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Literature DB >> 18504476

A man with new onset of ascites and edema.

Melvin Lau¹.

Abstract

Entities: Disease Species

Mesh：

Year: 2008 PMID： 18504476 PMCID： PMC2390687

Source DB: PubMed Journal: Medscape J Med ISSN： 1934-1997

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18 in total

1. Long-term outcome of patients with AL amyloidosis treated with high-dose melphalan and stem-cell transplantation.

Authors: Vaishali Sanchorawala; Martha Skinner; Karen Quillen; Kathleen T Finn; Gheorghe Doros; David C Seldin
Journal: Blood Date: 2007-08-02 Impact factor: 22.113

Review 2. Light-chain (AL) amyloidosis: diagnosis and treatment.

Authors: Vaishali Sanchorawala
Journal: Clin J Am Soc Nephrol Date: 2006-10-11 Impact factor: 8.237

Review 3. Amyloidosis and bleeding: pathophysiology, diagnosis, and therapy.

Authors: Christoph Sucker; Gerd Ruediger Hetzel; Bernd Grabensee; Marcus Stockschlaeder; Ruediger E Scharf
Journal: Am J Kidney Dis Date: 2006-06 Impact factor: 8.860

4. Risk factors for bleeding complications in percutaneous renal biopsy.

Authors: Masaaki Eiro; Tetsuo Katoh; Tsuyoshi Watanabe
Journal: Clin Exp Nephrol Date: 2005-03 Impact factor: 2.801

Review 5. Tubulointerstitial nephritis and Fanconi syndrome in primary biliary cirrhosis.

Authors: Marie Lino; Raynald Binaut; Laure-Hélène Noël; Natacha Patey; Pierre Rustin; Laurent Daniel; Jeanne Serpaggi; Anne Varaut; Philippe Vanhille; Bertrand Knebelmann; Jean-Pierre Grünfeld; Fadi Fakhouri
Journal: Am J Kidney Dis Date: 2005-09 Impact factor: 8.860

A man with new onset of ascites and edema.

1. Long-term outcome of patients with AL amyloidosis treated with high-dose melphalan and stem-cell transplantation.

Review 2. Light-chain (AL) amyloidosis: diagnosis and treatment.

Review 3. Amyloidosis and bleeding: pathophysiology, diagnosis, and therapy.

4. Risk factors for bleeding complications in percutaneous renal biopsy.

Review 5. Tubulointerstitial nephritis and Fanconi syndrome in primary biliary cirrhosis.

Review 6. AL amyloidosis with renal involvement.

Review 7. Diagnosis and management of cholestatic liver disease.

Review 8. Primary amyloidosis and severe intrahepatic cholestatic jaundice.

Review 9. New insights into systemic amyloidosis: the importance of diagnosis of specific type.

10. Hepatic amyloidosis. A histopathologic analysis of primary (AL) and secondary (AA) forms.