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Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation Everman, D. B.; Morgan, C. T.; Lyle, Robert; Laughridge, M. E.; ... Schwartz, C. E. 2006
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A child with a systemic febrile illness - differential diagnosis and management Hofer, Michael; Mahlaoui, Nizar; Prieur, Anne-Marie 2006
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Borréliose de Lyme - 3ème partie : Prévention, grossesse, états d'immunodéficience, syndrome post-borréliose de Lyme Evison, J; Aebi, Christoph; Francioli, P; Péter, O; ... Weber, R 2006
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Differential role of three major New Zealand Black-derived loci linked with Yaa-induced murine lupus nephritis Kikuchi, Shuichi; Fossati-Jimack, Liliane; Moll, Thomas; Amano, Hirofumi; ... Izui, Shozo 2005
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Eosinophilic cellulitis (Wells' syndrome) associated with colon carcinoma Hirsch, Katrin; Ludwig, Ralf J.; Wolter, Manfred; Zollner, Thomas Matthias; ... Boehncke, Wolf-Henning 2005
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Utilité du dosage plasmatique de la procalcitonine chez l'adulte et chez l'enfant Gervaix, Alain; Pugin, Jérôme 2005
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Surfactant lavage for extracorporeal membrane oxygenation-requiring meconium aspiration syndrome--a cheap alternative Lejeune, Thierry; Pfister, Riccardo 2005
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Diagnosis of allergy syndromes: do symptoms always mean allergy? Eigenmann, Philippe 2005
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The space of senses: impaired crossmodal interactions in a patient with Balint syndrome after bilateral parietal damage Valenza, Nathalie; Murray, M. M.; Ptak, Radek; Vuilleumier, Patrik 2004
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The incubation period of acute retroviral syndrome as a multistep process: a parametric survival analysis Vanhems, Philippe; Voirin, Nicolas; Philippe, Pierre; Hirschel, Bernard; ... Allard, Robert 2004
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Knobloch syndrome: novel mutations in COL18A1, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatin Menzel, Olivier; Bekkeheien, R. C.; Reymond, Alexandre; Fukai, Naomi; ... Guipponi, Michel 2004
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Presence of autoantibodies to apolipoprotein A-1 in patients with acute coronary syndrome further links autoimmunity to cardiovascular disease Vuilleumier, Nicolas; Reber, Guido; James, Richard William; Burger, Danielle; ... Mach, François 2004
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Lymphoid enhancer factor-1 links two hereditary leukemia syndromes through core-binding factor alpha regulation of ELA2 Li, Feng-Qian; Person, Richard E; Takemaru, Ken-Ichi; Williams, Kayleen; ... Horwitz, Marshall 2004
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Brief report: incubation and duration of specific symptoms at acute retroviral syndrome as independent predictors of progression to AIDS Vanhems, Philippe; Voirin, Nicolas; Hirschel, Bernard; Cooper, David; ... Perrin, Luc 2003
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Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome Deutsch, Samuel; Rideau, Alexandra; Bochaton-Piallat, Marie-Luce; Merla, Giuseppe; ... Beris, Photis 2003
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Gene symbol: GLI3. Disease: Greig cephalopolysyndactyly syndrome Driess, S.; Freese, K.; Bornholdt, D.; Kobelt, A.; ... Kalff-Suske, M. 2003
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FOXL2-mutations in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES); challenges for genetic counseling in female patients Fokstuen, Siv; Antonarakis, Stylianos; Blouin, Jean-Louis 2003
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Kjellin's syndrome: fundus autofluorescence, angiographic, and electrophysiologic findings Frisch, Inez B; Haag, Peter; Steffen, Heimo; Weber, Bernhard H F; Holz, Frank G 2002
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The CD4 cell count 3 months after acute retroviral syndrome is associated with the presence of AIDS in the source individual Vanhems, Philippe; Caillat-Vallet, Emmanuelle; Hirschel, Bernard; Routy, J. P.; ... Perrin, Luc 2002
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Clinical features of acute retroviral syndrome differ by route of infection but not by gender and age Vanhems, Philippe; Routy, J. P.; Hirschel, Bernard; Baratin, Dominique; ... Perrin, Luc 2002
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