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  • Laura Preston Barnes, Msn, Cnaa, Is Nursing Direct

LAURA PRESTON BARNES, MSN, CNAA, is nursing direct: Influence Statistics

LAURA PRESTON BARNES MSN CNAA : Expert Impact

Concepts for which LAURA PRESTON BARNES MSN CNAA has direct influence: Pediatric patients , Peer victimization , Intravenous lipid emulsion , Newborn screening , Neonatal abstinence syndrome , Functional impairment , Therapeutic assessment .

LAURA PRESTON BARNES MSN CNAA : KOL impact

Concepts related to the work of other authors for which for which LAURA PRESTON BARNES MSN CNAA has influence: Fabry disease , Chronic pain , Pyloric stenosis , Eosinophilic esophagitis , Agalsidase alfa , Selenium deficiency , Juvenile fibromyalgia .

KOL Resume for LAURA PRESTON BARNES, MSN, CNAA, is nursing direct

Year

Prominent publications by LAURA PRESTON BARNES, MSN, CNAA, is nursing direct

KOL-Index: 11443 . Children not accepted or actively rejected by peers are at greater risk for peer victimization. We examined whether a positive teacher-student relationship can potentially buffer these children from the risk of peer victimization. Participants were 361 elementary school children in the 4th or 5th grade. Peer-report measures were used to assess teacher-student relationship quality (TSRQ), ...
Known for Peer Victimization | Social Preference | Protective Role | School Children
KOL-Index: 9172 . Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal dysplasia due to mutations causing haploinsufficiency of RUNX2, an osteoblast transcription factor specific for bone and cartilage. The classic form of CCD is characterized by delayed closure of the fontanels, hypoplastic or aplastic clavicles and dental anomalies. Clinical reports suggest that a subset of patients with ...
Known for Cleidocranial Dysplasia | Runx2 Ccd | Dental Anomalies | Delayed Closure
KOL-Index: 9113 . Background: Lamin A/C (LMNA) gene mutations cause a heterogeneous group of progeroid disorders, including Hutchinson-Gilford progeria syndrome, mandibuloacral dysplasia, and atypical progeroid syndrome (APS). Five of the 31 previously reported patients with APS harbored a recurrent de novo heterozygous LMNA p.T10I mutation. All five had generalized lipodystrophy, as well as similar ...
Known for Generalized Lipodystrophy | Progeroid Syndrome | Heterozygous Lmna | Metabolic Complications
KOL-Index: 9090 . BACKGROUND: Acute viral bronchiolitis is the most common diagnosis resulting in hospital admission in pediatrics. Utilization of non-evidence-based therapies and testing remains common despite a large volume of evidence to guide quality improvement efforts. OBJECTIVE: Our objective was to reduce utilization of unnecessary therapies in the inpatient care of bronchiolitis across a diverse ...
Known for Acute Bronchiolitis | Chest Radiography | Viral Testing | United States
KOL-Index: 8641 . BACKGROUND: In February, 1999, a local US health department identified a cluster of pertussis cases among neonates born at a community hospital and recommended oral erythromycin for post-exposure prophylaxis for about 200 neonates born at that hospital between Feb 1 and Feb 24, 1999. We investigated a cluster of seven cases of infantile hypertrophic pyloric stenosis (IHPS) that occurred ...
Known for Erythromycin Ihps | Pyloric Stenosis | Infantile Hypertrophic | Pertussis Cases
KOL-Index: 8393 . PurposeWe explore whether Machiavellianism—a personality trait which describes the extent to which individuals ignore values and ethical considerations when the ends justify the means—will influence their responses to their employing organizations’ failure to fulfil promised obligations (psychological contracts). Specifically, we draw on psychological contracts theory and the group value ...
Known for Organizational Identification | Psychological Contract | Time Employees | Personality Trait
KOL-Index: 7958 . The developmental and epileptic encephalopathies (DEEs) are heterogeneous disorders with a strong genetic contribution, but the underlying genetic etiology remains unknown in a significant proportion of individuals. To explore whether statistical support for genetic etiologies can be generated on the basis of phenotypic features, we analyzed whole-exome sequencing data and phenotypic ...
Known for Adaptor Protein | Mediated Endocytosis | Ap2 Complex | Neurodevelopmental Disorders
KOL-Index: 7681 . OBJECTIVE: To identify and summarize published cases in which intravenous lipid emulsion was used to treat pediatric patients with acute drug toxicities. DATA SOURCES: PubMed, SCOPUS, and EMBASE were searched up to December 2012 for relevant publications using the terms fat emulsion, lipid emulsion, Intralipid, Liposyn, Medialipide, Medialipid, lipid rescue, ILE, IVLE, IFE, IVFE, or lipid ...
Known for Intravenous Lipid Emulsion | Pediatric Patients | Local Anesthetics | Systemic Toxicity
KOL-Index: 7543 . OBJECTIVE: Family factors and emotional functioning can play an important role in the ability of adolescents with juvenile primary fibromyalgia syndrome (JPFS) to cope with their condition and function in their everyday lives. The primary objectives of this study were to determine 1) whether adolescents with JPFS and their caregivers differed from healthy age-matched comparison peers and ...
Known for Functional Impairment | Adolescents Jpfs | Emotional Functioning | Fibromyalgia Syndrome
KOL-Index: 6919 . PURPOSE: To prospectively determine if children who present with a unilateral inguinal hernia can be identified as at risk for developing a metachronous inguinal hernia (MIH) based on risk factors and laparoscopic findings of the contralateral internal ring. MATERIALS AND METHODS: Between April 2000 and October 2004, 299 patients with a unilateral inguinal hernia were followed ...
Known for Inguinal Hernia | Laparoscopic Findings | Bilateral Repair | 14 Girls
KOL-Index: 6767 . WHIM syndrome is an autosomal dominant immunodeficiency disease caused by mutations affecting the carboxy-terminus of CXCR4. To characterize novel genetic causes of the syndrome, we recruited a pediatric patient with possible WHIM syndrome, performed CXCR4 gene sequencing and compared his clinical phenotype and CXCR4 tail amino acid sequences with other patients with WHIM syndrome carrying ...
Known for Cxcr4 Gene | Receptor Downregulation | Syndrome Caused | Immunodeficiency Diseases
KOL-Index: 6668 . OBJECTIVE: To determine if high-dose cyclophosphamide is an effective therapy for children with refractory severe aplastic anemia (SAA). BACKGROUND: SAA is an illness characterized by the depletion of hematopoietic precursors associated with life-threatening complications. Hematopoietic stem cell transplant (HSCT) is the treatment of choice if a human leukocyte antigen (HLA)-related donor ...
Known for Dose Cyclophosphamide | Aplastic Anemia | Children Saa | Immunosuppressive Therapy
KOL-Index: 6477 . Three cases of meningitis due to multidrug-resistant serotype 14 Streptococcus pneumoniae occurred at a day care center (DCC) over 5 days. Cultures of nasopharyngeal samples were done at the index DCC, 2 comparison DCCs, and a pediatrics practice. Isolates were serotyped and subtyped by pulsed-field gel electrophoresis (PFGE) with SmaI. Pneumococcal carriage rates ranged from 44%-65% at ...
Known for Streptococcus Pneumoniae | Microbial Drug Resistance | Day Center | Pneumococcal Carriage
KOL-Index: 6063 . Enzyme-based newborn screening for Mucopolysaccharidosis type I (MPS I) has a high false-positive rate due to the prevalence of pseudodeficiency alleles, often resulting in unnecessary and costly follow up. The glycosaminoglycans (GAGs), dermatan sulfate (DS) and heparan sulfate (HS) are both substrates for α-l-iduronidase (IDUA). These GAGs are elevated in patients with MPS I and have ...
Known for Newborn Screening | Mucopolysaccharidosis Type | Patients Mps | Heparan Sulfate
KOL-Index: 6054 . BACKGROUND: To evaluate the role of in utero exposure to metronidazole (a carcinogen in some animal models) and the risk of subsequent cancer, the authors conducted a retrospective cohort study of childhood cancer. METHODS: The cohort included 328,846 children younger than 5 years born to women enrolled in Tennessee Medicaid at any time between the last menstrual period (LMP) and the date ...
Known for Childhood Cancer | Prenatal Exposure | Metronidazole Risk | Tennessee Medicaid

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