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1. Mademoiselle de Clermont
by Genlis, Stéphanie Félicité, comtesse de, 1746-1830 and Duras, Claire de Durfort, duchesse de, 1777-1828
1994, Littératures, ISBN 9782862604589, 161
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2. Full Text Forelimb Treatment in a Large Cohort of Dystrophic Dogs Supports Delivery of a Recombinant AAV for Exon Skipping in Duchenne Patients
by Le Guiner, Caroline and Montus, Marie and Servais, Laurent and Cherel, Yan and Francois, Virginie and Thibaud, Jean-Laurent and Wary, Claire and Matot, Béatrice and Larcher, Thibaut and Guigand, Lydie and Dutilleul, Maeva and Domenger, Claire and Allais, Marine and Beuvin, Maud and Moraux, Amélie and Le Duff, Johanne and Devaux, Marie and Jaulin, Nicolas and Guilbaud, Mickaël and Latournerie, Virginie and Veron, Philippe and Boutin, Sylvie and Leborgne, Christian and Desgue, Diana and Deschamps, Jack-Yves and Moullec, Sophie and Fromes, Yves and Vulin, Adeline and Smith, Richard H and Laroudie, Nicolas and Barnay-Toutain, Frédéric and Rivière, Christel and Bucher, Stéphanie and Le, Thanh-Hoa and Delaunay, Nicolas and Gasmi, Mehdi and Kotin, Robert M and Bonne, Gisèle and Adjali, Oumeya and Masurier, Carole and Hogrel, Jean-Yves and Carlier, Pierre and Moullier, Philippe and Voit, Thomas
Molecular Therapy, ISSN 1525-0016, 11/2014, Volume 22, Issue 11, pp. 1923 - 1935
Duchenne muscular dystrophy (DMD) is a severe muscle-wasting disorder caused by mutations in the dystrophin gene, without curative treatment yet available. Our... 
MEDICINE, RESEARCH & EXPERIMENTAL | EFFICACY | SAFETY | RESTORATION | DEFICIENCY | SKELETAL-MUSCLE | RETRIEVER MUSCULAR-DYSTROPHY | MODELS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | GENE-TRANSFER | EXPRESSION | VECTORS | Dependovirus - genetics | Genetic Therapy | Genetic Vectors - administration & dosage | Exons | Humans | Dose-Response Relationship, Drug | Forelimb - physiopathology | Animals | Dystrophin - genetics | Muscular Dystrophy, Duchenne - physiopathology | RNA, Small Nuclear - genetics | Dogs | Infusions, Intravenous | Muscular Dystrophy, Duchenne - genetics | RNA, Small Nuclear - metabolism | Muscular Dystrophy, Duchenne - therapy | Cohort Studies | Disease Models, Animal | Original
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3. Full Text Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy
by Azibani, Feriel and Brull, Astrid and Arandel, Ludovic and Beuvin, Maud and Nelson, Isabelle and Jollet, Arnaud and Ziat, Esma and Prudhon, Bernard and Benkhelifa-Ziyyat, Sofia and Bitoun, Marc and Lorain, Stéphanie and Bonne, Gisèle and Bertrand, Anne T
Molecular Therapy - Nucleic Acids, ISSN 2162-2531, 03/2018, Volume 10, Issue C, pp. 376 - 386
We assessed the potential of mRNA repair by spliceosome-mediated RNA trans-splicing as a therapeutic approach for -related congenital muscular dystrophy. This... 
Lmna | lamin A/C | LMNA-related congenital muscular dystrophy | gene therapy | trans-splicing | MEDICINE, RESEARCH & EXPERIMENTAL | LAMINOPATHIES | CELLS | REPAIR | MESSENGER-RNA | PARTIAL LIPODYSTROPHY | A/C | MOUSE MODEL | MUSCLE | MICE | EXPRESSION | Phenotypes | Immunoglobulins | Myotubes | Transcription | Splicing | Exons | Gene expression | Experiments | Muscular dystrophy | Myoblasts | Mutation | Dystrophy | Gene therapy
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4. Full Text Emergence and Transmission of Arbovirus Evolutionary Intermediates with Epidemic Potential
by Stapleford, Kenneth A and Coffey, Lark L and Lay, Sreyrath and Bordería, Antonio V and Duong, Veasna and Isakov, Ofer and Rozen-Gagnon, Kathryn and Arias-Goeta, Camilo and Blanc, Hervé and Beaucourt, Stéphanie and Haliloğlu, Türkan and Schmitt, Christine and Bonne, Isabelle and Ben-Tal, Nir and Shomron, Noam and Failloux, Anna-Bella and Buchy, Philippe and Vignuzzi, Marco
Cell Host & Microbe, ISSN 1931-3128, 06/2014, Volume 15, Issue 6, pp. 706 - 716
The high replication and mutation rates of RNA viruses can result in the emergence of new epidemic variants. Thus, the ability to follow host-specific... 
CHIKUNGUNYA | VIROLOGY | AEDES-ALBOPICTUS | LANDSCAPE | WEST-NILE-VIRUS | DISEASE | FERRETS | MICROBIOLOGY | MECHANISMS | INFECTION | OUTBREAK | PARASITOLOGY | Epidemics | Cambodia | Chikungunya virus - genetics | Mammals - virology | Arbovirus Infections - virology | Virus Replication - genetics | Humans | Viral Load | Genetic Variation | Culicidae - virology | Aedes - virology | Female | Chikungunya virus - pathogenicity | Disease Models, Animal | Insect Vectors | Arbovirus Infections - epidemiology | Mice, Inbred C57BL | Arbovirus Infections - transmission | Chikungunya Fever - virology | Chikungunya Fever - transmission | Arboviruses - physiology | Biological Evolution | Host-Pathogen Interactions | Saliva - virology | Animals | Arboviruses - pathogenicity | Disease transmission | RNA | Analysis | Chikungunya Fever | Arbovirus Infections | Arboviruses | Mammals | Aedes | Virology | Life Sciences | Microbiology and Parasitology | Virus Replication | Chikungunya virus | Culicidae | Saliva
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5. Full Text High-Risk But Not Low-Risk HPV E2 Proteins Bind to the APC Activators Cdh1 and Cdc20 and Cause Genomic Instability
by Bellanger, Sophie and Blachon, Stéphanie and Mechali, Francisca and Bonne-Andrea, Catherine and Thierry, Françoise
Cell Cycle, ISSN 1538-4101, 11/2005, Volume 4, Issue 11, pp. 1608 - 1615
Human papillomaviruses (HPVs) from the high-risk group are associated with cervicalcancer, in contrast to HPVs from the low-risk group which are associated... 
Binding | Proteins | Landes | Calcium | Bioscience | Biology | Cell | Cycle | Cancer | Organogenesis | APC | Genomic instability | HPV | SPINDLE CHECKPOINT | ANAPHASE-PROMOTING COMPLEX | G/M | UBIQUITIN | HUMAN-PAPILLOMAVIRUS | CERVICAL INTRAEPITHELIAL NEOPLASIA | CELL BIOLOGY | MITOSIS | MITOTIC REGULATOR | DEGRADATION | genomic instability | REPLICATIVE HELICASE E1 | EXPRESSION | Anaphase-Promoting Complex-Cyclosome | Protein Binding - genetics | Cadherins - metabolism | Humans | Ubiquitin-Protein Ligase Complexes - antagonists & inhibitors | Ubiquitin-Protein Ligase Complexes - genetics | Cell Cycle Proteins - antagonists & inhibitors | DNA-Binding Proteins - metabolism | Human papillomavirus 18 - metabolism | Cell Cycle Proteins - genetics | Cdc20 Proteins | Cadherins - genetics | Genomic Instability - genetics | Oncogene Proteins, Viral - metabolism | Oncogene Proteins, Viral - physiology | DNA-Binding Proteins - physiology | Human papillomavirus 16 - pathogenicity | Risk Factors | Cell Cycle Proteins - metabolism | Human papillomavirus 16 - metabolism | Human papillomavirus 6 - metabolism | Ubiquitin-Protein Ligase Complexes - metabolism | Human papillomavirus 18 - pathogenicity | Cell Line, Tumor | Cadherins - antagonists & inhibitors | Genomic Instability | Oncogene Proteins, Viral | Human papillomavirus 6 | Ubiquitin-Protein Ligase Complexes | Human papillomavirus 18 | Virology | Life Sciences | Human papillomavirus 16 | Microbiology and Parasitology | Protein Binding | Cadherins | Genetics | Cell Cycle Proteins | Human genetics | DNA-Binding Proteins
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6. Full Text Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea
by Bauché, Stéphanie and O’Regan, Seana and Azuma, Yoshiteru and Laffargue, Fanny and McMacken, Grace and Sternberg, Damien and Brochier, Guy and Buon, Céline and Bouzidi, Nassima and Topf, Ana and Lacène, Emmanuelle and Remerand, Ganaelle and Beaufrere, Anne-Marie and Pebrel-Richard, Céline and Thevenon, Julien and El Chehadeh-Djebbar, Salima and Faivre, Laurence and Duffourd, Yannis and Ricci, Federica and Mongini, Tiziana and Fiorillo, Chiara and Astrea, Guja and Burloiu, Carmen Magdalena and Butoianu, Niculina and Sandu, Carmen and Servais, Laurent and Bonne, Gisèle and Nelson, Isabelle and Desguerre, Isabelle and Nougues, Marie-Christine and Bœuf, Benoit and Romero, Norma and Laporte, Jocelyn and Boland, Anne and Lechner, Doris and Deleuze, Jean-François and Fontaine, Bertrand and Strochlic, Laure and Lochmuller, Hanns and Eymard, Bruno and Mayer, Michèle and Nicole, Sophie
The American Journal of Human Genetics, ISSN 0002-9297, 09/2016, Volume 99, Issue 3, pp. 753 - 761
The neuromuscular junction (NMJ) is one of the best-studied cholinergic synapses. Inherited defects of peripheral neurotransmission result in congenital... 
BUTYRYLCHOLINESTERASE | RESPIRATORY RHYTHM | NEUROTRANSMISSION | GENETICS & HEREDITY | MUTATIONS | NEUROMUSCULAR-JUNCTION | RECEPTORS | EXPRESSION | KNOCKOUT MOUSE | ACETYLTRANSFERASE | DEFICIENCY | Myasthenia Gravis - complications | Presynaptic Terminals - pathology | Genes, Recessive - genetics | Neuromuscular Junction - metabolism | Apnea - metabolism | Humans | Muscle Weakness - complications | Child, Preschool | Infant | Male | Muscle Weakness - genetics | Mutation, Missense - genetics | Synaptic Transmission | Myasthenia Gravis - metabolism | Butyrylcholinesterase - metabolism | DNA Mutational Analysis | HEK293 Cells | Muscle Weakness - pathology | Female | Neuromuscular Junction - enzymology | Child | Infant, Newborn | Neuromuscular Junction - pathology | Myasthenia Gravis - pathology | Apnea - complications | Muscle Hypotonia - genetics | Cholinergic Neurons - metabolism | Arthrogryposis - complications | Symporters - deficiency | Arthrogryposis - genetics | Mutation - genetics | Symporters - metabolism | Homozygote | Exome - genetics | Apnea - pathology | Symporters - genetics | Adolescent | Presynaptic Terminals - metabolism | Apnea - genetics | Heterozygote | Myasthenia Gravis - genetics | Cholinergic Neurons - pathology | Life Sciences | Human health and pathology | Report
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7. Full Text Influence of medically assisted reproduction techniques on crown-rump length and biochemical markers of trisomy 21 in the first trimester of pregnancy
by Bonne, Stéphanie, M.D and Sauleau, Eric, M.D., Ph.D and Sananes, Nicolas, M.D and Akaladios, Cherif, M.D and Rongières, Catherine, M.D and Pirrello, Olivier, M.D
Fertility and Sterility, ISSN 0015-0282, 2016, Volume 105, Issue 2, pp. 410 - 416
Objective To determine whether there is a difference between the known gestational age in pregnancies conceived after IVF and the estimated gestational age... 
Internal Medicine | Obstetrics and Gynecology | PAPP-A | Robinson's curve | ART | hCG | early fetal growth | DOWNS-SYNDROME | HUMAN CHORIONIC-GONADOTROPIN | OBSTETRICS & GYNECOLOGY | 1ST-TRIMESTER SCREENING MARKERS | OOCYTE RETRIEVAL | TECHNOLOGIES ART | REPRODUCTIVE BIOLOGY | GESTATIONAL-AGE | SERUM PAPP-A | IN-VITRO FERTILIZATION | NUCHAL TRANSLUCENCY | PLASMA PROTEIN-A | Pregnancy-Associated Plasma Protein-A - analysis | Humans | Treatment Outcome | Biomarkers - blood | Gestational Age | Pregnancy Trimester, First | Pregnancy | Fertilization in Vitro | Infertility - diagnosis | Crown-Rump Length | Fertility | Ultrasonography, Prenatal | Chorionic Gonadotropin - blood | Down Syndrome - blood | Down Syndrome - genetics | Adult | Female | Infertility - physiopathology | Retrospective Studies | Down Syndrome - diagnosis | Infertility - therapy | Pregnant women | Methods | Medical informatics
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8. Full Text Myoblasts and Embryonic Stem Cells Differentially Engraft in a Mouse Model of Genetic Dilated Cardiomyopathy
by Catelain, Cyril and Riveron, Stéphanie and Papadopoulos, Aurélie and Mougenot, Nathalie and Jacquet, Adeline and Vauchez, Karine and Yada, Erica and Pucéat, Michel and Fiszman, Marc and Butler-Browne, Gillian and Bonne, Gisèle and Vilquin, Jean-Thomas
Molecular Therapy, ISSN 1525-0016, 05/2013, Volume 21, Issue 5, pp. 1064 - 1075
The functional and architectural benefits of embryonic stem cells (ESC) and myoblasts (Mb) transplantations into infarcted myocardium have been investigated... 
CARDIAC-FUNCTION | MEDICINE, RESEARCH & EXPERIMENTAL | MYOCARDIAL-INFARCTION | INDUCED HEART-FAILURE | SKELETAL MYOBLASTS | MUSCLE-CELLS | TRANSPLANTATION | ISCHEMIC CARDIOMYOPATHY | THERAPY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | IMPROVEMENT | STRIATED-MUSCLE | Cardiomyopathy, Dilated - genetics | Myocardial Contraction | Cell Line | Embryonic Stem Cells - metabolism | Embryonic Stem Cells - cytology | Graft Survival | Male | Myocardium - pathology | Cell- and Tissue-Based Therapy | Myoblasts - transplantation | Muscle Development | Myoblasts - metabolism | Phenotype | Animals | Cardiomyopathy, Dilated - physiopathology | Embryonic Stem Cells - transplantation | Myocardium - metabolism | Myoblasts - cytology | Female | Cell Differentiation | Mice | Cardiomyopathy, Dilated - mortality | Cardiomyopathy, Dilated - therapy | Disease Models, Animal | Index Medicus | Original
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9. Full Text European Society of Gene and Cell TherapyFrench Society of Cell and Gene TherapyCollaborative Congress 2012October 25–29, 2012Palais des Congrès de VersaillesVersailles, France
by Schmidt, Manfred and Verhoeyen, Els and Gobbo, Emilie and Divers, Dominique and Oudrhiri, Noufissa and Griscelli, Frank and Bennaceur-Griscelli, Annelise and Klatzmann, David and Anguela, Xavier M and Sharma, Rajiv and Sharma, Rajiv and Li, Hojun and Li, Hojun and Haurigot, Virginia and Haurigot, Virginia and Haurigot, Virginia and Bhagwat, Anand and Bhagwat, Anand and Davidson, Robert and Davidson, Robert and Zhou, Shangzhen and Zhou, Shangzhen and Zhou, Shangzhen and Doyon, Yannick and Gregory, Philip D and Gregory, Philip D and Gregory, Philip D and Holmes, Michael C and Holmes, Michael C and Holmes, Michael C and High, Katherine A and Carbonaro, Denise and Shaw, Kit and Jin, Xiangyang and Geiger, Sabine and Mishra, Suparna and Cooper, Aaron and DeOliveira, Satiro and Sokolic, Rob and Candotti, Fabio and Carmo, Marlene and Arumugam, Paritha and Alonso-Ferrero, Maria and Schambach, Axel and Schambach, Axel and Baum, Christopher and Baum, Christopher and Baum, Christopher and Risma, Kimberly and Malik, Punam and Jordan, Michael and Rivat, Christine and Booth, Claire and Thrasher, Adrian and Whilding, Lynsey and Archibald, Kyra and Oberg, Daniel and Golan, Talia and Hubert, Ayala and Shemi, Amotz and Khvalevsky, Elina Zorde and Gabai-Malka, Racheli and Focht, Gili and Brunschwig, Zivia and Raskin, Stephen and Goldberg, Nahum and Ben-David, Eli and Peretz, Tamar and Eliakim, Rami and Dankur, Alan and Galun and Rachmur, Itzik and Domb, Avi and Kopelman, Yael and Hantz, Yael and Lahav, Mor and Arbel-Alon, Sagit and Dickson, George and Barkats, Martine and Daboussi, Fayza and Silva, Georges and Cedrone, Frederic and Epinat, Jean Charles and Juillerat, Alexandre and Valton, Julien and Montini, Eugenio and Biffi, Alessandra and Biffi, Alessandra and Calabria, Andrea and Calabria, Andrea and Biasco, Luca and Biasco, Luca and Cesani, Martina and Cesani, Martina and Benedicenti, Fabrizio and Benedicenti, Fabrizio and Plati, Tiziana and Leo, Simone and Zanetti, Gianluigi and Aiuti, Alessandro and ...
Human Gene Therapy, ISSN 1043-0342, 10/2012, Volume 23, Issue 10, pp. A1 - A173
Abstracts
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10. Full Text Uropathogenic Escherichia coli AL511 requires flagellum to enter renal collecting duct cells
by Pichon, Christophe and Hechard, Celine and du Merle, Laurence and Chaudray, Christelle and Bonne, Isabelle and Guadagnini, Stephanie and Vandewalle, Alain and Le Bouguenec, Chantal
Cellular Microbiology, ISSN 1462-5814, 04/2009, Volume 11, Issue 4, pp. 616 - 628
Summary Escherichia coli is the leading cause of urinary tract infections, but the mechanisms governing renal colonization by this bacterium remain poorly... 
URINARY-TRACT-INFECTION | STRAINS | P-FIMBRIAE | LOCALIZATION | PYELONEPHRITIS | MICROBIOLOGY | COLONIZATION | AFA | EXPRESSION | EPIDEMIOLOGY | ADHESINS | CELL BIOLOGY | Flagella - physiology | Humans | Bacterial Proteins - genetics | Cystitis - microbiology | Escherichia coli Infections - microbiology | Escherichia coli Proteins - metabolism | Kidney Tubules, Collecting - cytology | Pyelonephritis - microbiology | Host-Pathogen Interactions | Kidney Tubules, Collecting - microbiology | Animals | Flagella - metabolism | Escherichia coli - genetics | Escherichia coli - isolation & purification | Epithelial Cells - microbiology | Escherichia coli - pathogenicity | Flagellin - metabolism | Escherichia coli Proteins - genetics | Bacterial Proteins - metabolism | Mice | Escherichia coli - physiology | Urine - microbiology | Proteins | Cell research | Analysis | Myosin | Water quality | Urinary tract infections | Kidney diseases
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11. Romans de femmes du XVIIIe siècle
by Trousson, Raymond
1996, Bouquins., ISBN 9782221080979, lxxv, 1085
French fiction | Women authors
Book
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12. Full Text Comment optimiser le dossier transfusionnel papier pour une efficience sécuritaire et vigilante par la pertinence d’un audit clinique au CHG d’Auch en Gascogne
by Vaillant, Willy and Mellier, Joëlle and Roques, Philippe and Dore, Nadine and Cibin, Stéphane and Arnon, Stéphanie and Bonne, Emilie and Soumoulou, Martine Came and Courtes, Nais and Gomez, Lisa and Jaffres, Marie Louise and Paumier, Régine and Ferraro, Pierre
Transfusion clinique et biologique, ISSN 1246-7820, 11/2018, Volume 25, Issue 4, pp. 343 - 344
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13. Full Text Assembly and role of pili in group B streptococci
by Dramsi, Shaynoor and Caliot, Elise and Bonne, Isabelle and Guadagnini, Stéphanie and Prévost, Marie‐Christine and Kojadinovic, Mila and Lalioui, Lila and Poyart, Claire and Trieu‐Cuot, Patrick
Molecular Microbiology, ISSN 0950-382X, 06/2006, Volume 60, Issue 6, pp. 1401 - 1413
Summary Streptococcus agalactiae[group B streptococcus (GBS)] is the leading cause of neonatal pneumonia, sepsis and meningitis. An in silico genome analysis... 
GRAM-POSITIVE BACTERIA | CELL-WALL | EPITHELIAL-CELLS | RLRA PATHOGENICITY ISLET | ACTINOMYCES-NAESLUNDII | BIOCHEMISTRY & MOLECULAR BIOLOGY | SURFACE-PROTEINS | GENE-EXPRESSION | MICROBIOLOGY | STAPHYLOCOCCUS-AUREUS | GENOME ANALYSIS | C5A PEPTIDASE | Streptococcus agalactiae - pathogenicity | Fimbriae Proteins - metabolism | Humans | Aminoacyltransferases - genetics | Bacterial Proteins - genetics | Streptococcus agalactiae - ultrastructure | Fimbriae, Bacterial - genetics | Streptococcus agalactiae - metabolism | Bacterial Adhesion | Cysteine Endopeptidases - metabolism | Cysteine Endopeptidases - genetics | Epithelial Cells - microbiology | Aminoacyltransferases - metabolism | Bacterial Proteins - metabolism | Fimbriae Proteins - analysis | Fimbriae, Bacterial - metabolism
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14. Evaluation and Management of Necrotizing Soft Tissue Infections
by Bonne, Stephanie L and Kadri, Sameer S
Infectious Disease Clinics of North America, ISSN 0891-5520, 09/2017, Volume 31, Issue 3, pp. 497 - 511
Despite advances in antibiotic and surgical management and supportive care for necrotizing soft tissue infections, morbidity and mortality remain substantial.... 
Gangrene | Sepsis | Soft tissue infection | Necrotizing fasciitis | HYPERBARIC-OXYGEN | INFECTIOUS DISEASES | PRACTICE GUIDELINES | INTRAVENOUS IMMUNOGLOBULIN THERAPY | CLINICAL CHARACTERISTICS | IMMUNOLOGY | RESISTANT STAPHYLOCOCCUS-AUREUS | COMPUTED-TOMOGRAPHY | FOURNIERS GANGRENE | SUBINHIBITORY CONCENTRATIONS | TOXIC-SHOCK-SYNDROME | LABORATORY RISK INDICATOR | Soft Tissue Infections - diagnosis | Humans | Fasciitis, Necrotizing - therapy | Soft Tissue Infections - therapy | Immunoglobulins - administration & dosage | Fasciitis, Necrotizing - drug therapy | Soft Tissue Infections - complications | Gangrene - drug therapy | Anti-Bacterial Agents - therapeutic use | Debridement | Sepsis - drug therapy | Administration, Intravenous | Sepsis - therapy | Fasciitis, Necrotizing - complications | Gangrene - microbiology | Disease Management | Soft Tissue Infections - drug therapy | Fasciitis, Necrotizing - diagnosis | Immunoglobulins - therapeutic use | Hyperbaric Oxygenation | Sepsis - microbiology
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15. Full Text Cardiometabolic assessment of lamin A/C gene mutation carriers: a phenotype–genotype correlation
by Kwapich, M and Lacroix, D and Espiard, S and Ninni, S and Brigadeau, F and Kouakam, C and Degroote, P and Laurent, J.M and Tiffreau, V and Jannin, A and Humbert, L and Ben Hamou, A and Tard, C and Ben Yaou, R and Lamblin, N and Klug, D and Richard, P and Vigouroux, C and Bonne, G and Vantyghem, M.C and Diamenord-AEDNL Working Grp and Diamenord–AEDNL Working Group
Diabetes & Metabolism, ISSN 1262-3636, 09/2019, Volume 45, Issue 4, pp. 382 - 389
Mutations of the gene encoding lamin A/C induce heterogeneous phenotypes ranging from cardiopathies and myopathies to lipodystrophies. The aim of this study... 
Lipodystrophy | Rhythm disorders | Laminopathy | Coronary artery disease | LMNAgene | MANAGEMENT | FAMILIAL PARTIAL LIPODYSTROPHY | GIRDLE MUSCULAR-DYSTROPHY | RISK | DILATED CARDIOMYOPATHY | SOCIETY | ENDOCRINOLOGY & METABOLISM | DUNNIGAN VARIETY | Life Sciences
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16. Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea
by Stéphanie Bauché and Seana O'Regan and Yoshiteru Azuma and Fanny Laffargue and Grace McMacken and Damien Sternberg and Guy Brochier and Céline Buon and Nassima Bouzidi and Ana Topf and Emmanuelle Lacène and Ganaelle Remerand and Anne-Marie Beaufrere and Céline Pebrel-Richard and Julien Thevenon and Salima ElChehadeh-Djebbar and Laurence Faivre and Yannis Duffourd and Federica Ricci and Tiziana Mongini and Chiara Fiorillo and Guja Astrea and Carmen Magdalena Burloiu and Niculina Butoianu and Carmen Sandu and Laurent Servais and Gisèle Bonne and Isabelle Nelson and Isabelle Desguerre and Marie-Christine Nougues and Benoit Boeuf and Norma Romero and Jocelyn Laporte and Anne Boland and Doris Lechner and Jean-François Deleuze and Bertrand Fontaine and Laure Strochlic and Hanns Lochmuller and Bruno Eymard and Michèle Mayer and Sophie Nicole
American Journal of Human Genetics, ISSN 0002-9297, 09/2016, Volume 99, Issue 3, p. 753
  The neuromuscular junction (NMJ) is one of the best-studied cholinergic synapses. Inherited defects of peripheral neurotransmission result in congenital... 
Neurotransmitters | Cognition & reasoning | Mutation | Metabolism | Cells
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17. Full Text Maladies aiguës non obstétricales chez la femme enceinte et place de l'obstétricie
by Ducarme, Guillaume and Bonne, Stéphanie and Khater, Carine and Ceccaldi, Pierre-François and Poujade, Olivier and Luton, Dominique
Presse Medicale, ISSN 0755-4982, 02/2012, Volume 41, Issue 2, pp. 125 - 133
The management of a pregnant woman with an acute non-obstetrical disease must be made in narrow collaboration with an obstetrician. This one must be warned... 
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18. Full Text Assembly of pili in group B Streptococci
by Dramsi, Shaynoor and Caliot, Elise and Bonne, Isabelle and Guadagnini, Stéphanie and Prévost, Marie-Christine and Kojadinovic, Mila and Lalioui, Lila and Poyart, Claire and Trieu-Cuot, Patrick
Molecular Microbiology, ISSN 0950-382X, 06/2006, Volume 60, Issue 6, pp. 1401 - 1413
Streptococcus agalactiae[group B streptococcus (GBS)] is the leading cause of neonatal pneumonia, sepsis and meningitis. An in silico genome analysis indicated... 
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