The impact of embryo vitrification on placental histopathology features and perinatal outcome in singleton live births
Volodarsky-Perel, A, Ton Nu, T N, Orvieto, R, Mashiach, R, Machado-Gedeon, A, Cui, Y, Shaul, J, Dahan, M H
Published in Human reproduction (Oxford) (30.09.2022)
Published in Human reproduction (Oxford) (30.09.2022)
Get full text
Journal Article
Beckmann rearrangement reaction: About the role of defect groups in high silica zeolite catalysts
Bonelli, B., Forni, L., Aloise, A., Nagy, J.B., Fornasari, G., Garrone, E., Gedeon, A., Giordano, G., Trifirò, F.
Published in Microporous and mesoporous materials (19.04.2007)
Published in Microporous and mesoporous materials (19.04.2007)
Get full text
Journal Article
Conference Proceeding
Mutations in GDI1 are responsible for X-linked non-specific mental retardation
Toniolo, Daniela, D'Adamo, Patrizia, Menegon, Andrea, Lo Nigro, Cristiana, Grasso, Marina, Gulisano, Massimo, Tamanini, Filippo, Bienvenu, Thierry, Gedeon, Agi K, Oostra, Ben, Wu, Shih-Kwang, Tandon, Anurag, Valtorta, Flavia, Balch, William E, Chelly, Jamel
Published in Nature genetics (01.06.1998)
Published in Nature genetics (01.06.1998)
Get full text
Journal Article
Identification of the gene ( SEDL ) causing X-linked spondyloepiphyseal dysplasia tarda
Gécz, Jozef, Colley, Alison, Tiller, George E, Rogers, John, Gedeon, Ági K, Jamieson, Robyn, Sillence, David, Thompson, Elizabeth M, Mulley, John C
Published in Nature genetics (01.08.1999)
Published in Nature genetics (01.08.1999)
Get full text
Journal Article
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene
Davis, M.R, Haan, E, Jungbluth, H, Sewry, C, North, K, Muntoni, F, Kuntzer, T, Lamont, P, Bankier, A, Tomlinson, P, Sánchez, A, Walsh, P, Nagarajan, L, Oley, C, Colley, A, Gedeon, A, Quinlivan, R, Dixon, J, James, D, Müller, C.R, Laing, N.G
Published in Neuromuscular disorders : NMD (01.02.2003)
Published in Neuromuscular disorders : NMD (01.02.2003)
Get full text
Journal Article
Identification of the gene FMR2 , associated with FRAXE mental retardation
Gecz, Jozef, Gedeon, Agi K, Sutherland, Grant R, Mulley, John C
Published in Nature genetics (01.05.1996)
Published in Nature genetics (01.05.1996)
Get full text
Journal Article
The Molecular Basis of X-Linked Spondyloepiphyseal Dysplasia Tarda
Gedeon, A.K., Tiller, G.E., Le Merrer, M., Heuertz, S., Tranebjaerg, L., Chitayat, D., Robertson, S., Glass, I.A., Savarirayan, R., Cole, W.G., Rimoin, D.L., Kousseff, B.G., Ohashi, H., Zabel, B., Munnich, A., Gecz, J., Mulley, J.C.
Published in American journal of human genetics (01.06.2001)
Published in American journal of human genetics (01.06.2001)
Get full text
Journal Article
A novel X-linked gene, G4.5. is responsible for Barth syndrome
Bione, S, D'Adamo, P, Maestrini, E, Gedeon, A K, Bolhuis, P A, Toniolo, D
Published in Nature genetics (01.04.1996)
Published in Nature genetics (01.04.1996)
Get full text
Journal Article
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy
Lower, Karen M, Lütcherath, Viggo, Gécz, Jozef, Frints, Suzanna G.M, Partington, Michael, Strømme, Petter, Scheffer, Ingrid E, Gedeon, Ági K, Lewis, Suzanne M.E, Turner, Gillian, Fryns, Jean-Pierre, Sutherland, Grant R, Wallace, Robyn H, Mangelsdorf, Marie E, Shaw, Marie A, Mulley, John C, Bruyere, Helene
Published in Nature genetics (01.04.2002)
Published in Nature genetics (01.04.2002)
Get full text
Journal Article
Surface acidity diagnosis and catalytic activity of AlSBA materials obtained by direct synthesis
Gédéon, A., Lassoued, A., Bonardet, J.L., Fraissard, J.
Published in Microporous and mesoporous materials (01.04.2001)
Published in Microporous and mesoporous materials (01.04.2001)
Get full text
Journal Article
Conference Proceeding
Probing the pore space in mesoporous materials by laser enhanced hyperpolarised 129Xe NMR
Guenneau, F., Nader, M., Salamé, P., Launay, F., Semmer-Herledan, V., Gédéon, A.
Published in Catalysis today (01.03.2006)
Published in Catalysis today (01.03.2006)
Get full text
Journal Article
A novel X-linked gene, G4.5 . is responsible for Barth syndrome
Bione, Silvia, D'Adamo, Patrizia, Maestrini, Elena, Gedeon, Agi K, Bolhuis, Pieter A, Toniolo, Daniela
Published in Nature genetics (01.04.1996)
Published in Nature genetics (01.04.1996)
Get full text
Journal Article
Fragile X syndrome without CCG amplification has an FMR1 deletion
Gedeon, A.K, Baker, E, Robinson, H, Partington, M.W, Gross, B, Manca, A, Korn, B, Poustka, A, Yu, S, Sutherland 1, G.R, Mulley, J.C
Published in Nature genetics (01.08.1992)
Published in Nature genetics (01.08.1992)
Get full text
Journal Article
Comparative textural study of highly ordered silicate and aluminosilicate mesoporous mesophase materials having different pore sizes
Fenelonov, V.B., Derevyankin, A.Yu, Kirik, S.D., Solovyov, L.A., Shmakov, A.N., Bonardet, J.-L., Gedeon, A., Romannikov, V.N.
Published in Microporous and mesoporous materials (01.06.2001)
Published in Microporous and mesoporous materials (01.06.2001)
Get full text
Journal Article
Conference Proceeding
In situ magnetic resonance imaging study of the impregnation of γ-alumina pellets
Nowacka, A., Moughames, J., Adem, Z., Quoineaud, A.-A., Rolland, M., Guenneau, F., Gédéon, A.
Published in Applied catalysis. A, General (25.08.2015)
Published in Applied catalysis. A, General (25.08.2015)
Get full text
Journal Article
Fragile-X syndrome : unique genetics of the heritable unstable element
YU, S, MULLEY, J, SUTHERLAND, G. R, RICHARDS, R. I, LOESCH, D, TURNER, G, DONNELLY, A, GEDEON, A, HILLEN, D, KREMER, E, LYNCH, M, PRITCHARD, M
Published in American journal of human genetics (01.05.1992)
Get full text
Published in American journal of human genetics (01.05.1992)
Journal Article
Genotype-phenotype relationships in fragile X syndrome : a family study
LOESCH, D. Z, HUGGINS, R, HAY, D. A, GEDEON, A. K, MULLEY, J. C, SUTHERLAND, G. R
Published in American journal of human genetics (01.11.1993)
Get full text
Published in American journal of human genetics (01.11.1993)
Journal Article