 |
|
Asymptomatic maternal 3-methylcrotonylglycinuria detected by her unaffected baby's neonatal screening test
Sun Hee Lee (Lee SH), Yong Hee Hong (Hong YH)
Clin Exp Pediatr. 2014;57(7):329-332. Published online 2014 Jul 23 DOI: https://doi.org/10.3345/kjp.2014.57.7.329
|
|
Citations to this article as recorded by
 Epidemiology of inherited metabolic disorders in newborn screening: insights from three years of experience in Southern Iran
Leila Salarian, Homa Ilkhanipoor, Anis Amirhakimi, Zhila Afshar, Saman Nahid, Fariba Moradi Ardekani, Nazila Rahimi, Negar Yazdani, Abdolhossein Nikravesh, Zahra Beyzaei, Hossein Moravej
Orphanet Journal of Rare Diseases.2025;[Epub] CrossRef An asymptomatic father diagnosed with 3-methylcrotonyl-CoA carboxylase deficiency following his son newborn screening test
Rosamaria Terracciano, Margherita Ruoppolo, Ferdinando Barretta, Lucia Albano, Daniela Crisci, Giovanna Gallo, Fabiana Uomo, Pietro Strisciuglio, Giancarlo Parenti, Giulia Frisso, Alessandro Rossi
Molecular Genetics and Metabolism Reports.2024; 40: 101116. CrossRef Newborn screening and genetic diagnosis of 3-methylcrotonyl-CoA carboxylase deficiency in Quanzhou,China
Weihua Lin, Kunyi Wang, Yanru Chen, Zhenzhu Zheng, Yiming Lin
Molecular Genetics and Metabolism Reports.2024; 40: 101127. CrossRef Newborn Screening by DNA-First: Systematic Evaluation of the Eligibility of Inherited Metabolic Disorders Based on Treatability
Abigail Veldman, Birgit Sikkema-Raddatz, Terry G. J. Derks, Clara D. M. van Karnebeek, M. B. Gea Kiewiet, Margaretha F. Mulder, Marcel R. Nelen, M. Estela Rubio-Gozalbo, Richard J. Sinke, Monique G. de Sain-van der Velden, Gepke Visser, Maaike C. de Vries
International Journal of Neonatal Screening.2024; 11(1): 1. CrossRef Discovery, structure, and function of filamentous 3-methylcrotonyl-CoA carboxylase
Jason J. Hu, Jane K.J. Lee, Yun-Tao Liu, Clinton Yu, Lan Huang, Inna Aphasizheva, Ruslan Aphasizhev, Z. Hong Zhou
Structure.2023; 31(1): 100. CrossRef Primary and maternal 3‐methylcrotonyl‐CoA carboxylase deficiency: insights from the Israel newborn screening program
Jonathan Rips, Shlomo Almashanu, Hanna Mandel, Sagi Josephsberg, Tally Lerman‐Sagie, Ayelet Zerem, Ben Podeh, Yair Anikster, Avraham Shaag, Anthony Luder, Orna Staretz Chacham, Ronen Spiegel
Journal of Inherited Metabolic Disease.2016; 39(2): 211. CrossRef
|