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

Por Van Calcar, Sandra C., Ney, Denise M.
Publicado em 2012

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

Por Werts, Rachel L., Van Calcar, Sandra C., Wargowski, David S., Smith, Susan M.
Publicado em 2013

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

Por MacLeod, Erin L., Gleason, Sally T., van Calcar, Sandra C., Ney, Denise M.
Publicado em 2009

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

Por Lim, Kyungwha, van Calcar, Sandra C., Nelson, Kathryn L., Gleason, Sally T., Ney, Denise M.
Publicado em 2007

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

Por MacLeod, Erin L., Clayton, Murray K., van Calcar, Sandra C., Ney, Denise M.
Publicado em 2010

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

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

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

Por Amos-Kroohs, Robyn M., Fink, Birgit A., Smith, Carol J., Chin, Lyanne, Van Calcar, Sandra C., Wozniak, Jeffrey R., Smith, Susan M.
Publicado no J Pediatr (2015)

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

Por 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
Publicado em 2013

Recommendations for the nutrition management of phenylalanine hydroxylase deficiency

Por 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.
Publicado em 2014

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

Por 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.
Publicado no JIMD Rep (2016)

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

Por 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
Publicado no Mol Genet Metab (2016)

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

Por 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.
Publicado no Mol Genet Metab (2013)

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

Por 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.
Publicado no J Inherit Metab Dis (2016)