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 Custom Filters

Results by year

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

Year Number of Results
1962 1
1995 1
1996 2
1997 2
1998 2
1999 8
2000 6
2001 3
2002 1
2003 7
2004 2
2005 4
2006 5
2007 4
2008 5
2009 4
2010 7
2011 5
2012 4
2013 4
2014 4
2015 6
2016 5
2017 5
2018 5
2019 6
2020 5
2021 9
2022 5
2023 7
2024 13
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

135 results

Results by year

Filters applied: . Clear all
Page 1
Syndromic Hearing Loss in Children.
Lewis M, Robson CD, D'Arco F. Lewis M, et al. Among authors: robson cd. Neuroimaging Clin N Am. 2023 Nov;33(4):563-580. doi: 10.1016/j.nic.2023.05.007. Epub 2023 Jul 4. Neuroimaging Clin N Am. 2023. PMID: 37741658 Review.
Conductive Hearing Loss in Children.
Robson CD. Robson CD. Neuroimaging Clin N Am. 2023 Nov;33(4):543-562. doi: 10.1016/j.nic.2023.05.006. Epub 2023 Jul 11. Neuroimaging Clin N Am. 2023. PMID: 37741657 Review.
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
Jurgens JA, Barry BJ, Chan WM, MacKinnon S, Whitman MC, Matos Ruiz PM, Pratt BM, England EM, Pais L, Lemire G, Groopman E, Glaze C, Russell KA, Singer-Berk M, Di Gioia SA, Lee AS, Andrews C, Shaaban S, Wirth MM, Bekele S, Toffoloni M, Bradford VR, Foster EE, Berube L, Rivera-Quiles C, Mensching FM, Sanchis-Juan A, Fu JM, Wong I, Zhao X, Wilson MW, Weisburd B, Lek M; Ocular CCDD Phenotyping Consortium; Brand H, Talkowski ME, MacArthur DG, O'Donnell-Luria A, Robson CD, Hunter DG, Engle EC. Jurgens JA, et al. Among authors: robson cd. Genet Med. 2024 Jul 17:101216. doi: 10.1016/j.gim.2024.101216. Online ahead of print. Genet Med. 2024. PMID: 39033378 Free article.
Non-Syndromic Sensorineural Hearing Loss in Children.
Robson CD, Lewis M, D'Arco F. Robson CD, et al. Neuroimaging Clin N Am. 2023 Nov;33(4):531-542. doi: 10.1016/j.nic.2023.05.005. Epub 2023 Jul 11. Neuroimaging Clin N Am. 2023. PMID: 37741656 Review.
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Tenney AP, Di Gioia SA, Webb BD, Chan WM, de Boer E, Garnai SJ, Barry BJ, Ray T, Kosicki M, Robson CD, Zhang Z, Collins TE, Gelber A, Pratt BM, Fujiwara Y, Varshney A, Lek M, Warburton PE, Van Ryzin C, Lehky TJ, Zalewski C, King KA, Brewer CC, Thurm A, Snow J, Facio FM, Narisu N, Bonnycastle LL, Swift A, Chines PS, Bell JL, Mohan S, Whitman MC, Staffieri SE, Elder JE, Demer JL, Torres A, Rachid E, Al-Haddad C, Boustany RM, Mackey DA, Brady AF, Fenollar-Cortés M, Fradin M, Kleefstra T, Padberg GW, Raskin S, Sato MT, Orkin SH, Parker SCJ, Hadlock TA, Vissers LELM, van Bokhoven H, Jabs EW, Collins FS, Pennacchio LA, Manoli I, Engle EC. Tenney AP, et al. Among authors: robson cd. Nat Genet. 2023 Jul;55(7):1149-1163. doi: 10.1038/s41588-023-01424-9. Epub 2023 Jun 29. Nat Genet. 2023. PMID: 37386251 Free PMC article.
Fetal Head and Neck Imaging.
Patino M, Jaimes C, Robson CD. Patino M, et al. Among authors: robson cd. Magn Reson Imaging Clin N Am. 2024 Aug;32(3):413-430. doi: 10.1016/j.mric.2024.03.003. Epub 2024 Apr 24. Magn Reson Imaging Clin N Am. 2024. PMID: 38944431 Review.
Imaging of Pediatric Orbital Diseases.
Vachha BA, Robson CD. Vachha BA, et al. Among authors: robson cd. Neuroimaging Clin N Am. 2015 Aug;25(3):477-501. doi: 10.1016/j.nic.2015.05.009. Neuroimaging Clin N Am. 2015. PMID: 26208421 Review.
Prenatal Imaging of Craniosynostosis Syndromes.
Ketwaroo PD, Robson CD, Estroff JA. Ketwaroo PD, et al. Among authors: robson cd. Semin Ultrasound CT MR. 2015 Dec;36(6):453-64. doi: 10.1053/j.sult.2015.06.002. Epub 2015 Jun 16. Semin Ultrasound CT MR. 2015. PMID: 26614129 Review.
Congenital hearing impairment.
Robson CD. Robson CD. Pediatr Radiol. 2006 Apr;36(4):309-24. doi: 10.1007/s00247-005-0042-9. Epub 2006 Feb 8. Pediatr Radiol. 2006. PMID: 16465539 Review.
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
Jurgens JA, Barry BJ, Chan WM, MacKinnon S, Whitman MC, Matos Ruiz PM, Pratt BM, England EM, Pais L, Lemire G, Groopman E, Glaze C, Russell KA, Singer-Berk M, Di Gioia SA, Lee AS, Andrews C, Shaaban S, Wirth MM, Bekele S, Toffoloni M, Bradford VR, Foster EE, Berube L, Rivera-Quiles C, Mensching FM, Sanchis-Juan A, Fu JM, Wong I, Zhao X, Wilson MW, Weisburd B, Lek M; Ocular CCDD Phenotyping Consortium; Brand H, Talkowski ME, MacArthur DG, O'Donnell-Luria A, Robson CD, Hunter DG, Engle EC. Jurgens JA, et al. Among authors: robson cd. medRxiv [Preprint]. 2024 Mar 26:2024.03.22.24304594. doi: 10.1101/2024.03.22.24304594. medRxiv. 2024. Update in: Genet Med. 2024 Jul 17:101216. doi: 10.1016/j.gim.2024.101216. PMID: 38585811 Free PMC article. Updated. Preprint.
135 results