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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1887 1
1930 1
1944 1
1946 3
1947 1
1948 1
1949 4
1950 4
1951 4
1952 3
1953 5
1954 5
1955 7
1956 8
1957 8
1958 1
1959 2
1960 5
1961 8
1962 5
1963 8
1964 4
1965 9
1966 3
1967 8
1968 7
1969 14
1970 13
1971 17
1972 8
1973 13
1974 16
1975 15
1976 14
1977 12
1978 18
1979 14
1980 21
1981 18
1982 18
1983 18
1984 25
1985 17
1986 16
1987 18
1988 13
1989 7
1990 22
1991 23
1992 25
1993 22
1994 18
1995 21
1996 18
1997 30
1998 16
1999 20
2000 28
2001 30
2002 20
2003 25
2004 30
2005 44
2006 54
2007 56
2008 42
2009 50
2010 42
2011 50
2012 50
2013 74
2014 92
2015 80
2016 130
2017 82
2018 83
2019 100
2020 105
2021 89
2022 96
2023 94
2024 38

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2,054 results

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Page 1
Krabbe disease: New hope for an old disease.
Bradbury AM, Bongarzone ER, Sands MS. Bradbury AM, et al. Neurosci Lett. 2021 May 1;752:135841. doi: 10.1016/j.neulet.2021.135841. Epub 2021 Mar 22. Neurosci Lett. 2021. PMID: 33766733 Free PMC article. Review.
Krabbe disease (globoid cell leukodystrophy) is a lysosomal storage disease (LSD) characterized by progressive and profound demyelination. Infantile, juvenile and adult-onset forms of Krabbe disease have been described, with infantile being the most common. ...
Krabbe disease (globoid cell leukodystrophy) is a lysosomal storage disease (LSD) characterized by progressive and profound demyelina …
Krabbe Disease.
Orsini JJ, Escolar ML, Wasserstein MP, Caggana M. Orsini JJ, et al. 2000 Jun 19 [updated 2018 Oct 11]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2000 Jun 19 [updated 2018 Oct 11]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301416 Free Books & Documents. Review.
Although historically 85%-90% of symptomatic individuals with Krabbe disease diagnosed by enzyme activity alone have infantile-onset Krabbe disease and 10%-15% have later-onset Krabbe disease, the experience with newborn screening (NBS) suggests that the prop …
Although historically 85%-90% of symptomatic individuals with Krabbe disease diagnosed by enzyme activity alone have infantile-onset …
Globoid Cell Leukodystrophy (Krabbe Disease): An Update.
Maghazachi AA. Maghazachi AA. Immunotargets Ther. 2023 Oct 31;12:105-111. doi: 10.2147/ITT.S424622. eCollection 2023. Immunotargets Ther. 2023. PMID: 37928748 Free PMC article. Review.
Globoid cell leukodystrophy or Krabbe is a disease that affects children as well as adults who have mutations in the gene encoding the enzyme galactosylceramidase/galctocerebrosidase (GALC), resulting in the deposition of the toxic lipid D-galactosyl-beta1-1' sphingosine ( …
Globoid cell leukodystrophy or Krabbe is a disease that affects children as well as adults who have mutations in the gene encoding th …
Krabbe Disease.
Jain M, De Jesus O. Jain M, et al. 2023 Aug 23. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Aug 23. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 32965986 Free Books & Documents.
Krabbe disease is an autosomal recessive neurodegenerative disorder. ...Krabbe disease is subdivided into four sub-categories based on the age of presentation of symptoms; however, many experts disagree with the age range allotted to different subtypes. ...
Krabbe disease is an autosomal recessive neurodegenerative disorder. ...Krabbe disease is subdivided into four sub-categories …
Krabbe's leukodystrophy: Approaches and models in vitro.
Avola R, Graziano AC, Pannuzzo G, Alvares E, Cardile V. Avola R, et al. J Neurosci Res. 2016 Nov;94(11):1284-92. doi: 10.1002/jnr.23846. J Neurosci Res. 2016. PMID: 27638610 Review.
This Review describes some in vitro approaches used to investigate the mechanisms involved in Krabbe's disease, with particular regard to the cellular systems employed to study processes of inflammation, apoptosis, and angiogenesis. ...For a long time, the nonavaila …
This Review describes some in vitro approaches used to investigate the mechanisms involved in Krabbe's disease, with particula …
Krabbe's disease; A rare case report.
Jaiswani AK, Kulkarni V, Paliwal A. Jaiswani AK, et al. Leg Med (Tokyo). 2023 Feb;60:102155. doi: 10.1016/j.legalmed.2022.102155. Epub 2022 Oct 17. Leg Med (Tokyo). 2023. PMID: 36272395
Krabbe's disease (globoid cell leukodystrophy) is a rare lysosomal storage disorder in which galactocerebroside and psychosine accumulate in macrophages and demyelination of white matter of the cerebrum. We present a case of Krabbe's disease with enlar …
Krabbe's disease (globoid cell leukodystrophy) is a rare lysosomal storage disorder in which galactocerebroside and psychosine …
Neuroimmune mechanisms in Krabbe's disease.
Potter GB, Petryniak MA. Potter GB, et al. J Neurosci Res. 2016 Nov;94(11):1341-8. doi: 10.1002/jnr.23804. J Neurosci Res. 2016. PMID: 27638616 Free PMC article. Review.
Moreover, the therapeutic effect underlying hematopoietic stem cell transplantation, the only treatment for Krabbe's disease, has been demonstrated to occur via immunomodulation. This Review highlights recent advances in elaboration of the immune cascade involved in …
Moreover, the therapeutic effect underlying hematopoietic stem cell transplantation, the only treatment for Krabbe's disease, …
Ethical issues with testing and treatment for Krabbe disease.
Ehmann P, Lantos JD. Ehmann P, et al. Dev Med Child Neurol. 2019 Dec;61(12):1358-1361. doi: 10.1111/dmcn.14258. Epub 2019 May 15. Dev Med Child Neurol. 2019. PMID: 31090922 Free article. Review.
WHAT THIS PAPER ADDS: Current tests to identify which children are likely to develop Krabbe diseased are inadequate. Many children identified as being 'at risk' for early infantile Krabbe disease remain asymptomatic. Psychosine appears to be more specific than low g …
WHAT THIS PAPER ADDS: Current tests to identify which children are likely to develop Krabbe diseased are inadequate. Many children id …
Newborn screening for Krabbe's disease.
Orsini JJ, Saavedra-Matiz CA, Gelb MH, Caggana M. Orsini JJ, et al. J Neurosci Res. 2016 Nov;94(11):1063-75. doi: 10.1002/jnr.23781. J Neurosci Res. 2016. PMID: 27638592 Free PMC article. Review.
Live newborn screening for Krabbe's disease (KD) was initiated in New York on August 7, 2006, and started in Missouri in August, 2012. ...Although current treatment options for infants with early-infantile Krabbe's disease are not curative, over time t …
Live newborn screening for Krabbe's disease (KD) was initiated in New York on August 7, 2006, and started in Missouri in Augus …
Hospitalization Burden and Incidence of Krabbe Disease.
Ghabash G, Wilkes J, Barney BJ, Bonkowsky JL. Ghabash G, et al. J Child Neurol. 2022 Jan;37(1):12-19. doi: 10.1177/08830738211027717. Epub 2021 Oct 20. J Child Neurol. 2022. PMID: 34670440 Free PMC article.
OBJECTIVE: The purpose of our study was to understand the healthcare burden and incidence of Krabbe disease (Krabbe). METHODS: Retrospective analysis of Krabbe patients identified October 1, 2015 through December 31, 2020, ages birth through age 3, evaluated …
OBJECTIVE: The purpose of our study was to understand the healthcare burden and incidence of Krabbe disease (Krabbe). METHODS: …
2,054 results

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