Publications by authors named "Sandra van Calcar"

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Corrigendum to "Evaluating change in diet with pegvaliase treatment in adults with phenylketonuria: Analysis of phase 3 clinical trial data" [Molecular Genetics and Metabolism 141, Issue 3 (2024) 108122].
Fran Rohr, Barbara Burton, Anne Dee, Cary O Harding, Joshua Lilienstein, Sandra van Calcar

Mol Genet Metab· December 2024

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The efficacy of Carbamylglutamate impacts the nutritional management of patients with N-Acetylglutamate synthase deficiency.
Rani H Singh, Marie-Hélène Bourdages, Angela Kurtz, Erin MacLoed, Chelsea Norman, Sandra C van Calcar

Orphanet J Rare Dis· April 2024

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Evaluating change in diet with pegvaliase treatment in adults with phenylketonuria: Analysis of phase 3 clinical trial data.
Fran Rohr, Barbara Burton, Anne Dee, Cary O Harding, Joshua Lilienstein, Sandra van Calcar

Mol Genet Metab· March 2024

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The Effect of Preoperative Carbohydrate Intake on Length of Stay and Postoperative Recovery Following Laparoscopic Living Donor Nephrectomy.
Morgan Kuiper, Melanie Gillingham, Julie Martin, Daniella Gardner, Sandra Van Calcar

J Ren Nutr· May 2023

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Simplified Diet for nutrition management of phenylketonuria: A survey of U.S. metabolic dietitians.
Joyanna Hansen, Suzanne Hollander, Nicoletta Drilias, Sandra Van Calcar, Fran Rohr

JIMD Rep· May 2020

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Metabolomic Insights into the Nutritional Status of Adults and Adolescents with Phenylketonuria Consuming a Low-Phenylalanine Diet in Combination with Amino Acid and Glycomacropeptide Medical Foods.
Bridget M Stroup, Denise M Ney, Sangita G Murali, Frances Rohr, Sally T Gleason, Sandra C van Calcar

J Nutr Metab· December 2017

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Development of carrier testing for common inborn errors of metabolism in the Wisconsin Plain population.
Ashley Kuhl, Sandra van Calcar, Mei Baker, Christine M Seroogy, Gregory Rice

Genet Med· March 2017

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International clinical guideline for the management of classical galactosemia: diagnosis, treatment, and follow-up.
Lindsey Welling, Laurie E Bernstein, Gerard T Berry, Alberto B Burlina, François Eyskens, Sandra C Van Calcar

J Inherit Metab Dis· March 2017

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Bone Health in Classic Galactosemia: Systematic Review and Meta-Analysis.
Britt van Erven, Lindsey Welling, Sandra C van Calcar, Artemis Doulgeraki, François Eyskens

JIMD Rep· December 2016

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Successful pregnancy and delivery in a woman with propionic acidemia from the Amish community.
Jessica Scott Schwoerer, Sandra van Calcar, Gregory M Rice, James Deline

Mol Genet Metab Rep· September 2016

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Outcomes and genotype-phenotype correlations in 52 individuals with VLCAD deficiency diagnosed by NBS and enrolled in the IBEM-IS database.
Loren D M Pena, Sandra C van Calcar, Joyanna Hansen, Mathew J Edick, Cate Walsh Vockley

Mol Genet Metab· August 2016

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Role of medical food in MMA.
Amy Cunningham, Dianne Frazier, Barbara Marriage, Shideh Mofidi, Beth Ogata, Sandra Van Calcar

Genet Med· April 2016

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Abnormal Eating Behaviors Are Common in Children with Fetal Alcohol Spectrum Disorder.
Robyn M Amos-Kroohs, Birgit A Fink, Carol J Smith, Lyanne Chin, Sandra C Van Calcar

J Pediatr· February 2016

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Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency.
Jessica Scott Schwoerer, Gena Cooper, Sandra van Calcar

Mol Genet Metab Rep· June 2015

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A re-evaluation of life-long severe galactose restriction for the nutrition management of classic galactosemia.
Sandra C Van Calcar, Laurie E Bernstein, Frances J Rohr, Christine H Scaman, Steven Yannicelli

Mol Genet Metab· July 2014

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Prevalence and mutation analysis of short/branched chain acyl-CoA dehydrogenase deficiency (SBCADD) detected on newborn screening in Wisconsin.
Sandra C Van Calcar, Mei W Baker, Phillip Williams, Susan A Jones, Blia Xiong

Mol Genet Metab· March 2014

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Inappropriate feeding behaviors and dietary intakes in children with fetal alcohol spectrum disorder or probable prenatal alcohol exposure.
Rachel L Werts, Sandra C Van Calcar, David S Wargowski, Susan M Smith

Alcohol Clin Exp Res· March 2014

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Recommendations for the nutrition management of phenylalanine hydroxylase deficiency.
Rani H Singh, Fran Rohr, Dianne Frazier, Amy Cunningham, Shideh Mofidi, Sandra C Van Calcar

Genet Med· February 2014

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Galactose content of legumes, caseinates, and some hard cheeses: implications for diet treatment of classic galactosemia.
Sandra C Van Calcar, Laurie E Bernstein, Frances J Rohr, Steven Yannicelli, Gerard T Berry

J Agric Food Chem· February 2014

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Newborn screening 50 years later: access issues faced by adults with PKU.
Susan A Berry, Christine Brown, Mitzie Grant, Carol L Greene, Elaina Jurecki, Sandra C van Calcar

Genet Med· August 2013

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Use of Gastrostomy Tube to Prevent Maternal PKU Syndrome.
Jessica A Scott Schwoerer, Lisa Obernolte, Sandra Van Calcar, Susan Heighway, Heather Bankowski

JIMD Rep· February 2013

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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.
Sandra C van Calcar, Denise M Ney

J Acad Nutr Diet· August 2012

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Breakfast with glycomacropeptide compared with amino acids suppresses plasma ghrelin levels in individuals with phenylketonuria.
Erin L MacLeod, Murray K Clayton, Sandra C van Calcar, Denise M Ney

Mol Genet Metab· August 2010

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Reassessment of phenylalanine tolerance in adults with phenylketonuria is needed as body mass changes.
Erin L MacLeod, Sally T Gleason, Sandra C van Calcar, Denise M Ney

Mol Genet Metab· December 2009

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Improved nutritional management of phenylketonuria by using a diet containing glycomacropeptide compared with amino acids.
Sandra C van Calcar, Erin L MacLeod, Sally T Gleason, Mark R Etzel, Murray K Clayton

Am J Clin Nutr· April 2009

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