Molekulargenetisches Labor
Zentrum für Nephrologie und Stoffwechsel
Diese Gruppe umfasst alle Nierenerkrankungen mit einem genetischen Hintergrund.
| 1. |
Granel B et al. (2006) Lysozyme amyloidosis: report of 4 cases and a review of the literature. 
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| 2. |
Baroncelli GI et al. (2004) Genetic advances, biochemical and clinical features and critical approach to treatment of patients with X-linked hypophosphatemic rickets.
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| 3. |
None (2005) ADPKD: molecular characterization and quest for treatment.
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| 4. |
El-Shanti H et al. (2006) Familial mediterranean fever in Arabs.
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| 5. |
None (2006) The podocyte's response to injury: role in proteinuria and glomerulosclerosis.
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| 6. |
None (2005) Renal phosphate--wasting disorders in childhood.
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| 7. |
Weber S et al. (2005) Recurrence of focal-segmental glomerulosclerosis in children after renal transplantation: clinical and genetic aspects.
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| 8. |
Tahvanainen E et al. (2005) Polycystic liver and kidney diseases.
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| 9. |
None (2006) Genetic alterations and histopathologic findings in familial renal cell carcinoma.
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| 10. |
Tryggvason K et al. (2006) Thin basement membrane nephropathy.
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| 11. |
None (2005) The von Hippel-Lindau tumor suppressor protein: roles in cancer and oxygen sensing.
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Genetisch bedingte Erkrankungen
