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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 | Life Sciences
Journal Article
Laboratory Investigation, ISSN 0023-6837, 03/2014, Volume 94, Issue 3, pp. 275 - 285
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 09/2012, Volume 122, Issue 9, pp. 3355 - 3367
Tight regulation of calcium levels is required for many critical biological functions. The Ca2+-sensing receptor (CaSR) expressed by parathyroid cells controls... 
MEDICINE, RESEARCH & EXPERIMENTAL | EXTRACELLULAR CA2+-SENSING RECEPTOR | PRIMARY HYPERPARATHYROIDISM | LUMINAL MEMBRANE | COLLECTING DUCT | RAT-KIDNEY | PARATHYROID-HORMONE SECRETION | FAMILIAL HYPOCALCIURIC HYPERCALCEMIA | HENLES LOOP | CALCEMIC RESPONSE | THICK ASCENDING LIMB | Calcium - metabolism | Loop of Henle - metabolism | Male | Parathyroidectomy | Receptors, Calcium-Sensing - metabolism | Sodium-Potassium-Chloride Symporters - metabolism | Calcium - blood | Osteocalcin - blood | Parathyroid Hormone - metabolism | Diphosphonates - therapeutic use | Receptors, Calcium-Sensing - antagonists & inhibitors | Hypoparathyroidism - drug therapy | Parathyroid Hormone - secretion | Permeability - drug effects | Receptors, Calcium-Sensing - physiology | Amino Acids - urine | Bone Density Conservation Agents - therapeutic use | Rats | Calcium - urine | Creatinine - urine | Rats, Sprague-Dawley | Bone Density Conservation Agents - pharmacology | Naphthalenes - pharmacology | Sodium-Potassium-Exchanging ATPase - metabolism | Solute Carrier Family 12, Member 1 | Animals | Hypoparathyroidism - blood | Diphosphonates - pharmacology | Naphthalenes - therapeutic use | Measurement | Calcium, Dietary | Analysis and chemistry | Parathyroid hormone | Research | Gene expression | Health aspects | Blood | Methods | Organic chemistry | Chemical Sciences
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 02/2012, Volume 109, Issue 7, pp. 2567 - 2572
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 12/2018, Volume 19, Issue 1, pp. 143 - 6
BackgroundWilson’s disease (WD) is a rare autosomal recessive metabolic disease caused by ATP7B gene mutations tat cause excessively high copper levels,... 
Ceruloplasmin | Phenotypes | Excretion | Genomics | Genes | Liver | Epidemiology | Data bases | ATP7B gene | Next-generation sequencing | Alleles | Software | Chelating agents | Mutation | Copper | Wilson's disease | Metabolic disorders | Life Sciences | Genetics | Santé publique et épidémiologie | Clinical prevalence | Wilson’s disease | ATP7B | Heterozygous carrier frequency
Journal Article