Publications by authors named "Sandra C Van Calcar"

20Publications

Bone Health in Classic Galactosemia: Systematic Review and Meta-Analysis.

JIMD Rep 2017 20;35:87-96. Epub 2016 Dec 20.

Department of Pediatrics, Academic Medical Center, Emma Children's Hospital, University of Amsterdam, Amsterdam, The Netherlands.

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December 2016

Abnormal Eating Behaviors Are Common in Children with Fetal Alcohol Spectrum Disorder.

J Pediatr 2016 Feb 19;169:194-200.e1. Epub 2015 Nov 19.

Department of Nutritional Sciences, University of Wisconsin-Madison, Madison, WI; Waisman Center for Neurodisabilities, University of Wisconsin-Madison, Madison, WI. Electronic address:

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February 2016

A re-evaluation of life-long severe galactose restriction for the nutrition management of classic galactosemia.

Mol Genet Metab 2014 Jul 2;112(3):191-7. Epub 2014 May 2.

Division of Genetics and Genomics, Metabolism Program, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA. Electronic address:

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July 2014

Galactose content of legumes, caseinates, and some hard cheeses: implications for diet treatment of classic galactosemia.

J Agric Food Chem 2014 Feb 3;62(6):1397-402. Epub 2014 Feb 3.

Division of Genetics and Metabolism, Department of Pediatrics, School of Medicine and Public Health, University of Wisconsin-Madison , 1500 Highland Avenue, Madison, Wisconsin 53705, United States.

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February 2014

Recommendations for the nutrition management of phenylalanine hydroxylase deficiency.

Genet Med 2014 Feb 2;16(2):121-31. Epub 2014 Jan 2.

Division of Genetics and Metabolism, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

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February 2014

Inappropriate feeding behaviors and dietary intakes in children with fetal alcohol spectrum disorder or probable prenatal alcohol exposure.

Alcohol Clin Exp Res 2014 Mar 24;38(3):871-8. Epub 2013 Oct 24.

Waisman Center, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin; Department of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin.

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March 2014

Newborn screening 50 years later: access issues faced by adults with PKU.

Genet Med 2013 Aug 7;15(8):591-9. Epub 2013 Mar 7.

Department of Pediatrics, Division of Genetics and Metabolism, University of Minnesota, Minneapolis, MN, USA.

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August 2013

Food products made with glycomacropeptide, a low-phenylalanine whey protein, provide a new alternative to amino Acid-based medical foods for nutrition management of phenylketonuria.

J Acad Nutr Diet 2012 Aug;112(8):1201-10

Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, WI 53703, USA.

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August 2012

Breakfast with glycomacropeptide compared with amino acids suppresses plasma ghrelin levels in individuals with phenylketonuria.

Mol Genet Metab 2010 Aug 14;100(4):303-8. Epub 2010 Apr 14.

Department of Nutritional Sciences, 1415 Linden Dr., University of Wisconsin, Madison, Wisconsin 53706, USA.

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August 2010

Reassessment of phenylalanine tolerance in adults with phenylketonuria is needed as body mass changes.

Mol Genet Metab 2009 Dec 8;98(4):331-7. Epub 2009 Aug 8.

Department of Nutritional Sciences, 1415 Linden Drive, University of Wisconsin, Madison, WI 53705, USA.

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December 2009

Acceptable low-phenylalanine foods and beverages can be made with glycomacropeptide from cheese whey for individuals with PKU.

Mol Genet Metab 2007 Sep-Oct;92(1-2):176-8. Epub 2007 Jul 23.

Wisconsin Center for Dairy Research, University of Wisconsin, Madison, WI 53706, USA.

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November 2007

L-carnitine administration reduces number of episodes in cyclic vomiting syndrome.

Clin Pediatr (Phila) 2002 Apr;41(3):171-4

Biochemical Genetics Program, Waisman Center, University of Wisconsin-Madison, USA.

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April 2002