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Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant.
Am J Med Genet A. 2018 Mar;176(3):692-698. doi: 10.1002/ajmg.a.38602. Epub 2018 Feb 1.
Am J Med Genet A. 2018.
PMID: 29388319
Free PMC article.
Review.
Does adherence to epilepsy quality measures correlate with reduced epilepsy-related adverse hospitalizations? A retrospective experience.
Ladner TR, Morgan CD, Pomerantz DJ, Kennedy VE, Azar N, Haas K, Lagrange A, Gallagher M, Singh P, Abou-Khalil BW, Arain AM.
Ladner TR, et al. Among authors: pomerantz dj.
Epilepsia. 2015 May;56(5):e63-7. doi: 10.1111/epi.12965. Epub 2015 Mar 23.
Epilepsia. 2015.
PMID: 25809720
Free article.
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Dilated cardiomyopathy associated with a mutation in the dispatched RND transporter family member 1 gene.
Torpoco Rivera DM, Hafzalah M, Pomerantz DJ, Garcia RU.
Torpoco Rivera DM, et al. Among authors: pomerantz dj.
Cardiol Young. 2022 Jul;32(7):1166-1168. doi: 10.1017/S1047951121004625. Epub 2021 Dec 2.
Cardiol Young. 2022.
PMID: 34852870
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A case study: service delivery and parents with disabilities.
Pomerantz P, Pomerantz DJ, Colca LA.
Pomerantz P, et al. Among authors: pomerantz dj.
Child Welfare. 1990 Jan-Feb;69(1):65-73.
Child Welfare. 1990.
PMID: 2295270
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