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The Diagnostic Journey of a Patient with Prader-Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature.
Pellikaan K, van Woerden GM, Kleinendorst L, Rosenberg AGW, Horsthemke B, Grosser C, van Zutven LJCM, van Rossum EFC, van der Lely AJ, Resnick JL, Brüggenwirth HT, van Haelst MM, de Graaff LCG. Pellikaan K, et al. Among authors: kleinendorst l. Genes (Basel). 2021 Jun 7;12(6):875. doi: 10.3390/genes12060875. Genes (Basel). 2021. PMID: 34200226 Free PMC article. Review.
[Genetic obesity: new diagnostic options].
de Vries TI, Alsters SI, Kleinendorst L, van Haaften G, van der Zwaag B, Van Haelst MM. de Vries TI, et al. Among authors: kleinendorst l. Ned Tijdschr Geneeskd. 2017;161:D688. Ned Tijdschr Geneeskd. 2017. PMID: 28351432 Dutch.
Young girl with severe early-onset obesity and hyperphagia.
Kleinendorst L, van Haelst MM, van den Akker ELT. Kleinendorst L, et al. BMJ Case Rep. 2017 Sep 25;2017:bcr2017221067. doi: 10.1136/bcr-2017-221067. BMJ Case Rep. 2017. PMID: 28951511 Free PMC article.
Genetic obesity: next-generation sequencing results of 1230 patients with obesity.
Kleinendorst L, Massink MPG, Cooiman MI, Savas M, van der Baan-Slootweg OH, Roelants RJ, Janssen ICM, Meijers-Heijboer HJ, Knoers NVAM, Ploos van Amstel HK, van Rossum EFC, van den Akker ELT, van Haaften G, van der Zwaag B, van Haelst MM. Kleinendorst L, et al. J Med Genet. 2018 Sep;55(9):578-586. doi: 10.1136/jmedgenet-2018-105315. Epub 2018 Jul 3. J Med Genet. 2018. PMID: 29970488
The pathogenesis of obesity.
Oussaada SM, van Galen KA, Cooiman MI, Kleinendorst L, Hazebroek EJ, van Haelst MM, Ter Horst KW, Serlie MJ. Oussaada SM, et al. Among authors: kleinendorst l. Metabolism. 2019 Mar;92:26-36. doi: 10.1016/j.metabol.2018.12.012. Epub 2019 Jan 9. Metabolism. 2019. PMID: 30639246 Review.
[A girl with 16p11.2 deletion syndrome].
Kleinendorst L, Sno M, van Haelst MM. Kleinendorst L, et al. Ned Tijdschr Geneeskd. 2019 Mar 21;163:D3441. Ned Tijdschr Geneeskd. 2019. PMID: 30945833 Dutch.
Genetic analysis in the bariatric clinic; impact of a PTEN gene mutation.
Cooiman MI, Kleinendorst L, van der Zwaag B, Janssen IMC, Berends FJ, van Haelst MM. Cooiman MI, et al. Among authors: kleinendorst l. Mol Genet Genomic Med. 2019 Jun;7(6):e00632. doi: 10.1002/mgg3.632. Epub 2019 May 4. Mol Genet Genomic Med. 2019. PMID: 31055886 Free PMC article.
33 results