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Withdrawn as duplicate: Expanding the phenotypic spectrum of Kenny-Caffey syndrome: a case series and systematic literature review.
Schigt H, Bald M, van der Eerden BCJ, Gal L, Ilenwabor BP, Konrad M, Levine MA, Li D, Mache CJ, Mackin S, Perry C, Rios FJ, Schlingmann KP, Storey B, Trapp CM, Verkerk AJMH, Zillikens MC, Touyz RM, Hoorn EJ, Hoenderop JGJ, de Baaij JHF. Schigt H, et al. Among authors: schlingmann kp. J Clin Endocrinol Metab. 2023 Jun 16;108(7):e501. doi: 10.1210/clinem/dgad154. J Clin Endocrinol Metab. 2023. PMID: 36919775 Free PMC article.
Expanding the Phenotypic Spectrum of Kenny-Caffey Syndrome.
Schigt H, Bald M, van der Eerden BCJ, Gal L, Ilenwabor BP, Konrad M, Levine MA, Li D, Mache CJ, Mackin S, Perry C, Rios FJ, Schlingmann KP, Storey B, Trapp CM, Verkerk AJMH, Zillikens MC, Touyz RM, Hoorn EJ, Hoenderop JGJ, de Baaij JHF. Schigt H, et al. Among authors: schlingmann kp. J Clin Endocrinol Metab. 2023 Aug 18;108(9):e754-e768. doi: 10.1210/clinem/dgad147. J Clin Endocrinol Metab. 2023. PMID: 36916904 Free PMC article.
[No title available]
[No authors listed] [No authors listed] PMID: 35851051
The genetic spectrum of Gitelman(-like) syndromes.
Schlingmann KP, de Baaij JHF. Schlingmann KP, et al. Curr Opin Nephrol Hypertens. 2022 Sep 1;31(5):508-515. doi: 10.1097/MNH.0000000000000818. Epub 2022 Jul 11. Curr Opin Nephrol Hypertens. 2022. PMID: 35894287 Free PMC article. Review.
Autoimmune Renal Calcium and Magnesium Wasting.
Schlingmann KP, Konrad M. Schlingmann KP, et al. J Am Soc Nephrol. 2022 Jul;33(7):1231-1233. doi: 10.1681/ASN.2022050545. Epub 2022 Jun 21. J Am Soc Nephrol. 2022. PMID: 35728888 Free PMC article. No abstract available.
CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemia.
Arjona FJ, de Baaij JH, Schlingmann KP, Lameris AL, van Wijk E, Flik G, Regele S, Korenke GC, Neophytou B, Rust S, Reintjes N, Konrad M, Bindels RJ, Hoenderop JG. Arjona FJ, et al. Among authors: schlingmann kp. PLoS Genet. 2014 Apr 3;10(4):e1004267. doi: 10.1371/journal.pgen.1004267. eCollection 2014 Apr. PLoS Genet. 2014. PMID: 24699222 Free PMC article.
Juvenile onset IIH and CYP24A1 mutations.
Schlingmann KP, Cassar W, Konrad M. Schlingmann KP, et al. Bone Rep. 2018 Jun 21;9:42-46. doi: 10.1016/j.bonr.2018.06.005. eCollection 2018 Dec. Bone Rep. 2018. PMID: 30591926 Free PMC article.
Author's Reply: The Subcellular Localization of RRAGD.
Schlingmann KP, Jouret F, Knoers NVAM, de Baaij JHF. Schlingmann KP, et al. J Am Soc Nephrol. 2022 May;33(5):1048-1049. doi: 10.1681/ASN.2022030252. Epub 2022 Mar 31. J Am Soc Nephrol. 2022. PMID: 35361709 Free PMC article. No abstract available.
[No title available]
[No authors listed] [No authors listed] PMID: 35556292
70 results