skip to main content
Results 1 2 3 4 5 next page
Show only
Refined by: topic: Middle Aged remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
BCL6 gene rearrangements also occur in marginal zone B-cell lymphoma
Material Type:
Article
Add to e-Shelf

BCL6 gene rearrangements also occur in marginal zone B-cell lymphoma

DIERLAMM J ; PITTALUGA S ; STUL M ; WLODARSKA I ; MICHAUX L ; THOMAS J ; VERHOEF G ; VERHEST A ; DEPARDIEU C ; CASSIMAN J.J ; HAGEMEIJER A ; DE WOLF-PEETERS C ; VAN DEN BERGHE H

British Journal of Haematology, 1997-09, Vol.98 (3), p.719-725 [Peer Reviewed Journal]

Full text available

2
A rare cause of hyperferritinemia without iron overload
Material Type:
Article
Add to e-Shelf

A rare cause of hyperferritinemia without iron overload

Jacobs, B ; Cassiman, David ; Meersseman, Wouter 2013

Full text available

3
Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features [see comments]
Material Type:
Article
Add to e-Shelf

Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features [see comments]

Dierlamm, J ; Pittaluga, S ; Wlodarska, I ; Stul, M ; Thomas, J ; Boogaerts, M ; Michaux, L ; Driessen, A ; Mecucci, C ; Cassiman, JJ

Blood, 1996-01-01, Vol.87 (1), p.299-307 [Peer Reviewed Journal]

Full text available

4
Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization
Material Type:
Article
Add to e-Shelf

Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization

Dierlamm, J ; Rosenberg, C ; Stul, M ; Pittaluga, S ; Wlodarska, I ; Michaux, L ; Dehaen, M ; Verhoef, G ; Thomas, J ; de Kelver, W ; Bakker-Schut, T ; Cassiman, J J ; Raap, A K ; De Wolf-Peeters, C ; Van den Berghe, H ; Hagemeijer, A

Leukemia, 1997-05, Vol.11 (5), p.747-758 [Peer Reviewed Journal]

Full text available

5
FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12
Material Type:
Article
Add to e-Shelf

FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12

Dierlamm, J ; Wlodarska, I ; Michaux, L ; Vermeesch, J R ; Meeus, P ; Stul, M ; Criel, A ; Verhoef, G ; Thomas, J ; Delannoy, A ; Louwagie, A ; Cassiman, J J ; Mecucci, C ; Hagemeijer, A ; Van den Berghe, H

Genes chromosomes & cancer, 1997-10, Vol.20 (2), p.155-166 [Peer Reviewed Journal]

Full text available

6
FISH identifies different types of duplications with 12q13‐15 as the commonly involved segment in B‐cell lymphoproliferative malignancies characterized by partial trisomy 12
Material Type:
Article
Add to e-Shelf

FISH identifies different types of duplications with 12q13‐15 as the commonly involved segment in B‐cell lymphoproliferative malignancies characterized by partial trisomy 12

Dierlamm, Judith ; Wlodarska, Iwona ; Michaux, Lucienne ; Vermeesch, Joris R ; Meeus, Peter ; Stul, Michel ; Criel, Arnold ; Verhoef, Gregor ; Thomas, José ; Delannoy, André ; Louwagie, Andries ; Cassiman, Jean‐Jacques ; Mecucci, Cristina ; Hagemeijer, Anne ; Van den Berghe, Herman

Genes chromosomes & cancer, 1997-10, Vol.20 (2), p.155-166 [Peer Reviewed Journal]

Full text available

7
The Storage and Use of Biological Tissue Samples from Minors for Research: A Focus Group Study
Material Type:
Article
Add to e-Shelf

The Storage and Use of Biological Tissue Samples from Minors for Research: A Focus Group Study

K. Hens ; H. Nys ; J.-J. Cassiman ; K. Dierickx

Public health genomics, 2011-01-01, Vol.14 (2), p.68-76 [Peer Reviewed Journal]

Full text available

8
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1
Material Type:
Article
Add to e-Shelf

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1

Suls, A ; Dedeken, P ; Goffin, K ; Van Esch, H ; Dupont, P ; Cassiman, D ; Kempfle, J ; Wuttke, T. V ; Weber, Y ; Lerche, H ; Afawi, Z ; Vandenberghe, W ; Korczyn, A. D ; Berkovic, S. F ; Ekstein, D ; Kivity, S ; Ryvlin, P ; Claes, L. R. F ; Deprez, L ; Maljevic, S ; Vargas, A ; Van Dyck, T ; Goossens, D ; Del-Favero, J ; Van Laere, K ; De Jonghe, P ; Van Paesschen, W

Brain (London, England : 1878), 2008-06-24, Vol.131 (7), p.1831-1844 [Peer Reviewed Journal]

Full text available

9
Elafibranor, an Agonist of the Peroxisome Proliferator−Activated Receptor−α and −δ, Induces Resolution of Nonalcoholic Steatohepatitis Without Fibrosis Worsening
Material Type:
Article
Add to e-Shelf

Elafibranor, an Agonist of the Peroxisome Proliferator−Activated Receptor−α and −δ, Induces Resolution of Nonalcoholic Steatohepatitis Without Fibrosis Worsening

Ratziu, Vlad ; Harrison, Stephen A ; Francque, Sven ; Bedossa, Pierre ; Lehert, Philippe ; Serfaty, Lawrence ; Romero-Gomez, Manuel ; Boursier, Jérôme ; Abdelmalek, Manal ; Caldwell, Steve ; Drenth, Joost ; Anstee, Quentin M ; Hum, Dean ; Hanf, Remy ; Roudot, Alice ; Megnien, Sophie ; Staels, Bart ; Sanyal, Arun ; Mathurin, P ; Gournay, J ; Nguyen-Khac, E ; De Ledinghen, V ; Larrey, D ; Tran, A ; Bourliere, M ; Maynard-Muet, M ; Asselah, T ; Henrion, J ; Nevens, F ; Cassiman, D ; Geerts, A ; Moreno, C ; Beuers, U.H ; Galle, P.R ; Spengler, U ; Bugianesi, E ; Craxi, A ; Angelico, M ; Fargion, S ; Voiculescu, M ; Gheorghe, L ; Preotescu, L ; Caballeria, J ; Andrade, R.J ; Crespo, J ; Callera, J.L ; Ala, A ; Aithal, G ; Abouda, G ; Luketic, V ; Huang, M.A ; Gordon, S ; Pockros, P ; Poordad, F ; Shores, N ; Moehlen, M.W ; Bambha, K ; Clark, V ; Satapathy, S ; Parekh, S ; Reddy, R.K ; Sheikh, M.Y ; Szabo, G ; Vierling, J ; Foster, T ; Umpierrez, G ; Chang, C ; Box, T ; Gallegos-Orozco, J

Gastroenterology (New York, N.Y. 1943), 2016-05, Vol.150 (5), p.1147-1159.e5 [Peer Reviewed Journal]

Full text available

10
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats
Material Type:
Article
Add to e-Shelf

Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats

Rubinsztein, D C ; Leggo, J ; Coles, R ; Almqvist, E ; Biancalana, V ; Cassiman, J J ; Chotai, K ; Connarty, M ; Crauford, D ; Curtis, A ; Curtis, D ; Davidson, M J ; Differ, A M ; Dode, C ; Dodge, A ; Frontali, M ; Ranen, N G ; Stine, O C ; Sherr, M ; Abbott, M H ; Franz, M L ; Graham, C A ; Harper, P S ; Hedreen, J C ; Hayden, M R

American journal of human genetics, 1996-07, Vol.59 (1), p.16-22 [Peer Reviewed Journal]

Full text available

Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Show only

  1. Peer-reviewed Journals (555)

Refine My Results

Topic 

  1. Science & Technology  (562)
  2. Female  (553)
  3. Life Sciences & Biomedicine  (538)
  4. Male  (534)
  5. Adult  (476)
  6. Aged  (355)
  7. Adolescent  (177)
  8. Genetics & Heredity  (134)
  9. Aged, 80 And Over  (129)
  10. Child  (99)
  11. Young Adult  (98)
  12. Risk Factors  (91)
  13. Oncology  (85)
  14. Research  (84)
  15. Mutation  (78)
  16. Genetic Aspects  (77)
  17. Pathology  (68)
  18. Hematology  (62)
  19. More options open sub menu

Creation Date 

From To
  1. Before 1991  (7)
  2. 1991 To 1998  (59)
  3. 1999 To 2005  (182)
  4. 2006 To 2013  (237)
  5. After 2013  (180)
  6. More options open sub menu

Language 

  1. Portuguese  (4)
  2. Spanish  (2)
  3. More options open sub menu

Searching Remote Databases, Please Wait

  • Searching for
  • inscope:(TRAILS-PRINT),scope:(D-01TRAILS_MSU_GFC),scope:(E-01TRAILS_MSU_GFC),primo_central_multiple_fe
  • Show me what you have so far