Rare kidney diseases:
Patients with rare disorders are often condemned to neglect: their disease is difficult to recognize, the information available on possible therapies is scanty (if there exists one at all) and, due to small patient populations, little research is done in the field. However, there are several example...
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| Weitere Verfasser: | , , , |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Basel
Karger
2001
|
| Schriftenreihe: | Contributions to nephrology
Vol. 136 |
| Schlagworte: | |
| Online-Zugang: | BFB01 BSB01 BTW01 EUV01 FAN01 FAW01 FFW01 FHI01 FHM01 FHN01 FHR01 FKE01 FNU01 FWS01 FWS02 GEM01 LCO01 SAB01 SAM01 SBG01 SBR01 SND01 TUM01 UBA01 UBG01 UBM01 UBR01 UBT01 UBW01 UER01 UPA01 Volltext |
| Zusammenfassung: | Patients with rare disorders are often condemned to neglect: their disease is difficult to recognize, the information available on possible therapies is scanty (if there exists one at all) and, due to small patient populations, little research is done in the field. However, there are several examples of how research into the etiology and pathogenesis of rare renal disorders has provided important information on the normal physiology of the kidney. Featuring reviews by leading experts in their field, this volume offers up-to-date information on a number of uncommon renal disorders, including Fabry Disease, von Hippel-Lindau Disease, tuberous sclerosis, autosomal recessive polycystic disease, medullary cystic disease, Alport Syndrome, Liddle’s Syndrome, primary hyperoxaluria, systemic vasculitis and familial and recurrent hemolytic uremic syndrome. A chapter on gene therapy in nephrology is also included.This book will be important reading for all those involved in basic and clinical research of the kidney. Moreover, it will provide valuable information for the practicing nephrologist wishing to learn more about how to recognize serious but neglected renal disorders |
| Beschreibung: | from clinical manifestations to diagnosis |
| Beschreibung: | 1 Online-Ressource (X, 340 Seiten) Illustrationen, Diagramme |
| ISBN: | 9783318007510 |
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| 520 | |a Patients with rare disorders are often condemned to neglect: their disease is difficult to recognize, the information available on possible therapies is scanty (if there exists one at all) and, due to small patient populations, little research is done in the field. However, there are several examples of how research into the etiology and pathogenesis of rare renal disorders has provided important information on the normal physiology of the kidney. Featuring reviews by leading experts in their field, this volume offers up-to-date information on a number of uncommon renal disorders, including Fabry Disease, von Hippel-Lindau Disease, tuberous sclerosis, autosomal recessive polycystic disease, medullary cystic disease, Alport Syndrome, Liddle’s Syndrome, primary hyperoxaluria, systemic vasculitis and familial and recurrent hemolytic uremic syndrome. A chapter on gene therapy in nephrology is also included.This book will be important reading for all those involved in basic and clinical research of the kidney. Moreover, it will provide valuable information for the practicing nephrologist wishing to learn more about how to recognize serious but neglected renal disorders | ||
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| genre | (DE-588)4143413-4 Aufsatzsammlung gnd-content |
| genre_facet | Aufsatzsammlung |
| id | DE-604.BV036069372 |
| illustrated | Not Illustrated |
| indexdate | 2024-08-01T11:41:42Z |
| institution | BVB |
| isbn | 9783318007510 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-018960677 |
| oclc_num | 873639874 |
| open_access_boolean | |
| owner | DE-384 DE-473 DE-BY-UBG DE-703 DE-29 DE-19 DE-BY-UBM DE-91 DE-BY-TUM DE-739 DE-355 DE-BY-UBR DE-20 DE-1102 DE-1028 DE-573 DE-859 DE-M347 DE-1049 DE-92 DE-898 DE-BY-UBR DE-863 DE-BY-FWS DE-862 DE-BY-FWS DE-128 DE-54 DE-22 DE-BY-UBG DE-150 DE-155 DE-BY-UBR DE-521 DE-522 DE-526 DE-12 DE-83 DE-M382 DE-70 DE-578 DE-11 DE-1046 |
| owner_facet | DE-384 DE-473 DE-BY-UBG DE-703 DE-29 DE-19 DE-BY-UBM DE-91 DE-BY-TUM DE-739 DE-355 DE-BY-UBR DE-20 DE-1102 DE-1028 DE-573 DE-859 DE-M347 DE-1049 DE-92 DE-898 DE-BY-UBR DE-863 DE-BY-FWS DE-862 DE-BY-FWS DE-128 DE-54 DE-22 DE-BY-UBG DE-150 DE-155 DE-BY-UBR DE-521 DE-522 DE-526 DE-12 DE-83 DE-M382 DE-70 DE-578 DE-11 DE-1046 |
| physical | 1 Online-Ressource (X, 340 Seiten) Illustrationen, Diagramme |
| psigel | ZDB-1-KEB |
| publishDate | 2001 |
| publishDateSearch | 2001 |
| publishDateSort | 2001 |
| publisher | Karger |
| record_format | marc |
| series | Contributions to nephrology |
| series2 | Contributions to nephrology |
| spellingShingle | Rare kidney diseases Contributions to nephrology Nephrology Genetics Metabolism Pediatrics Nierenkrankheit (DE-588)4075399-2 gnd |
| subject_GND | (DE-588)4075399-2 (DE-588)4143413-4 |
| title | Rare kidney diseases |
| title_auth | Rare kidney diseases |
| title_exact_search | Rare kidney diseases |
| title_full | Rare kidney diseases volume editors: Arrigo Schieppati, Erica Daina, Adalberto Sessa, Giuseppe Remuzzi |
| title_fullStr | Rare kidney diseases volume editors: Arrigo Schieppati, Erica Daina, Adalberto Sessa, Giuseppe Remuzzi |
| title_full_unstemmed | Rare kidney diseases volume editors: Arrigo Schieppati, Erica Daina, Adalberto Sessa, Giuseppe Remuzzi |
| title_short | Rare kidney diseases |
| title_sort | rare kidney diseases |
| topic | Nephrology Genetics Metabolism Pediatrics Nierenkrankheit (DE-588)4075399-2 gnd |
| topic_facet | Nephrology Genetics Metabolism Pediatrics Nierenkrankheit Aufsatzsammlung |
| url | https://karger.com/books/book/2392 |
| volume_link | (DE-604)BV039142755 |
| work_keys_str_mv | AT schieppatiarrigo rarekidneydiseases AT dainaerica rarekidneydiseases AT sessaadalberto rarekidneydiseases AT remuzzigiusepppe rarekidneydiseases |