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

Year Number of Results
1969 1
1970 1
1977 2
1978 1
1979 5
1980 7
1981 4
1982 5
1983 2
1984 3
1985 8
1986 8
1987 6
1988 2
1989 4
1990 6
1991 6
1992 5
1993 6
1994 4
1995 3
1996 3
1997 7
1998 6
1999 5
2000 7
2001 7
2002 8
2003 1
2004 15
2005 7
2006 4
2007 6
2008 7
2009 14
2010 11
2011 9
2012 17
2013 8
2014 16
2015 12
2016 11
2017 10
2018 5
2019 15
2020 11
2021 18
2022 9
2023 18
2024 12

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340 results

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Page 1
Congenital and perinatal infections.
Ostrander B, Bale JF. Ostrander B, et al. Among authors: bale jf. Handb Clin Neurol. 2019;162:133-153. doi: 10.1016/B978-0-444-64029-1.00006-0. Handb Clin Neurol. 2019. PMID: 31324308 Review.
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations.
Rodan LH, Spillmann RC, Kurata HT, Lamothe SM, Maghera J, Jamra RA, Alkelai A, Antonarakis SE, Atallah I, Bar-Yosef O, Bilan F, Bjorgo K, Blanc X, Van Bogaert P, Bolkier Y, Burrage LC, Christ BU, Granadillo JL, Dickson P, Donald KA, Dubourg C, Eliyahu A, Emrick L, Engleman K, Gonfiantini MV, Good JM, Kalser J, Kloeckner C, Lachmeijer G, Macchiaiolo M, Nicita F, Odent S, O'Heir E, Ortiz-Gonzalez X, Pacio-Miguez M, Palomares-Bralo M, Pena L, Platzer K, Quinodoz M, Ranza E, Rosenfeld JA, Roulet-Perez E, Santani A, Santos-Simarro F, Pode-Shakked B, Skraban C, Slaugh R, Superti-Furga A, Thiffault I, van Jaabrsveld RH, Vincent M, Wang HG, Zacher P; Undiagnosed Diseases Network; Rush E, Pitt GS, Au PYB, Shashi V. Rodan LH, et al. Genet Med. 2021 Oct;23(10):1922-1932. doi: 10.1038/s41436-021-01232-8. Epub 2021 Jun 23. Genet Med. 2021. PMID: 34163037 Free PMC article.
Changes in medical errors after implementation of a handoff program.
Starmer AJ, Spector ND, Srivastava R, West DC, Rosenbluth G, Allen AD, Noble EL, Tse LL, Dalal AK, Keohane CA, Lipsitz SR, Rothschild JM, Wien MF, Yoon CS, Zigmont KR, Wilson KM, O'Toole JK, Solan LG, Aylor M, Bismilla Z, Coffey M, Mahant S, Blankenburg RL, Destino LA, Everhart JL, Patel SJ, Bale JF Jr, Spackman JB, Stevenson AT, Calaman S, Cole FS, Balmer DF, Hepps JH, Lopreiato JO, Yu CE, Sectish TC, Landrigan CP; I-PASS Study Group. Starmer AJ, et al. Among authors: bale jf jr. N Engl J Med. 2014 Nov 6;371(19):1803-12. doi: 10.1056/NEJMsa1405556. N Engl J Med. 2014. PMID: 25372088 Free article.
Bi-allelic variants in INTS11 are associated with a complex neurological disorder.
Tepe B, Macke EL, Niceta M, Weisz Hubshman M, Kanca O, Schultz-Rogers L, Zarate YA, Schaefer GB, Granadillo De Luque JL, Wegner DJ, Cogne B, Gilbert-Dussardier B, Le Guillou X, Wagner EJ, Pais LS, Neil JE, Mochida GH, Walsh CA, Magal N, Drasinover V, Shohat M, Schwab T, Schmitz C, Clark K, Fine A, Lanpher B, Gavrilova R, Blanc P, Burglen L, Afenjar A, Steel D, Kurian MA, Prabhakar P, Gößwein S, Di Donato N, Bertini ES; Undiagnosed Diseases Network; Wangler MF, Yamamoto S, Tartaglia M, Klee EW, Bellen HJ. Tepe B, et al. Am J Hum Genet. 2023 May 4;110(5):774-789. doi: 10.1016/j.ajhg.2023.03.012. Epub 2023 Apr 12. Am J Hum Genet. 2023. PMID: 37054711 Free PMC article.
Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome.
Kozycki CT, Kodati S, Huryn L, Wang H, Warner BM, Jani P, Hammoud D, Abu-Asab MS, Jittayasothorn Y, Mattapallil MJ, Tsai WL, Ullah E, Zhou P, Tian X, Soldatos A, Moutsopoulos N, Kao-Hsieh M, Heller T, Cowen EW, Lee CR, Toro C, Kalsi S, Khavandgar Z, Baer A, Beach M, Long Priel D, Nehrebecky M, Rosenzweig S, Romeo T, Deuitch N, Brenchley L, Pelayo E, Zein W, Sen N, Yang AH, Farley G, Sweetser DA, Briere L, Yang J, de Oliveira Poswar F, Schwartz IVD, Silva Alves T, Dusser P, Koné-Paut I, Touitou I, Titah SM, van Hagen PM, van Wijck RTA, van der Spek PJ, Yano H, Benneche A, Apalset EM, Jansson RW, Caspi RR, Kuhns DB, Gadina M, Takada H, Ida H, Nishikomori R, Verrecchia E, Sangiorgi E, Manna R, Brooks BP, Sobrin L, Hufnagel RB, Beck D, Shao F, Ombrello AK, Aksentijevich I, Kastner DL; Undiagnosed Diseases Network. Kozycki CT, et al. Ann Rheum Dis. 2022 Oct;81(10):1453-1464. doi: 10.1136/annrheumdis-2022-222629. Epub 2022 Jul 22. Ann Rheum Dis. 2022. PMID: 35868845 Free PMC article.
Congenital infections.
Bale JF Jr. Bale JF Jr. Neurol Clin. 2002 Nov;20(4):1039-60, vii. doi: 10.1016/s0733-8619(02)00014-2. Neurol Clin. 2002. PMID: 12616680 Review.
Emerging viral infections.
Bale JF Jr. Bale JF Jr. Semin Pediatr Neurol. 2012 Sep;19(3):152-7. doi: 10.1016/j.spen.2012.02.001. Semin Pediatr Neurol. 2012. PMID: 22889544 Free PMC article. Review.
A Pediatric Department's Innovative Grant Writing Workshops.
Joss-Moore LA, Keenan HT, Bale JF Jr, Dean JM, Albertine KH. Joss-Moore LA, et al. Among authors: bale jf jr. J Pediatr. 2018 Jun;197:5-7.e1. doi: 10.1016/j.jpeds.2018.02.060. J Pediatr. 2018. PMID: 29801547 Free PMC article. No abstract available.
Cysticercosis.
Bale JF Jr. Bale JF Jr. Curr Treat Options Neurol. 2000 Jul;2(4):355-360. doi: 10.1007/s11940-000-0052-8. Curr Treat Options Neurol. 2000. PMID: 11096760
340 results