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

Year Number of Results
2003 1
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2005 5
2006 4
2007 5
2008 2
2009 1
2010 2
2011 4
2012 3
2013 7
2014 5
2015 5
2016 1
2017 3
2018 3
2019 5
2020 4
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2022 2
2023 4
2024 3

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64 results

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Page 1
Editorial: Copy Number Variation in Rare Disorders.
Komlósi K, Gyenesei A, Bene J. Komlósi K, et al. Front Genet. 2022 Apr 5;13:898059. doi: 10.3389/fgene.2022.898059. eCollection 2022. Front Genet. 2022. PMID: 35450215 Free PMC article. No abstract available.
Ein neues Forum für seltene Hauterkrankungen.
Emmert S, Iben S, Fischer J, Komlosi K, Betz RC, Frank J J, Has C. Emmert S, et al. Among authors: komlosi k. J Dtsch Dermatol Ges. 2019 Jun;17(6):672-673. doi: 10.1111/ddg.13863. J Dtsch Dermatol Ges. 2019. PMID: 31241841 No abstract available.
Obsessive-compulsive symptoms and 15q11.2q13.1 duplication syndrome.
Göbel T, Maier A, Schlump A, Runge K, Nickel K, Tebartz van Elst L, Schiele MA, Domschke K, Gläser B, Tzschach A, Komlosi K, Endres D. Göbel T, et al. Among authors: komlosi k. Eur Neuropsychopharmacol. 2024 Jan;78:67-69. doi: 10.1016/j.euroneuro.2023.09.009. Epub 2023 Dec 1. Eur Neuropsychopharmacol. 2024. PMID: 38041926 No abstract available.
Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis.
Hotz A, Kopp J, Bourrat E, Oji V, Süßmuth K, Komlosi K, Bouadjar B, Tantcheva-Poór I, Hellström Pigg M, Betz RC, Giehl K, Schedel F, Weibel L, Schulz S, Stölzl DV, Tadini G, Demiral E, Berggard K, Zimmer AD, Alter S, Fischer J. Hotz A, et al. Among authors: komlosi k. Genes (Basel). 2023 Mar 15;14(3):717. doi: 10.3390/genes14030717. Genes (Basel). 2023. PMID: 36980989 Free PMC article.
The Clinical and Molecular Spectrum of GM1 Gangliosidosis.
Arash-Kaps L, Komlosi K, Seegräber M, Diederich S, Paschke E, Amraoui Y, Beblo S, Dieckmann A, Smitka M, Hennermann JB. Arash-Kaps L, et al. Among authors: komlosi k. J Pediatr. 2019 Dec;215:152-157.e3. doi: 10.1016/j.jpeds.2019.08.016. J Pediatr. 2019. PMID: 31761138
Neonatal presentation of COG6-CDG with prominent skin phenotype.
Komlosi K, Gläser S, Kopp J, Hotz A, Alter S, Zimmer AD, Beger C, Heinzel S, Schmidt C, Fischer J. Komlosi K, et al. JIMD Rep. 2020 Aug 7;55(1):51-58. doi: 10.1002/jmd2.12154. eCollection 2020 Sep. JIMD Rep. 2020. PMID: 32905044 Free PMC article.
Fatal Neonatal DOLK-CDG as a Rare Form of Syndromic Ichthyosis.
Komlosi K, Claris O, Collardeau-Frachon S, Kopp J, Hausser I, Mazereeuw-Hautier J, Jonca N, Zimmer AD, Sanlaville D, Fischer J. Komlosi K, et al. Front Genet. 2021 Dec 8;12:719624. doi: 10.3389/fgene.2021.719624. eCollection 2021. Front Genet. 2021. PMID: 34956305 Free PMC article.
64 results