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
2003 2
2004 1
2009 1
2010 3
2011 1
2012 6
2013 4
2014 2
2015 4
2016 2
2017 2
2018 2
2019 2
2021 1
Text availability
Article attribute
Article type
Publication date

Search Results

29 results
Results by year
Filters applied: . Clear all
Page 1
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.
Cameron-Christie SR, Wells CF, Simon M, Wessels M, Tang CZN, Wei W, Takei R, Aarts-Tesselaar C, Sandaradura S, Sillence DO, Cordier MP, Veenstra-Knol HE, Cassina M, Ludwig K, Trevisson E, Bahlo M, Markie DM, Jenkins ZA, Robertson SP. Cameron-Christie SR, et al. Among authors: ludwig k. Am J Hum Genet. 2018 Jun 7;102(6):1115-1125. doi: 10.1016/j.ajhg.2018.04.008. Epub 2018 May 24. Am J Hum Genet. 2018. PMID: 29805041 Free PMC article.
Recurrent BCOR Internal Tandem Duplication and YWHAE-NUTM2B Fusions in Soft Tissue Undifferentiated Round Cell Sarcoma of Infancy: Overlapping Genetic Features With Clear Cell Sarcoma of Kidney.
Kao YC, Sung YS, Zhang L, Huang SC, Argani P, Chung CT, Graf NS, Wright DC, Kellie SJ, Agaram NP, Ludwig K, Zin A, Alaggio R, Antonescu CR. Kao YC, et al. Among authors: ludwig k. Am J Surg Pathol. 2016 Aug;40(8):1009-20. doi: 10.1097/PAS.0000000000000629. Am J Surg Pathol. 2016. PMID: 26945340 Free PMC article.
Photosensitive epilepsy and long QT: expanding Timothy syndrome phenotype.
Po' C, Zordan R, Vecchi M, Cerutti A, Sartori S, Trevisson E, Ludwig K, Castaldi B, Salviati L, Leoni L, Toldo I. Po' C, et al. Among authors: ludwig k. Clin Neurophysiol. 2019 Nov;130(11):2134-2136. doi: 10.1016/j.clinph.2019.09.003. Epub 2019 Sep 17. Clin Neurophysiol. 2019. PMID: 31563812 No abstract available.
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.
Cameron-Christie SR, Wells CF, Simon M, Wessels M, Tang CZN, Wei W, Takei R, Aarts-Tesselaar C, Sandaradura S, Sillence DO, Cordier MP, Veenstra-Knol HE, Cassina M, Ludwig K, Trevisson E, Bahlo M, Markie DM, Jenkins ZA, Robertson SP. Cameron-Christie SR, et al. Among authors: ludwig k. Am J Hum Genet. 2019 Sep 5;105(3):669. doi: 10.1016/j.ajhg.2019.08.007. Am J Hum Genet. 2019. PMID: 31491409 Free PMC article. No abstract available.
Rare uterine cancer: carcinosarcomas. Review from histology to treatment.
Artioli G, Wabersich J, Ludwig K, Gardiman MP, Borgato L, Garbin F. Artioli G, et al. Among authors: ludwig k. Crit Rev Oncol Hematol. 2015 Apr;94(1):98-104. doi: 10.1016/j.critrevonc.2014.10.013. Epub 2014 Nov 7. Crit Rev Oncol Hematol. 2015. PMID: 25468677 Review.
Apert syndrome with fused thalami.
Ludwig K, Salmaso R, Manara R, Cosmi E, Baldi M, Rugge M. Ludwig K, et al. Fetal Pediatr Pathol. 2012 Dec;31(6):410-4. doi: 10.3109/15513815.2012.659407. Epub 2012 Mar 23. Fetal Pediatr Pathol. 2012. PMID: 22443264
Oral-facial-digital syndrome type VI: is C5orf42 really the major gene?
Romani M, Mancini F, Micalizzi A, Poretti A, Miccinilli E, Accorsi P, Avola E, Bertini E, Borgatti R, Romaniello R, Ceylaner S, Coppola G, D'Arrigo S, Giordano L, Janecke AR, Lituania M, Ludwig K, Martorell L, Mazza T, Odent S, Pinelli L, Poo P, Santucci M, Signorini S, Simonati A, Spiegel R, Stanzial F, Steinlin M, Tabarki B, Wolf NI, Zibordi F, Boltshauser E, Valente EM. Romani M, et al. Among authors: ludwig k. Hum Genet. 2015 Jan;134(1):123-6. doi: 10.1007/s00439-014-1508-3. Epub 2014 Nov 19. Hum Genet. 2015. PMID: 25407461 Free PMC article.
Ichthyosis and Kallmann syndrome: not always a contiguous gene syndrome.
Trevisson E, Ludwig K, Casarin A, Di Meglio A, Greggio NA, Manara R, Lenzini E, Clementi M, Salviati L. Trevisson E, et al. Among authors: ludwig k. J Dermatol Sci. 2015 May;78(2):158-60. doi: 10.1016/j.jdermsci.2015.02.005. Epub 2015 Feb 16. J Dermatol Sci. 2015. PMID: 25726327 No abstract available.
29 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page