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Year | Number of Results |
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2002 | 1 |
2018 | 1 |
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Page 1
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Kidney Int. 2021 Sep;100(3):650-659. doi: 10.1016/j.kint.2021.04.019. Epub 2021 Apr 30.
Kidney Int. 2021.
PMID: 33940108
Haematological characteristics and spontaneous haematological recovery in Pearson syndrome.
Yoshimi A, Grünert SC, Cario H, Fisch A, Gross-Wieltsch U, Timmermann K, Kontny U, Lobitz S, Odenthal HS, Schmid I, Uetz B, Höll T, Rötig A, Lücke T, Borkhardt A, Strauß G, Hohnecker A, Metzler M, Karall D, Niemeyer CM.
Yoshimi A, et al. Among authors: uetz b.
Br J Haematol. 2021 Jun;193(6):1283-1287. doi: 10.1111/bjh.17434. Epub 2021 Apr 10.
Br J Haematol. 2021.
PMID: 33837965
No abstract available.
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[Transient Pseudohypoaldosteronism - an Important Differential Diagnosis to Congenital Adrenal Hyperplasia].
Metz J, Kesper MS, Uetz B, Burdach S, Warncke K.
Metz J, et al. Among authors: uetz b.
Klin Padiatr. 2018 Jul;230(4):229-230. doi: 10.1055/a-0575-4068. Epub 2018 Mar 21.
Klin Padiatr. 2018.
PMID: 29564839
German.
No abstract available.
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Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies.
Riedhammer KM, Braunisch MC, Günthner R, Wagner M, Hemmer C, Strom TM, Schmaderer C, Renders L, Tasic V, Gucev Z, Nushi-Stavileci V, Putnik J, Stajić N, Weidenbusch M, Uetz B, Montoya C, Strotmann P, Ponsel S, Lange-Sperandio B, Hoefele J.
Riedhammer KM, et al. Among authors: uetz b.
Am J Kidney Dis. 2020 Oct;76(4):460-470. doi: 10.1053/j.ajkd.2019.12.008. Epub 2020 Apr 28.
Am J Kidney Dis. 2020.
PMID: 32359821
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Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome.
Karle SM, Uetz B, Ronner V, Glaeser L, Hildebrandt F, Fuchshuber A.
Karle SM, et al. Among authors: uetz b.
J Am Soc Nephrol. 2002 Feb;13(2):388-393. doi: 10.1681/ASN.V132388.
J Am Soc Nephrol. 2002.
PMID: 11805166
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