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  1. A “Set Point” for Water Homeostasis Disturbed with Altered Kidney Transplantation Outcome
  2. GNAS: A New Nephrogenic Cause of Inappropriate Antidiuresis
  3. ACUTE AND CHRONIC HYPERGLYCEMIC EFFECTS OF VASOPRESSIN IN NORMAL RATS, INVOLVEMENT OF V 1A RECEPTORS
  4. Impaired Left Atrial Function in Fabry Disease: A Longitudinal Speckle-Tracking Echocardiography Study
  5. The validation of pharmacogenetics for the identification of Fabry patients to be treated with migalastat
  6. Functional Recovery of AQP2 Recessive Mutations Through Hetero-Oligomerization with Wild-Type Counterpart
  7. β3-Adrenoreceptors in the thick ascending limb of Henle and in principal cells of the collecting duct work to concentrate urine
  8. MAP17 Is a Necessary Activator of Renal Na + /Glucose Cotransporter SGLT2
  9. Time to treatment benefit for adult patients with Fabry disease receiving agalsidase β: data from the Fabry Registry
  10. A need for a systematic genetic evaluation of hereditary polyuric patients
  11. Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant)
  12. Phenotype of Fabry disease in patients with mutations amenable to migalastat
  13. The validation of pharmacogenetics in the identification of patients with Fabry disease for treatment with migalastat
  14. Vasopressin at Central Levels and Consequences of Dehydration
  15. Approach to the patient with polyuria
  16. Total Kidney Volume in Autosomal Dominant Polycystic Kidney Disease: A Biomarker of Disease Progression and Therapeutic Efficacy
  17. Un diabète insipide peut en cacher un autre ! À propos d’un cas de diabète insipide néphrogénique
  18. Oral Migalastat HCl Leads to Greater Systemic Exposure and Tissue Levels of Active α-Galactosidase A in Fabry Patients when Co-Administered with Infused Agalsidase
  19. Pathophysiology, diagnosis and management of nephrogenic diabetes insipidus
  20. Characterization of Early Disease Status in Treatment-Naive Male Paediatric Patients with Fabry Disease Enrolled in a Randomized Clinical Trial
  21. Les années 2000
  22. Improvement in gastrointestinal symptoms observed in the phase 3 FACETS (AT1001-011) study of migalastat in patients affected with Fabry disease
  23. Long-term efficacy and safety of migalastat compared to enzyme replacement therapy in Fabry disease: Phase 3 study results
  24. Accurate quantitation of plasma globotriaosylsphingosine (lyso-Gb3) in normal individuals and Fabry disease patients by liquid chromatography–tandem mass spectrometry (LC–MS/MS)
  25. Vasopressin and hydration play a major role in the development of glucose intolerance and hepatic steatosis in obese rats
  26. Urinary biomarker investigation in children with Fabry disease using tandem mass spectrometry
  27. Diabetes Insipidus: Celebrating a Century of Vasopressin Therapy
  28. Comparison Between Copeptin and Vasopressin in a Population From the Community and in People With Chronic Kidney Disease
  29. Erratum to: Clinical practice guideline on diagnosis and treatment of hyponatraemia
  30. Erratum
  31. Central vasopressin: dendritic and axonal secretion and renal actions
  32. A Copeptin-Based Classification of the Osmoregulatory Defects in the Syndrome of Inappropriate Antidiuresis
  33. Outcomes of patients treated through the Canadian Fabry disease initiative
  34. Erratum to: Clinical practice guideline on diagnosis and treatment of hyponatraemia
  35. The physiological and pathophysiological functions of renal and extrarenal vasopressin V2 receptors
  36. The syndrome of inappropriate antidiuresis: a copeptin-based classification and identification of a novel subtype
  37. Clinical practice guideline on diagnosis and treatment of hyponatraemia
  38. Clinical Practice Guideline on Diagnosis and Treatment of Hyponatraemia
  39. Section Introduction: Emergent Management of Sodium Disorders
  40. G Protein-Coupled Receptor Mutations and Human Genetic Disease
  41. Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families
  42. Diabètes insipides : nouvelles données génétiques et physiopathologiques
  43. Diabète insipide néphrogénique héréditaire : quelle prise en charge à l’âge adulte ?
  44. Transient nephrogenic syndrome of inappropriate antidiuresis: Table 1.
  45. Urinary concentration: different ways to open and close the tap
  46. A Phase 2 study of migalastat hydrochloride in females with Fabry disease: Selection of population, safety and pharmacodynamic effects
  47. A phase 2a study to investigate the effect of a single dose of migalastat HCl, a pharmacological chaperone, on agalsidase activity in subjects with Fabry disease
  48. Benefit of enzyme replacement therapy in Fabry disease: Comparison of outcomes in the Canadian Fabry Disease Initiative study
  49. Clinical effects of neutralizing anti-agalsidase antibodies in patients receiving enzyme replacement therapy in the Canadian Fabry Disease Initiative Study
  50. A randomized, multicenter, multinational, phase 3B, open-label, parallel-group study of agalsidase beta in treatment-naive male pediatric patients with Fabry disease without severe symptoms: Baseline demographics and clinical data
  51. Inherited secondary nephrogenic diabetes insipidus: concentrating on humans
  52. Polyuria and Diabetes Insipidus
  53. Lixivaptan safely and effectively corrects serum sodium concentrations in hospitalized patients with euvolemic hyponatremia
  54. Oral lixivaptan effectively increases serum sodium concentrations in outpatients with euvolemic hyponatremia
  55. A defect in vasopressin secretion in autosomal dominant polycystic kidney disease
  56. Identification and Characterization of an Activating F229V Substitution in the V2 Vasopressin Receptor in an Infant with NSIAD
  57. 4. Renal Actions of Vasopressin
  58. Physiopathology of hereditary polyuric states: a molecular view of renal function
  59. Polycystic kidney disease: An early urea-selective urine-concentrating defect in ADPKD
  60. Vaptans vs medicinal urea
  61. Genetics and diagnosis of central diabetes insipidus
  62. A Family With Hyponatremia and the Nephrogenic Syndrome of Inappropriate Antidiuresis
  63. P19—Influence of Anti-Agalsidase Antibodies on Clinical Outcomes in the Canadian Fabry Disease Initiative Study
  64. P18—Agalsidase Alfa and Agalsidase Beta have Similar Effects on Outcomes in Fabry Disease: Results From the Canadian Fabry Disease Initiative
  65. Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus--update and epidemiology
  66. 025 L’hormone antidiurétique (ou vasopressine) est un nouveau facteur de risque du diabète, indépendant. Résultats de la cohorte D.E.S.I.R.
  67. Prospective Results of Switching Enzyme Replacement Therapy from Agalsidase beta to Agalsidase alfa in the Canadian Fabry Disease Initiative Study
  68. Oral Migalastat HCL (AT1001/GR181314A) as an Investigational Therapy Evaluated in Females with Fabry Disease
  69. Fabry Disease Mutations Addressable with Migalastat HCl, an Investigational Chaperone Therapy. Screening Results from FACETS, a Phase 3 Study in Male and Female Patients
  70. Inherited Disorders of the Renal Tubule
  71. Response of the Renal Inner Medulla to Hypoxia: Possible Defense Mechanisms
  72. Tolvaptan inhibition of desmopressin effects on coagulation factors in a patient with decreased von Willebrand factor and polycystic kidney disease
  73. Desmopressin duration of antidiuretic action in patients with central diabetes insipidus
  74. Novel mutation in the AVPR2 gene in a Danish male with nephrogenic diabetes insipidus caused by ER retention and subsequent lysosomal degradation of the mutant receptor
  75. A patient with polyuria and hydronephrosis: answer
  76. A patient with polyuria and hydronephrosis: question
  77. Agalsidase Alfa and Agalsidase beta Have Similar Effects on Outcomes in Fabry disease– results from the canadian Fabry disease initiative
  78. The Posterior Pituitary
  79. Endocrine Control of Water Balance
  80. Contributors
  81. How well does urinary lyso-Gb3 function as a biomarker in Fabry disease?
  82. Kidney and liver cysts in autosomal dominant polycystic kidney disease
  83. A de novo novel missense mutation in AVPR2 with severe nephrogenic diabetes insipidus
  84. Vasopressin V2 receptors, ENaC, and sodium reabsorption: a risk factor for hypertension?
  85. Stimulating Effect of External Myo-Inositol on the Expression of Mutant Forms of Aquaporin 2
  86. Race, sex, and the regulation of urine osmolality: observations made during water deprivation
  87. New autosomal recessive mutations in aquaporin‐2 causing nephrogenic diabetes insipidus through deficient targeting display normal expression in Xenopus oocytes
  88. Baseline characteristics of patients enrolled in the Canadian Fabry Disease Initiative
  89. A validated disease severity scoring system for Fabry disease
  90. Oral Tolvaptan Is Safe and Effective in Chronic Hyponatremia
  91. Targeted Inactivation of EGF Receptor Inhibits Renal Collecting Duct Development and Function
  92. 140. A validated disease severity scoring system for Fabry disease
  93. 148.A randomized controlled trial of enzyme replacement therapy in Fabry disease: The Canadian Fabry disease initiative at year three
  94. Assessment of Renal Pathology and Dysfunction in Children with Fabry Disease
  95. Vasopressin Type 2 Receptor V88M Mutation: Molecular Basis of Partial and Complete Nephrogenic Diabetes Insipidus
  96. Secondary Nephrogenic Diabetes Insipidus as a Complication of Inherited Renal Diseases
  97. The Canadian Fabry Disease Initiative: a randomized controlled trial of agalsidase therapy in Fabry nephropathy
  98. Hereditary nephrogenic diabetes insipidus: a major conundrum during labour and delivery
  99. Characterization of D150E and G196D aquaporin-2 mutations responsible for nephrogenic diabetes insipidus: importance of a mild phenotype
  100. Wilms tumor arising in a child with X-linked nephrogenic diabetes insipidus
  101. Nephrogenic Diabetes Insipidus
  102. Chapter 2 V2R Mutations and Nephrogenic Diabetes Insipidus
  103. Is Testing with dDAVP Useful in Detecting Carriers of the Nephrogenic Diabetes insipidus Gene?
  104. Rolipram, a Phosphodiesterase Inhibitor, in the Treatment of Two Male Patients with Congenital Nephrogenic Diabetes insipidus
  105. A novel disease-causing mutation in AVPR2: Q96H
  106. Sodium Excretion in Response to Vasopressin and Selective Vasopressin Receptor Antagonists
  107. Ethnic Differences in Renal Responses to Furosemide
  108. Vasopressin Receptor Mutations in Nephrogenic Diabetes Insipidus
  109. Urinary globotriaosylceramide excretion correlates with the genotype in children and adults with Fabry disease
  110. Polyuria and Diabetes Insipidus
  111. Expression and functionality of the Na+/myo-inositol cotransporter SMIT2 in rabbit kidney
  112. Diabetes insípidas nefrógenas
  113. Diabètes insipides néphrogéniques
  114. Clinical benefits of early treatment with Fabrazyme in Fabry disease
  115. Deterioration of renal function in young adult patients with fabry disease and proteinuria
  116. Diabètes insipides néphrogéniques
  117. Elaboration of a novel technique for purification of plasma membranes from Xenopus laevis oocytes
  118. Severe combined immunodeficiency associated with nephrogenic diabetes insipidus and a deletion in the Xq28 region
  119. Water Metabolism
  120. Hereditary Polyuric Disorders: New Concepts and Differential Diagnosis
  121. Nephrogenic Diabetes Insipidus
  122. Lithium, Cyclic AMP Signaling, A-Kinase Anchoring Proteins, and Aquaporin-2
  123. The dilemma of diagnosing the cause of hypernatraemia: drinking habits vs diabetes insipidus
  124. Pharmacological chaperone action on G-protein-coupled receptors
  125. P011 - Une forme rare de diabète insipide familial : la mutation du gène de la pré-pro AVP
  126. The quest for the gene responsible for medullarycystic kidney disease type 1
  127. Functional Rescue of the Constitutively Internalized V2 Vasopressin Receptor Mutant R137H by the Pharmacological Chaperone Action of SR49059
  128. Pharmacological chaperones: potential treatment for conformational diseases
  129. Reabsorption of Sodium Chloride — Lessons from the Chloride Channels
  130. Diabètes insipides néphrogéniques
  131. Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus
  132. Prix Nobel de Chimie 2003 : canaux hydriques et ioniques
  133. Influence of plasma amino acid level on vasopressin secretion
  134. Un an déjà!
  135. Two Novel Aquaporin-2 Mutations Responsible for Congenital Nephrogenic Diabetes Insipidus in Chinese Families
  136. Life : une étude qui vaprobablement modifiernotre approchedans le traitement del’hypertension artérielle
  137. Intrafamilial phenotype variability in nephrogenic diabetes insipidus
  138. Le changement dans la continuité et la continuité dans le changement
  139. Three Families with Autosomal Dominant Nephrogenic Diabetes Insipidus Caused by Aquaporin-2 Mutations in the C-Terminus
  140. Arginine-vasopressin and oxytocin response to cholecystokinin-tetrapeptide
  141. A patient with partial central diabetes insipidus: Clarifying pathophysiology and designing treatment
  142. Association of Calnexin with Wild Type and Mutant AVPR2 that Cause Nephrogenic Diabetes Insipidus†
  143. Nephrogenic Diabetes Insipidus
  144. 2001, Odyssée de la Science.
  145. Structure de l'aquaporine 1 ou comment bloquer un bâton de relais (le proton) qui se déplace plus vite que le coureur (l'eau) ?
  146. Pharmacological chaperones: a new twist on receptor folding
  147. Pharmacological chaperones rescue cell-surface expression and function of misfolded V2 vasopressin receptor mutants
  148. Des chaperons pharmacologiques pour corriger le diabète insipide néphrogénique ?
  149. The Relationship Among Carbon Dioxide Pneumoperitoneum, Vasopressin Release, and Hemodynamic Changes
  150. The Relationship Among Carbon Dioxide Pneumoperitoneum, Vasopressin Release, and Hemodynamic Changes
  151. Metabolic and Antihypertensive Effects of Nebivolol and Atenolol in Normometabolic Patients with Mild-to-Moderate Hypertension
  152. Diversity of nephrogenic diabetes insipidus mutations and importance of early recognition and treatment
  153. Nephrogenic diabetes insipidus11In collaboration with The American Physiological Society, Thomas E. Andreoli, MD, Editor
  154. The role of the β-noradrenergic system in cholecystokinin-tetrapeptide-induced panic symptoms
  155. Hyponatremia in cirrhosis: From pathogenesis to treatment
  156. Nephrogenic Diabetes Insipidus and Vasopressin Receptor Mutations
  157. Chapter 7 Two genes-one disease: The molecular basis of congenital nephrogenic diabetes insipidus
  158. Diabètes insipides héréditaires : un nouveau gène responsable du syndrome de Wolfram.
  159. Functional Study of Two V2 Vasopressin Mutant Receptors Related to NDI
  160. Étude fonctionnelle de mutations du gène due récepteur V2 responsables d'un diabète insipide néphrogénique congénital
  161. Biochemical Basis of Partial Nephrogenic Diabetes Insipidus Phenotypes
  162. Influence of type A behaviour pattern on response to CCK-4
  163. Chloride channels and hypercalciuria: an unturned stone.
  164. Posterior Pituitary Hormones
  165. Les diabètes insipides néphrogéniques héréditaires
  166. Étude fonctionnelle de mutations du gène du récepteur V2 responsables d'un diabète insipide néphrogénique congénital
  167. Étude fonctionnelle de deux mutations du gène du RV2, responsables d'un diabète insipide néphrogénique lié à l'X
  168. Two novel mutations in the aquaporin-2 and the vasopressin V2 receptor genes in patients with congenital nephrogenic diabetes insipidus
  169. A Peptide Derived from a  2-Adrenergic Receptor Transmembrane Domain Inhibits Both Receptor Dimerization and Activation
  170. Vasopressin receptors in health and disease
  171. Molecular analysis of X-linked nephrogenic diabetes insipidus
  172. Effect of a major depressive episode history on the CCK-4 response in women
  173. The role of the seta adrenergic system in CCK-4 induced panic symptoms
  174. Evidence for a third genetic locus for autosomal dominant polycystic kidney disease
  175. P-1-4 The effects of CCK-4 on plasma arginine-vasopressin and oxytocin levels in women with and without premenstrual dysphoric disorder
  176. Diabetes insipidus
  177. Urinary Excretion of Aquaporin-2 in Patients with Diabetes Insipidus
  178. Evidence for a third genetic locus for autosomal dominant polycystic kidney disease
  179. MOLECULAR BIOLOGY OF DIABETES INSIPIDUS
  180. Prognostic value of neurohumoral activation in patients with an acute myocardial infarction: Effect of captopril
  181. Autosomal dominant polycystic kidney disease in the fetus
  182. N-terminal proatrial natriuretic factor. An independent predictor of long-term prognosis after myocardial infarction
  183. Atrial natriuretic peptide release from the ventricles in response to exercise in dogs with atrioventricular block
  184. Molecular and cellular biology of vasopressin and oxytocin receptor and action in the kidney
  185. X-linked nephrogenic diabetes insipidus mutations in North America and the Hopewell hypothesis.
  186. Activation of neurohumoral systems in postinfarction left ventricular dysfunction
  187. The vasopressin type 2 receptor gene. Chromosomal localization and its role in nephrogenic diabetes insipidus
  188. The Hemodynamic and Coagulant Effects of DDAVP Are Specific Extrarenal V2- Receptor Responses
  189. The Vasopressin Antagonist Sk&F 105494 Inhibits Desmopressin-Stimulated Clotting Factor Release in Vivo
  190. Influence of the level of hydration on the renal response to a protein meal
  191. Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus
  192. Activation of neurohumoral systems following acute myocardial infarction
  193. Platelet vasopressin receptors in patients with congenital nephrogenic diabetes insipidus
  194. Pharmacokinetics of intravenous diltiazem and five of its metabolites in patients with chronic renal failure and in healthy volunteers
  195. Pharmacokinetics of oral diltiazem and five of its metabolites in patients with chronic renal failure
  196. Selective activation of neurohormonal systems in post-infarction left ventricular dysfunction
  197. Sustained beneficial effect of a seventy-two hour intravenous infusion of nitroglycerin in patients with severe chronic congestive heart failure
  198. Epinephrine and dDAVP administration in patients with congenital nephrogenic diabetes insipidus
  199. 12 Water disturbances in cardiac failure
  200. Arginine-vasopressin in congenital nephrogenic diabetes insipidus
  201. Effect of induced ventricular tachycardia on atrial natriuretic peptide in humans
  202. Neurohumoral and hemodynamic changes in congestive heart failure: Lack of correlation and evidence of compensatory mechanisms
  203. Atrial natriuretic peptide in congestive heart failure: Postural changes and reset with chronic captopril therapy
  204. Hemodynamic and Coagulation Responses to 1-Desamino[8-D-Arginine] Vasopressin in Patients with Congenital Nephrogenic Diabetes Insipidus
  205. Chronic renal and neurohumoral effects of the calcium entry blocker nisoldipine in patients with congestive heart failure
  206. Human platelet fraction arginine-vasopressin. Potential physiological role.
  207. Modulation of plasma and platelet vasopressin by cardiac function in patients with heart failure
  208. Sodium excretion in advanced cirrhosis: Effect of expansion of central blood volume and suppression of plasma aldosterone
  209. Differential long-term intrarenal and neurohormonal effects of captopril and prazosin in patients with chronic congestive heart failure: importance of initial plasma renin activity
  210. Hypersécrétion de l'hormone antidiurétique chez l'homme
  211. Syndrome of Inappropriate Antidiuresis in the Absence of Arginine Vasopressin*
  212. Vasopressin in Congestive Heart Failure
  213. Interrelationship between cardiac output and vascular resistance as determinants of effective arterial blood volume in cirrhotic patients
  214. Elevated plasma norepinephrine concentrations in decompensated cirrhosis. Association with increased secretion rates, normal clearance rates, and suppressibility by central blood volume expansion
  215. Role of Arginine-Vasopressin (AVP) in Stress-Induced Inhibition of Testicular Steroidogenesis in Normal and in AVP-Deficient Rats*
  216. Treatment of Hypoosmolar and Hyperosmolar States
  217. Effect of Head-Out Water Immersion on Hepatorenal Syndrome
  218. Sodium and Water Excretion in Patients with Congestive Heart Failure and Cirrhosis
  219. Mechanisms of improvement of water and sodium excretion by immersion in decompensated cirrhotic patients
  220. Potential Role of Increased Sympathetic Activity in Impaired Sodium and Water Excretion in Cirrhosis
  221. Role of Vasopressin in Abnormal Water Excretion in Cirrhotic Patients
  222. EVIDENCE AGAINST CONCEPT OF HYPONATRAEMIA AND "SICK CELLS"
  223. Renal intracortical blood flow and renin secretion after denervation by 6-hydroxydopamine
  224. Radioimmunoassay of Plasma Arginine Vasopressin in Hyponatremic Patients with Congestive Heart Failure
  225. Prevention and Pathogenesis of Acute Renal Failure
  226. Increased circulating plasma catecholamines and plasma renin activity in dogs after chemical sympathectomy with 6-hydroxydopamine
  227. Posterior Pituitary Hormones
  228. Nephrogenic Diabetes Insipidus st[Water and Urea Transport
  229. Insuffisance posthypophysaire au cours de la grossesse