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1958 6
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1960 3
1961 3
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1964 4
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1966 4
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1968 2
1969 1
1970 9
1971 6
1972 3
1973 3
1974 4
1975 2
1976 10
1977 6
1978 11
1979 10
1980 12
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1982 8
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1984 24
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1988 32
1989 37
1990 35
1991 22
1992 35
1993 40
1994 34
1995 51
1996 55
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1998 82
1999 99
2000 96
2001 130
2002 127
2003 141
2004 151
2005 167
2006 182
2007 206
2008 231
2009 232
2010 231
2011 269
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2013 313
2014 340
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Page 1
Reply to Beaulieu.
Moore A, Fisher E, Eccleston C. Moore A, et al. Pain. 2021 Aug 1;162(8):2310. doi: 10.1097/j.pain.0000000000002295. Pain. 2021. PMID: 34256384 No abstract available.
Novel CNS malformations and skeletal anomalies in a patient with Beaulieu-boycott-Innes syndrome.
Accogli A, Scala M, Calcagno A, Castello R, Torella A, Musacchia F, Allegri AME, Mancardi MM, Maghnie M, Severino M; Telethon Undiagnosed Diseases Program; Nigro V, Capra V. Accogli A, et al. Am J Med Genet A. 2018 Dec;176(12):2835-2840. doi: 10.1002/ajmg.a.40534. Epub 2018 Sep 20. Am J Med Genet A. 2018. PMID: 30238602 Review.
Bi-allelic mutations in THOC6 have been associated to Beaulieu-Boycott-Innes syndrome (BBIS), a syndromic form of intellectual disability (ID). ...
Bi-allelic mutations in THOC6 have been associated to Beaulieu-Boycott-Innes syndrome (BBIS), a syndromic form of intellectual disabi …
Cultural responsiveness in applied behavior analysis: Research and practice.
Jimenez-Gomez C, Beaulieu L. Jimenez-Gomez C, et al. J Appl Behav Anal. 2022 Jun;55(3):650-673. doi: 10.1002/jaba.920. Epub 2022 Apr 12. J Appl Behav Anal. 2022. PMID: 35411945
The content of this paper is grounded in the framework described by Beaulieu and Jimenez-Gomez (2022)....
The content of this paper is grounded in the framework described by Beaulieu and Jimenez-Gomez (2022)....
La maladie de Crohn.
Fitaire C, Michetti P. Fitaire C, et al. Rev Med Suisse. 2023 Sep 27;19(843):1761. doi: 10.53738/REVMED.2023.19.843.1761. Rev Med Suisse. 2023. PMID: 37753916 French. No abstract available.
Finding MYCure.
Beaulieu ME, Soucek L. Beaulieu ME, et al. Mol Cell Oncol. 2019 Jun 20;6(5):e1618178. doi: 10.1080/23723556.2019.1618178. eCollection 2019. Mol Cell Oncol. 2019. PMID: 31528695 Free PMC article.
Beaulieu v. Clausen.
Minnesota. Court of Appeals. Minnesota. Court of Appeals. Wests North West Rep. 1992 Oct 20;491:662-8. Wests North West Rep. 1992. PMID: 12041144
The Court of Appeals of Minnesota affirmed an administrative law judge's determination that a dentist, Clausen, was not permitted to refuse treatment to a patient, Beaulieu, when he learned that the patient had tested HIV-positive. The appellate court further held that the …
The Court of Appeals of Minnesota affirmed an administrative law judge's determination that a dentist, Clausen, was not permitted to refuse …
Proteinuria in Two Sisters with Beaulieu-Boycott-Innes Syndrome, A Case Report.
Hassanvand Amouzadeh M, Akhavan Sepahi M, Abasi E. Hassanvand Amouzadeh M, et al. Iran J Kidney Dis. 2020 Jul;14(4):312-314. Iran J Kidney Dis. 2020. PMID: 32655027 Free article.
Direct Sanger sequencing confirmed that they are homozygote for the pathogenic variant mutations in the THOC6 gene, which is associated with Beaulieu-Boycott-Innes syndrome (BBIS). These patients also had proteinuria and subsequently developed hematuria. ...
Direct Sanger sequencing confirmed that they are homozygote for the pathogenic variant mutations in the THOC6 gene, which is associated with …
Floquet-Bloch valleytronics.
Fragkos S, Fabre B, Tkach O, Petit S, Descamps D, Schönhense G, Mairesse Y, Schüler M, Beaulieu S. Fragkos S, et al. Nat Commun. 2025 Jul 1;16(1):5799. doi: 10.1038/s41467-025-61076-7. Nat Commun. 2025. PMID: 40593831 Free PMC article.
Beaulieu-Boycott-Innes syndrome: an intellectual disability syndrome with characteristic facies.
Casey J, Jenkinson A, Magee A, Ennis S, Monavari A, Green A, Lynch SA, Crushell E, Hughes J. Casey J, et al. Clin Dysmorphol. 2016 Oct;25(4):146-51. doi: 10.1097/MCD.0000000000000134. Clin Dysmorphol. 2016. PMID: 27295358
Whole-exome sequencing identified three linked homozygous missense variants in THOC6 (c.298T>A, p.Trp100Arg; c.700G>C, p.Val234Leu; c.824G>A, p.Gly275Asp) as the likely cause of this child's intellectual disability syndrome, resulting in a molecular diagnosis of Beaul …
Whole-exome sequencing identified three linked homozygous missense variants in THOC6 (c.298T>A, p.Trp100Arg; c.700G>C, p.Val234Leu; c. …
6,833 results