Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1998 2
1999 2
2001 1
2002 3
2004 2
2005 1
2006 2
2007 6
2008 2
2009 3
2010 1
2011 3
2012 5
2013 1
2014 2
2015 5
2016 5
2017 2
2018 1
2019 2
2021 3
2022 3
2023 3
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

52 results

Results by year

Filters applied: . Clear all
Page 1
Umbilical Cord Hemangioma with Significant Cord Edema.
Zhang L, Delisle MF, Hendson G, Liauw J. Zhang L, et al. Among authors: hendson g. J Obstet Gynaecol Can. 2023 Nov;45(11):101785. doi: 10.1016/j.jogc.2021.06.012. Epub 2021 Jul 22. J Obstet Gynaecol Can. 2023. PMID: 34303858 No abstract available.
Comment.
Connolly M, Steinbok P, Hendson G. Connolly M, et al. Among authors: hendson g. Childs Nerv Syst. 1999 Aug;15(8):403. doi: 10.1007/s003810050424. Childs Nerv Syst. 1999. PMID: 10447612 No abstract available.
Infantile cardioencephalopathy due to a COX15 gene defect: report and review.
Alfadhel M, Lillquist YP, Waters PJ, Sinclair G, Struys E, McFadden D, Hendson G, Hyams L, Shoffner J, Vallance HD. Alfadhel M, et al. Among authors: hendson g. Am J Med Genet A. 2011 Apr;155A(4):840-4. doi: 10.1002/ajmg.a.33881. Epub 2011 Mar 15. Am J Med Genet A. 2011. PMID: 21412973 Review.
Low-grade diffusely infiltrative tumour (LGDIT), SMARCB1-mutant: A clinical and histopathological distinct entity showing epigenetic similarity with ATRT-MYC.
Hasselblatt M, Thomas C, Federico A, Bens S, Hellström M, Casar-Borota O, Kordes U, Neumann JE, Dottermusch M, Rodriguez FJ, Lo AC, Cheng S, Hendson G, Hukin J, Hartmann C, Koch A, Capper D, Siebert R, Paulus W, Nemes K, Johann PD, Frühwald MC, Kool M. Hasselblatt M, et al. Among authors: hendson g. Neuropathol Appl Neurobiol. 2022 Jun;48(4):e12797. doi: 10.1111/nan.12797. Epub 2022 Feb 18. Neuropathol Appl Neurobiol. 2022. PMID: 35152461
Dental abnormalities in Schimke immuno-osseous dysplasia.
Morimoto M, Kérourédan O, Gendronneau M, Shuen C, Baradaran-Heravi A, Asakura Y, Basiratnia M, Bogdanovic R, Bonneau D, Buck A, Charrow J, Cochat P, Dehaai KA, Fenkçi MS, Frange P, Fründ S, Fryssira H, Keller K, Kirmani S, Kobelka C, Kohler K, Lewis DB, Massella L, McLeod DR, Milford DV, Nobili F, Olney AH, Semerci CN, Stajic N, Stein A, Taque S, Zonana J, Lücke T, Hendson G, Bonnaure-Mallet M, Boerkoel CF. Morimoto M, et al. Among authors: hendson g. J Dent Res. 2012 Jul;91(7 Suppl):29S-37S. doi: 10.1177/0022034512450299. J Dent Res. 2012. PMID: 22699664 Free PMC article.
Are CUL3 variants an underreported cause of congenital heart disease?
Di Francesco D, Swenerton A, Li WL, Dunham C, Hendson G, Boerkoel CF. Di Francesco D, et al. Among authors: hendson g. Am J Med Genet A. 2023 Dec;191(12):2903-2907. doi: 10.1002/ajmg.a.63387. Epub 2023 Sep 4. Am J Med Genet A. 2023. PMID: 37665043
52 results