IPG - Institut de Pathologie et de Génétique

Publications de 2007

Voici quelques publications réalisées par les membres de l'IPG.

Prix :

Publications :

• H. El Housni, J. Vandesompele, Dr Sc. P. VANNUFFEL , B. Gulbis, J. Parma and P. Cochaux.
  Rapid and esay prenatal diagnosis of sickle cell anemia using double-dye LNA probe technology.
  British Journal of Haematology, (2007) 136, 509.
• Courtmans I ., Mancilla V., Ligny C., Dr Sc. P. Hilbert, Mansbach AL., Van Maldergem L.
  Clinical findings and PDS mutations in fifteen patients with hearing loss and dilatation of the vestibular aqueduct.
  J Laryngol Otol. 2007 Apr;121(4):312-7. Epub 2006 Nov 24.
• Rice G, Patrick T, Parmar R, Taylor CF, Aeby A, Aicardi J, Artuch R, Montalto SA, Bacino CA, Barroso B, Baxter P, Benko WS, Bergmann C, Bertini E, Biancheri R, Blair EM, Blau N, Bonthron DT, Briggs T, Brueton LA, Brunner HG, Burke CJ, Carr IM, Carvalho DR, Chandler KE, Christen HJ, Corry PC, Cowan FM, Cox H, D'Arrigo S, Dean J, De Laet C, De Praeter C, Dery C, Ferrie CD, Flintoff K, Frints SG, Garcia-Cazorla A, Gener B, Goizet C, Goutieres F, Green AJ, Guet A, Hamel BC, Hayward BE, Heiberg A, Hennekam RC, Husson M, Jackson AP, Jayatunga R, Jiang YH, Kant SG, Kao A, King MD, Kingston HM, Klepper J, van der Knaap MS, Kornberg AJ, Kotzot D, Kratzer W, Lacombe D, Lagae L, Landrieu PG, Lanzi G, Leitch A, Lim MJ, Livingston JH, Lourenco CM, Lyall EG, Lynch SA, Lyons MJ, Marom D, McClure JP, McWilliam R, Melancon SB, Mewasingh LD, Moutard ML, Nischal KK, Ostergaard JR, Prendiville J, Rasmussen M, Rogers RC, Dr D. Roland, Rosser EM, Rostasy K, Roubertie A, Sanchis A, Schiffmann R, Scholl-Burgi S, Seal S, Shalev SA, Corcoles CS, Sinha GP, Soler D, Spiegel R, Stephenson JB, Tacke U, Tan TY, Till M, Tolmie JL, Tomlin P, Vagnarelli F, Valente EM, Van Coster RN, Van der Aa N, Vanderver A, Vles JS, Voit T, Wassmer E, Weschke B, Whiteford ML, Willemsen MA, Zankl A, Zuberi SM, Orcesi S, Fazzi E, Lebon P, Crow YJ.
  Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
  Am J Hum Genet 2007 (4) : 713-725.
• Houinato D, Laleye A , Adjien C, Adjagba M, Sternberg D, Dr Sc. P. Hilbert, Vallat JM, Darboux RB, Funalot B, Avode DG.
  Hypokalaemic periodic paralysis due to the CACNA1S R1239H mutation in a large African family.
  Neuromuscul Disord. 2007 May;17(5):419-22
• Dr I. MAYSTADT, Rezsöhazy R, Barkats M, Duque S, Dr Sc. P. VANNUFFEL, Remacle S, Lambert B, Najimi M, Sokal E, Munnich A, Viollet L, Pr Ch. VERELLEN-DUMOULIN
  The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onset.
  Am J Hum Genet. 2007 July; 81(1):67-76
• Vanhooteghem O, Dr G. Müller, de la Brassinne M.
  Anogenital condylomata in the children. Practice guidelines for a medical expertise
  Rev Med Liege. 2007 Mar;62(3):151-4. Review. French.
• Laporte M, Trakatelli M, Vereecken P, Blocklet D, Lespagnard M, Dr M. Petein, Goldman M, Velu T, Heenen M.
  Skin biopsies in DC vaccines for stage III-IV melanoma patients: Role of Neutrophils ?
  Arch Dermatol Res. 2007 Dec; 299(10):483-6
• Heimann M, Beco L, Dr M. Petein, Nishifuji K, Amagai M, Olivry T.
  Canine hyperplastic intraepidermal pustular and suprabasal acantholytic Dermatosis with features of human pemphigus vegetans.
  Vet Pathol . 2007 July; 44(4):550-5
• Decelle L, D'Hondt L, Andre M, Dr P.DELREE , Calicis B, Lonchay C, Ide C, Canon JL.
  Ovarian cancer associated with carcinomatous meningitis: a case report and review of the literature.
  Int J Gynecol Cancer. 2007 Sep-Oct;17(5):1136-40. Epub 2007 Mar 15. Review.
• Giuliani R, Durbecq V, Di Leo A, Paesmans M, Larsimont D, Leroy JY, Borms M, Vindevoghel A, Jerusalem G, D'Hondt V, Dirix L, Canon JL, Richard V, Cocquyt V, Majois F, Reginster M, Demol J, Kains JP, Dr P.DELREE , Keppens C, Sotiriou C, Piccart MJ, Cardoso F.
  Phosphorylated HER-2 tyrosine kinase and Her-2/neu gene amplification as predictive factors of response to trastuzumab in patients with HER-2 overexpressing metastatic breast cancer (MBC).
  Eur J Cancer. 2007 Mar;43(4):725-35. Epub 2007 Jan 23.
• Zouaoui Boudjeltia K, Roumeguere T, Dr P.DELREE , Moguilevsky N, Ducobu J, Vanhaeverbeek M, Wespes E.
  Presence of LDL modified by myeloperoxidase in the penis in patients with vascular erectile dysfunction: a preliminary study.
  Eur Urol. 2007 Jan;51(1):262-8; discussion 268-9. Epub 2006 Sep 8.
• Dr P. Ribai, Nguyen K, Hahn-Barma V, Gourfinkel-An I, Vidailhet M, Legout A, et al.
  Psychiatric and cognitive difficulties as indicators of juvenile huntington disease onset in 29 patients.
  Archives of neurology. 2007 Jun;64(6):813-9.
  IF2007: ??
• Dr P. Ribai, Pousset F, Tanguy ML, Rivaud-Pechoux S, Le Ber I, Gasparini F, et al.
  Neurological, cardiological, and oculomotor progression in 104 patients with Friedreich ataxia during long-term follow-up
  Archives of neurology. 2007 Apr;64(4):558-64.
  IF2007: ??
• Depienne C, Fedirko E, Forlani S, Cazeneuve C, Dr P. Ribai, Feki I, et al.
  Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia.
  Journal of medical genetics. 2007 Apr;44(4):281-4.
  IF2007: ??
• Cotton RG, Auerbach AD, Brown AF, Carrera P, Christodoulou J, Claustres M, Compton J , Cox DW , De Baere E , den Dunnen JT , Greenblatt M , Fujiwara M , Dr Sc. P. Hilbert, Jani A , Lehvaslaiho H , Nebert DW , et al.
  A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases.
  Human mutation. 2007 Oct;28(10):931-2.
  IF2007: ??

Communications :

• Dr Sc. P. Hilbert, S. Boulanger , Van Maldergem L., Gillerot Y., Pr Ch. VERELLEN-DUMOULIN
  Preconceptional or prenatal Fragile X screening. Experience of 14 years in a Belgian Center for Human Genetics
  Belgian Society of Human Genetics , Marcinelle, avril 2007
• Dr Sc. B. Grisart, Dr Sc. K. RACK, Sébastien Vidrequin, Dr A. Destrée, Dr Sc. P. Hilbert, Pr Ch. VERELLEN-DUMOULIN
  NF1 microduplication : phenotypic observation and segregation in a familial pedigree.
  Genomic disorders, Cambridge du 21-23 mars 2007
• Dr D. Roland
  Fulminant onset (japanese) type 1 diabetes in a caucasian boy, triggered by Lyme disease.
  Société Belge de Pédiatrie, 2007
• Grégoire Y, Agneessens E, Navez J-F, Dr P.DELREE
  Dyspnee progressive chez un homme de 26 ans.
  2007
• N. Nijs-De Wolf, X. Holy, L. Bégot, Dr P.DELREE, V. Coulic, R. Karmali, P.J. Bergmann
  Decreased PTHrP mRNA expression in the periosteum of hind limb long bones in tail suspended rats.
  IBMS, 17th meeting, Montreal June 2007
• V. Coulic, Dr P.DELREE, C. Deprez, E. Dekoster.
  Foetal organ ectopic growth on artificial biopolymer support for replacement of circular oesophagus defects..
  Materialstoday, Asia (Beijing), September 2007
• Dr P.DELREE, C. Deprez, E. Dekoster.
  Participation of the host and graft cells in the ectopic development of the fetal intestine implanted into a syngenoic adult organism.
  Belgian Week of Gastroenterology, 19th meeting, Oostende, February 2007
• Dr P.DELREE, Coulic V., MC. Lallemand, Duprez L.
  Green Fluorescent Protein (GFP) marking for the study of host and graft participation in the foetal intestine ectopic growth.
  German Society of Cytometry, 17th annual meeting, Regensburg, October 2007
• DeBock F., Kiwit U., Dr Sc. P. Hilbert, Horneff G.
  Akromegalie und generalisierte Lipodystrophie.
  Monatsschrift Kinderheilkunde 2007

Ouvrages :

• Dr A. DESTREE, Van Maldergem L., Vokaer A.
  Epidémiologie et déterminants génétiques et psychosociaux du handicap mental dans différents groupes de patients institutionnalisés.
  Handicap mental: prévention et accueil, de boeck éditeur, Collection Questions de personne, pg 49-64, 2007

Dernière mise à jour : 22 avril 10