Results for &quot;&quot;Phenylketonuria, Maternal&quot;&quot;[mesh_terms]

Finding the fertile woman with phenylketonuria.

William B Hanley

European journal of obstetrics, gynecology, and reproductive biology 2008;137(2):131-5

Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature.

Annamaria Sapuppo, Alessia Arena, Maria Grazia Pappalardo, Luisa La Spina, Marianna Messina, Concetta Meli, Andrea Domenico Praticò, Agata Polizzi, Michele Vecchio, Martino Ruggieri, Raffaele Falsaperla, Guido Leone, Federica Gullo, Laura Licciardello, Manuela Lo Bianco, Riccardo Iacobacci

Nutrients 2025;17(4):

The First 1000 Days of PKU: A Narrative Review of Maternal PKU and Early Life Management After Positive Newborn Screening.

Elvira Verduci, Martina Tosi, Juri Zuvadelli, Sara Giorda, Giacomo Biasucci, Vincenzo Leuzzi, Marco Spada, Alberto Burlina, Carlo Dionisi Vici

Nutrients 2026;18(2):

Phenylalanine hydroxylase deficiency treatment and management: A systematic evidence review of the American College of Medical Genetics and Genomics (ACMG).

April D Adams, Moisés Ó Fiesco-Roa, Lawrence Wong, Gabrielle P Jenkins, Jennifer Malinowski, Olivia M Demarest, Paul G Rothberg, Judith A Hobert

Genetics in medicine : official journal of the American College of Medical Genetics 2023;25(9):100358

Similarities and differences in key diagnosis, treatment, and management approaches for PAH deficiency in the United States and Europe.

Tracy Brock Lowe, Jane DeLuca, Georgianne L Arnold

Orphanet journal of rare diseases 2021;15(1):266

Phenylketonuria and maternal phenylketonuria.

H Purnell

Breastfeeding review : professional publication of the Nursing Mothers' Association of Australia 2001;9(2):19-21

The Impact of the Quality of Nutrition and Lifestyle in the Reproductive Years of Women with PKU on the Long-Term Health of Their Children.

Júlio César Rocha, Maria Inês Gama, Anita MacDonald, Anne Daly, Alex Pinto

Nutrients 2022;14(5):1021

Sapropterin dihydrochloride use in pregnant women with phenylketonuria: an interim report of the PKU MOMS sub-registry.

Dorothy K Grange, Richard E Hillman, Barbara K Burton, Shoji Yano, Chin-To Fong, Joellen Hunt, John J Mahoney, Jessica L Cohen-Pfeffer, Jerry Vockley

Molecular genetics and metabolism 2014;112(1):9-16

A practical approach to maternal phenylketonuria management.

F Maillot, P Cook, M Lilburn, P J Lee

Journal of inherited metabolic disease 2007;30(2):198-201

Management of Women With Phenylalanine Hydroxylase Deficiency (Phenylketonuria): ACOG Committee Opinion, Number 802.

Obstetrics and gynecology 2020;135(4):e167-e170

Management of Women With Phenylalanine Hydroxylase Deficiency (Phenylketonuria): ACOG Committee Opinion Summary, Number 802.

Obstetrics and gynecology 2020;135(4):987-988

Maternal phenylketonuria and hyperphenylalaninemia in pregnancy: pregnancy complications and neonatal sequelae in untreated and treated pregnancies.

Wim C J Hop, Johannes J Duvekot, Babette W Prick

The American journal of clinical nutrition 2012;95(2):374-82

Maternal phenylketonuria syndrome and case management implications.

Patricia J Gambol

Journal of pediatric nursing 2007;22(2):129-38