Georgianne L Arnold

Summary

Affiliation: University of Rochester
Country: USA

Publications

  1. ncbi Iron and protein sufficiency and red cell indices in phenylketonuria
    G L Arnold
    Department of Pediatrics, University of Rochester School of Medicine and Dentistry, New York 14642, USA
    J Am Coll Nutr 20:65-70. 2001
  2. ncbi Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State
    Georgianne L Arnold
    Department of Pediatrics, University of Rochester School of Medicine and Dentistry, 601 Elmwood Avenue, Box 777, Rochester, NY 14642, USA
    Mol Genet Metab 99:263-8. 2010
  3. ncbi A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency
    Georgianne L Arnold
    Department of Pediatrics, University of Rochester, School of Medicine and Dentistry, Rochester, NY 14642, USA
    Mol Genet Metab 96:85-90. 2009
  4. ncbi A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency
    Georgianne L Arnold
    Department of Pediatrics, University of Rochester School of Medicine and Dentistry, 601 Elmwood Avenue, Box 777, Rochester, NY 14642, USA
    Mol Genet Metab 93:363-70. 2008
  5. ncbi Prevalence of stimulant use for attentional dysfunction in children with phenylketonuria
    G L Arnold
    Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
    J Inherit Metab Dis 27:137-43. 2004
  6. ncbi Plasma amino acids profiles in children with autism: potential risk of nutritional deficiencies
    Georgianne L Arnold
    Department of Pediatrics, University of Rochester Medical Center, Rochester, New York 14642, USA
    J Autism Dev Disord 33:449-54. 2003
  7. ncbi Protein insufficiency and linear growth restriction in phenylketonuria
    Georgianne L Arnold
    Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, New York 14642, USA
    J Pediatr 141:243-6. 2002
  8. ncbi Universal nephroblastomatosis with bilateral hyperplastic nephromegaly in siblings
    Philip J Katzman
    Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA
    Pediatr Dev Pathol 12:47-52. 2009
  9. ncbi Parents' experiences of expanded newborn screening evaluations
    Jane M Deluca
    University of Rochester, School of Nursing, 601 Elmwood Ave, Box SON, Rochester, NY 14642, USA
    Pediatrics 128:53-61. 2011
  10. ncbi Improved growth and nutrition status in children with methylmalonic or propionic acidemia fed an elemental medical food
    Steven Yannicelli
    Ross Products Division, Abbott Laboratories, 625 Cleveland Avenue, Columbus, OH 43215-1724, USA
    Mol Genet Metab 80:181-8. 2003

Research Grants

  1. Attentional Dysfunction in Children with Phenylketonuria
    Georgianne Arnold; Fiscal Year: 2007

Collaborators

Detail Information

Publications10

  1. ncbi Iron and protein sufficiency and red cell indices in phenylketonuria
    G L Arnold
    Department of Pediatrics, University of Rochester School of Medicine and Dentistry, New York 14642, USA
    J Am Coll Nutr 20:65-70. 2001
    ..We reviewed records of 41 children with treated phenylketonuria (PKU) in order to evaluate hematopoiesis and the effect of iron and protein sufficiency...
  2. ncbi Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State
    Georgianne L Arnold
    Department of Pediatrics, University of Rochester School of Medicine and Dentistry, 601 Elmwood Avenue, Box 777, Rochester, NY 14642, USA
    Mol Genet Metab 99:263-8. 2010
    ..We reviewed the outcome of patients identified with MCAD deficiency by the New York State NBS process to identify biochemical or genotypic markers which might predict outcome...
  3. ncbi A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency
    Georgianne L Arnold
    Department of Pediatrics, University of Rochester, School of Medicine and Dentistry, Rochester, NY 14642, USA
    Mol Genet Metab 96:85-90. 2009
    ..This consensus protocol is intended to assist clinicians in the diagnosis and management of screen-positive newborns for VLCAD deficiency until evidence-based guidelines are available...
  4. ncbi A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency
    Georgianne L Arnold
    Department of Pediatrics, University of Rochester School of Medicine and Dentistry, 601 Elmwood Avenue, Box 777, Rochester, NY 14642, USA
    Mol Genet Metab 93:363-70. 2008
    ..This consensus protocol is intended to assist clinicians in the diagnosis and management of screen-positive newborns for 3-MCC deficiency and to encourage the development of evidence-based guidelines...
  5. ncbi Prevalence of stimulant use for attentional dysfunction in children with phenylketonuria
    G L Arnold
    Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
    J Inherit Metab Dis 27:137-43. 2004
    ..Stimulant use and parent reports of attentional dysfunction are quite common in our PKU patients and appear to be strongly related to higher phenylalanine concentrations...
  6. ncbi Plasma amino acids profiles in children with autism: potential risk of nutritional deficiencies
    Georgianne L Arnold
    Department of Pediatrics, University of Rochester Medical Center, Rochester, New York 14642, USA
    J Autism Dev Disord 33:449-54. 2003
    ..The high rate of tryptophan and tyrosine deficiency in this group is also of concern given their role as neurotransmitter precursors...
  7. ncbi Protein insufficiency and linear growth restriction in phenylketonuria
    Georgianne L Arnold
    Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, New York 14642, USA
    J Pediatr 141:243-6. 2002
    ..We suggest that a plasma prealbumin level of at least 20 mg/dL is necessary for optimal growth in children with PKU...
  8. ncbi Universal nephroblastomatosis with bilateral hyperplastic nephromegaly in siblings
    Philip J Katzman
    Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA
    Pediatr Dev Pathol 12:47-52. 2009
    ..The pathology was most consistent with universal nephroblastomatosis with nephromegaly, a rare entity described in only 4 cases and in only 1 of these as a possible inherited disorder...
  9. ncbi Parents' experiences of expanded newborn screening evaluations
    Jane M Deluca
    University of Rochester, School of Nursing, 601 Elmwood Ave, Box SON, Rochester, NY 14642, USA
    Pediatrics 128:53-61. 2011
    ..Abnormal results of newborn screening for common metabolic diseases are known to create substantial distress for parents. We explored parents' perceptions during diagnostic evaluations for newer disorders that are less well understood...
  10. ncbi Improved growth and nutrition status in children with methylmalonic or propionic acidemia fed an elemental medical food
    Steven Yannicelli
    Ross Products Division, Abbott Laboratories, 625 Cleveland Avenue, Columbus, OH 43215-1724, USA
    Mol Genet Metab 80:181-8. 2003
    ..Providing energy and protein for patients with FTT at intakes recommended for catch-up growth may have resulted in even better growth...

Research Grants2

  1. Attentional Dysfunction in Children with Phenylketonuria
    Georgianne Arnold; Fiscal Year: 2007
    ....