Kirmse B - Search Results

1

Short-term follow-up systems for positive newborn screens in the Washington Metropolitan Area and the United States.

Viall S, Jain S, Chapman K, Ah Mew N, Summar M, Kirmse B; Members of the Division of Genetics & Metabolism at Children's National Health System. Viall S, et al. Among authors: kirmse b. Mol Genet Metab. 2015 Dec;116(4):226-30. doi: 10.1016/j.ymgme.2015.11.002. Epub 2015 Nov 4. Mol Genet Metab. 2015. PMID: 26549574

2

Mind the gap.

Summar M, Kirmse B, Monaco J. Summar M, et al. Among authors: kirmse b. Mol Genet Metab. 2014 Sep-Oct;113(1-2):1. doi: 10.1016/j.ymgme.2014.08.005. Mol Genet Metab. 2014. PMID: 25261244 No abstract available.

3

The incidence of urea cycle disorders.

Summar ML, Koelker S, Freedenberg D, Le Mons C, Haberle J, Lee HS, Kirmse B; European Registry and Network for Intoxication Type Metabolic Diseases (E-IMD). Electronic address: http://www.e-imd.org/en/index.phtml; Members of the Urea Cycle Disorders Consortium (UCDC). Electronic address: http://rarediseasesnetwork.epi.usf.edu/ucdc/. Summar ML, et al. Among authors: kirmse b. Mol Genet Metab. 2013 Sep-Oct;110(1-2):179-80. doi: 10.1016/j.ymgme.2013.07.008. Epub 2013 Jul 18. Mol Genet Metab. 2013. PMID: 23972786 Free PMC article.

4

Plasma fibroblast growth factor-21 levels in patients with inborn errors of metabolism.

Kirmse B, Cabrerra-Luque J, Ayyub O, Cusmano K, Chapman K, Summar M. Kirmse B, et al. Mol Genet Metab Rep. 2017 Sep 4;13:52-54. doi: 10.1016/j.ymgmr.2017.04.001. eCollection 2017 Dec. Mol Genet Metab Rep. 2017. PMID: 28920014 Free PMC article.

5

LPIN1 rhabdomyolysis: A single site cohort description and treatment recommendations.

Kanderi N, Kirmse B, Regier DS, Chapman KA. Kanderi N, et al. Among authors: kirmse b. Mol Genet Metab Rep. 2022 Feb 5;30:100844. doi: 10.1016/j.ymgmr.2022.100844. eCollection 2022 Mar. Mol Genet Metab Rep. 2022. PMID: 35242575 Free PMC article.

6

Deconstructing Black Swans: An Introductory Approach to Inherited Metabolic Disorders in the Neonate.

Mew NA, Viall S, Kirmse B, Chapman KA. Mew NA, et al. Among authors: kirmse b. Adv Neonatal Care. 2015 Aug;15(4):241-7; quiz E1-2. doi: 10.1097/ANC.0000000000000206. Adv Neonatal Care. 2015. PMID: 26225592

7

Abnormal newborn screens and acylcarnitines in HIV-exposed and ARV-exposed infants.

Kirmse B, Hobbs CV, Peter I, Laplante B, Caggana M, Kloke K, Raymond K, Summar M, Borkowsky W. Kirmse B, et al. Pediatr Infect Dis J. 2013 Feb;32(2):146-50. doi: 10.1097/INF.0b013e31827030a6. Pediatr Infect Dis J. 2013. PMID: 22935866 Free PMC article.

8

Concurrent non-ketotic hyperglycinemia and propionic acidemia in an eight year old boy.

Kruszka PS, Kirmse B, Zand DJ, Cusmano-Ozog K, Spector E, Van Hove JL, Chapman KA. Kruszka PS, et al. Among authors: kirmse b. Mol Genet Metab Rep. 2014 May 22;1:237-240. doi: 10.1016/j.ymgmr.2014.04.007. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896094 Free PMC article.

9

Acylcarnitine Profiles in HIV-Exposed, Uninfected Neonates in the United States.

Kirmse B, Yao TJ, Hofherr S, Kacanek D, Williams PL, Hobbs CV, Hazra R, Borkowsky W, Van Dyke RB, Summar M. Kirmse B, et al. AIDS Res Hum Retroviruses. 2016 Apr;32(4):339-48. doi: 10.1089/AID.2015.0112. Epub 2016 Jan 19. AIDS Res Hum Retroviruses. 2016. PMID: 26548585 Free PMC article.

10

Acylcarnitines and Genetic Variation in Fat Oxidation Genes in HIV-infected, Antiretroviral-treated Children With and Without Myopathy.

Kirmse B, Hobbs C, Aaron L, Montepiedra G, Summar M, Williams PL, Smith CJ, Van Dyke R, Yu C, Ryckman KK, Borkowsky W; Pediatric HIV/AIDS Cohort Study. Kirmse B, et al. Pediatr Infect Dis J. 2022 Aug 1;41(8):e306-e311. doi: 10.1097/INF.0000000000003586. Epub 2022 Jul 13. Pediatr Infect Dis J. 2022. PMID: 35622436 Free PMC article.

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