Lennert T - Search Results

1

Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene.

Köhler B, Schumacher V, Schulte-Overberg U, Biewald W, Lennert T, l'Allemand D, Royer-Pokora B, Grüters A. Köhler B, et al. Among authors: lennert t. Pediatr Res. 1999 Feb;45(2):187-90. doi: 10.1203/00006450-199902000-00005. Pediatr Res. 1999. PMID: 10022588

2

Multicystic renal dysplasia: nephrectomy versus conservative treatment.

Lennert T, Tetzner M, Er M, Jung F, Kaufmann HJ, Biewald W. Lennert T, et al. Contrib Nephrol. 1988;67:183-7. doi: 10.1159/000415399. Contrib Nephrol. 1988. PMID: 3061739 Review. No abstract available.

3

Aminoglycoside pretreatment partially restores the function of truncated V(2) vasopressin receptors found in patients with nephrogenic diabetes insipidus.

Schulz A, Sangkuhl K, Lennert T, Wigger M, Price DA, Nuuja A, Grüters A, Schultz G, Schöneberg T. Schulz A, et al. Among authors: lennert t. J Clin Endocrinol Metab. 2002 Nov;87(11):5247-57. doi: 10.1210/jc.2002-020286. J Clin Endocrinol Metab. 2002. PMID: 12414899

4

Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities.

Zenker M, Aigner T, Wendler O, Tralau T, Müntefering H, Fenski R, Pitz S, Schumacher V, Royer-Pokora B, Wühl E, Cochat P, Bouvier R, Kraus C, Mark K, Madlon H, Dötsch J, Rascher W, Maruniak-Chudek I, Lennert T, Neumann LM, Reis A. Zenker M, et al. Among authors: lennert t. Hum Mol Genet. 2004 Nov 1;13(21):2625-32. doi: 10.1093/hmg/ddh284. Epub 2004 Sep 14. Hum Mol Genet. 2004. PMID: 15367484

5

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen.

Zerres K, Mücher G, Bachner L, Deschennes G, Eggermann T, Kääriäinen H, Knapp M, Lennert T, Misselwitz J, von Mühlendahl KE, et al. Zerres K, et al. Among authors: lennert t. Nat Genet. 1994 Jul;7(3):429-32. doi: 10.1038/ng0794-429. Nat Genet. 1994. PMID: 7920664

6

Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndrome.

Zenker M, Tralau T, Lennert T, Pitz S, Mark K, Madlon H, Dötsch J, Reis A, Müntefering H, Neumann LM. Zenker M, et al. Among authors: lennert t. Am J Med Genet A. 2004 Oct 1;130A(2):138-45. doi: 10.1002/ajmg.a.30310. Am J Med Genet A. 2004. PMID: 15372515 Review.

7

Kidneys on vacation: the notion of renal work and the introduction of nonpharmacological therapies.

Lennert T, Luft FC. Lennert T, et al. Am J Kidney Dis. 1997 May;29(5):777-80. doi: 10.1016/s0272-6386(97)90134-7. Am J Kidney Dis. 1997. PMID: 9159316

8

Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome.

Mann N, Mzoughi S, Schneider R, Kühl SJ, Schanze D, Klämbt V, Lovric S, Mao Y, Shi S, Tan W, Kühl M, Onuchic-Whitford AC, Treimer E, Kitzler TM, Kause F, Schumann S, Nakayama M, Buerger F, Shril S, van der Ven AT, Majmundar AJ, Holton KM, Kolb A, Braun DA, Rao J, Jobst-Schwan T, Mildenberger E, Lennert T, Kuechler A, Wieczorek D, Gross O, Ermisch-Omran B, Werberger A, Skalej M, Janecke AR, Soliman NA, Mane SM, Lifton RP, Kadlec J, Guccione E, Schmeisser MJ, Zenker M, Hildebrandt F. Mann N, et al. Among authors: lennert t. J Am Soc Nephrol. 2021 Mar;32(3):580-596. doi: 10.1681/ASN.2020040490. Epub 2021 Feb 16. J Am Soc Nephrol. 2021. PMID: 33593823 Free PMC article.

9

Fulminant metastatic calcinosis with cutaneous necrosis in a child with end-stage renal disease and tertiary hyperparathyroidism.

Zouboulis CC, Blume-Peytavi U, Lennert T, Stavropoulos PG, Schwarz A, Runkel N, Trautmann C, Orfanos CE. Zouboulis CC, et al. Among authors: lennert t. Br J Dermatol. 1996 Oct;135(4):617-22. Br J Dermatol. 1996. PMID: 8915159

10

Autosomal recessive and dominant forms of polycystic kidney disease are not allelic.

Wirth B, Zerres K, Fischbach M, Claus D, Neumann HP, Lennert T, Brodehl J, Neugebauer M, Müller-Wiefel DE, Geisert J, et al. Wirth B, et al. Among authors: lennert t. Hum Genet. 1987 Nov;77(3):221-2. doi: 10.1007/BF00284473. Hum Genet. 1987. PMID: 3479385

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