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1. Full Text Test of Martin's overkill hypothesis using radiocarbon dates on extinct megafauna
by Surovell, Todd A and Pelton, Spencer R and Anderson-Sprecher, Richard and Myers, Adam D
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 01/2016, Volume 113, Issue 4, pp. 886 - 891
Following Martin [Martin PS (1973) Science 179: 969-974], we propose the hypothesis that the timing of human arrival to the New World can be assessed by... 
Pleistocene extinctions | Temporal frequency distributions | Radiocarbon | Overkill | overkill | temporal frequency distributions | CHRONOLOGY | MULTIDISCIPLINARY SCIENCES | HUMAN ARRIVAL | ARCHAEOLOGICAL SITES | CLOVIS | COLLAPSE | TEMPORAL FREQUENCY-DISTRIBUTIONS | SOUTH-AMERICA | radiocarbon | NORTH-AMERICA | AGE | South America | History, Ancient | Paleontology - methods | Body Size | Humans | Extinction, Biological | Mammals | North America | Fossils | Human Migration - history | Animals | Radiometric Dating | Models, Biological | Ecosystem | Archaeology - methods | Human Activities | Biological research | Animal populations | Extinction (Biology) | Research | Natural history | Biology, Experimental | Hypothesis testing | Ecology | Carbon dating | Geological time | Extinction | Paleontology | Index Medicus
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2. Full Text Genotype–phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France
by Mariani, Louise‐Laure and Lozeron, Pierre and Théaudin, Marie and Mincheva, Zoia and Signate, Aissatou and Ducot, Beatrice and Algalarrondo, Vincent and Denier, Christian and Adam, Clovis and Nicolas, Guillaume and Samuel, Didier and Slama, Michel S and Lacroix, Catherine and Misrahi, Micheline and Adams, David and French Familial Amyloid Polyneurop and French Familial Amyloid Polyneuropathies Network (CORNAMYL) Study Group
Annals of Neurology, ISSN 0364-5134, 12/2015, Volume 78, Issue 6, pp. 901 - 916
Objective: To compare the natural history of familial transthyretin amyloid polyneuropathies (FAP) due to the Val30Met, Ser77Tyr, and Ile107Val mutations in... 
LIVER-TRANSPLANTATION | NEUROPATHY | FAP | JAPAN | DENERVATION | INFLAMMATORY DEMYELINATING POLYNEUROPATHY | LATE-ONSET | CARPAL-TUNNEL-SYNDROME | NEUROSCIENCES | VAL30MET | CLINICAL NEUROLOGY | FEATURES | Amyloid - genetics | Prealbumin - genetics | Amyloid Neuropathies, Familial - genetics | Humans | Middle Aged | Genotype | Male | Portugal | Disease Progression | Amyloid Neuropathies, Familial - physiopathology | Phenotype | Prealbumin - metabolism | Age of Onset | Aged, 80 and over | Adult | Female | Aged | Amyloid Neuropathies, Familial - mortality | Retrospective Studies | Mutation | France | Genotype & phenotype | Genetic counseling | Biopsy | Index Medicus | Life Sciences
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3. Full Text Mitochondrial myopathy associated with anti-programmed cell death 1 therapy
by Ibrahim, Tony and Adam, Clovis and Routier, Emilie and Slama, Abdelhamid and Robert, Caroline
European Journal of Cancer, ISSN 0959-8049, 03/2019, Volume 110, pp. 71 - 73
ONCOLOGY | DIAGNOSIS | DISEASE | Mitochondria | Cell death | Myopathy | Apoptosis
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4. Full Text Clinical features and prognostic factors of listeriosis: the MONALISA national prospective cohort study
by Charlier, Caroline, Dr and Perrodeau, Élodie, MSc and Leclercq, Alexandre, MSc and Cazenave, Benoît, MD and Pilmis, Benoît, MD and Henry, Benoît, MD and Lopes, Amanda, MD and Maury, Mylène M, PhD and Moura, Alexandra, PhD and Goffinet, François, MD and Dieye, Hélène Bracq and Thouvenot, Pierre and Ungeheuer, Marie-Noëlle, MD and Tourdjman, Mathieu, MD and Goulet, Véronique, MD and de Valk, Henriette, MD and Lortholary, Olivier, Prof and Ravaud, Philippe, Prof and Lecuit, Marc, Prof and MONALISA Study Grp and MONALISA study group
Lancet Infectious Diseases, The, ISSN 1473-3099, 2017, Volume 17, Issue 5, pp. 510 - 519
Summary Background Listeriosis is a severe foodborne infection and a notifiable disease in France. We did a nationwide prospective study to characterise its... 
Infectious Disease | MORTALITY | MENINGITIS | INFECTIOUS DISEASES | MONOCYTOGENES | RISK-FACTORS | MANAGEMENT | GUIDELINES | SURVEILLANCE | PREGNANCY | Foodborne Diseases - microbiology | Infant, Newborn, Diseases - epidemiology | Prognosis | Prospective Studies | Humans | Listeriosis - diagnosis | Bacteremia - mortality | Male | Infant, Newborn, Diseases - microbiology | Listeriosis - epidemiology | Mandatory Reporting | Listeria monocytogenes - classification | Adult | Female | Pregnancy Complications, Infectious - microbiology | Infant, Newborn | Meningoencephalitis - epidemiology | France - epidemiology | Meningoencephalitis - mortality | Pregnancy Complications, Infectious - epidemiology | Risk Factors | Listeria monocytogenes - isolation & purification | Hospitalization | Infectious Disease Transmission, Vertical | Pregnancy | Meningoencephalitis - microbiology | Bacteremia - epidemiology | Listeriosis - microbiology | Aged | Population Surveillance | Listeriosis | Neonates | Food-borne diseases | Disease | Brain stem | Clinical trials | Infections | Genomes | Gestation | Epidemiology | Risk factors | Windows (intervals) | Listeria | Meningitis | Public health | Food | Dexamethasone | Bacterial infections | Mortality | Fetuses | Regression analysis | Clustering | Patients | Bacteremia | Meningoencephalitis | Studies | Surveillance | Medical prognosis | Health risk assessment | Cancer | Index Medicus | Life Sciences
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5. Full Text Genomic Alterations and Complex Subclonal Architecture in Sporadic GH-Secreting Pituitary Adenomas
by Hage, Mirella and Viengchareun, Say and Brunet, Erika and Villa, Chiara and Pineau, Dominique and Bouligand, Jérôme and Teglas, Jean-Paul and Adam, Clovis and Parker, Fabrice and Lombès, Marc and Tachdjian, Gérard and Gaillard, Stéphane and Chanson, Philippe and Tosca, Lucie and Kamenický, Peter
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 05/2018, Volume 103, Issue 5, pp. 1929 - 1939
Purpose: The molecular pathogenesis of growth hormone-secreting pituitary adenomas is not fully understood. Cytogenetic alterations might serve as alternative... 
HETEROGENEITY | GERMLINE | LANDSCAPE | ENDOCRINOLOGY & METABOLISM | AIP | HYBRIDIZATION | MUTATIONS | CHROMOTHRIPSIS | CANCER | TUMORS | Adenoma - genetics | Humans | Middle Aged | Growth Hormone-Secreting Pituitary Adenoma - genetics | In Situ Hybridization, Fluorescence | Male | Clonal Evolution - genetics | DNA Copy Number Variations | Comparative Genomic Hybridization | Chromosome Aberrations | Adenoma - pathology | Adult | Female | Cytogenetic Analysis | Mutation | Acromegaly - genetics | Acromegaly - pathology | Growth Hormone-Secreting Pituitary Adenoma - pathology | Profiling | Pathogenesis | Acromegaly | Fluorescence | Adenoma | Chromosome rearrangements | Subgroups | Gene sequencing | Genomic instability | Heterogeneity | Alterations | Fluorescence in situ hybridization | DNA fingerprinting | Deoxyribonucleic acid--DNA | Gigantism | Stability | Architecture | Abnormalities | Stability analysis | Ribonucleic acid--RNA | Patients | Molecular chains | Pituitary | Hybridization analysis | Growth hormone | Tumors | Index Medicus | Abridged Index Medicus
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6. Full Text Neuroprotective effect of kinin B1 receptor activation in acute cerebral ischemia in diabetic mice
by Desposito, Dorinne and Zadigue, Georges and Taveau, Christopher and Adam, Clovis and Alhenc-Gelas, François and Bouby, Nadine and Roussel, Ronan
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 9410 - 11
Activation of the kallikrein-kinin system enhances cardiac and renal tolerance to ischemia. Here we investigated the effects of selective agonists of kinin B1... 
TISSUE KALLIKREIN | SECONDARY BRAIN-DAMAGE | MULTIDISCIPLINARY SCIENCES | B2 RECEPTORS | REPERFUSION INJURY | B-2 RECEPTORS | MYOCARDIAL-ISCHEMIA | BRADYKININ B-1 | UP-REGULATION | EXPRESSION | AGONISTS | Receptor, Bradykinin B1 - agonists | Receptor, Bradykinin B2 - agonists | Animals | Infarction, Middle Cerebral Artery | Neuroprotective Agents - pharmacology | Renal Insufficiency | Mice, Inbred C57BL | Diabetes Mellitus, Type 1 | Male | Brain Ischemia - prevention & control | Diabetes Mellitus, Experimental - chemically induced | Hemodynamics | Neuroprotection | Renal function | Mortality | Diabetes mellitus | Kinins | Kallikrein | mRNA | Renal insufficiency | Tissue kallikrein | Reperfusion | Ischemia | Cerebral blood flow | Rodents | Cerebrum | Renal failure | Water content | Diabetes | Receptor mechanisms | Heart diseases | Life Sciences | Human health and pathology | Endocrinology and metabolism | Pharmacology | Neurons and Cognition | Pharmaceutical sciences
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7. Full Text Decreased expression of megalin and cubilin and altered mitochondrial activity in tenofovir nephrotoxicity
by Cez, Alexandre and Brocheriou, Isabelle and Lescure, François-Xavier and Adam, Clovis and Girard, Pierre-Marie and Pialoux, Gilles and Moestrup, Søren K and Fellahi, Soraya and Bastard, Jean-Philippe and Ronco, Pierre and Plaisier, Emmanuelle
Human Pathology, ISSN 0046-8177, 03/2018, Volume 73, pp. 89 - 101
Tenofovir disoproxil fumarate (TDF) is a commonly used antiretroviral drug for HIV, rarely causing Fanconi syndrome and acute kidney injury. We retrospectively... 
Tenofovir | Fanconi syndrome | Megalin | Nephrotoxicity | Cubilin | Tubulopathy | CELLS | SAFETY | ADEFOVIR | RISK | TOXICITY | PATHOLOGY | ENDOCYTOSIS | THERAPY | DISOPROXIL FUMARATE | CHRONIC KIDNEY-DISEASE | Immunoglobulins | Fasting | Statistical analysis | Infections | Uric acid | Glucose | Variables | Pathology | Hepatitis | Mitochondria | Microscopy | Biopsy | Human immunodeficiency virus--HIV | Rodents | Diabetes | Kidney diseases | Deoxyribonucleic acid--DNA | Index Medicus
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