Glycerol phenylbutyrate efficacy and safety from an open label study in pediatric patients under 2 months of age with urea cycle disorders by Longo, Nicola, Diaz, George A., Lichter-Konecki, Uta, Schulze, Andreas, Inbar-Feigenberg, Michal, Conway, Robert L., Bannick, Allison A., McCandless, Shawn E., Zori, Roberto, Hainline, Bryan, Ah Mew, Nicholas, Canavan, Colleen, Vescio, Thomas, Kok, Teresa, Porter, Marty H., Berry, Susan A.

Get full text

Outcomes of referrals to Child Protective Services for medical neglect in patients with phenylketonuria: Experiences at a single treatment center by Bannick, Allison A., Laufman, Jason D., Edwards, Heidi L., Ventimiglia, June, Feldman, Gerald L.

Get full text

ELEVATION OF HEPTADECANOYLCARNITINE DETECTED VIA NEWBORN SCREENING IS A STRONG PREDICTOR OF NEONATAL-ONSET DISEASE AMONG INBORN ERRORS OF METABOLISM AFFECTING PROPIONYLCARNITINE ME... by Conway, Robert, Moloney, Shawn, Bannick, Allison, Pappas, Kara, Seeterlin, Mary

Get full text

ARGININOSUCCINIC ACID IS EXQUISITELY SENSITIVE AND SPECIFIC COMPARED TO CITRULLINE IN SCREENING FOR ARGININOSUCCINIC ACID LYASE DEFICIENCY VIA NEWBORN SCREENING: MICHIGAN'S 10 YEAR... by Ellenberg, Elisheva, Kaur, Shagun, Pappas, Kara, Bannick, Allison, Beltran, Carolina, Evans, Lisa, Moloney, Shawn, Seeterlin, Mary, Conway, Robert L.

Get full text

Parental strategies to help children with phenylketonuria (PKU) cope with feeling different by Zwiesele, Sheila, Bannick, Allison, Trepanier, Angela

Get full text

Methionine adenosyltransferase I/III deficiency: Long-term follow-up and treatment of 3 adult siblings by Bannick, Allison, Chase, Sara, Miner, Alyson, Seeterlin, Mary, Conway, Robert L.

Get full text

O08: Long-term efficacy and safety of pegzilarginase for arginase 1 deficiency: 2 years of experience in the phase 2 extension study by McNutt, Markey, Diaz, George, Schulze, Andreas, Bubb, Gillian, Sloan, Leslie, Leão-Teles, Elisa, Batzios, Spyros, Sun, Angela, Bannick, Allison, Zori, Roberto, Enns, Gregory

Get full text

Clinical effect and safety profile of pegzilarginase in patients with arginase 1 deficiency by Diaz, George A., Schulze, Andreas, McNutt, Markey C., Leão‐Teles, Elisa, Merritt, J. Lawrence, Enns, Gregory M., Batzios, Spyros, Bannick, Allison, Zori, Roberto T., Sloan, Leslie S., Potts, Susan L., Bubb, Gillian, Quinn, Anthony G.

Get full text

Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes by Chien, Yin-Hsiu, Abdenur, Jose E, Baronio, Federico, Bannick, Allison Anne, Corrales, Fernando, Couce, Maria, Donner, Markus G, Ficicioglu, Can, Freehauf, Cynthia, Frithiof, Deborah, Gotway, Garrett, Hirabayashi, Koichi, Hofstede, Floris, Hoganson, George, Hwu, Wuh-Liang, James, Philip, Kim, Sook, Korman, Stanley H, Lachmann, Robin, Levy, Harvey, Lindner, Martin, Lykopoulou, Lilia, Mayatepek, Ertan, Muntau, Ania, Okano, Yoshiyuki, Raymond, Kimiyo, Rubio-Gozalbo, Estela, Scholl-Bürgi, Sabine, Schulze, Andreas, Singh, Rani, Stabler, Sally, Stuy, Mary, Thomas, Janet, Wagner, Conrad, Wilson, William G, Wortmann, Saskia, Yamamoto, Shigenori, Pao, Maryland, Blom, Henk J

Get full text

Mild Persistent Isolated Hypermethioninemia Identified through Newborn Screening in Michigan by Sen, Kuntal, Felice, Michael D., Bannick, Allison, Colombo, Roberto, Conway, Robert L.

Get full text