Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations
Voermans, N. C., van der Bilt, R. C., IJspeert, J., Hogrel, J. Y., Jeanpierre, M., Behin, A., Laforet, P., Stojkovic, T., van Engelen, B. G., Padberg, G. W., Sacconi, S., Lemmers, R. J. L. F., van der Maarel, S. M., Eymard, B., Bassez, G.
Published in Journal of neurology (01.12.2019)
Published in Journal of neurology (01.12.2019)
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G.P.144
Stojkovic, T, Richard, P, Charron, P, Rondeau, S, JeanPierre, M
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Common SNPs of AmelogeninX (AMELX) and Dental Caries Susceptibility
Gasse, B., Grabar, S., Lafont, A.G., Quinquis, L., Opsahl Vital, S., Davit-Béal, T., Moulis, E., Chabadel, O., Hennequin, M., Courson, F., Droz, D., Vaysse, F., Laboux, O., Tassery, H., Al-Hashimi, N., Boillot, A., Carel, J.C., Treluyer, J.M., Jeanpierre, M., Beldjord, C., Sire, J.Y., Chaussain, C.
Published in Journal of dental research (01.05.2013)
Published in Journal of dental research (01.05.2013)
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Infantile facioscapulohumeral muscular dystrophy (FSHD): A severe multi-systemic disease
Walther-Louvier, U, Meyer, P, Mercier, M, Manel, V, Cances, C, Espil-Taris, C, Richelme, C, Jeanpierre, M, Rivier, F
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
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Comparison of Autologous vs Homologous Costal Cartilage Grafts in Dorsal Augmentation Rhinoplasty: A Systematic Review and Meta-analysis
Vila, Peter M, Jeanpierre, Latoya M, Rizzi, Christopher J, Yaeger, Lauren H, Chi, John J
Published in JAMA otolaryngology-- head & neck surgery (01.04.2020)
Published in JAMA otolaryngology-- head & neck surgery (01.04.2020)
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Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophy
Laforêt, P, de Toma, C, Eymard, B, Becane, H M, Jeanpierre, M, Fardeau, M, Duboc, D
Published in Neurology (01.11.1998)
Published in Neurology (01.11.1998)
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An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome
Jeanpierre, M, Turleau, C, Aurias, A, Prieur, M, Ledeist, F, Fischer, A, Viegas-Pequignot, E
Published in Human molecular genetics (01.06.1993)
Published in Human molecular genetics (01.06.1993)
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A Founder Mutation in the γ-Sarcoglycan Gene of Gypsies Possibly Predating Their Migration Out of India
Piccolo, F., Jeanpierre, M., Leturcq, F., Dodé, C., Azibi, K., Toutain, A., Merlini, L., Jarre, L., Navarro, C., Krishnamoorthy, R., Tomé, F. M. S., Urtizberea, J. A., Beckmann, J. S., Campbell, K. P., Kaplan, J.-C.
Published in Human molecular genetics (01.12.1996)
Published in Human molecular genetics (01.12.1996)
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Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
Piccolo, F, Chaouch, M, Jeanpierre, M, Romero, N.B, Campbell, K.P, Voit, T, Kaplan, J-C, El Kerch, F, Collin, H, Roberds, S.L, Eymard, B, Fardeau, M, Leturcq, F, Beckmann, J.S, Sefiani, A, Tomé, F.M.S, Azibi, K, Récan, D, Reghis, A, Merlini, L, Beldjord, C, Carrié, A
Published in Nature genetics (01.06.1995)
Published in Nature genetics (01.06.1995)
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G.P.7.11 Digenism as a cause of oculopharyngodistal myopathy
Behin, A, Laforêt, P, Dubourg, O, Maisonobe, T, Richard, P, Jeanpierre, M, Eymard, B
Published in Neuromuscular disorders : NMD (2007)
Published in Neuromuscular disorders : NMD (2007)
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Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy
Eymard, B, Romero, N B, Leturcq, F, Piccolo, F, Carrié, A, Jeanpierre, M, Collin, H, Deburgrave, N, Azibi, K, Chaouch, M, Merlini, L, Thémar-Noël, C, Penisson, I, Mayer, M, Tanguy, O, Campbell, K P, Kaplan, J C, Tomé, F M, Fardeau, M
Published in Neurology (01.05.1997)
Published in Neurology (01.05.1997)
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Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)
Carrié, A, Piccolo, F, Leturcq, F, de Toma, C, Azibi, K, Beldjord, C, Vallat, J M, Merlini, L, Voit, T, Sewry, C, Urtizberea, J A, Romero, N, Tomé, F M, Fardeau, M, Sunada, Y, Campbell, K P, Kaplan, J C, Jeanpierre, M
Published in Journal of medical genetics (01.06.1997)
Published in Journal of medical genetics (01.06.1997)
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M.P.4.02 Permanent muscle weakness in McArdle disease
Nadaj-Pakleza, A, Vincitorio, C, Laforêt, P, Eymard, B, Teijeira, S, Jeanpierre, M, Navarro, C, Stojkovic, T
Published in Neuromuscular disorders : NMD (2007)
Published in Neuromuscular disorders : NMD (2007)
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Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders : rearrangements of DNA satellite II and new recurrent translocations
BUSSON-LE CONIAT, M, SALOMON-NGUYEN, F, BERNARD, O. A, BERGER, R, DASTUGUE, N, MAAREK, O, LAFAGE-POCHITALOFF, M, MOZZICONACCI, M.-J, BARANGER, L, BRIZARD, F, RADFORD, I, JEANPIERRE, M
Published in Leukemia (01.12.1999)
Published in Leukemia (01.12.1999)
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Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy
GINJAAR, H. B, VAN DER KOOI, A. J, JEANPIERRE, M, BOLHUIS, P. A, MOORMAN, A. F. M, DE VISSER, M, BAKKER, E, OMMEN, G. J. B. V, CEELIE, H, KNEPPERS, A. L. J, VAN MEEGEN, M, BARTH, P. G, BUSCH, H. F. M, WOKKE, J. H. J, ANDERSON, L. V. B, BÖNNEMANN, C. G
Published in Journal of neurology (01.07.2000)
Published in Journal of neurology (01.07.2000)
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Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin
Kokalj-Vokac, N, Almeida, A, Viegas-Péquignot, E, Jeanpierre, M, Malfoy, B, Dutrillaux, B
Published in Cytogenetics and cell genetics (1993)
Published in Cytogenetics and cell genetics (1993)
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Undermethylation of Alu sequences in ICF syndrome : molecular and in situ analysis
MINIOU, P, BOURC'HIS, D, MOLINA GOMES, D, JEANPIERRE, M, VIEGAS-PEQUIGNOT, E
Published in Cytogenetic and genome research (01.01.1997)
Published in Cytogenetic and genome research (01.01.1997)
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