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1. Full Text Determination of the solar parallax from photographs of Eros made with the Crossley reflector of the Lick observatory, University of California
by Perrine, Charles Dillon, 1867
1910, Carnegie Institution of Washington. Publication no. 119, Volume 119
Sun | Parallax | Planets, Minor
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2. Permaculture
: guérir la Terre, nourrir les hommes
by Hervé-Gruyer, Perrine and Hervé-Gruyer, Charles
2014, Domaine du possible, ISBN 9782330034344, 367, [1]
Le Bec-Hellouin (France) Rural conditions | Organic farming
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3. Full Text A comprehensive repertoire of prokaryotic species identified in human beings
by Hugon, Perrine, PharmD and Dufour, Jean-Charles, MCU and Colson, Philippe, Prof and Fournier, Pierre-Edouard, Prof and Sallah, Kankoe, MD and Raoult, Didier, Prof
Lancet Infectious Diseases, The, ISSN 1473-3099, 2015, Volume 15, Issue 10, pp. 1211 - 1219
Summary The compilation of the complete prokaryotic repertoire associated with human beings as commensals or pathogens is a major goal for the scientific and... 
Infectious Disease | GEN. NOV | INFECTIOUS DISEASES | FINISHED GENOME SEQUENCE | SENEGALENSIS SP-NOV | HUMAN GUT MICROBIOTA | ANAEROBIC-BACTERIA | MASSILIENSIS SP-NOV | HUMAN FECES | PATHOGENIC BACTERIA | CLINICAL MICROBIOLOGY | MOLECULAR ANALYSIS | Bacteria - isolation & purification | Microbiota | Humans | Bacteria - classification | Carrier State - microbiology | Archaea - isolation & purification | Archaea - classification | Bacterial Infections - microbiology | Databases, Factual | Microbiota (Symbiotic organisms) | Usage | Pathogenesis | Taxonomy | Prokaryotes | Laboratories | Genomes | Bacteriology | Investigations | Biological diversity | Names | Microorganisms | Classification | Bacteria | Deoxyribonucleic acid--DNA | Methods | Life Sciences | Microbiology and Parasitology | Human health and pathology | Infectious diseases
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4. Problems in retailing
by McNair, Malcolm Perrine, 1894 and Graag, Charles Insco and Teele, Stanley Ferdinand
1937, xv, 676 p. illus., diag., form.
Retail trade
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5. Problems in retail distribution
by McNair, Malcolm Perrine, 1894 and Gragg, Charles I. (Charles Insco)
1930, 1st ed., xx, 559
Retail trade
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6. Full Text Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study
by Jacobi, Heike, MD and du Montcel, Sophie Tezenas, PhD and Bauer, Peter, MD and Giunti, Paola, PhD and Cook, Arron, MBBS and Labrum, Robyn, MD and Parkinson, Michael H, MBBS and Durr, Alexandra, PhD and Brice, Alexis, Prof and Charles, Perrine, MD and Marelli, Cecilia, MD and Mariotti, Caterina, MD and Nanetti, Lorenzo, MD and Panzeri, Marta, MD and Rakowicz, Maria, MD and Sulek, Anna, PhD and Sobanska, Anna, MD and Schmitz-Hübsch, Tanja, MD and Schöls, Ludger, MD and Hengel, Holger, MD and Baliko, Laszlo, MD and Melegh, Bela, Prof and Filla, Alessandro, Prof and Antenora, Antonella, MD and Infante, Jon, MD and Berciano, José, Prof and van de Warrenburg, Bart P, PhD and Timmann, Dagmar, MD and Szymanski, Sandra, MD and Boesch, Sylvia, MD and Kang, Jun-Suk, MD and Pandolfo, Massimo, Prof and Schulz, Jörg B, Prof and Molho, Sonia, MSc and Diallo, Alhassane, MD and Klockgether, Thomas, Prof
Lancet Neurology, The, ISSN 1474-4422, 2015, Volume 14, Issue 11, pp. 1101 - 1108
Summary Background Spinocerebellar ataxias are dominantly inherited neurodegenerative diseases. As potential treatments for these diseases are being developed,... 
Neurology | RELIABILITY | SCALE | NATURAL-HISTORY | DOMINANT CEREBELLAR-ATAXIA | POLYGLUTAMINE EXPANSIONS | CALCIUM-CHANNEL | CLINICAL NEUROLOGY | Humans | Middle Aged | Spinocerebellar Ataxias - classification | Repressor Proteins - genetics | Male | Spinocerebellar Ataxias - physiopathology | Disease Progression | Ataxin-2 - genetics | Young Adult | PubMed - statistics & numerical data | Adult | Female | Calcium Channels - genetics | Ataxin-1 - genetics | Ataxin-3 - genetics | Cohort Studies | Spinocerebellar Ataxias - genetics | Development and progression | Ataxia | Nervous system diseases | Neurosciences | Analysis | Medical genetics | Studies | Genotype & phenotype | Biomedical research | Disease | Funding | Grants | Patients | Age
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7. Full Text Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data
by Reetz, Kathrin, Prof and Dogan, Imis, PhD and Costa, Ana S, MSc and Dafotakis, Manuel, MD and Fedosov, Kathrin, MSc and Giunti, Paola, MD and Parkinson, Michael H, MBBS and Sweeney, Mary G, BSc and Mariotti, Caterina, MD and Panzeri, Marta, MD and Nanetti, Lorenzo, MD and Arpa, Javier, MD and Sanz-Gallego, Irene, MD and Durr, Alexandra, Prof and Charles, Perrine, MD and Boesch, Sylvia, MD and Nachbauer, Wolfgang, MD and Klopstock, Thomas, MD and Karin, Ivan, MD and Depondt, Chantal, MD and vom Hagen, Jennifer Müller, MD and Schöls, Ludger, Prof and Giordano, Ilaria A, MD and Klockgether, Thomas, Prof and Bürk, Katrin, MD and Pandolfo, Massimo, Prof and Schulz, Jörg B, Prof Dr
Lancet Neurology, The, ISSN 1474-4422, 2015, Volume 14, Issue 2, pp. 174 - 182
Summary Background Friedreich's ataxia is a rare autosomal recessive neurodegenerative disorder. Here we report cross-sectional baseline data to establish the... 
Neurology | POINT MUTATIONS | REGRESSION-COEFFICIENTS | SCALES | FRDA | NATURAL-HISTORY | PROGRESSION | CLINICAL NEUROLOGY | Prospective Studies | Cross-Sectional Studies | Humans | Middle Aged | Friedreich Ataxia - diagnosis | Europe - epidemiology | Male | Trinucleotide Repeats - genetics | Friedreich Ataxia - genetics | Activities of Daily Living | Young Adult | Friedreich Ataxia - epidemiology | Adolescent | Adult | Female | Aged | Translational Medical Research - methods | Child | Longitudinal Studies | Cohort Studies | Databases, Factual | Ataxia | Nervous system diseases | Neurosciences | Studies | Age | Inventory
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8. Full Text Adherence to antiretroviral treatment in HIV-positive patients in the Cameroon context: Promoting the use of medication reminder methods
by Perrine, Roux and Kouanfack, Charles and Cohen, Julien and Marcellin, Fabienne and Boyer, Sylvie and Delaporte, Eric and Carrieri, Patrizia and Laurent, Christian and Spire, Bruno and Stratall ANRS 12110 ESTHER Study and Stratall ANRS 12110/ESTHER Study Group
Journal of Acquired Immune Deficiency Syndromes, ISSN 1525-4135, 07/2011, Volume 57, Issue 1, pp. S40 - S43
Objectives: Antiretroviral treatment (ART) scale-up in sub-Saharan Africa has made it possible to investigate the maintenance of adherence to HIV medications.... 
HIV | reminder | antiretroviral treatment | adherence | Africa | DEPRESSION | INFECTIOUS DISEASES | SUB-SAHARAN AFRICA | IMMUNOLOGY | TRIAL | THERAPY | NONADHERENCE | INFECTED PATIENTS | HAART | Cameroon | Reminder Systems | Prospective Studies | Humans | Adult | Anti-HIV Agents - therapeutic use | Female | HIV Infections - drug therapy | Male | Patient Compliance | Antiretroviral drugs | Drug therapy | Patients | Human immunodeficiency virus--HIV
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9. Full Text Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data
by Jacobi, Heike, MD and Reetz, Kathrin, MD and du Montcel, Sophie Tezenas, PhD and Bauer, Peter, MD and Mariotti, Caterina, MD and Nanetti, Lorenzo, MD and Rakowicz, Maria, PhD and Sulek, Anna, PhD and Durr, Alexandra, PhD and Charles, Perrine, PhD and Filla, Alessandro, Prof and Antenora, Antonella, MD and Schöls, Ludger, MD and Schicks, Julia, MD and Infante, Jon, MD and Kang, Jun-Suk, MD and Timmann, Dagmar, MD and Fabio, Roberto Di, MD and Masciullo, Marcella, MD and Baliko, Laszlo, MD and Melegh, Bela, Prof and Boesch, Sylvia, MD and Bürk, Katrin, MD and Peltz, Annkathrin and Schulz, Jörg B, Prof and Dufaure-Garé, Isabelle, PhD and Klockgether, Thomas, Prof
Lancet Neurology, The, ISSN 1474-4422, 2013, Volume 12, Issue 7, pp. 650 - 658
Summary Background Spinocerebellar ataxias (SCAs) are autosomal, dominantly inherited, fully penetrant neurodegenerative diseases. Our aim was to study the... 
Neurology | INSTRUMENT | GENE CARRIERS | DOMINANT CEREBELLAR ATAXIAS | RESTLESS LEGS SYNDROME | DISEASE | VALIDATION | SYMPTOMS | PREVALENCE | NATURAL-HISTORY | SEVERITY | CLINICAL NEUROLOGY | Prospective Studies | Humans | Middle Aged | Male | Risk | DNA - blood | Young Adult | Mutation - physiology | Spinocerebellar Ataxias - diagnosis | Brain Stem - pathology | Adult | Female | Spinocerebellar Ataxias - psychology | Sleep Wake Disorders - etiology | Europe | Spinocerebellar Ataxias - physiopathology | Mutation - genetics | Disease Progression | DNA - genetics | Neuropsychological Tests | Magnetic Resonance Imaging | Neurologic Examination | Image Processing, Computer-Assisted | Restless Legs Syndrome - complications | Adolescent | Age of Onset | Heterozygote | Aged | Health Status | Longitudinal Studies
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10. Full Text Early Energy Deficit in Huntington Disease: Identification of a Plasma Biomarker Traceable during Disease Progression
by Mochel, F and Charles, P and Seguin, F and Barritault, J and Coussieu, C and Perin, L and Le Bouc, Y and Gervais, C and Carcelain, G and Vassault, A and Feingold, J and Rabier, D and Durr, A
PLOS ONE, ISSN 1932-6203, 07/2007, Volume 2, Issue 7, p. e647
Huntington disease (HD) is a fatal neurodegenerative disorder, with no effective treatment. The pathogenic mechanisms underlying HD have not been elucidated,... 
BIOLOGY | Predictive Value of Tests | Amino Acids - blood | Body Weight | Humans | Middle Aged | Male | Reference Values | Cognition Disorders - genetics | Biomarkers - blood | Loss of Heterozygosity | Motor Activity | Huntington Disease - metabolism | Disease Progression | Energy Metabolism | Aged, 80 and over | Huntington Disease - genetics | Adult | Female | Heterozygote | Huntington Disease - blood | Aged | Mutation | Weight Loss - genetics | Huntington Disease - physiopathology | Medical research | Nervous system diseases | Huntington's chorea | Branched chain amino acids | Body weight | Physiological aspects | Medicine, Experimental | Development and progression | Nuclear magnetic resonance spectroscopy | High-definition television | Diagnostic imaging | Comparative analysis | Huntingtons disease | Tricarboxylic acid cycle | Brain | Phosphorylation | Nuclear magnetic resonance--NMR | Dehydrogenases | Insulin-like growth factor I | Chorea | Cognitive ability | Chain branching | Amino acids | Nervous system | Insulin-like growth factors | Body weight loss | Family medical history | Leucine | Kinases | Krebs cycle | Defects | Magnetic resonance spectroscopy | Body mass index | Energy resources | Rodents | Questionnaires | Bioindicators | Isoleucine | Enzymes | Statistical analysis | Neurodegenerative diseases | Weight loss | Inflammation | Metabolism | Huntington's disease | Patients | HD1 gene | Disease control | Substrates | Carriers | Multivariate statistical analysis | Valine | Biomarkers | Plasma levels | NMR spectroscopy | Plasmas (physics) | Magnetic resonance | Nuclear magnetic resonance | NMR
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11. Full Text Objective comparison of particle tracking methods
by Chenouard, Nicolas and Smal, Ihor and Chaumont, Fabrice and Maška, Martin and Sbalzarini, Ivo and Gong, Yuanhao and Cardinale, A.E and Carthel, Craig and Coraluppi, Stefano and Winter, Mark and Cohen, Anew and Godinez, William and Rohr, Karl and Kalaidzidis, Yannis and Liang, Liang and Duncan, James and Shen, Hongying and Xu, Ying and Magnusson, Klas E and Jaldén, Joakim and Blau, Helen and Paul-Gilloteaux, Perrine and Roudot, Philippe and Kervrann, Charles and Waharte, François and Tinevez, Jean-Yves and Shorte, Spencer and Willemse, José and Celler, Katherine and Wezel, Gilles and Dan, Sorin and Tsai, Yuh-Show and Solórzano, Carlos Ortiz and Olivo-Marin, Jean-Christophe and Meijering, Erik and Centra and Signalbehandling and Skolan för elektro- och systemteknik (EES) and KTH and ACCESS Linnaeus Centre
Nature Methods, ISSN 1548-7091, 03/2014, Volume 11, Issue 3, pp. 281 - 289
textabstractParticle tracking is of key importance for quantitative analysis of intracellular dynamic processes from time-lapse microscopy image data. Because... 
DYNAMIC PROPERTIES | TRANSPORT | ATOMIC-FORCE MICROSCOPY | FLUORESCENCE MICROSCOPY | VIDEO MICROSCOPY | IMAGES | BIOCHEMICAL RESEARCH METHODS | SEGMENTATION | AUTOMATED TRACKING | ALGORITHMS | LIVING CELLS | Microscopy, Fluorescence - methods | Image Interpretation, Computer-Assisted - standards | Microscopy, Fluorescence - standards | Physiological aspects | Particle tracks (Nuclear physics) | Research | Comparative studies | Atoms & subatomic particles | Life Sciences | Image Processing | Computer Science | Biological Sciences | Segmentation | Images | Video Microscopy | Living Cells | Fluorescence Microscopy | Automated Tracking | Naturvetenskap | Algorithms | Biokemi och molekylärbiologi | Biologiska vetenskaper | Biochemistry and Molecular Biology | Natural Sciences | Dynamic Properties | Transport | Atomic-Force Microscopy
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12. Full Text Lower incidence of fracture after IV bisphosphonates in girls with Rett syndrome and severe bone fragility
by Lambert, Anne-Sophie and Rothenbuhler, Anya and Charles, Perrine and Brailly-Tabard, Sylvie and Trabado, Séverine and Célestin, Elisabeth and Durand, Emmanuel and Fontaine, Isabelle and Miladi, Lotfi and Wicart, Philippe and Bahi-Buisson, Nadia and Linglart, Agnès
PLoS ONE, ISSN 1932-6203, 10/2017, Volume 12, Issue 10, p. e0186941
Background Classic Rett Syndrome (RS) is a disabling condition mainly caused by MECP2 mutations. Girls with RS are at risk of developing bone fragility and... 
MECP2 | POPULATION | PAMIDRONATE | MANAGEMENT | MULTIDISCIPLINARY SCIENCES | MASS | MUTATIONS | CEREBRAL-PALSY | OSTEOPOROSIS | TREAT OSTEOPENIA | CHILDREN | Rett Syndrome - complications | Bone Density | Humans | Bone Density Conservation Agents - therapeutic use | Fractures, Bone - epidemiology | Calcium - urine | Creatinine - urine | Incidence | Young Adult | Fractures, Bone - etiology | Adolescent | Diphosphonates - therapeutic use | Adult | Female | Imidazoles - therapeutic use | Child | Fractures, Bone - prevention & control | Pediatrics | Cerebral palsy | Calcium | Spine | Parents | Bisphosphonates | Disability | Osteoporosis | Pain | Methyl-CpG binding protein | Scoliosis | Mineralization | Zoledronic acid | Bone density | Drug dosages | Creatinine | Calcium (urinary) | Excretion | Metabolism | Patients | Girls | Pamidronic acid | Fragility | Quality of life | Fractures | MeCP2 protein | Orthopedics | Rett syndrome | Bone mineral density | Mutation | Bone | Endocrinology
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