Baker MW - Search Results

1

Newborn screening for spinal muscular atrophy: The Wisconsin first year experience.

Baker MW, Mochal ST, Dawe SJ, Wiberley-Bradford AE, Cogley MF, Zeitler BR, Piro ZD, Harmelink MM, Kwon JM. Baker MW, et al. Neuromuscul Disord. 2022 Feb;32(2):135-141. doi: 10.1016/j.nmd.2021.07.398. Epub 2021 Jul 27. Neuromuscul Disord. 2022. PMID: 35120759

2

Development of a routine newborn screening protocol for severe combined immunodeficiency.

Baker MW, Grossman WJ, Laessig RH, Hoffman GL, Brokopp CD, Kurtycz DF, Cogley MF, Litsheim TJ, Katcher ML, Routes JM. Baker MW, et al. J Allergy Clin Immunol. 2009 Sep;124(3):522-7. doi: 10.1016/j.jaci.2009.04.007. Epub 2009 May 31. J Allergy Clin Immunol. 2009. PMID: 19482345

3

Statewide newborn screening for severe T-cell lymphopenia.

Routes JM, Grossman WJ, Verbsky J, Laessig RH, Hoffman GL, Brokopp CD, Baker MW. Routes JM, et al. Among authors: baker mw. JAMA. 2009 Dec 9;302(22):2465-70. doi: 10.1001/jama.2009.1806. JAMA. 2009. PMID: 19996402

4

Implementing routine testing for severe combined immunodeficiency within Wisconsin's newborn screening program.

Baker MW, Laessig RH, Katcher ML, Routes JM, Grossman WJ, Verbsky J, Kurtycz DF, Brokopp CD. Baker MW, et al. Public Health Rep. 2010 May-Jun;125 Suppl 2(Suppl 2):88-95. doi: 10.1177/00333549101250S211. Public Health Rep. 2010. PMID: 20518449 Free PMC article.

5

Newborn screening for severe combined immunodeficiency; the Wisconsin experience (2008-2011).

Verbsky JW, Baker MW, Grossman WJ, Hintermeyer M, Dasu T, Bonacci B, Reddy S, Margolis D, Casper J, Gries M, Desantes K, Hoffman GL, Brokopp CD, Seroogy CM, Routes JM. Verbsky JW, et al. Among authors: baker mw. J Clin Immunol. 2012 Feb;32(1):82-8. doi: 10.1007/s10875-011-9609-4. Epub 2011 Nov 10. J Clin Immunol. 2012. PMID: 22068910

6

Prevalence and mutation analysis of short/branched chain acyl-CoA dehydrogenase deficiency (SBCADD) detected on newborn screening in Wisconsin.

Van Calcar SC, Baker MW, Williams P, Jones SA, Xiong B, Thao MC, Lee S, Yang MK, Rice GM, Rhead W, Vockley J, Hoffman G, Durkin MS. Van Calcar SC, et al. Among authors: baker mw. Mol Genet Metab. 2013 Sep-Oct;110(1-2):111-5. doi: 10.1016/j.ymgme.2013.03.021. Epub 2013 Apr 15. Mol Genet Metab. 2013. PMID: 23712021 Free PMC article.

7

Genotypes of patients with phenylalanine hydroxylase deficiency in the Wisconsin Amish.

Schwoerer JS, Drilias N, Kuhl A, Mochal S, Baker M. Schwoerer JS, et al. Mol Genet Metab Rep. 2018 Mar 8;15:75-77. doi: 10.1016/j.ymgmr.2018.02.005. eCollection 2018 Jun. Mol Genet Metab Rep. 2018. PMID: 29560316 Free PMC article.

8

Increased Congenital Hypothyroidism Detection in Preterm Infants with Serial Newborn Screening.

Kaluarachchi DC, Allen DB, Eickhoff JC, Dawe SJ, Baker MW. Kaluarachchi DC, et al. Among authors: baker mw. J Pediatr. 2019 Apr;207:220-225. doi: 10.1016/j.jpeds.2018.11.044. Epub 2018 Dec 20. J Pediatr. 2019. PMID: 30579585

9

Progress in treatment and newborn screening for Duchenne muscular dystrophy and spinal muscular atrophy.

Ke Q, Zhao ZY, Mendell JR, Baker M, Wiley V, Kwon JM, Alfano LN, Connolly AM, Jay C, Polari H, Ciafaloni E, Qi M, Griggs RC, Gatheridge MA. Ke Q, et al. World J Pediatr. 2019 Jun;15(3):219-225. doi: 10.1007/s12519-019-00242-6. Epub 2019 Mar 23. World J Pediatr. 2019. PMID: 30904991 Review.

10

Thyroid-Stimulating Hormone Reference Ranges for Preterm Infants.

Kaluarachchi DC, Allen DB, Eickhoff JC, Dawe SJ, Baker MW. Kaluarachchi DC, et al. Among authors: baker mw. Pediatrics. 2019 Aug;144(2):e20190290. doi: 10.1542/peds.2019-0290. Epub 2019 Jul 16. Pediatrics. 2019. PMID: 31311840

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

108 results

Search Page