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

Year Number of Results
1946 1
2005 1
2007 2
2008 5
2009 6
2010 8
2011 3
2012 8
2013 9
2014 8
2015 11
2016 18
2017 15
2018 31
2019 21
2020 45
2021 41
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195 results
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Page 1
Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia.
Yap ZY, Efthymiou S, Seiffert S, Vargas Parra K, Lee S, Nasca A, Maroofian R, Schrauwen I, Pendziwiat M, Jung S, Bhoj E, Striano P, Mankad K, Vona B, Cuddapah S, Wagner A, Alvi JR, Davoudi-Dehaghani E, Fallah MS, Gannavarapu S, Lamperti C, Legati A, Murtaza BN, Nadeem MS, Rehman MU, Saeidi K, Salpietro V, von Spiczak S, Sandoval A, Zeinali S, Zeviani M, Reich A; SYNaPS Study Group; University of Washington Center for Mendelian Genomics, Jang C, Helbig I, Barakat TS, Ghezzi D, Leal SM, Weber Y, Houlden H, Yoon WH. Yap ZY, et al. Among authors: mankad k. Am J Hum Genet. 2021 Nov 17:S0002-9297(21)00415-8. doi: 10.1016/j.ajhg.2021.11.003. Online ahead of print. Am J Hum Genet. 2021. PMID: 34800363
MRI Patterns in Pediatric CNS Hemophagocytic Lymphohistiocytosis.
Malik P, Antonini L, Mannam P, Aboobacker FN, Merve A, Gilmour K, Rao K, Kumar S, Mani SE, Eleftheriou D, Rao A, Hemingway C, Sudhakar SV, Bartram J, Mankad K. Malik P, et al. Among authors: mankad k. AJNR Am J Neuroradiol. 2021 Nov;42(11):2077-2085. doi: 10.3174/ajnr.A7292. Epub 2021 Oct 7. AJNR Am J Neuroradiol. 2021. PMID: 34620587
L1CAM variants cause two distinct imaging phenotypes on fetal MRI.
Accogli A, Goergen S, Izzo G, Mankad K, Krajden Haratz K, Parazzini C, Fahey M, Menzies L, Baptista J, Carpineta L, Tortora D, Fulcheri E, Gaetano Vellone V, Paladini D, Spaccini L, Toto V, Trayers C, Ben Sira L, Reches A, Malinger G, Salpietro V, De Marco P, Srour M, Zara F, Capra V, Rossi A, Severino M. Accogli A, et al. Among authors: mankad k. Ann Clin Transl Neurol. 2021 Oct;8(10):2004-2012. doi: 10.1002/acn3.51448. Epub 2021 Sep 12. Ann Clin Transl Neurol. 2021. PMID: 34510796 Free PMC article.
Machine Assist for Pediatric Posterior Fossa Tumor Diagnosis: A Multinational Study.
Zhang M, Wong SW, Wright JN, Toescu S, Mohammadzadeh M, Han M, Lummus S, Wagner MW, Yecies D, Lai H, Eghbal A, Radmanesh A, Nemelka J, Harward S, Malinzak M, Laughlin S, Perreault S, Braun KRM, Vossough A, Poussaint T, Goetti R, Ertl-Wagner B, Ho CY, Oztekin O, Ramaswamy V, Mankad K, Vitanza NA, Cheshier SH, Said M, Aquilina K, Thompson E, Jaju A, Grant GA, Lober RM, Yeom KW. Zhang M, et al. Among authors: mankad k. Neurosurgery. 2021 Oct 13;89(5):892-900. doi: 10.1093/neuros/nyab311. Neurosurgery. 2021. PMID: 34392363
Giant pattern VEPs in children.
Thompson DA, Marmoy OR, Prise KL, Reynolds VM, Handley SE, Versace DM, Kafiabadi S, Mankad K, Panteli V, Schwiebert K, James G, Bowman R. Thompson DA, et al. Among authors: mankad k. Eur J Paediatr Neurol. 2021 Sep;34:33-42. doi: 10.1016/j.ejpn.2021.07.008. Epub 2021 Jul 30. Eur J Paediatr Neurol. 2021. PMID: 34388649
Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformation.
Haldipur P, Bernardo S, Aldinger KA, Sivakumar T, Millman J, Sjoboen AH, Dang D, Dubocanin D, Deng M, Timms AE, Davis BD, Plummer JT, Mankad K, Oztekin O, Manganaro L, Guimiot F, Adle-Biassette H, Russo R, Siebert JR, Kidron D, Petrilli G, Roux N, Razavi F, Glass IA, Di Gioia C, Silvestri E, Millen KJ. Haldipur P, et al. Among authors: mankad k. Acta Neuropathol. 2021 Oct;142(4):761-776. doi: 10.1007/s00401-021-02355-7. Epub 2021 Aug 4. Acta Neuropathol. 2021. PMID: 34347142
195 results