Publications by authors named "Thomas Lennert"

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Mutations in Are a Novel Cause of Galloway-Mowat Syndrome.
Nina Mann, Slim Mzoughi, Ronen Schneider, Susanne J Kühl, Denny Schanze, Thomas Lennert

J Am Soc Nephrol· March 2021

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Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities.
Martin Zenker, Thomas Aigner, Olaf Wendler, Tim Tralau, Horst Müntefering, Thomas Lennert

Hum Mol Genet· November 2004

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Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndrome.
Martin Zenker, Tim Tralau, Thomas Lennert, Susanne Pitz, Karlheinz Mark

Am J Med Genet A· October 2004

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A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2.
Rainer G Ruf, Matthias T F Wolf, Hans C Hennies, Barbara Lucke, Christina Zinn, Thomas Lennert

J Am Soc Nephrol· June 2003

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Pulmonary re-occurrence of post-transplant lymphoproliferative disease with hypogammaglobulinaemia.
Matthias T F Wolf, Eva Mildenberger, Thomas Lennert, Ioannis Anagnostopoulos, Christina Zinn

Eur J Pediatr· March 2003

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Aminoglycoside pretreatment partially restores the function of truncated V(2) vasopressin receptors found in patients with nephrogenic diabetes insipidus.
Angela Schulz, Katrin Sangkuhl, Thomas Lennert, Marianne Wigger, David Anthony Price

J Clin Endocrinol Metab· November 2002

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