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

Year Number of Results
2002 1
2009 2
2010 2
2011 2
2013 2
2014 3
2015 1
2019 1
2021 1
2022 1
2023 1
2024 2
2025 0

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18 results

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Page 1
Ophthalmic findings in Alström syndrome.
Zhou Y, Shoala TS, Kline AD, Francomano CA, Collins MLZ, Ferguson M, Billiet J, Sunness JS, Bianchi M, Payne S, Guan B, Yousaf S, Levin AV. Zhou Y, et al. Among authors: collins mlz. Ophthalmic Genet. 2024 Dec;45(6):596-601. doi: 10.1080/13816810.2024.2402534. Epub 2024 Sep 12. Ophthalmic Genet. 2024. PMID: 39264219
Retinoblastoma: the Zimmerman family story.
Collins ML. Collins ML. JAMA Ophthalmol. 2014 May;132(5):519-20. doi: 10.1001/jamaophthalmol.2014.467. JAMA Ophthalmol. 2014. PMID: 24626469 No abstract available.
Refractive Error Change and Overminus Lens Therapy for Childhood Intermittent Exotropia.
Writing Committee for the Pediatric Eye Disease Investigator Group; Pediatric Eye Disease Investigator Group; Chen AM, Erzurum SA, Chandler DL, Hercinovic A, Wu R, Vricella M, Waters AL, Ticho BH, Erickson JW, Han S, McDowell PS, Li Z, Kraker RT, Holmes JM, Cotter SA. Writing Committee for the Pediatric Eye Disease Investigator Group, et al. JAMA Ophthalmol. 2024 May 1;142(5):417-428. doi: 10.1001/jamaophthalmol.2024.0276. JAMA Ophthalmol. 2024. PMID: 38536764 Free PMC article. Clinical Trial.
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.
Tischfield MA, Baris HN, Wu C, Rudolph G, Van Maldergem L, He W, Chan WM, Andrews C, Demer JL, Robertson RL, Mackey DA, Ruddle JB, Bird TD, Gottlob I, Pieh C, Traboulsi EI, Pomeroy SL, Hunter DG, Soul JS, Newlin A, Sabol LJ, Doherty EJ, de Uzcátegui CE, de Uzcátegui N, Collins ML, Sener EC, Wabbels B, Hellebrand H, Meitinger T, de Berardinis T, Magli A, Schiavi C, Pastore-Trossello M, Koc F, Wong AM, Levin AV, Geraghty MT, Descartes M, Flaherty M, Jamieson RV, Møller HU, Meuthen I, Callen DF, Kerwin J, Lindsay S, Meindl A, Gupta ML Jr, Pellman D, Engle EC. Tischfield MA, et al. Cell. 2010 Jan 8;140(1):74-87. doi: 10.1016/j.cell.2009.12.011. Cell. 2010. PMID: 20074521 Free PMC article.
CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX.
Engle EC, McIntosh N, Yamada K, Lee BA, Johnson R, O'Keefe M, Letson R, London A, Ballard E, Ruttum M, Matsumoto N, Saito N, Collins ML, Morris L, Del Monte M, Magli A, de Berardinis T. Engle EC, et al. BMC Genet. 2002;3:3. doi: 10.1186/1471-2156-3-3. Epub 2002 Mar 6. BMC Genet. 2002. PMID: 11882252 Free PMC article.
18 results