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

door Van Calcar, Sandra C., Ney, Denise M.
Gepubliceerd in 2012

Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency

door Scott Schwoerer, Jessica, Cooper, Gena, van Calcar, Sandra
Gepubliceerd in Mol Genet Metab Rep (2015)

Successful pregnancy and delivery in a woman with propionic acidemia from the Amish community()

door Scott Schwoerer, Jessica, van Calcar, Sandra, Rice, Gregory M., Deline, James
Gepubliceerd in Mol Genet Metab Rep (2016)

Inappropriate Feeding Behaviors and Dietary Intakes in Children with FASD or Probable PAE

door Werts, Rachel L., Van Calcar, Sandra C., Wargowski, David S., Smith, Susan M.
Gepubliceerd in 2013

Reassessment of Phenylalanine Tolerance in Adults with Phenylketonuria is Needed as Body Mass Changes

door MacLeod, Erin L., Gleason, Sally T., van Calcar, Sandra C., Ney, Denise M.
Gepubliceerd in 2009

Simplified Diet for nutrition management of phenylketonuria: A survey of U.S. metabolic dietitians

door Hansen, Joyanna, Hollander, Suzanne, Drilias, Nicoletta, Van Calcar, Sandra, Rohr, Fran, Bernstein, Laurie
Gepubliceerd in JIMD Rep (2020)

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

door Lim, Kyungwha, van Calcar, Sandra C., Nelson, Kathryn L., Gleason, Sally T., Ney, Denise M.
Gepubliceerd in 2007

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

door MacLeod, Erin L., Clayton, Murray K., van Calcar, Sandra C., Ney, Denise M.
Gepubliceerd in 2010

Use of Gastrostomy Tube to Prevent Maternal PKU Syndrome

door Schwoerer, Jessica A. Scott, Obernolte, Lisa, Van Calcar, Sandra, Heighway, Susan, Bankowski, Heather, Williams, Phillip, Rice, Gregory
Gepubliceerd in 2012

Metabolomic Insights into the Nutritional Status of Adults and Adolescents with Phenylketonuria Consuming a Low-Phenylalanine Diet in Combination with Amino Acid and Glycomacropept...

door Stroup, Bridget M., Ney, Denise M., Murali, Sangita G., Rohr, Frances, Gleason, Sally T., van Calcar, Sandra C., Levy, Harvey L.
Gepubliceerd in J Nutr Metab (2017)

Improved nutritional management of phenylketonuria by using a diet containing glycomacropeptide compared with amino acids

door van Calcar, Sandra C, MacLeod, Erin L, Gleason, Sally T, Etzel, Mark R, Clayton, Murray K, Wolff, Jon A, Ney, Denise M
Gepubliceerd in 2009

Abnormal Eating Behaviors are Common in Children with Fetal Alcohol Spectrum Disorders

door Amos-Kroohs, Robyn M., Fink, Birgit A., Smith, Carol J., Chin, Lyanne, Van Calcar, Sandra C., Wozniak, Jeffrey R., Smith, Susan M.
Gepubliceerd in J Pediatr (2015)

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

door Berry, Susan A., Brown, Christine, Grant, Mitzie, Greene, Carol L., Jurecki, Elaina, Koch, Jean, Moseley, Kathryn, Suter, Ruth, van Calcar, Sandra C., Wiles, Judy, Cederbaum, Stephen
Gepubliceerd in 2013

Recommendations for the nutrition management of phenylalanine hydroxylase deficiency

door Singh, Rani H., Rohr, Fran, Frazier, Dianne, Cunningham, Amy, Mofidi, Shideh, Ogata, Beth, Splett, Patricia L., Moseley, Kathryn, Huntington, Kathleen, Acosta, Phyllis B., Vockley, Jerry, Van Calcar, Sandra C.
Gepubliceerd in 2014

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

door van Erven, Britt, Welling, Lindsey, van Calcar, Sandra C., Doulgeraki, Artemis, Eyskens, François, Gribben, Joanna, Treacy, Eileen P., Vos, Rein, Waisbren, Susan E., Rubio-Gozalbo, M. Estela, Bosch, Annet M.
Gepubliceerd in JIMD Rep (2016)

Outcomes and genotype-phenotype correlations in 52 individuals with VLCAD deficiency diagnosed by NBS and enrolled in the IBEM-IS database

door Pena, Loren D.M., van Calcar, Sandra C., Hansen, Joyanna, Edick, Mathew J., Vockley, Cate Walsh, Leslie, Nancy, Cameron, Cynthia, Mohsen, Al-Walid, Berry, Susan A, Arnold, Georgianne L, Vockley, Jerry
Gepubliceerd in Mol Genet Metab (2016)

Prevalence and mutation analysis of short/branched chain acyl-CoA dehydrogenase deficiency (SBCADD) detected on newborn screening in Wisconsin

door Van Calcar, Sandra C., Baker, Mei W., Williams, Phillip, Jones, Susan A., Xiong, Blia, Thao, Mai Choua, Lee, Sheng, Yang, Mai Khou, Rice, Greg M., Rhead, William, Vockley, Jerry, Hoffman, Gary, Durkin, Maureen S.
Gepubliceerd in Mol Genet Metab (2013)

International clinical guideline for the management of classical galactosemia: diagnosis, treatment, and follow-up

door Welling, Lindsey, Bernstein, Laurie E., Berry, Gerard T., Burlina, Alberto B., Eyskens, François, Gautschi, Matthias, Grünewald, Stephanie, Gubbels, Cynthia S., Knerr, Ina, Labrune, Philippe, van der Lee, Johanna H., MacDonald, Anita, Murphy, Elaine, Portnoi, Pat A., Õunap, Katrin, Potter, Nancy L., Rubio-Gozalbo, M. Estela, Spencer, Jessica B., Timmers, Inge, Treacy, Eileen P., Van Calcar, Sandra C., Waisbren, Susan E., Bosch, Annet M.
Gepubliceerd in J Inherit Metab Dis (2016)