Hello,
Here is a long list (sorry) of papers/posters/etc. presented to congress, symposia, conferences... The question is : where have they been published ? I've tried Pubmed, national catalogues (antilope and libis), the national library (who at least should have a copy of the Belgian meetings), Copernic, ... without success... Thank you very much for your help.
Bonjour !
Voici une longue (désolée) liste de communica tions prsentées à des congrès/conférences/symposiums... La question est : où ont-ils été publiés ? J'ai essayé Pubmed, Antilope et Libis, la bibliothèque nationale, Copernic, etc. sans succès. Merci pour votre aide.
Angélique
1. Broeckx W, Song M, Van Maldergem L, Ledoux M.
Pseudodermatomyositis in Bruton disease (oral communication)
Congressus Mundi Dermatologicae - Berlin (Germany) , July 1987.
2. Van Maldergem L, Jeghers O, de Prez C, Piepsz A and Ham H.
Détection du shunt portosystémique à l'aide du thallium injecté par voie rectale (poster)
6e Congrès National de Recherche en Pédiatrie - Toulouse (France) , Sept 1988.
3. Van Maldergem L, Capel P and Boeynaems J-M.
Increased prostacyclin biosynthesis in a patient with homocystinuria (oral communication).
24e Congrès International de Pédiatrie - Paris (France) , July 1989.
4. Gillerot Y, Van Maldergem M, Koulischer L.
Intérêt de l'autopsie en période néonatale : expérience personnelle à propos de 1100 observations (oral communication).
24e Congrès International de Pédiatrie - Paris (France) , July 1989.
5. Gillerot Y, Van Maldergem L, Koulischer L.
A propos du retard mental dit léger. Etude portant sur 500 familles (poster)
24e Congrès International de Pédiatrie - Paris (France) , July 1989.
6. Van Maldergem L, Gillerot Y, Roels F, Wanders RJA, Koulischer L.
X-linked recessive chondrodysplasia punctata associated with X-Y translocation (poster)
5th International Congress in Inborn Errors of Metabolism - Asilomar (California - USA) , June 1990.
7. Van Maldergem L, Gérard C, Kempeneers M-C, Van Alphen P, Koulischer L.
Détection du papillomavirus humain à l'aide de sondes biotinylées (poster)
1es Journées Franco-Belges de Gynéco-Pathologie - Namur (Belgium) , June 1990. Lauréat de la Société Franco-Belge de Gynéco-Pathologie.
8. Roels F, Espeel M, Rehder H, Van Maldergem L, Litwin J, Yokota S, Tager J, Hashimoto T.
Liver pathology and immunocytochemistry in congenital peroxisomal disorders (poster)
28th Annual Symposium of the Society for the Study of Inborn Errors of Metabolism (SSIEM) - Birmingham (United Kingdom) , Sept 1990.
9. Gillerot Y, Van Maldergem L, Koulischer L.
Lethal MCA of unknown aetiology : experience from 1200 neonatal necropsies (oral communication)
1st European Meeting of Dysmorphology - Zaragoza (Spain) , Sept 1990.
10. Gillerot Y, Van Maldergem L, Koulischer L.
Fetal hypokinesia sequence with rapidly fatal outcome (poster)
1st European Meeting of Dysmorphology - Zaragoza (Spain) , Sept 1990.
11. Van Maldergem L, Roels F, Espeel M, Wanders RJA, Koulischer L, Gillerot Y.
Peroxisomal workup in a 27-week-old stillborn with X-L recessive chondrodysplasia punctata and X-Y translocation (poster)
5th International Congress on Inborn Errors of Metabolism - Asilomar (California - USA) , June 1990.
12. Van Maldergem L, Delberghe X, Marneth P, Fourneau C, Gillerot Y. Oculocerebral hypopigmentation (Cross syndrome) : two new cases with hypochromic anemia (poster)
23rd Annual Meeting of the European Society of Human Genetics - Leuven (Belgium) , July 1991.
13. Fourneau C, Luyx A, Van Maldergem L, Gillerot Y. "Cytomegalic" degeneration of the adrenals in a case of triploidy retrospective diagnosis on fetal curetage debris (poster)
23rd Annual Meeting of the European Society of Human Genetics - Leuven (Belgium) , July 1991.
14. Verloes A, Journel H, Kaplan J, Le Merrer M, Van Maldergem L.
Heterogeneity of Neuheuser-megalocornea-mental retardation syndrome (oral communication)
2nd European Meeting of dysmorphology - Strasbourg (France) , Sept 1991.
15. Van Maldergem L, Bachy A, Tuerlinckx D, Van Hoof F, Wanders R, Vianey C, Martin J-J, Gillerot Y. Long-chain 3-hydroxyacyl-Co A dehydrogenase deficiency presenting as hepatic cirrhosis in two siblings (oral communication)
6th International Congress on Inborn Errors of Metabolism - Milano (Italy) , May 1994.
16. Jaeken J, Detheux M, Van Maldergem L, Fryns JP, Alliet P, Foulon M, Carchon H, Van Schaftingen E.
3-Phosphoglycerate dehydrogenase deficiency and 3-phosphoserine phosphatase deficiency : Inborn errors of serine biosynthesis. (oral communication)
33rd Annual Symposium of the Society for the Study of Inborn Errors of Metabolism - Toledo (Spain) Sept 12-15, 1995. SSIEM award
17. Van Maldergem L.
Update in the work-up of patients suffering from mental retardation (invited lecture).
Réunion annuelle des Généticiens de l'Est de la France, organized by Prof. J.L. Mandel. Novembre 1995.
18. Van Maldergem L.
Genetic heterogeneity in autistic conditions (invited lecture).
3rd International symposium on neurogenetics - Antwerp (Belgium) Dec 1996.
19. Van Maldergem L, Van Steirteghem S, Seemanova E, Loret H, Savasta S, Medina JL, Bonnici F, Nivelon-Chevalier A, Khallouf E, Capeau J, O'Rahilly S, D'Abronzo F, Verloes A, Gillerot Y. Clinical features in 36 new patients with Berardinelli-Seip congenital lipodystrophy (oral communication).
First international Conference on Congenital Lipodystrophies - Brussels, (Belgium) Sept 19-20, 1997.
20. Gedde-Dahl Jr, Trygstad O, Van Maldergem L, Magré J, van der Hagen CB,Olaisen O, Stenersen M, Mevag B and the Berardinelli-Seip Study group.
Genetics of B-S syndrome in Norway. (oral communication)
First international Conference on Congenital Lipodystrophies - Brussels, (Belgium) Sept 19-20, 1997.
21. Magré J, Vigouroux C, Hilbert P, Fauré S, Gedde-Dahl Jr, Khallouf E, Robert JJ, Weissenbach J, Capeau J, Van Maldergem L, the Berardinelli-Seip Study group.
Search for the genes responsible for lipoatrophic diabetes. (oral communication)
First international Conference on Congenital Lipodystrophies - Brussels, (Belgium) Sept 19-20, 1997.
22. Van Maldergem L.
CMT2 and distal HMN in Belgian families (1) Classification and diagnostic guidelines for Charcot-Marie-Tooth type 2 (CMT2 - HMSN II) and distal hereditary motor neuropathy (distal HMN spinal CMT)(oral communication).
53rd International workshop - European Neuromuscular Centre - Naarden, (The Netherlands), Sept 1997.
23. Van Maldergem L.
A registry of DNA laboratories in Europe: The EDDNAL experience. (Invited lecture) .
First Conference on Human Genome Research : Implications for Health in Latin America - SanJuan del Rio, Querétaro, (Mexico), Nov 1997.
24. Destrée A, Hennecker J-L, Stevart O, Collard L, Van Maldergem L.
Syndrome de GAPO : diagnostic préliminaire chez un nourrisson avec mégafontanelle (poster). 26e Annual meeting of the Belgian Society of Paediatrics - La Hulpe (Belgium) , March 20-21, 1998.
25. Van Maldergem L, Fagnart D, Ducastel L, Louis J, Dacremont G, Gillerot Y.
Supplementation of three patients presenting Smith-Lemli-Opitz syndrome (SLOS) with oral cholesterol : preliminary results (poster).
26th Annual meeting of the Belgian Society of Paediatrics - La Hulpe (Belgium), March 20-21, 1998.
26. Destrée A, Beauduin P, El Bouz S, Bartholomé J, Van Maldergem L.
Syndrome de Holt-Oram transmis en dominance : nouveau-né polymalformé et forme mineure atypique chez la mère. (poster)
26th Annual meeting of the Belgian Society of Paediatrics - La Hulpe, (Belgium) March 20-21, 1998.
27. Defresne P, Godfroid N, Provis P, Moser A, Van Maldergem L.
Chondroplasie ponctuée rhizomélique / une maladie péroxysomiale reconnaissable à la naissance (poster).
26th Annual meeting of the Belgian Society of Paediatrics - La Hulpe, (Belgium) March 20-21, 1998.
28. Destrée A, Foulon M, Christiaens F, Rombouts JJ, Christophe C, Van Maldergem L. Arthrogrypose, hypotonie, dysmorphie faciale, hypomélanose cutanée : triploïdie en mosaïque (poster)
26th Annual meeting of the Belgian Society of Paediatrics - La Hulpe, (Belgium) March 20-21, 1998.
29. Jordan I, Heymans C, Van Maldergem L.
Ambiguité sexuelle liée au syndrome 9p- (poster).
26th Annual meeting of the Belgian Society of Paediatrics - La Hulpe, (Belgium) March 20-21, 1998.
30. Gillerot Y, Destrée A, Van Maldergem L.
Expressivité variable et hétérogénéité dans le syndrome de Treacher-Collins (poster).
26th Annual meeting of the Belgian Society of Paediatrics - La Hulpe, (Belgium) March 20-21, 1998.
31. Van Maldergem L.
Cutis laxa and other progeroid states. (invited lecture)
Symposium organized by SE Antonorakis in the Department of Medical Genetics, University of Geneva - Switzerland May 1998.
32. Mortier G, Craen M, Leroy J, Verloes A, Van Maldergem L, De Paepe A, Nuytinck L.
Clinical and radiologic features of hypochondroplasia due to different mutations in the FGFR3 gene. (poster)
8th Birth defects conference - Manchester (United Kingdom) , November 1998.
33. Van Maldergem L, Hilbert P, Gillerot Y. Pitfalls in the molecular diagnosis of trinucleotide expansion (invited lecture). Euro-Ataxia Conference - Westende (Belgium) Oct 29-31, 1999.
34. Van Maldergem L, Hilbert P, Tavares P, Coelho T.
Mosaicism in Facioscapulohumeral Muscular Dystrophy. (invited lecture)
Conference on the Cause and Treatment of Facioscapulohumeral Muscular Dystrophy, 3rd International Symposium, NIH - Bethesda, Maryland (USA) May 7-9, 2000.
35. Van Maldergem L.
Diagnostic Work-Up in the Autistic Child (invited lecture). International Conference on Autism and related Disorders, University of Thessalonique (Greece), Oct 21, 2000.
36. Andries S, Hilbert P, Fourneau A-F, Gillerot Y, Van Maldergem L.
Unsuspected diagnosis of Connexin 26 deafness in patients with presumably other etiologies. (poster)
30th Annual Meeting of the Belgian Society of Pediatrics - La Hulpe (Belgium), March 23-24, 2001.
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