Liver failure and neurologic disease in a patient with homocystinuria von Snyderman, Selma E.

Volltext

In response to R.E. Roux et al (2006) The longest surviving patient with classical maple syrup urine disease. J Inherit Metab Dis 29:190–194 von Snyderman, Selma E.

Volltext

Maple Syrup Urine Disease: Identification and Carrier-Frequency Determination of a Novel Founder Mutation in the Ashkenazi Jewish Population von Edelmann, Lisa, Wasserstein, Melissa P., Kornreich, Ruth, Sansaricq, Claude, Snyderman, Selma E., Diaz, George A.

Volltext

Influence of metabolic control on growth in homocystinuria due to cystathionine B-synthase deficiency von TOPALOGLU, Ali Kemal, SANSARICQ, Claude, SNYDERMAN, Selma E

Volltext

Succinyl-CoA:3-Ketoacid CoA-Transferase Deficiency von Snyderman, Selma E, Sansaricq, Claude, Middleton, Bruce

Volltext

Newborn screening for homocystinuria von Snyderman, Selma E, Sansaricq, Claude

Volltext

Baclofen in the Treatment of Polymyoclonus and Ataxia in a Patient With Homocystinuria von Awaad, Yasser, Sansaricq, Claude, Moroney, Joan, Fish, Irving, Kyriakakos, Anastassios, Snyderman, Selma E.

Volltext

The pathobiochemistry of uremia and hyperargininemia further demonstrates a metabolic relationship between urea and guanidinosuccinic acid von Marescau, Bart, De Deyn, Peter P., Qureshi, Ijaz A., De Broe, Marc E., Antonozzi, Italo, Cederbaum, Stephen D., Cerone, Roberto, Chamoles, Nestor, Gatti, Rosa, Kang, Soo-Sang, Lambert, Marie, Possemiers, Ilse, Snyderman, Selma E., Yoshino, Makoto

Volltext

The relationship between the branched chain amino acids and their α-ketoacids in maple syrup urine disease von SNYDERMAN, S. E, GOLDSTEIN, F, SANSARICQ, C, NORTON, P. M

Volltext

Molecular basis of phenotypic variation in patients with argininemia von UCHINO, T, SNYDERMAN, S. E, LAMBERT, M, QURESHI, I. A, SHAPIRA, S. K, SANSARICQ, C, SMIT, L. M. E, JAKOBS, C, MATSUDA, I

Volltext

Treatment of phenylketonuria von Duell, P Barton, David, S Weigle, William, E Connor, Selma, E Snyderman, Bessman, Samuel

Volltext

The plasma aminogram. I. Influence of the level of protein intake and a comparison of whole protein and amino acid diets von Snyderman, S E, Holt, Jr, L E, Nortn, P M, Roitman, E, Phansalkar, S V

Volltext

The histidine requirement of the infant von SNYDERMAN, S E, BOYER, A, ROITMAN, E, HOLT, Jr, L E, PROSE, P H

Volltext

Disturbances of amino acid metabolism von HOLT, Jr, L E, SNYDERMAN, S E

Volltext

The Absorption of Short-chain Fats by Premature Infants von Snyderman, Selma E., Morales, Soledad, Holt, L. Emmett

Volltext

PROPIONYL CoA CARBOXYLASE ACTIVITY OF OBLIGATE HETEROZYGOTE FOR PROPIONIC ACIDEMIA von Sansaricq, Claude, Snyderman, Selma E

Volltext

IN VIVO PHENYLALANINE HYDROXYLASE ACTIVITY von Sansaricq, Claude, Snyderman, Selma E, Arcay, Ann

Volltext

Dietary and Genetic Therapy of Inborn Errors of Metabolism: A Summary von SNYDERMAN, SELMA E.

Volltext

Biotinidase deficiency in black children von Lara, Emily B., Sansaricq, Claude, Wolf, Barry, Snyderman, Selma E.

Volltext

Newborn screening for maple syrup urine disease von Snyderman, Selma E., Sansaricq, Claude

Volltext