PubMed (Bookshelf cited) for id: 44131

Year	Number of Results
1980	1
1991	1
1995	2
1996	2
1997	4
1999	2
2003	1
2004	1
2005	2
2006	1
2007	1
2010	3
2011	2
2012	3
2013	4
2014	5
2015	5
2016	4
2017	3
2018	5
2024	0

1

A prospective natural history study of Krabbe disease in a patient cohort with onset between 6 months and 3 years of life.

Bascou N, DeRenzo A, Poe MD, Escolar ML. Bascou N, et al. Orphanet J Rare Dis. 2018 Aug 9;13(1):126. doi: 10.1186/s13023-018-0872-9. Orphanet J Rare Dis. 2018. PMID: 30089515 Free PMC article.

2

Adult-onset Krabbe disease in two generations of a Chinese family.

Zhang T, Yan C, Ji K, Lin P, Chi L, Zhao X, Zhao Y. Zhang T, et al. Ann Transl Med. 2018 May;6(10):174. doi: 10.21037/atm.2018.04.30. Ann Transl Med. 2018. PMID: 29951496 Free PMC article.

3

Hematopoietic Stem Cell Transplantation in Late-Onset Krabbe Disease: No Evidence of Worsening Demyelination and Axonal Loss 4 Years Post-allograft.

Laule C, Vavasour IM, Shahinfard E, Mädler B, Zhang J, Li DKB, MacKay AL, Sirrs SM. Laule C, et al. J Neuroimaging. 2018 May;28(3):252-255. doi: 10.1111/jon.12502. Epub 2018 Feb 26. J Neuroimaging. 2018. PMID: 29479774

4

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. 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.

5

Precision newborn screening for lysosomal disorders.

Minter Baerg MM, Stoway SD, Hart J, Mott L, Peck DS, Nett SL, Eckerman JS, Lacey JM, Turgeon CT, Gavrilov D, Oglesbee D, Raymond K, Tortorelli S, Matern D, Mørkrid L, Rinaldo P. Minter Baerg MM, et al. Genet Med. 2018 Aug;20(8):847-854. doi: 10.1038/gim.2017.194. Epub 2017 Nov 9. Genet Med. 2018. PMID: 29120458 Free article.

6

Developmental outcomes of cord blood transplantation for Krabbe disease: A 15-year study.

Wright MD, Poe MD, DeRenzo A, Haldal S, Escolar ML. Wright MD, et al. Neurology. 2017 Sep 26;89(13):1365-1372. doi: 10.1212/WNL.0000000000004418. Epub 2017 Aug 30. Neurology. 2017. PMID: 28855403 Free PMC article.

7

Psychosine, a marker of Krabbe phenotype and treatment effect.

Escolar ML, Kiely BT, Shawgo E, Hong X, Gelb MH, Orsini JJ, Matern D, Poe MD. Escolar ML, et al. Mol Genet Metab. 2017 Jul;121(3):271-278. doi: 10.1016/j.ymgme.2017.05.015. Epub 2017 May 22. Mol Genet Metab. 2017. PMID: 28579020 Free PMC article.

8

Clinical management of Krabbe disease.

Escolar ML, West T, Dallavecchia A, Poe MD, LaPoint K. Escolar ML, et al. J Neurosci Res. 2016 Nov;94(11):1118-25. doi: 10.1002/jnr.23891. J Neurosci Res. 2016. PMID: 27638597 Review.

9

Expression of individual mutations and haplotypes in the galactocerebrosidase gene identified by the newborn screening program in New York State and in confirmed cases of Krabbe's disease.

Saavedra-Matiz CA, Luzi P, Nichols M, Orsini JJ, Caggana M, Wenger DA. Saavedra-Matiz CA, et al. J Neurosci Res. 2016 Nov;94(11):1076-83. doi: 10.1002/jnr.23905. J Neurosci Res. 2016. PMID: 27638593

10

Clinical outcomes of children with abnormal newborn screening results for Krabbe disease in New York State.

Wasserstein MP, Andriola M, Arnold G, Aron A, Duffner P, Erbe RW, Escolar ML, Estrella L, Galvin-Parton P, Iglesias A, Kay DM, Kronn DF, Kurtzberg J, Kwon JM, Langan TJ, Levy PA, Naidich TP, Orsini JJ, Pellegrino JE, Provenzale JM, Wenger DA, Caggana M. Wasserstein MP, et al. Genet Med. 2016 Dec;18(12):1235-1243. doi: 10.1038/gim.2016.35. Epub 2016 May 12. Genet Med. 2016. PMID: 27171547 Free article.

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