Newborn Screening and the Pediatric Practitioner von Seashore, Margretta R., Seashore, Carl J.

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Diagnosis of Very Long Chain Acyl-Dehydrogenase Deficiency From an Infant's Newborn Screening Card von Wood, John C, Magera, Mark J, Rinaldo, Piero, Seashore, Margretta Reed, Strauss, Arnold W, Friedman, Alan

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Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC) von Rosenblatt, D. S., Aspler, A. L., Shevell, M. I., Pletcher, B. A., Fenton, W. A., Seashore, M. R.

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Tetrahydrobiopterin and Dietary Restriction in Mild Phenylketonuria von Seashore, Margretta R

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Management of Phenylketonuria for Optimal Outcome: A Review of Guidelines for Phenylketonuria Management and a Report of Surveys of Parents, Patients, and Clinic Directors von Wappner, Rebecca, Cho, Sechin, Kronmal, Richard A, Schuett, Virginia, Seashore, Margretta Reed

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Newborn Screening for Congenital Hypothyroidism: Recommended Guidelines von AAP Section on Endocrinology and Committee on Genetics, and American Thyroid Association Committee on Public Health

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Newborn screening fact sheets von Committee on Genetics

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Glucose transporter type 1 deficiency : a study of two cases with video-EEG von BOLES, R. G, SEASHORE, M. R, MITCHELL, W. G, KOLLROS, P. R, MOFIDI, S, NOVOTNY, E. J

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In vivo measurement of phenylalanine in human brain by proton nuclear magnetic resonance spectroscopy von NOVOTNY, E. J, AVISON, M. J, HERSCHKOWITZ, N, PETROFF, O. A. C, PRICHARD, J. W, SEASHORE, M. R, ROTHMAN, D. L

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Development of Guidelines for Treatment of Children With Phenylketonuria: Report of a Meeting at the National Institute of Child Health and Human Development Held August 15, 1995,... von Seashore, Margretta Reed, Wappner, Rebecca, Cho, Sechin, de la Cruz, Felix

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HUMAN DERMATOSPARAXIS - A FORM OF EHLERS-DANLOS SYNDROME THAT RESULTS FROM FAILURE TO REMOVE THE AMINO-TERMINAL PROPEPTIDE OF TYPE-I PROCOLLAGEN von SMITH, LT, WERTELECKI, W, MILSTONE, LM, PETTY, EM, SEASHORE, MR, BRAVERMAN, IM, JENKINS, TG, BYERS, PH

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Health Supervision for Children With Achondroplasia von Seashore, Margretta R, Cho, Sechin, Desposito, Franklin, Sherman, Jack

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Familial apple peel jejunal atresia: surgical, genetic, and radiographic aspects von SEASHORE, J. H, COLLINS, F. S, MARKOWITZ, R. I, SEASHORE, M. R

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Health Supervision for Children With Down Syndrome von Sherman, Jack, Wappner, Rebecca S, Wilson, Miriam G, Seashore, Margretta R

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Health Supervision for Children With Neurofibromatosis von Committee on Genetics, 1994 to 1995

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Health supervision for children with Turner syndrome von Seashore, Margretta R, Cho, Sechin, Desposito, Franklin, Sherman, Jack

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New England Consortium: A model for medical evaluation of expanded newborn screening with tandem mass spectrometry von Albers, S., Waisbren, S. E., Ampola, M. G., Brewster, T. G., Burke, L. W., Demmer, L. A., Filiano, J., Greenstein, R. M. G., Ingham, C. L., Korson, M. S., Marsden, D., Schwartz, R. C., Seashore, M. R., Shih, V. E., Levy, H. L.

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Health Supervision for Children With Marfan Syndrome von Committee on Genetics

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ISSUES IN NEWBORN SCREENING von MCCABE, ERB, LEONARD, CO, MEDICI, FN, SEASHORE, MR, WEISS, L

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Loss of intellectual function in children with phenylketonuria after relaxation of dietary phenylalanine restriction von Seashore, Margretta R, Friedman, Estelle, Novelly, Robert A, Bapat, Vijaya

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