Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1988 1
1989 1
1990 2
1992 1
1993 2
1995 1
1996 1
1997 2
1998 3
1999 2
2000 4
2001 5
2003 1
2004 1
2005 1
2007 1
2008 4
2009 1
2010 5
2011 3
2013 2
2014 1
2016 1
2022 0
Text availability
Article attribute
Article type
Publication date

Search Results

43 results
Results by year
Filters applied: . Clear all
Page 1
Molecular Diagnosis of Myotonic Dystrophy.
Chakraborty S, Vatta M, Bachinski LL, Krahe R, Dlouhy S, Bai S. Chakraborty S, et al. Among authors: bachinski ll. Curr Protoc Hum Genet. 2016 Oct 11;91:9.29.1-9.29.19. doi: 10.1002/cphg.22. Curr Protoc Hum Genet. 2016. PMID: 27727437
New theories. Causes of dilated cardiomyopathy.
Bachinski LL, Roberts R. Bachinski LL, et al. Cardiol Clin. 1998 Nov;16(4):603-10, vii. doi: 10.1016/s0733-8651(05)70037-0. Cardiol Clin. 1998. PMID: 9891590 Review.
Molecular signatures of metastasis in head and neck cancer.
Colella S, Richards KL, Bachinski LL, Baggerly KA, Tsavachidis S, Lang JC, Schuller DE, Krahe R. Colella S, et al. Among authors: bachinski ll. Head Neck. 2008 Oct;30(10):1273-83. doi: 10.1002/hed.20871. Head Neck. 2008. PMID: 18642293 Free PMC article.
Premutation allele pool in myotonic dystrophy type 2.
Bachinski LL, Czernuszewicz T, Ramagli LS, Suominen T, Shriver MD, Udd B, Siciliano MJ, Krahe R. Bachinski LL, et al. Neurology. 2009 Feb 10;72(6):490-7. doi: 10.1212/01.wnl.0000333665.01888.33. Epub 2008 Nov 19. Neurology. 2009. PMID: 19020295 Free PMC article.
Desmin mutation responsible for idiopathic dilated cardiomyopathy.
Li D, Tapscoft T, Gonzalez O, Burch PE, Quiñones MA, Zoghbi WA, Hill R, Bachinski LL, Mann DL, Roberts R. Li D, et al. Among authors: bachinski ll. Circulation. 1999 Aug 3;100(5):461-4. doi: 10.1161/01.cir.100.5.461. Circulation. 1999. PMID: 10430757
Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromes.
Müller JS, Herczegfalvi A, Vilchez JJ, Colomer J, Bachinski LL, Mihaylova V, Santos M, Schara U, Deschauer M, Shevell M, Poulin C, Dias A, Soudo A, Hietala M, Aärimaa T, Krahe R, Karcagi V, Huebner A, Beeson D, Abicht A, Lochmüller H. Müller JS, et al. Among authors: bachinski ll. Brain. 2007 Jun;130(Pt 6):1497-506. doi: 10.1093/brain/awm068. Epub 2007 Apr 17. Brain. 2007. PMID: 17439981
Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2.
Vihola A, Bachinski LL, Sirito M, Olufemi SE, Hajibashi S, Baggerly KA, Raheem O, Haapasalo H, Suominen T, Holmlund-Hampf J, Paetau A, Cardani R, Meola G, Kalimo H, Edström L, Krahe R, Udd B. Vihola A, et al. Among authors: bachinski ll. Acta Neuropathol. 2010 Apr;119(4):465-79. doi: 10.1007/s00401-010-0637-6. Epub 2010 Jan 12. Acta Neuropathol. 2010. PMID: 20066428 Free PMC article.
Identification of a gene responsible for familial Wolff-Parkinson-White syndrome.
Gollob MH, Green MS, Tang AS, Gollob T, Karibe A, Ali Hassan AS, Ahmad F, Lozado R, Shah G, Fananapazir L, Bachinski LL, Roberts R. Gollob MH, et al. Among authors: bachinski ll. N Engl J Med. 2001 Jun 14;344(24):1823-31. doi: 10.1056/NEJM200106143442403. N Engl J Med. 2001. PMID: 11407343 Free article.
43 results