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

Year Number of Results
2018 2
2019 1
2020 6
2021 2
2022 2
2023 0

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13 results

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Page 1
Myalgia in 30 Patients with Suspected Myopathy.
Lehmann Urban D, Lehmann E, Motlagh Scholle L, Kraya T. Lehmann Urban D, et al. Among authors: motlagh scholle l. Int J Environ Res Public Health. 2020 Apr 6;17(7):2502. doi: 10.3390/ijerph17072502. Int J Environ Res Public Health. 2020. PMID: 32268560 Free PMC article.
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly.
Klöckner C, Fernández-Murray JP, Tavasoli M, Sticht H, Stoltenburg-Didinger G, Scholle LM, Bakhtiari S, Kruer MC, Darvish H, Firouzabadi SG, Pagnozzi A, Shukla A, Girisha KM, Narayanan DL, Kaur P, Maroofian R, Zaki MS, Noureldeen MM, Merkenschlager A, Gburek-Augustat J, Cali E, Banu S, Nahar K, Efthymiou S, Houlden H, Jamra RA, Williams J, McMaster CR, Platzer K. Klöckner C, et al. Among authors: scholle lm. Brain. 2022 Jun 30;145(6):1916-1923. doi: 10.1093/brain/awac074. Brain. 2022. PMID: 35202461 Free PMC article.
Camptocormia as a Novel Phenotype in a Heterozygous POLG2 Mutation.
Lehmann Urban D, Motlagh Scholle L, Alt K, Ludolph AC, Rosenbohm A. Lehmann Urban D, et al. Among authors: motlagh scholle l. Diagnostics (Basel). 2020 Jan 26;10(2):68. doi: 10.3390/diagnostics10020068. Diagnostics (Basel). 2020. PMID: 31991853 Free PMC article.
13 results