L. Bernstein

发表

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

J. H. van der Lee, S. Waisbren, K. Õunap, 2016, Journal of Inherited Metabolic Disease.

Improved growth and nutrition status in children with methylmalonic or propionic acidemia fed an elemental medical food.

H. Bock, R. Steiner, P. Galvin-Parton, 2003, Molecular genetics and metabolism.

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

C. Scaman, G. Berry, F. Rohr, 2014, Molecular genetics and metabolism.

The Diet for Galactosemia

L. Bernstein, S. V. Calcar, S. C. Calcar, 2015 .

Nutrient intakes and physical growth of children with phenylketonuria undergoing nutrition therapy.

R. Steiner, Rani H. Singh, E. Jurecki, 2003, Journal of the American Dietetic Association.

8th Annual Conference of the European Nutraceutical Association (ENA)

J. Moreno-Navarrete, J. Fernández-Real, A. Pontecorvi, 2012, Annals of Nutrition and Metabolism.

Evaluation of the Efficacy and Effectiveness of Metabolic University: A Didactic Training Program for the Metabolic Clinician

Janet A. Thomas, C. Freehauf, L. Bernstein, 2011 .

Inconsistencies in the Nutrition Management of Glutaric Aciduria Type 1: An International Survey

F. Rohr, C. Coughlin, L. Bernstein, 2020, Nutrients.

Network Phenylketonuria Conference: An Effective Tool for Facilitating Adherence to Diet Therapy in Individuals With Phenylketonuria

Janet A. Thomas, C. Freehauf, Dexiang Gao, 2009 .

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

J. Hansen, F. Rohr, S. V. van Calcar, 2020, JIMD reports.

Nutrition education tools used in phenylketonuria: clinician, parent and patient perspectives from three international surveys.

J. Rocha, M. Giżewska, F. Feillet, 2014, Journal of human nutrition and dietetics : the official journal of the British Dietetic Association.

Adherence Issues in Inherited Metabolic Disorders Treated by Low Natural Protein Diets

A. Bosch, F. V. van Spronsen, M. Giżewska, 2012, Annals of Nutrition and Metabolism.

Impact on Isoleucine and Valine Supplementation When Decreasing Use of Medical Food in the Nutritional Management of Methylmalonic Acidemia

P. Baker II, Sommer Gaughan, M. Sailer, 2020, Nutrients.

Nutritional therapy improves growth and protein status of children with a urea cycle enzyme defect.

G. Arnold, A. Ryan, M. Plewinska, 2005, Molecular genetics and metabolism.

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

C. Scaman, G. Berry, F. Rohr, 2014, Journal of agricultural and food chemistry.

REVIEW: Practical strategies to maintain anabolism by intravenous nutritional management in children with inborn metabolic diseases.

S. McCandless, A. Larson, J. V. Van Hove, 2021, Molecular genetics and metabolism.

Acute nutrition management in the prevention of metabolic illness: a practical approach with glucose polymers.

J. V. Van Hove, C. Freehauf, S. Myers, 2009, Molecular genetics and metabolism.

Nutrient intake and growth of infants with phenylketonuria undergoing therapy.

B. Gaffield, B. Marriage, L. Bernstein, 1998, Journal of pediatric gastroenterology and nutrition.

Nutrition Management of Glutaric Acidemia Type 1

L. Bernstein, 2015 .

Intake and Blood Levels of Fatty Acids in Treated Patients With Phenylketonuria

R. Koch, Rani H. Singh, F. Rohr, 2001, Journal of pediatric gastroenterology and nutrition.

Impact of geographic access to care on compliance and metabolic control in phenylketonuria.

J. V. Van Hove, C. Freehauf, Dexiang Gao, 2013, Molecular genetics and metabolism.

International practices in the dietary management of fructose 1-6 biphosphatase deficiency

F. de Boer, M. Dixon, A. Macdonald, 2018, Orphanet Journal of Rare Diseases.

Multiclinic Observations on the Simplified Diet in PKU

F. Rohr, L. Bernstein, C. Burns, 2017, Journal of nutrition and metabolism.

Normalizing Diet in Individuals with Phenylketonuria Treated with Pegvaliase: A Case Series and Patient Perspective

J. Hansen, F. Rohr, J. Rocha, 2021, Nutrition and Dietary Supplements.

Development of a practical dietitian road map for the nutritional management of phenylketonuria (PKU) patients on pegvaliase

A. Macdonald, F. Rohr, J. Rocha, 2021, Molecular genetics and metabolism reports.

NDS_A_337135 145..154

J. Hansen, F. Rohr, J. Rocha, 2021 .

Effects of etanercept in patients with the metabolic syndrome.

L. Bernstein, S. Grinspoon, J. Berry, 2006, Archives of internal medicine.

Amino Acids and Inherited Amino Acid-Related Disorders

J. Sass, I. Knerr, E. Crushell, 2018, Journal of nutrition and metabolism.