David A Wenger - Search Results

Year	Number of Results
2002	3
2003	4
2004	5
2005	7
2006	1
2008	1
2009	5
2010	1
2011	1
2012	2
2013	5
2014	3
2015	6
2016	5
2018	2
2019	4
2020	5
2021	3
2024	0

1

Advances in the Diagnosis and Treatment of Krabbe Disease.

Wenger DA, Luzi P, Rafi MA. Wenger DA, et al. Int J Neonatal Screen. 2021 Aug 18;7(3):57. doi: 10.3390/ijns7030057. Int J Neonatal Screen. 2021. PMID: 34449528 Free PMC article. Review.

2

Consensus guidelines for newborn screening, diagnosis and treatment of infantile Krabbe disease.

Kwon JM, Matern D, Kurtzberg J, Wrabetz L, Gelb MH, Wenger DA, Ficicioglu C, Waldman AT, Burton BK, Hopkins PV, Orsini JJ. Kwon JM, et al. Among authors: wenger da. Orphanet J Rare Dis. 2018 Feb 1;13(1):30. doi: 10.1186/s13023-018-0766-x. Orphanet J Rare Dis. 2018. PMID: 29391017 Free PMC article. Review.

3

A closer look at ARSA activity in a patient with metachromatic leukodystrophy.

Doherty K, Frazier SB, Clark M, Childers A, Pruthi S, Wenger DA, Duis J. Doherty K, et al. Among authors: wenger da. Mol Genet Metab Rep. 2019 Feb 20;19:100460. doi: 10.1016/j.ymgmr.2019.100460. eCollection 2019 Jun. Mol Genet Metab Rep. 2019. PMID: 30828547 Free PMC article.

4

Krabbe disease: One Hundred years from the bedside to the bench to the bedside.

Wenger DA, Rafi MA, Luzi P. Wenger DA, et al. J Neurosci Res. 2016 Nov;94(11):982-9. doi: 10.1002/jnr.23743. J Neurosci Res. 2016. PMID: 27638583 Review.

5

Chemical mutagenesis of a GPCR ligand: Detoxifying "inflammo-attraction" to direct therapeutic stem cell migration.

Lee JP, Zhang R, Yan M, Duggineni S, Wakeman DR, Niles WL, Feng Y, Chen J, Hamblin MH, Han EB, Gonzalez R, Fang X, Zhu Y, Wang J, Xu Y, Wenger DA, Seyfried TN, An J, Sidman RL, Huang Z, Snyder EY. Lee JP, et al. Among authors: wenger da. Proc Natl Acad Sci U S A. 2020 Dec 8;117(49):31177-31188. doi: 10.1073/pnas.1911444117. Epub 2020 Nov 20. Proc Natl Acad Sci U S A. 2020. PMID: 33219123 Free PMC article.

6

Rare Saposin A deficiency: Novel variant and psychosine analysis.

Calderwood L, Wenger DA, Matern D, Dahmoush H, Watiker V, Lee C. Calderwood L, et al. Among authors: wenger da. Mol Genet Metab. 2020 Feb;129(2):161-164. doi: 10.1016/j.ymgme.2019.08.001. Epub 2019 Aug 5. Mol Genet Metab. 2020. PMID: 31439510

7

A Patient With Atypical Multiple Sulfatase Deficiency.

Miskin C, Melvin JJ, Legido A, Wenger DA, Harasink SM, Khurana DS. Miskin C, et al. Among authors: wenger da. Pediatr Neurol. 2016 Apr;57:98-100. doi: 10.1016/j.pediatrneurol.2015.10.023. Epub 2015 Dec 24. Pediatr Neurol. 2016. PMID: 26825355

8

Sixteen novel mutations in the arylsulfatase A gene causing metachromatic leukodystrophy.

Luzi P, Rafi MA, Rao HZ, Wenger DA. Luzi P, et al. Among authors: wenger da. Gene. 2013 Nov 10;530(2):323-8. doi: 10.1016/j.gene.2013.08.065. Epub 2013 Aug 31. Gene. 2013. PMID: 24001781

9

The Lysosomal Diseases Testing Laboratory: A review of the past 47 years.

Wenger DA, Luzi P. Wenger DA, et al. JIMD Rep. 2020 Apr 4;54(1):61-67. doi: 10.1002/jmd2.12117. eCollection 2020 Jul. JIMD Rep. 2020. PMID: 32685352 Free PMC article.

10

Insights into the diagnosis and treatment of lysosomal storage diseases.

Wenger DA, Coppola S, Liu SL. Wenger DA, et al. Arch Neurol. 2003 Mar;60(3):322-8. doi: 10.1001/archneur.60.3.322. Arch Neurol. 2003. PMID: 12633142 Review.

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