Pilot Study on Neonatal Screening for Methylmalonic Acidemia Caused by Defects in the Adenosylcobalamin Synthesis Pathway and Homocystinuria Caused by Defects in Homocysteine Remet... by Reiko Kagawa, Go Tajima, Takako Maeda, Fumiaki Sakura, Akari Nakamura-Utsunomiya, Keiichi Hara, Yutaka Nishimura, Miori Yuasa, Yosuke Shigematsu, Hiromi Tanaka, Saki Fujihara, Chiyoko Yoshii, Satoshi Okada

“…International Journal of Neonatal Screening…”
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Genomic-Based Newborn Screening for Inborn Errors of Immunity: Practical and Ethical Considerations by Jovanka R. King, Kalle Grill, Lennart Hammarström

“…International Journal of Neonatal Screening…”
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Successful Implementation of Newborn Screening for Hemoglobin Disorders in the Philippines by Carmencita D. Padilla, Bradford L. Therrell, Maria Melanie Liberty B. Alcausin, Reynaldo C. de Castro, Maria Beatriz P. Gepte, Ma. Elouisa L. Reyes, Charity M. Jomento, Riza Concordia N. Suarez, Ebner Bon G. Maceda, Conchita G. Abarquez, J. Edgar Winston C. Posecion, Alma P. Andal, Anna Lea G. Elizaga, Bernadette C. Halili-Mendoza, Maria Paz Virginia K. Otayza, Carolyn C. Hoppe

“…International Journal of Neonatal Screening…”
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Processing of Positive Newborn Screening Results for Congenital Hypothyroidism: A Qualitative Exploration of Current Practice in England by Pru Holder, Tim Cheetham, Alessandra Cocca, Holly Chinnery, Jane Chudleigh

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A Roadmap to Newborn Screening for Duchenne Muscular Dystrophy by Samiah A. Al-Zaidy, Michele Lloyd-Puryear, Annie Kennedy, Veronica Lopez, Jerry R. Mendell

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Newborn Screening in a Pandemic—Lessons Learned by Matej Mlinaric, James R. Bonham, Viktor Kožich, Stefan Kölker, Ondrej Majek, Tadej Battelino, Ana Drole Torkar, Vanesa Koracin, Dasa Perko, Ziga Iztok Remec, Barbka Repic Lampret, Maurizio Scarpa, Peter C. J. I. Schielen, Rolf H. Zetterström, Urh Groselj

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Genomics and Newborn Screening: Perspectives of Public Health Programs by Aaron J. Goldenberg, Roselle Ponsaran, Amy Gaviglio, Dalton Simancek, Beth A. Tarini

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Newborn Screening for SCID: Experience in Spain (Catalonia) by Ana Argudo-Ramírez, Andrea Martín-Nalda, Jose Manuel González de Aledo-Castillo, Rosa López-Galera, Jose Luis Marín-Soria, Sonia Pajares-García, Mónica Martínez-Gallo, Marina García-Prat, Roger Colobran, Jacques G. Riviere, Yania Quintero, Tatiana Collado, Antonia Ribes, Judit García-Villoria, Pere Soler-Palacín

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Setting up a Newborn Hearing Screening Programme in a Low-Income Country: Initial Findings from Malawi by Helen Brough

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Post-Analytical Tools for the Triage of Newborn Screening Results in Follow-up Can Reduce Confirmatory Testing and Guide Performance Improvement by Patricia L. Hall, Angela Wittenauer, Arthur Hagar

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Gunnar Jungner and the Principles and Practice of Screening for Disease by Lars Jungner, Ingmar Jungner, Martin Engvall, Ulrika von Döbeln

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A Newborn Screening, Presymptomatically Identified Infant With Late-Onset Pompe Disease: Case Report, Parental Experience, and Recommendations by Raymond Y. Wang

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CCHD Screening Implementation Efforts in Latin American Countries by the Ibero American Society of Neonatology (SIBEN) by Augusto Sola, Susana Rodríguez, Alejandro Young, Lourdes Lemus Varela, Ramón Mir Villamayor, Marcelo Cardetti, Jorge Pleitez Navarrete, María Verónica Favareto, Victoria Lima, Hernando Baquero, Lorena Velandia Forero, María Elena Venegas, Carmen Davila, Fernando Dominguez Dieppa, Taína Malena Germosén, Ada Nidia Oviedo Barrantes, Ana Lorena Alvarez Castañeda, Mónica Morgues, Aldana Avila, Diana Fariña, Jose Luis Oliva, Erika Sosa, Sergio Golombek

“…International Journal of Neonatal Screening…”
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Neonatal Urine Screening Program in the Province of Quebec: Technological Upgrade from Thin Layer Chromatography to Tandem Mass Spectrometry by Christiane Auray-Blais, Michel Boutin, Pamela Lavoie, Bruno Maranda

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Including Classical Galactosaemia in the Expanded Newborn Screening Panel Using Tandem Mass Spectrometry for Galactose-1-Phosphate by Arieh S. Cohen, Marta Baurek, Allan M. Lund, Morten Dunø, David M. Hougaard

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Zoltan Lukacs Passed Away by Joseph Orsini, Michael Gelb, Peter C. J. I. Schielen

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Leading Risk Factors for Congenital Deafness in the Context of Universal Neonatal Screening: Our Observations in a Four-Year Retrospective Study by Antoine Paul, Fanny Bense, Claire Boithias Guerot, Sofia De La Rubia, Cécile Lebeaux, Jean-François Papon

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Newborn Screening for Mucopolysaccharidosis Type II in Illinois: An Update by Barbara K. Burton, Rachel Hickey, Lauren Hitchins

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Evaluation of Technical Issues in a Pilot Multicenter Newborn Screening Program for Sickle Cell Disease by Maddalena Martella, Giampietro Viola, Silvia Azzena, Sara Schiavon, Andrea Biondi, Giuseppe Basso, Paola Corti, Raffaella Colombatti, Nicoletta Masera, Laura Sainati

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Provider Perspectives on the Impact of the COVID-19 Pandemic on Newborn Screening by Jessica I. Gold, Ian M. Campbell, Can Ficicioglu

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