP Hildebrandt, F Verellen-Dumoulin, C Pirson, Y
Citation: K. Dahan et al., Familial juvenile hyperuricemic nephropathy and autosomal dominant medullary cystic kidney disease type 2: Two facets of the same disease?, J AM S NEPH, 12(11), 2001, pp. 2348-2357
Trisomy 16 as the sole anomaly in hematological malignancies: three new cases and a short review
Authors: Guillaume, B Ameye, G Dierlamm, J Verhoef, G Duhem, C Ferrant, A Hagemeijer, A Verellen-Dumoulin, C Michaux, L
Citation: B. Guillaume et al., Trisomy 16 as the sole anomaly in hematological malignancies: three new cases and a short review, CANC GENET, 128(2), 2001, pp. 168-171
Frequency of cystic fibrosis transmembrane conductance regulator gene mutations and 5T allele in patients with allergic bronchopulmonary aspergillosis
Authors: Marchand, E Verellen-Dumoulin, C Mairesse, M Delaunois, L Brancaleone, P Rahier, JF Vandenplas, O
Citation: E. Marchand et al., Frequency of cystic fibrosis transmembrane conductance regulator gene mutations and 5T allele in patients with allergic bronchopulmonary aspergillosis, CHEST, 119(3), 2001, pp. 762-767
CNGA3 mutations in hereditary cone photoreceptor disorders
Authors: Wissinger, B Gamer, D Jagle, H Giorda, R Marx, T Mayer, S Tippmann, S Broghammer, M Jurklies, B Rosenberg, T Jacobson, SG Sener, EC Tatlipinar, S Hoyng, CB Castellan, C Bitoun, P Andreasson, S Rudolph, G Kellner, U Lorenz, B Wolff, G Verellen-Dumoulin, C Schwartz, M Cremers, FPM Apfelstedt-ylla, E Zrenner, E Salati, R Sharpe, LT Kohl, S
Citation: B. Wissinger et al., CNGA3 mutations in hereditary cone photoreceptor disorders, AM J HU GEN, 69(4), 2001, pp. 722-737
CF gene and cystic fibrosis transmembrane conductance regulator expressionin autosomal dominant polycystic kidney disease
Authors: Persu, A Devuyst, O Lannoy, N Materne, R Brosnahan, G Gabow, PA Pirson, Y Verellen-Dumoulin, C
Citation: A. Persu et al., CF gene and cystic fibrosis transmembrane conductance regulator expressionin autosomal dominant polycystic kidney disease, J AM S NEPH, 11(12), 2000, pp. 2285-2296
MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23
Authors: Michaux, L Wlodarska, I Stul, M Dierlamm, J Mugneret, F Herens, C Beverloo, B Verhest, A Verellen-Dumoulin, C Verhoef, G Selleslag, M Madoe, V Lecomte, M Deprijck, B Ferrant, A Delannoy, A Marichal, S Duhem, C Dicato, M Hagemeijer, A
Citation: L. Michaux et al., MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23, GENE CHROM, 29(1), 2000, pp. 40-47
The value of interphase fluorescence in situ hybridization for the detection of translocation t(12;21) in childhood acute lymphoblastic leukemia
Authors: Ameye, G Jacquy, C Zenebergh, A Stul, M Vaerman, JL Bilhou-Nabera, C Libouton, JM Deneys, V Martiat, P Hagemeijer, A Cornu, G Verellen-Dumoulin, C Michaux, L
Citation: G. Ameye et al., The value of interphase fluorescence in situ hybridization for the detection of translocation t(12;21) in childhood acute lymphoblastic leukemia, ANN HEMATOL, 79(5), 2000, pp. 259-268
Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;22;21)(q34;q11;q22)
Authors: Guillaume, B Ameye, G Libouton, JM Dierlamm, J Vaerman, JL Straetmans, N Ferrant, A Verellen-Dumoulin, C Michaux, L
Citation: B. Guillaume et al., Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;22;21)(q34;q11;q22), CANC GENET, 116(2), 2000, pp. 166-169
Congenital muscular dystrophy with central and peripheral nervous system involvement in a Belgian patient
Authors: Belpaire-Dethiou, MC Saito, K Fukuyama, Y Kondo-Iida, E Toda, T Duprez, T Verellen-Dumoulin, C Van den Bergh, PYK
Citation: Mc. Belpaire-dethiou et al., Congenital muscular dystrophy with central and peripheral nervous system involvement in a Belgian patient, NEUROMUSC D, 9(4), 1999, pp. 251-256
New possibilities for prenatal diagnosis of muscular dystrophies: forced myogenesis with an adenoviral MyoD-vector
Authors: Roest, PAM Bakker, E Fallaux, FJ Verellen-Dumoulin, C Murry, CE den Dunnen, JT
Citation: Pam. Roest et al., New possibilities for prenatal diagnosis of muscular dystrophies: forced myogenesis with an adenoviral MyoD-vector, LANCET, 353(9154), 1999, pp. 727-728
Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3 ' APC mutation
Authors: Kartheuser, A Walon, C West, S Breukel, C Detry, R Gribomont, AC Hamzehloei, T Hoang, P Maiter, D Pringot, J Rahier, J Khan, PM Curtis, A Burn, J Fodde, R Verellen-Dumoulin, C
Citation: A. Kartheuser et al., Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3 ' APC mutation, J MED GENET, 36(1), 1999, pp. 65-67
The A16V signal peptide cleavage site mutation in the cationic trypsinogengene and chronic pancreatitis
Authors: Chen, JM Raguenes, O Ferec, C Deprez, PH Verellen-Dumoulin, C Andriulli, A
Citation: Jm. Chen et al., The A16V signal peptide cleavage site mutation in the cationic trypsinogengene and chronic pancreatitis, GASTROENTY, 117(6), 1999, pp. 1508-1509
Risultati: 1-12 |