General Clinical Research Center View Homepage


Ontology type: schema:MonetaryGrant     


Grant Info

YEARS

1976-2006

FUNDING AMOUNT

15325906 USD

ABSTRACT

N/A

URL

http://projectreporter.nih.gov/project_info_description.cfm?aid=7015779

Related SciGraph Publications

  • 2017-12. Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus in NATURE COMMUNICATIONS
  • 2015-12. Total Energy Expenditure of Infants with Congenital Heart Disease Who Have Undergone Surgical Intervention in PEDIATRIC CARDIOLOGY
  • 2013-10. 22q11.2 Deletions in Patients with Conotruncal Defects: Data from 1,610 Consecutive Cases in PEDIATRIC CARDIOLOGY
  • 2012-02. Maternal obesity associated with inflammation in their children in WORLD JOURNAL OF PEDIATRICS
  • 2012. Use of Segmental Lengths for the Assessment of Growth in Children with Cerebral Palsy in HANDBOOK OF ANTHROPOMETRY
  • 2012. The Ketogenic Diet and Brain Metabolism in NEURAL METABOLISM IN VIVO
  • 2011-09. Pilot trial of late booster doses of surfactant for ventilated premature infants in JOURNAL OF PERINATOLOGY
  • 2010-04. Inhaled nitric oxide in premature infants: effect on tracheal aspirate and plasma nitric oxide metabolites in JOURNAL OF PERINATOLOGY
  • 2008-10. A T-cell-specific CD154 transcriptional enhancer located just upstream of the promoter in GENES & IMMUNITY
  • 2008-02. Perceived Stress is Associated with Impaired T-Cell Response to HPV16 in Women with Cervical Dysplasia in ANNALS OF BEHAVIORAL MEDICINE
  • 2007-12. The effect of inhaled nitric oxide on pulmonary function in preterm infants in JOURNAL OF PERINATOLOGY
  • 2007-07. Dietary energy density increases during early childhood irrespective of familial predisposition to obesity: results from a prospective cohort study in INTERNATIONAL JOURNAL OF OBESITY
  • 2007-05. Effects of Delayed Pubertal Development, Nutritional Status, and Disease Severity on Longitudinal Patterns of Growth Failure in Children With Sickle Cell Disease in PEDIATRIC RESEARCH
  • 2007-04. CD8+ T-cell responses to adeno-associated virus capsid in humans in NATURE MEDICINE
  • 2006-08. Loss of function polymorphisms in NAT1 protect against spina bifida in HUMAN GENETICS
  • 2006. Hyperinsulinism of Infancy: Localization of Focal Forms in PEDIATRIC PET IMAGING
  • 2006-01. Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism in MODERN PATHOLOGY
  • 2005-04. Molecular analysis of congenital scoliosis: a candidate gene approach in HUMAN GENETICS
  • 2005-04. Molecular characterization of histidinemia: identification of four missense mutations in the histidase gene in HUMAN GENETICS
  • 2005-01. Vitamin D insufficiency in steroid-sensitive nephrotic syndrome in remission in PEDIATRIC NEPHROLOGY
  • 2004-12. Dysfunction of Pulmonary Surfactant in Chronically Ventilated Premature Infants in PEDIATRIC RESEARCH
  • 2004-11. The human T locus and spina bifida risk in HUMAN GENETICS
  • 2004-04. Predictors of body size in the first 2 y of life: a high-risk study of human obesity in INTERNATIONAL JOURNAL OF OBESITY
  • 2004-01. Bone disease in pediatric rheumatologic disorders in CURRENT RHEUMATOLOGY REPORTS
  • 2003-09. Histopathology of Congenital Hyperinsulinism: Retrospective Study with Genotype Correlations in PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
  • 2003-01. Body composition and metabolic factors in obese children and adolescents in INTERNATIONAL JOURNAL OF OBESITY
  • 2002-03. Multiple Courses of Antenatal Corticosteroids are Associated With Early Severe Lung Disease in Preterm Neonates in JOURNAL OF PERINATOLOGY
  • 2001-09. Hyperinsulinism and Hyperammonemia Syndrome: Report of Twelve Unrelated Patients in PEDIATRIC RESEARCH
  • 2001-04. A diagnostic approach to identifying submicroscopic 7p21 deletions in Saethre-Chotzen syndrome: Fluorescence in situ hybridization and dosage-sensitive Southern blot analysis in GENETICS IN MEDICINE
  • 2001-03. Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Clinical Course and Description of Causal Mutations in Two Patients in PEDIATRIC RESEARCH
  • 2000-09. Galactose Breath Testing Distinguishes Variant and Severe Galactose-1-Phosphate Uridyltransferase Genotypes in PEDIATRIC RESEARCH
  • 1999-02. Weights of parents and infants: Is there a relationship? in INTERNATIONAL JOURNAL OF OBESITY
  • 1999-01. Bone marrow transplantation in pediatric patients with therapy-related myelodysplasia and leukemia in BONE MARROW TRANSPLANTATION
  • 1998-06. In vivo measurement of ureagenesis with stable isotopes in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1998-03. Linkage-disequilibrium mapping without genotyping in NATURE GENETICS
  • 1997-04. Purine Metabolism and Inhibition of Xanthine Oxidase in Severely Hypoxic Neonates Going onto Extracorporeal Membrane Oxygenation1 in PEDIATRIC RESEARCH
  • 1996-10. Prospective Evaluation of Resting Energy Expenditure, Nutritional Status, Pulmonary Function, and Genotype in Children with Cystic Fibrosis in PEDIATRIC RESEARCH
  • 1994-04. Energy Expenditure and Genotype of Children with Cystic Fibrosis in PEDIATRIC RESEARCH
  • 1994-01. In Vitro and In Vivo Effects of Granulocyte Colony-Stimulating Factor on Neutrophils in Glycogen Storage Disease Type IB: Granulocyte Colony-Stimulating Factor Therapy Corrects the Neutropenia and the Defects in Respiratory Burst Activity and Ca2+ Mobilization in PEDIATRIC RESEARCH
  • 1993-09. Interferon-γ Corrects the Respiratory Burst Defect In Vitro in Monocyte-Derived Macrophages from Glycogen Storage Disease Type 1b Patients in PEDIATRIC RESEARCH
  • 1993-07. Renal Handling of Carnitine in Secondary Carnitine Deficiency Disorders in PEDIATRIC RESEARCH
  • 1993-01. The effect of lovastatin on very low-density lipoprotein apolipoprotein B production by the liver in familial combined hyperlipidaemia in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1993-01. Impairment of calcium mobilization in phagocytic cells in glycogen storage disease type 1b in EUROPEAN JOURNAL OF PEDIATRICS
  • 1992-09. Elevated plasma carnitine in the hepatic form of carnitine palmitoyltransferase-1 deficiency in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1991-11. Familial combined hyperlipidaemia: Use of stable isotopes to demonstrate overproduction of very low-density lipoprotein apolipoprotein B by the liver in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1990-07. Bone mineral content in black pre-schoolers: Normative data using single photon absorptiometry in PEDIATRIC RADIOLOGY
  • 1989-06. Medium-chain acyl-CoA dehydrogenase deficiency: Metabolic effects and therapeutic efficacy of long-terml-carnitine supplementation in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989-06. Hyperfiltration and renal disease in glycogen storage disease, type I in KIDNEY INTERNATIONAL
  • 1987-01. Albumin Synthesis in Premature Infants: Determination of Turnover with [15N]Glycine in PEDIATRIC RESEARCH
  • 1986-05. Impaired Chemotaxis and Neutrophil (Polymorphonuclear Leukocyte) Function in Glycogenosis Type IB in PEDIATRIC RESEARCH
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