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

Year Number of Results
1992 1
1993 1
1995 1
2001 1
2002 3
2003 1
2004 1
2007 3
2008 3
2010 1
2011 1
2012 2
2013 1
2014 1
2015 1
2016 1
2017 1
2018 2
2019 2
2023 0
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23 results
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Page 1
ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation.
Alber M, Kalscheuer VM, Marco E, Sherr E, Lesca G, Till M, Gradek G, Wiesener A, Korenke C, Mercier S, Becker F, Yamamoto T, Scherer SW, Marshall CR, Walker S, Dutta UR, Dalal AB, Suckow V, Jamali P, Kahrizi K, Najmabadi H, Minassian BA. Alber M, et al. Among authors: korenke c. Neurol Genet. 2017 May 26;3(3):e148. doi: 10.1212/NXG.0000000000000148. eCollection 2017 Jun. Neurol Genet. 2017. PMID: 28589176 Free PMC article.
Neonatal screening for citrullinaemia.
Sander J, Janzen N, Sander S, Steuerwald U, Das AM, Scholl S, Trefz FK, Koch HG, Häberle J, Korall H, Marquardt I, Korenke C. Sander J, et al. Among authors: korenke c. Eur J Pediatr. 2003 Jun;162(6):417-20. doi: 10.1007/s00431-003-1177-z. Epub 2003 Apr 8. Eur J Pediatr. 2003. PMID: 12684898
EEG features of glut-1 deficiency syndrome.
von Moers A, Brockmann K, Wang D, Korenke CG, Huppke P, De Vivo DC, Hanefeld F. von Moers A, et al. Among authors: korenke cg. Epilepsia. 2002 Aug;43(8):941-5. doi: 10.1046/j.1528-1157.2002.50401.x. Epilepsia. 2002. PMID: 12181017 Free article.
Antibodies to MOG and AQP4 in children with neuromyelitis optica and limited forms of the disease.
Lechner C, Baumann M, Hennes EM, Schanda K, Marquard K, Karenfort M, Leiz S, Pohl D, Venkateswaran S, Pritsch M, Koch J, Schimmel M, Häusler M, Klein A, Blaschek A, Thiels C, Lücke T, Gruber-Sedlmayr U, Kornek B, Hahn A, Leypoldt F, Sandrieser T, Gallwitz H, Stoffels J, Korenke C, Reindl M, Rostásy K. Lechner C, et al. Among authors: korenke c. J Neurol Neurosurg Psychiatry. 2016 Aug;87(8):897-905. doi: 10.1136/jnnp-2015-311743. Epub 2015 Dec 8. J Neurol Neurosurg Psychiatry. 2016. PMID: 26645082
23 results