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Page 1
The diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?
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.
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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.
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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
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Correlation of surrogate markers of Gaucher disease. Implications for long-term follow up of enzyme replacement therapy.
Cabrera-Salazar MA, O'Rourke E, Henderson N, Wessel H, Barranger JA.
Cabrera-Salazar MA, et al. Among authors: henderson n.
Clin Chim Acta. 2004 Jun;344(1-2):101-7. doi: 10.1016/j.cccn.2004.02.018.
Clin Chim Acta. 2004.
PMID: 15149877
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