PubMed for id: 435926

Year	Number of Results
1981	1
1987	1
1988	3
1992	3
1993	2
1994	1
1995	7
1996	4
1997	1
1998	5
1999	7
2000	3
2001	8
2002	5
2003	1
2004	12
2005	2
2006	12
2007	6
2008	6
2009	7
2010	8
2011	7
2012	12
2013	18
2014	10
2015	11
2016	17
2017	8
2018	16
2019	15
2020	8
2021	12
2022	6
2023	9
2024	3

1

Periventricular white matter abnormalities and restricted repetitive behavior in autism spectrum disorder.

Blackmon K, Ben-Avi E, Wang X, Pardoe HR, Di Martino A, Halgren E, Devinsky O, Thesen T, Kuzniecky R. Blackmon K, et al. Neuroimage Clin. 2015 Oct 31;10:36-45. doi: 10.1016/j.nicl.2015.10.017. eCollection 2016. Neuroimage Clin. 2015. PMID: 26693400 Free PMC article.

2

Interleukin-10 high producer allele and ultrasound-defined periventricular white matter abnormalities in preterm infants: a preliminary study.

Dördelmann M, Kerk J, Dressler F, Brinkhaus MJ, Bartels DB, Dammann CE, Dörk T, Dammann O. Dördelmann M, et al. Neuropediatrics. 2006 Jun;37(3):130-6. doi: 10.1055/s-2006-924554. Neuropediatrics. 2006. PMID: 16967363

3

Spastic diplegia and periventricular white matter abnormalities in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, a defect of isoleucine metabolism: differential diagnosis with hypoxic-ischemic brain diseases.

Poll-The BT, Wanders RJ, Ruiter JP, Ofman R, Majoie CB, Barth PG, Duran M. Poll-The BT, et al. Mol Genet Metab. 2004 Apr;81(4):295-9. doi: 10.1016/j.ymgme.2003.11.013. Mol Genet Metab. 2004. PMID: 15059617

4

Magnetic resonance and cranial ultrasound characteristics of periventricular white matter abnormalities in newborn infants.

Childs AM, Cornette L, Ramenghi LA, Tanner SF, Arthur RJ, Martinez D, Levene MI. Childs AM, et al. Clin Radiol. 2001 Aug;56(8):647-55. doi: 10.1053/crad.2001.0754. Clin Radiol. 2001. PMID: 11467866

5

Partial loss of function of colony-stimulating factor 1 receptor in a patient with white matter abnormalities.

Konno T, Miura T, Harriott AM, Mezaki N, Edwards ES, Rademakers R, Ross OA, Meschia JF, Ikeuchi T, Wszolek ZK. Konno T, et al. Eur J Neurol. 2018 Jun;25(6):875-881. doi: 10.1111/ene.13611. Epub 2018 Apr 3. Eur J Neurol. 2018. PMID: 29509319 Free PMC article.

6

Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy.

Theisen BE, Rumyantseva A, Cohen JS, Alcaraz WA, Shinde DN, Tang S, Srivastava S, Pevsner J, Trifunovic A, Fatemi A. Theisen BE, et al. Am J Med Genet A. 2017 Sep;173(9):2505-2510. doi: 10.1002/ajmg.a.38339. Epub 2017 Jun 26. Am J Med Genet A. 2017. PMID: 28650581

7

Clinical, radiological, and genetic survey of patients with muscle-eye-brain disease caused by mutations in POMGNT1.

Yiş U, Uyanik G, Rosendahl DM, Carman KB, Bayram E, Heise M, Cömertpay G, Kurul SH. Yiş U, et al. Pediatr Neurol. 2014 May;50(5):491-7. doi: 10.1016/j.pediatrneurol.2014.01.008. Epub 2014 Jan 7. Pediatr Neurol. 2014. PMID: 24731844

8

Characteristic brain magnetic resonance imaging pattern in patients with macrocephaly and PTEN mutations.

Vanderver A, Tonduti D, Kahn I, Schmidt J, Medne L, Vento J, Chapman KA, Lanpher B, Pearl P, Gropman A, Lourenco C, Bamforth JS, Sharpe C, Pineda M, Schallner J, Bodamer O, Orcesi S, Oberstein SA, Sistermans EA, Yntema HG, Bonnemann C, Waldman AT, van der Knaap MS. Vanderver A, et al. Am J Med Genet A. 2014 Mar;164A(3):627-33. doi: 10.1002/ajmg.a.36309. Epub 2013 Dec 20. Am J Med Genet A. 2014. PMID: 24375884 Free PMC article.

9

6p25 microdeletion: white matter abnormalities in an adult patient.

Vernon HJ, Bytyci Telegrafi A, Batista D, Owegi M, Leigh R. Vernon HJ, et al. Am J Med Genet A. 2013 Jul;161A(7):1686-9. doi: 10.1002/ajmg.a.35937. Epub 2013 May 17. Am J Med Genet A. 2013. PMID: 23686687

10

Hypomyelination and congenital cataract: broadening the clinical phenotype.

Biancheri R, Zara F, Rossi A, Mathot M, Nassogne MC, Yalcinkaya C, Erturk O, Tuysuz B, Di Rocco M, Gazzerro E, Bugiani M, van Spaendonk R, Sistermans EA, Minetti C, van der Knaap MS, Wolf NI. Biancheri R, et al. Arch Neurol. 2011 Sep;68(9):1191-4. doi: 10.1001/archneurol.2011.201. Arch Neurol. 2011. PMID: 21911699 Review.

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