Lista de obras - Carlton Dampier - Dominio Público Uruguay

1-Deamino-8 D-arginine vasopressin decreases the production of 13-hydroxyoctadecadienoic acid by endothelial cells

artículo científico publicado en 1992

A "Narcotics Contract" for a Patient With Sickle Cell Disease and Chronic Pain

scientific article published on 20 June 2011

A prospective study of the role of coping and family functioning in health outcomes for adolescents with sickle cell disease

artículo científico publicado en 2007

AAAPT Diagnostic Criteria for Acute Sickle Cell Disease Pain

scientific article published on 19 December 2018

AAPT Diagnostic Criteria for Chronic Sickle Cell Disease Pain

artículo científico publicado en 2017

Airway hyperreactivity in children with sickle cell disease

artículo científico publicado en 1997

Arthralgias and acidosis

artículo científico publicado en 1995

Assessing responsiveness over time of the PROMIS® pediatric symptom and function measures in cancer, nephrotic syndrome, and sickle cell disease

artículo científico publicado en 2017

Association of red cell spherocytosis with deletion of the short arm of chromosome 8

artículo científico publicado en 1987

Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

artículo científico publicado en 2012

Caregiver report of pain in infants and toddlers with sickle cell disease: reliability and validity of a daily diary

artículo científico publicado en 2002

Characteristics of pain managed at home in children and adolescents with sickle cell disease by using diary self-reports

artículo científico publicado en 2002

Chronic Pain in Adolescent Patients

artículo científico publicado en 1987

Clinical and Laboratory Study of Two Caucasian Families with Hereditary Pyropoikilocytosis and Hereditary Elliptocytosis

scientific article published on 01 July 1987

Clinical trial designs and models for analgesic medications for acute pain in neonates, infants, toddlers, children, and adolescents: ACTTION recommendations

artículo científico publicado en 2017

Cognitive Testing of an Electronic Version of the Faces Pain Scale-Revised with Pediatric and Adolescent Sickle Cell Patients

artículo científico publicado en 2016

Comparing abstract numerical and visual depictions of risk in survey of parental assessment of risk in sickle cell hydroxyurea treatment.

artículo científico publicado en 2011

Definitions of the phenotypic manifestations of sickle cell disease

artículo científico publicado en 2010

Dependence of Ribonucleic Acid Synthesis on Continuous Protein Synthesis in Yeast ⬇️

artículo científico publicado el 1 de febrero de 1972

Development and validation of the self-reported PROMIS pediatric pain behavior item bank and short form scale

artículo científico publicado en 2017

Double-blind, randomized, multicenter phase 2 study of SC411 in children with sickle cell disease (SCOT trial)

artículo científico publicado en 2018

Estimating minimally important difference (MID) in PROMIS pediatric measures using the scale-judgment method

artículo científico publicado en 2015

Executive Functioning Mediates the Relationship Between Pain Coping and Quality of Life in Youth With Sickle Cell Disease

artículo científico publicado en 2018

Fetal hemoglobin in sickle cell anemia: relationship to erythrocyte adhesion markers and adhesion

artículo científico publicado en 2001

Health-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium

artículo científico publicado en 2011

Health-related quality of life in children with sickle cell disease: a report from the Comprehensive Sickle Cell Centers Clinical Trial Consortium

artículo científico publicado en 2010

High dose vitamin D therapy for chronic pain in children and adolescents with sickle cell disease: results of a randomized double blind pilot study

artículo científico publicado en 2012

High-dose cytosine arabinoside and fractionated total body irradiation as a preparative regimen for the treatment of children with acute lymphoblastic leukemia and Down syndrome by allogeneic bone marrow transplantation

artículo científico publicado en 1996

Home management of pain in sickle cell disease: a daily diary study in children and adolescents

artículo científico publicado en 2002

Hypoxaemia in sickle cell disease: biomarker modulation and relevance to pathophysiology

artículo científico publicado en 2003

IMPROVE trial: a randomized controlled trial of patient-controlled analgesia for sickle cell painful episodes: rationale, design challenges, initial experience, and recommendations for future studies

artículo científico publicado en 2013

Impact of PCA strategies on pain intensity and functional assessment measures in adults with sickle cell disease during hospitalized vaso-occlusive episodes.

artículo científico publicado en 2012

Impact of intranasal fentanyl in nurse initiated protocols for sickle cell vaso-occlusive pain episodes in a pediatric emergency department

artículo científico publicado en 2018

Increased levels of the inflammatory biomarker C-reactive protein at baseline are associated with childhood sickle cell vasocclusive crises.

artículo científico publicado en 2009

Increased von Willebrand factor antigen and high molecular weight multimers in sickle cell disease associated with nocturnal hypoxemia.

artículo científico publicado en 2008

Initial Evaluation of the Pediatric PROMIS® Health Domains in Children and Adolescents With Sickle Cell Disease

artículo científico publicado en 2016

Inpatient management of sickle cell pain: a 'snapshot' of current practice.

artículo científico publicado en 2012

Intravenous morphine pharmacokinetics in pediatric patients with sickle cell disease

artículo científico publicado en 1995

Management of Refractory Pain in Hospitalized Adolescents With Sickle Cell Disease

artículo científico publicado en 2014

Measurement of hemoglobin saturation by oxygen in children and adolescents with sickle cell disease

scientific article published on 01 December 1999

Mechanisms of nocturnal oxyhemoglobin desaturation in children and adolescents with sickle cell disease

artículo científico publicado en 1999

New and emerging treatments for vaso-occlusive pain in sickle cell disease

scientific article published on 06 August 2019

Nitric oxide for inhalation in the acute treatment of sickle cell pain crisis: a randomized controlled trial

artículo científico publicado en 2011

Normal saline bolus use in pediatric emergency departments is associated with poorer pain control in children with sickle cell anemia and vaso-occlusive pain.

artículo científico publicado en 2019

Novel findings from the multinational DOVE study on geographic and age-related differences in pain perception and analgesic usage in children with sickle cell anaemia.

artículo científico publicado en 2018

Opioid utilization patterns in United States individuals with sickle cell disease

artículo científico publicado en 2018

Overwhelming pneumococcal septicemia in a patient with HbSC disease and splenic dysfunction

scientific article published on 01 May 1984

PROMIS(®) pediatric self-report scales distinguish subgroups of children within and across six common pediatric chronic health conditions

artículo científico publicado en 2015

Pain characteristics and age-related pain trajectories in infants and young children with sickle cell disease

scientific article published on 24 September 2013

Pain in Children and Adolescents with Sickle Cell Disease: A Descriptive Study

artículo científico publicado en 1990

Parent pain catastrophizing predicts child depressive symptoms in youth with sickle cell disease.

artículo científico publicado en 2018

Pediatric Pain Management

artículo científico publicado en 1998

Pediatric Sickle Cell Disease and Parent and Child Catastrophizing

artículo científico publicado en 2016

Pediatric analgesic clinical trial designs, measures, and extrapolation: report of an FDA scientific workshop

artículo científico publicado en 2012

Pediatric pain screening identifies youth at risk of chronic pain in sickle cell disease

scholarly article by Soumitri Sil et al published 4 November 2018 in Pediatric Blood Cancer

Peripheral arterial tonometry in assessing endothelial dysfunction in pediatric sickle cell disease

artículo científico publicado en 2009

Physical and cognitive-behavioral activities used in the home management of sickle pain: A daily diary study in children and adolescents

scientific article published on 01 November 2004

Prenatally diagnosed non-immune hydrops caused by congenital transient leukaemia

artículo científico publicado en 1994

Psychometric Properties of a Modified Version of the Faces Pain Scale-Revised (Modified FPS-R) to Evaluate Worst Pain in Children and Adolescents With Sickle Cell Anemia

scientific article published on 01 October 2018

Psychosocial and Functional Outcomes in Youth With Chronic Sickle Cell Pain

artículo científico publicado en 2015

Quality of life among adolescents with sickle cell disease: mediation of pain by internalizing symptoms and parenting stress

artículo científico publicado en 2008

Red blood cell alloimmunization in sickle cell disease: prevalence in 2010.

artículo científico publicado en 2012

Reply to comment on: Hydroxyurea and pain history in relation to patient-reported outcomes using PROMIS® measures and the frequency of assessments in sickle cell disease patients

artículo científico publicado en 2016

Responsiveness of PROMIS® Pediatric Measures to Hospitalizations for Sickle Pain and Subsequent Recovery.

artículo científico publicado en 2016

Salmonella infection associated with a pet lizard in siblings with sickle cell anemia: an avoidable risk

artículo científico publicado en 2002

Self-Hypnosis Training as an Adjunctive Treatment in the Management of Pain Associated with Sickle Cell Disease

scientific article published on 01 October 1997

Severity of obstructive sleep apnea in children with sickle cell disease

artículo científico publicado en 2008

SickleREMOTE: A Two-Way Text Messaging System for Pediatric Sickle Cell Disease Patients

artículo científico publicado en 2012

Sleep patterns in pediatric sickle cell disease

artículo científico publicado en 2010

Splenic arteries and veins in pediatric sickle cell disease.

artículo científico publicado en 2001

Stigma and Pain in Adolescents Hospitalized for Sickle Cell Vaso-occlusive Pain Episodes

artículo científico publicado en 2017

Successful utilization of an electronic pain diary in a multinational phase 3 interventional study of pediatric sickle cell anemia

artículo científico publicado en 2017

Symptoms of depression and anxiety in adolescents with sickle cell disease: the role of intrapersonal characteristics and stress processing variables

artículo científico publicado en 2009

Trisomy 11 limited to trisomy 21 cells in a mosaic Down syndrome child with acute myeloid leukemia

artículo científico publicado en 2003

Vaso-occlusion in children with sickle cell disease: clinical characteristics and biologic correlates

artículo científico publicado en 2004

Vitamin D deficiency and chronic pain in sickle cell disease

iCanCope with Sickle Cell Pain: Design of a randomized controlled trial of a smartphone and web-based pain self-management program for youth with sickle cell disease

artículo científico publicado en 2018

Lista de obras de Carlton Dampier

1-Deamino-8 D-arginine vasopressin decreases the production of 13-hydroxyoctadecadienoic acid by endothelial cells

A "Narcotics Contract" for a Patient With Sickle Cell Disease and Chronic Pain

A prospective study of the role of coping and family functioning in health outcomes for adolescents with sickle cell disease

AAAPT Diagnostic Criteria for Acute Sickle Cell Disease Pain

AAPT Diagnostic Criteria for Chronic Sickle Cell Disease Pain

Airway hyperreactivity in children with sickle cell disease

Arthralgias and acidosis

Assessing responsiveness over time of the PROMIS® pediatric symptom and function measures in cancer, nephrotic syndrome, and sickle cell disease

Association of red cell spherocytosis with deletion of the short arm of chromosome 8

Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

Caregiver report of pain in infants and toddlers with sickle cell disease: reliability and validity of a daily diary

Characteristics of pain managed at home in children and adolescents with sickle cell disease by using diary self-reports

Chronic Pain in Adolescent Patients

Clinical and Laboratory Study of Two Caucasian Families with Hereditary Pyropoikilocytosis and Hereditary Elliptocytosis

Clinical trial designs and models for analgesic medications for acute pain in neonates, infants, toddlers, children, and adolescents: ACTTION recommendations

Cognitive Testing of an Electronic Version of the Faces Pain Scale-Revised with Pediatric and Adolescent Sickle Cell Patients

Comparing abstract numerical and visual depictions of risk in survey of parental assessment of risk in sickle cell hydroxyurea treatment.

Definitions of the phenotypic manifestations of sickle cell disease

Dependence of Ribonucleic Acid Synthesis on Continuous Protein Synthesis in Yeast ⬇️

Development and validation of the self-reported PROMIS pediatric pain behavior item bank and short form scale

Double-blind, randomized, multicenter phase 2 study of SC411 in children with sickle cell disease (SCOT trial)

Estimating minimally important difference (MID) in PROMIS pediatric measures using the scale-judgment method

Executive Functioning Mediates the Relationship Between Pain Coping and Quality of Life in Youth With Sickle Cell Disease

Fetal hemoglobin in sickle cell anemia: relationship to erythrocyte adhesion markers and adhesion

Health-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium

Health-related quality of life in children with sickle cell disease: a report from the Comprehensive Sickle Cell Centers Clinical Trial Consortium

High dose vitamin D therapy for chronic pain in children and adolescents with sickle cell disease: results of a randomized double blind pilot study

High-dose cytosine arabinoside and fractionated total body irradiation as a preparative regimen for the treatment of children with acute lymphoblastic leukemia and Down syndrome by allogeneic bone marrow transplantation

Home management of pain in sickle cell disease: a daily diary study in children and adolescents

Hypoxaemia in sickle cell disease: biomarker modulation and relevance to pathophysiology

IMPROVE trial: a randomized controlled trial of patient-controlled analgesia for sickle cell painful episodes: rationale, design challenges, initial experience, and recommendations for future studies

Impact of PCA strategies on pain intensity and functional assessment measures in adults with sickle cell disease during hospitalized vaso-occlusive episodes.

Impact of intranasal fentanyl in nurse initiated protocols for sickle cell vaso-occlusive pain episodes in a pediatric emergency department

Increased levels of the inflammatory biomarker C-reactive protein at baseline are associated with childhood sickle cell vasocclusive crises.

Increased von Willebrand factor antigen and high molecular weight multimers in sickle cell disease associated with nocturnal hypoxemia.

Initial Evaluation of the Pediatric PROMIS® Health Domains in Children and Adolescents With Sickle Cell Disease

Inpatient management of sickle cell pain: a 'snapshot' of current practice.

Intravenous morphine pharmacokinetics in pediatric patients with sickle cell disease

Management of Refractory Pain in Hospitalized Adolescents With Sickle Cell Disease

Measurement of hemoglobin saturation by oxygen in children and adolescents with sickle cell disease

Mechanisms of nocturnal oxyhemoglobin desaturation in children and adolescents with sickle cell disease

New and emerging treatments for vaso-occlusive pain in sickle cell disease

Nitric oxide for inhalation in the acute treatment of sickle cell pain crisis: a randomized controlled trial

Normal saline bolus use in pediatric emergency departments is associated with poorer pain control in children with sickle cell anemia and vaso-occlusive pain.

Novel findings from the multinational DOVE study on geographic and age-related differences in pain perception and analgesic usage in children with sickle cell anaemia.

Opioid utilization patterns in United States individuals with sickle cell disease

Overwhelming pneumococcal septicemia in a patient with HbSC disease and splenic dysfunction

PROMIS(®) pediatric self-report scales distinguish subgroups of children within and across six common pediatric chronic health conditions

Pain characteristics and age-related pain trajectories in infants and young children with sickle cell disease

Pain in Children and Adolescents with Sickle Cell Disease: A Descriptive Study

Parent pain catastrophizing predicts child depressive symptoms in youth with sickle cell disease.

Pediatric Pain Management

Pediatric Sickle Cell Disease and Parent and Child Catastrophizing

Pediatric analgesic clinical trial designs, measures, and extrapolation: report of an FDA scientific workshop

Pediatric pain screening identifies youth at risk of chronic pain in sickle cell disease

Peripheral arterial tonometry in assessing endothelial dysfunction in pediatric sickle cell disease

Physical and cognitive-behavioral activities used in the home management of sickle pain: A daily diary study in children and adolescents

Prenatally diagnosed non-immune hydrops caused by congenital transient leukaemia

Psychometric Properties of a Modified Version of the Faces Pain Scale-Revised (Modified FPS-R) to Evaluate Worst Pain in Children and Adolescents With Sickle Cell Anemia

Psychosocial and Functional Outcomes in Youth With Chronic Sickle Cell Pain

Quality of life among adolescents with sickle cell disease: mediation of pain by internalizing symptoms and parenting stress

Red blood cell alloimmunization in sickle cell disease: prevalence in 2010.

Reply to comment on: Hydroxyurea and pain history in relation to patient-reported outcomes using PROMIS® measures and the frequency of assessments in sickle cell disease patients

Responsiveness of PROMIS® Pediatric Measures to Hospitalizations for Sickle Pain and Subsequent Recovery.

Salmonella infection associated with a pet lizard in siblings with sickle cell anemia: an avoidable risk

Self-Hypnosis Training as an Adjunctive Treatment in the Management of Pain Associated with Sickle Cell Disease

Severity of obstructive sleep apnea in children with sickle cell disease

SickleREMOTE: A Two-Way Text Messaging System for Pediatric Sickle Cell Disease Patients

Sleep patterns in pediatric sickle cell disease

Splenic arteries and veins in pediatric sickle cell disease.

Stigma and Pain in Adolescents Hospitalized for Sickle Cell Vaso-occlusive Pain Episodes

Successful utilization of an electronic pain diary in a multinational phase 3 interventional study of pediatric sickle cell anemia

Symptoms of depression and anxiety in adolescents with sickle cell disease: the role of intrapersonal characteristics and stress processing variables

Trisomy 11 limited to trisomy 21 cells in a mosaic Down syndrome child with acute myeloid leukemia

Vaso-occlusion in children with sickle cell disease: clinical characteristics and biologic correlates

Vitamin D deficiency and chronic pain in sickle cell disease

iCanCope with Sickle Cell Pain: Design of a randomized controlled trial of a smartphone and web-based pain self-management program for youth with sickle cell disease