PubMed for id: 766850

Year	Number of Results
1973	1
1975	3
1978	2
1979	1
1980	1
1981	2
1983	4
1984	5
1985	6
1986	6
1987	8
1988	7
1989	12
1990	7
1991	6
1992	15
1993	19
1994	8
1995	16
1996	19
1997	17
1998	21
1999	22
2000	20
2001	15
2002	14
2003	19
2004	12
2005	12
2006	10
2007	6
2008	7
2009	10
2010	7
2011	9
2012	9
2013	13
2014	10
2015	12
2016	7
2017	17
2018	12
2019	14
2020	15
2021	9
2022	7
2023	8
2024	4

1

TFEB activation triggers pexophagy for functional adaptation during oxidative stress under calcium deficient-conditions.

Manandhar L, Dutta RK, Devkota P, Chhetri A, Wei X, Park C, Kwon HM, Park R. Manandhar L, et al. Cell Commun Signal. 2024 Feb 21;22(1):142. doi: 10.1186/s12964-024-01524-x. Cell Commun Signal. 2024. PMID: 38383392 Free PMC article.

2

Progress in leukodystrophies with zebrafish.

Shih HY, Raas Q, Bonkowsky JL. Shih HY, et al. Dev Growth Differ. 2024 Jan;66(1):21-34. doi: 10.1111/dgd.12907. Epub 2024 Jan 19. Dev Growth Differ. 2024. PMID: 38239149 Review.

3

[Zellweger syndrome caused by PEX6 gene variation in 2 cases and literature review].

Yang P, Zeng CZ, Tao XW, Rong SW, Long Y, Zeng LK. Yang P, et al. Zhonghua Er Ke Za Zhi. 2024 Jan 2;62(1):43-48. doi: 10.3760/cma.j.cn112140-20230914-00191. Zhonghua Er Ke Za Zhi. 2024. PMID: 38154976 Review. Chinese.

4

Abnormal activation of MAPKs pathways and inhibition of autophagy in a group of patients with Zellweger spectrum disorders and X-linked adrenoleukodystrophy.

Gragnaniello V, Gueraldi D, Puma A, Commone A, Cazzorla C, Loro C, Porcù E, Stornaiuolo M, Miglioranza P, Salviati L, Wanders RJA, Burlina A. Gragnaniello V, et al. Orphanet J Rare Dis. 2023 Nov 16;18(1):358. doi: 10.1186/s13023-023-02940-x. Orphanet J Rare Dis. 2023. PMID: 37974207 Free PMC article.

5

Severe Zellweger spectrum disorder due to a novel missense variant in the PEX13 gene: A case report and the literature review.

Su L, Peng MZ, Chen XD, Wu S, Liu L. Su L, et al. Mol Genet Genomic Med. 2024 Jan;12(1):e2315. doi: 10.1002/mgg3.2315. Epub 2023 Nov 14. Mol Genet Genomic Med. 2024. PMID: 37962062 Free PMC article.

6

A new test method for biochemical analysis of plasmalogens in dried blood spots and erythrocytes from patients with peroxisomal disorders.

Wegwerth PJ, White AL, Stoway SD, Loken PR, Oglesbee D, Matern D, Tortorelli S, Raymond KM, Braverman NE, Gavrilov DK. Wegwerth PJ, et al. J Inherit Metab Dis. 2023 Nov;46(6):1159-1169. doi: 10.1002/jimd.12682. Epub 2023 Oct 31. J Inherit Metab Dis. 2023. PMID: 37747296 Review.

7

Autosomal dominant Zellweger spectrum disorder caused by de novo variants in PEX14 gene.

Waterham HR, Koster J, Ebberink MS, Ješina P, Zeman J, Nosková L, Kmoch S, Devic P, Cheillan D, Wanders RJA, Ferdinandusse S. Waterham HR, et al. Genet Med. 2023 Nov;25(11):100944. doi: 10.1016/j.gim.2023.100944. Epub 2023 Jul 23. Genet Med. 2023. PMID: 37493040 Free article.

8

Novel PEX1 mutations in fibroblasts from children with Zellweger spectrum disorders exhibit temperature sensitive characteristics.

Liang JS, Hung KL, Lin LJ, Ong WP, Keng WT, Lu JF. Liang JS, et al. Epilepsy Behav. 2023 Aug;145:109266. doi: 10.1016/j.yebeh.2023.109266. Epub 2023 Jun 27. Epilepsy Behav. 2023. PMID: 37385119

9

A homozygous Gly470Ala variant in PEX6 causes severe Zellweger spectrum disorder.

Galarreta CI, Wong K, Carmichael J, Woods J, Tise CG, Niehaus AD, Schildt AJ, Verscaj CP, Cusmano-Ozog KP. Galarreta CI, et al. Am J Med Genet A. 2023 Aug;191(8):2057-2063. doi: 10.1002/ajmg.a.63234. Epub 2023 May 5. Am J Med Genet A. 2023. PMID: 37144748

10

Novel mutation causing Zellweger syndrome.

Adiyapatham S, Murugesan A. Adiyapatham S, et al. BMJ Case Rep. 2023 Mar 17;16(3):e252014. doi: 10.1136/bcr-2022-252014. BMJ Case Rep. 2023. PMID: 36931687

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

Results by year

Text availability

Article attribute

Article type

Publication date

459 results

Results by year