S. Mofidi

发表

Interpretation of commercial food ingredient labels by parents of food-allergic children.

S. Sicherer, P. Joshi, S. Mofidi, 2002, The Journal of allergy and clinical immunology.

Diagnostic guidelines for newborns who screen positive in newborn screening

N. Braverman, D. Kronn, S. Mofidi, 2010, Genetics in Medicine.

Allergic Eosinophilic Gastroenteritis With Protein-losing Enteropathy: Intestinal Pathology, Clinical Course, and Long-term Follow-up

H. Sampson, A. Nowak‐Wegrzyn, S. Sicherer, 2006, Journal of pediatric gastroenterology and nutrition.

Nutritional management of pediatric food hypersensitivity.

S. Mofidi, 2003, Pediatrics.

Skin prick test to egg white provides additional diagnostic utility to serum egg white-specific IgE antibody concentration in children.

H. Sampson, W. Shreffler, A. Nowak‐Wegrzyn, 2006, The Journal of allergy and clinical immunology.

Relevance of casual contact with peanut butter in children with peanut allergy.

S. Sicherer, Songhui Ma, S. Mofidi, 2003, The Journal of allergy and clinical immunology.

Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State.

Matthew J. Nichols, P. Galvin-Parton, M. Caggana, 2010, Molecular genetics and metabolism.

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.

Birch and ragweed pollen immunotherapy in the treatment of pollen-food allergy syndrome

L. Bardina, K. Beyer, A. Nowak‐Wegrzyn, 2004 .

Iron status of children with phenylketonuria undergoing nutrition therapy assessed by transferrin receptors

L. Elsas, R. Steiner, Rani H. Singh, 2004, Genetics in Medicine.

Systematic Review Materials and Methods Recommendations Were Developed by a Cooperative Effort among Genetic Metabolic Dietitians International, the Southeast Regional Genetics Collaborative, and Dietitians from the Diet Control and Management and Maternal Pku Workgroups from the National Institutes

J. Vockley, K. Moseley, Rani H. Singh, 2022 .

Emergency management of inherited metabolic disorders.

D. Kronn, S. Mofidi, 2009 .

Phenylketonuria Scientific Review Conference: state of the science and future research needs.

Melissa L McPheeters, Mary Lou Lindegren, Anita MacDonald, 2014, Molecular genetics and metabolism.

Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach.

K. Moseley, Rani H. Singh, D. Frazier, 2016, Molecular genetics and metabolism.

Recommendations for the nutrition management of phenylalanine hydroxylase deficiency

Jerry Vockley, J. Vockley, K. Moseley, 2014, Genetics in Medicine.

THE PREVALENCY OF TOXOPLASMA ANTIBODIES IN WOMEN DURING MARRIAGE CONSULTATION IN GORGAN

M. Saeidi, N. Behnampour, E. Ghaemi, 2002 .

Glucose transporter type 1 deficiency: a study of two cases with video-EEG

M. Seashore, E. Novotny, R. Boles, 1999, European Journal of Pediatrics.

Nutrition management of PKU with pegvaliase therapy: update of the web-based PKU nutrition management guideline recommendations

A. Kenneson, Rani H. Singh, F. Rohr, 2023, Orphanet Journal of Rare Diseases.

417 Reactions to food products labeled dairy-free: Quantity of milk contaminant

H. Sampson, L. Bardina, P. Chatchatee, 2000 .