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Page 1
The diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?
Weinreb NJ, Goker-Alpan O, Kishnani PS, Longo N, Burrow TA, Bernat JA, Gupta P, Henderson N, Pedro H, Prada CE, Vats D, Pathak RR, Wright E, Ficicioglu C. Weinreb NJ, et al. Among authors: henderson n. Mol Genet Metab. 2022 May;136(1):4-21. doi: 10.1016/j.ymgme.2022.03.001. Epub 2022 Mar 9. Mol Genet Metab. 2022. PMID: 35367141 Free article. Review.
Fabry Disease practice resource: Focused revision.
Henderson N, Berry L, Laney DA. Henderson N, et al. J Genet Couns. 2020 Oct;29(5):715-717. doi: 10.1002/jgc4.1318. Epub 2020 Sep 3. J Genet Couns. 2020. PMID: 32885538 No abstract available.
Newborn Screening for Pompe Disease: Pennsylvania Experience.
Ficicioglu C, Ahrens-Nicklas RC, Barch J, Cuddapah SR, DiBoscio BS, DiPerna JC, Gordon PL, Henderson N, Menello C, Luongo N, Ortiz D, Xiao R. Ficicioglu C, et al. Among authors: henderson n. Int J Neonatal Screen. 2020 Nov 13;6(4):89. doi: 10.3390/ijns6040089. Int J Neonatal Screen. 2020. PMID: 33202836 Free PMC article.
Postnatal Pancraniosynostosis in a Patient With Infantile Hypophosphatasia.
Nahabet EH, Gatherwright J, Vockley J, Henderson N, Tomei KL, Grigorian AP, Kaminski B, Bass N, Selman WR, Lakin GE. Nahabet EH, et al. Among authors: henderson n. Cleft Palate Craniofac J. 2016 Nov;53(6):741-744. doi: 10.1597/15-027. Epub 2015 Jul 14. Cleft Palate Craniofac J. 2016. PMID: 26171568