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1. Full Text Sunitinib in pancreatic neuroendocrine tumors: Updated progression-free survival and final overall survival from a phase III randomized study
by Faivre, Sandrine and Niccoli, P and Castellano, D and Valle, J.W and Hammel, P and Raoul, J.-L and Vinik, A and Van Cutsem, E and Bang, Y.-J and Lee, S.-H and Borbath, I and Lombard-Bohas, C and Metrakos, P and Smith, D and Chen, J.-S and Ruszniewski, P and Seitz, J.-F and Patyna, S and Lu, D.R and Ishak, K.J and Raymond, E
Annals of oncology, ISSN 0923-7534, 2017, Volume 28, Issue 2, pp. 339 - 343
Blinded independent central review | VEGFR inhibitor | Crossover | Rank-preserving structural failure time (RPSFT) | Antiangiogenics | Life Sciences & Biomedicine | Oncology | Science & Technology | Cross-Sectional Studies | Double-Blind Method | Humans | Kaplan-Meier Estimate | Proportional Hazards Models | Survival Rate | Antineoplastic Agents - administration & dosage | Indoles - administration & dosage | Pancreatic Neoplasms - drug therapy | Disease-Free Survival | Sunitinib | Pyrroles - administration & dosage | Neuroendocrine Tumors - diagnostic imaging | Neuroendocrine Tumors - drug therapy | Pancreatic Neoplasms - diagnostic imaging | Index Medicus
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2. Full Text Neuro-glial interactions at the nodes of Ranvier: Implication in health and diseases
by Faivre-Sarrailh, Catherine and Devaux, Jérôme J
Frontiers in cellular neuroscience, ISSN 1662-5102, 10/2013, Volume 7, pp. 196 - 196
Node of Ranvier | Extracellular matrix | Axon-glial interactions | Neurological disease | Ion channel | Guillain-Barre syndrome | Demyelinating diseases | Excitability | Nervous system | Neuronal-glial interactions | Cell adhesion molecules | Cell adhesion & migration | Neurological diseases | Proteins | Axons | Demyelination | Sodium channels (voltage-gated) | Potassium channels (voltage-gated) | Ion channels | Localization | Nodes of Ranvier | Life Sciences | Biomolecules | Biochemistry, Molecular Biology | Neurological Disease | Extracellular Matrix | axon-glia interaction | ion channel | node of Ranvier
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3. Full Text Management of hypersensitivity reactions to iodinated contrast media
by K. Brockow and C. Christiansen and G. Kanny and O. Clement and A. Barbaud and A. Bircher and P. DeWachter and J.-L. Gueant and R.-M. Rodriguez Gueant and C. Mouton-Faivre and J. Ring and A. Romano and J. Sainte-Laudy and P. Demoly and W. J. Pichler and ENDA and EAACI Interest Grp Drug Hypersensi and EAACI interest group on drug hypersensitivity and the EAACI interest group on drug hypersensitivity
Allergy (Copenhagen), ISSN 0105-4538, 02/2005, Volume 60, Issue 2, pp. 150 - 158
skin tests | immediate reaction | nonimmediate reaction | diagnosis | premedication | contrast media | Nonimmediate reaction | Diagnosis | Immediate reaction | Contrast media | Skin tests | Premedication | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Drug Hypersensitivity - etiology | Drug Hypersensitivity - prevention & control | Contrast Media - adverse effects | Prevalence | Drug Hypersensitivity - epidemiology | Humans | Risk Factors | Drug Hypersensitivity - diagnosis | Iodine Compounds - adverse effects | Drug Hypersensitivity - physiopathology | Index Medicus
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4. Full Text Addendum: Faivre, R.; Colin, J.; Menenti, M. Evaluation of Methods for Aerodynamic Roughness Length Retrieval from Very High-Resolution Imaging LIDAR Observations over the Heihe Basin in China. Remote Sens. 2017, 9, 63
by Faivre, Robin and Colin, Jérôme and Menenti, Massimo
Remote sensing (Basel, Switzerland), ISSN 2072-4292, 02/2017, Volume 9, Issue 2, pp. 157 - 157
n/a
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5. Full Text Acromial J-bone graft on the acromion for surgical treatment of glenohumeral instability: an anatomical study
by Sanchez, Matthieu and Klouche, Shahnaz and Faivre, Bruno and Bauer, Thomas and Hardy, Philippe
Shoulder & elbow, ISSN 1758-5732, 10/2017, Volume 9, Issue 4, pp. 272 - 278
J bone graft | glenoid bone loss | shoulder instability | iliac graft | Latarjet | Shoulder
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6. Full Text J/ψ Suppression at Forward Rapidity in Pb-Pb Collisions at √sNN=2.76  TeV
by Abelev, B.I and Adam, J and Bjelogrlic, S and Chojnacki, M and Christakoglou, P and de Rooij, R. S and Grelli, A and Luparello, G and Mischke, A and Nooren, G.J.L and Peitzmann, T and Reicher, M and Snellings, R.J.M and Thomas, D and van Leeuwen, M and Veldhoen, M and Verweij, M and Zhou, Y and Zynovyev, M
Physical review letters, ISSN 0031-9007, 2012, Volume 109, Issue 7, p. 072301/1
Physics | High Energy Physics - Experiment
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7. Full Text Mosaic‐activating FGFR2 mutation in two fetuses with papillomatous pedunculated sebaceous naevus
by Kuentz, P and Fraitag, S and Gonzales, M and Dhombres, F and St‐Onge, J and Duffourd, Y and Joyé, N and Jouannic, J.‐M and Picard, A and Marle, N and Thevenon, J and Thauvin‐Robinet, C and Faivre, L and Rivière, J.‐B and Vabres, P
British journal of dermatology (1951), ISSN 0007-0963, 01/2017, Volume 176, Issue 1, pp. 204 - 208
Life Sciences & Biomedicine | Dermatology | Science & Technology | Receptor, Fibroblast Growth Factor, Type 3 - genetics | Humans | Mutation, Missense - genetics | Abortion, Induced | Pregnancy | Fetal Death | Skin Neoplasms - genetics | Nevus, Sebaceous of Jadassohn - genetics | Adult | Female | Mosaicism | Infant, Newborn | Receptor, Fibroblast Growth Factor, Type 2 - genetics | Tyrosine | Skin diseases | Genetic aspects | Skin | Neonates | Fetuses | Acne | K-Ras protein | Missense mutation | Scalp | Protein-tyrosine kinase receptors | Mutation | Protein-tyrosine kinase | Fibroblast growth factor receptor 2 | Fibroblast growth factor receptors | Tumors | Cancer | Life Sciences | Human health and pathology
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8. Recherches sur les superstitions en Chine
: [Zhongguo min jian xin yang] : table analytique et index de l'œuvre du Père Henri Doré S. J.
by Faivre, Gilles
1997, ISBN 2842790189, 441
Doré, Henri. Recherches sur les superstitions en Chine | China Religious life and customs | China Religion | China Social life and customs
Book
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9. Full Text Exclusive $\mathrm{J/}\psi$ photoproduction off protons in ultra-peripheral p-Pb collisions at $\sqrt{s_{\rm NN}}=5.02$ TeV
by Abelev, B and Aphecetche, Laurent and Batigne, Guillaume and Belikov, I and Cheshkov, C and Cheynis, B and Delagrange, H and Ducroux, L and Erazmus, B and Estienne, Magali and Grossiord, J.-Y and Guilbaud, M and Lardeux, A and Maire, A and Martinez Garcia, Gines and Martin Blanco, J and Mas, A and Massacrier, L and Molnar, L and Morreale, A and Pillot, Philippe and Ronflette, L and Roy, C and Schutz, Y and Shabetai, Alexandre and Stocco, Diego and Tieulent, R and Uras, A and Vernet, R and Wang, M and Zoccarato, Y and Baek, Y.W and Barret, V and Bastid, N and Batista Camejo, A and Crochet, P and Dupieux, P and Germain, Marie and Li, S and Lopez, X and Manso, F and Marchisone, M and Porteboeuf-Houssais, S and Rosnet, P and Valencia Palomo, L and Vulpescu, B and Conesa Balbastre, G and Faivre, J and Furget, C and Guernane, R and Kox, S and Real, J.S and Silvestre, C and Valle, Z. Conesa del and Das, I and Espagnon, B and Hadjidakis, C and Lakomov, I and Suire, C and Takaki, J. D. Tapia and Palomo, L. Valencia and Baldisseri, Alberto and Borel, Herve and Castillo Castellanos, Javier and Charvet, Jean-luc and Pereira Da Costa, Hugo and Rakotozafindrabe, A
Physical review letters, ISSN 0031-9007, 2014, Volume 113, p. 232504
Nuclear Experiment | Physics | High Energy Physics - Experiment
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10. Full Text Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis
by Bruel, A.‐L and Masurel‐Paulet, A and Rivière, J.‐B and Duffourd, Y and Lehalle, D and Bensignor, C and Huet, F and Borgnon, J and Roucher, F and Kuentz, P and Deleuze, J.‐F and Thauvin‐Robinet, C and Faivre, L and Thevenon, J
Clinical genetics, ISSN 0009-9163, 02/2017, Volume 91, Issue 2, pp. 333 - 338
scrotal agenesis | whole‐exome sequencing | MAB21L1 | intellectual disability | whole-exome sequencing | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Abnormalities, Multiple - pathology | Humans | Intellectual Disability - pathology | Male | Developmental Disabilities - genetics | Homeodomain Proteins - genetics | Intellectual Disability - genetics | Homozygote | Developmental Disabilities - pathology | Exome - genetics | Phenotype | Animals | Mice | Scrotum - pathology | Mutation | Child | Abnormalities, Multiple - genetics | Frameshift Mutation - genetics | Agenesis | Genetic aspects | Genetics | Reproductive system | Rodents | Index Medicus | Life Sciences | Human health and pathology
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11. Full Text Choosing a career in oncology: Results of a nationwide cross-sectional study
by Faivre, J.C and Bibault, J.E and Bellesoeur, A and Salleron, J and Wack, M and Biau, J and Cervellera, M and Janoray, G and Leroy, T and Lescut, N and Martin, V and Molina, S and Pichon, B and Teyssier, C and Thureau, S and Mazeron, J.J and Roché, H and Culine, S
BMC medical education, ISSN 1472-6920, 01/2018, Volume 18, Issue 1, pp. 15 - 15
Training | Research | Education | Career mobility | Internship and residency | Neoplasms | Education & Educational Research | Education, Scientific Disciplines | Social Sciences | Medical Oncology | Specialization | Cross-Sectional Studies | Internship and Residency | Employment | Humans | Career Choice | Students, Medical - statistics & numerical data | Surveys and Questionnaires | France | Education, Medical, Graduate | Medical students | Psychological aspects | Career choice | Analysis | Oncology | Social aspects | Index Medicus
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12. Full Text Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral–facial–digital syndrome with short stature and brachymesophalangia
by Thevenon, J and Duplomb, L and Phadke, S and Eguether, T and Saunier, A and Avila, M and Carmignac, V and Bruel, A.‐L and St‐Onge, J and Duffourd, Y and Pazour, G.J and Franco, B and Attie‐Bitach, T and Masurel‐Paulet, A and Rivière, J.‐B and Cormier‐Daire, V and Philippe, C and Faivre, L and Thauvin‐Robinet, C
Clinical genetics, ISSN 0009-9163, 12/2016, Volume 90, Issue 6, pp. 509 - 517
oral–facial–digital syndrome | exome sequencing | IFT57 | ciliopathy | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Male | Craniofacial Abnormalities - physiopathology | Ellis-Van Creveld Syndrome - genetics | Young Adult | Ciliopathies - genetics | Adult | Female | Thorax - physiopathology | Dwarfism - physiopathology | Neck - physiopathology | Craniofacial Abnormalities - genetics | Ear - physiopathology | Ellis-Van Creveld Syndrome - physiopathology | Ear - abnormalities | Orofaciodigital Syndromes - genetics | Neck - abnormalities | Genetic Heterogeneity | Dwarfism - genetics | Homozygote | Exome - genetics | Phenotype | Ciliopathies - physiopathology | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Consanguinity | High-Throughput Nucleotide Sequencing | Orofaciodigital Syndromes - physiopathology | Mutation | Thorax - abnormalities | Proteins | Dysplasia | Analysis | Genetic aspects | Nucleotide sequencing | Multiple abnormalities | DNA sequencing | Index Medicus | Life Sciences | Human health and pathology
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13. Full Text Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole‐exome sequencing as a first‐line diagnostic test
by Thevenon, J and Duffourd, Y and Masurel‐Paulet, A and Lefebvre, M and Feillet, F and El Chehadeh‐Djebbar, S and St‐Onge, J and Steinmetz, A and Huet, F and Chouchane, M and Darmency‐Stamboul, V and Callier, P and Thauvin‐Robinet, C and Faivre, L and Rivière, J.B
Clinical genetics, ISSN 0009-9163, 06/2016, Volume 89, Issue 6, pp. 700 - 707
ultra‐rare disorders | severe intellectual disability | clinical and genetic heterogeneity | epileptic encephalopathy | clinical whole‐exome sequencing | Clinical whole-exome sequencing | Epileptic encephalopathy | Clinical and genetic heterogeneity | Ultra-rare disorders | Severe intellectual disability | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease - genetics | Reproducibility of Results | Humans | Child, Preschool | Male | Neurodevelopmental Disorders - genetics | Diagnostic Tests, Routine - trends | Genetic Testing - methods | Epilepsy - diagnosis | Intellectual Disability - genetics | Young Adult | Exome - genetics | Diagnostic Tests, Routine - methods | Intellectual Disability - diagnosis | Sensitivity and Specificity | Adolescent | Adult | Epilepsy - genetics | Female | Polymorphism, Single Nucleotide | High-Throughput Nucleotide Sequencing - methods | Child | Cohort Studies | Neurodevelopmental Disorders - diagnosis | Molecular genetics | Medical tests | Genetic testing | Intellectual disabilities | Diagnostic tests | Neurological disorders | Index Medicus | Life Sciences | Human health and pathology
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14. Full Text Study of J/ψ azimuthal anisotropy at forward rapidity in Pb-Pb collisions at s N N = 5.02 \[ \sqrt{s_{\mathrm{NN}}}=5.02 \] TeV
by J Adolfsson and S U Ahn and A Akindinov and Y Ali and V Anguelov and S Arcelli and I C Arsene and R Averbeck and A Badalà and J L Bazo Alba and R Bellwied and V Belyaev and Y Berdnikov and P P Bhaduri and M Bonora and M Broz and R S Camacho and T Chowdhury and L Cifarelli and M Colocci and Z Conesa del Valle and P Cortese and B Di Ruzza and R Divià and A Dubla and E Endress and F Flor and V Grigoriev and B Hohlweger and P Huhn and M Jercic and P Karczmarczyk and S Khan and M M Kielbowicz and K Kindra and M Konyushikhin and A Kravčáková and F Krizek and S Kundu and S L La Pointe and K Lapidus and F Lehas and C Lippmann and C Loizides and L Malinina and D Mal’Kevich and J Mareš and Y Melikyan and M Meres and M M Mieskolainen and