Neonatal Screening for Medium-Chain Acyl-CoA Dehydrogenase Deficiency—Alternative Approaches

By Pollitt Rodney J.  

International Journal of Neonatal Screening, Vol. 2, Iss. 1, 2016-03 ,pp. : 1-1

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Utility of Genetic Testing for Confirmation of Abnormal Newborn Screening in Disorders of Long-Chain Fatty Acids: A Missed Case of Carnitine Palmitoyltransferase 1A (CPT1A) Deficiency

By Dowsett Leah   Lulis Lauren   Ficicioglu Can   Cuddapah Sanmati  

International Journal of Neonatal Screening, Vol. 3, Iss. 2, 2017-04 ,pp. : 10-10

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Lessons Learned from Protective Immune Responses to Optimize Vaccines against Cryptosporidiosis

By Lemieux Maxime W.   Sonzogni-Desautels Karine   Ndao Momar  

Pathogens, Vol. 7, Iss. 1, 2017-12 ,pp. : 2-2

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Newborn Screening for Krabbe Disease and Other Lysosomal Storage Disorders: Broad Lessons Learned

By Orsini Joseph J.   Caggana Michele  

International Journal of Neonatal Screening, Vol. 3, Iss. 1, 2017-03 ,pp. : 3-3

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Early Detection and Diagnosis of Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency Missed by Newborn Screening Using Tandem Mass Spectrometry

By Shigetomi Hiroko   Tanaka Toju   Nagao Masayoshi   Tsutsumi Hiroyuki  

International Journal of Neonatal Screening, Vol. 4, Iss. 1, 2018-01 ,pp. : 5-5

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