BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 17929708)

  • 1. [AL-amyloidosis and its treatment by eliminating the precursor protein].
    Verbeek DE; Hazenberg BP; Jager PL; Kremer Hovinga TK
    Ned Tijdschr Geneeskd; 2007 Sep; 151(37):2021-6. PubMed ID: 17929708
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Outcome in systemic AL amyloidosis in relation to changes in concentration of circulating free immunoglobulin light chains following chemotherapy.
    Lachmann HJ; Gallimore R; Gillmore JD; Carr-Smith HD; Bradwell AR; Pepys MB; Hawkins PN
    Br J Haematol; 2003 Jul; 122(1):78-84. PubMed ID: 12823348
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Immunoglobulin-related (AL) amyloidosis.
    Husby G
    Clin Exp Rheumatol; 1983; 1(4):353-8. PubMed ID: 6442636
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Systemic immunoglobulin light-chain amyloidosis.
    Comenzo RL
    Clin Lymphoma Myeloma; 2006 Nov; 7(3):182-5. PubMed ID: 17229332
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Immunoglobulin light chain amyloidosis is diagnosed late in patients with preexisting plasma cell dyscrasias.
    Kourelis TV; Kumar SK; Go RS; Kapoor P; Kyle RA; Buadi FK; Gertz MA; Lacy MQ; Hayman SR; Leung N; Dingli D; Lust JA; Lin Y; Zeldenrust SR; Rajkumar SV; Dispenzieri A
    Am J Hematol; 2014 Nov; 89(11):1051-4. PubMed ID: 25111004
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The challenge of systemic immunoglobulin light-chain amyloidosis (Al).
    Palladini G; Comenzo RL
    Subcell Biochem; 2012; 65():609-42. PubMed ID: 23225018
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Systemic light-chain amyloidosis presenting with rapid progressive heart failure.
    Sunbul M; Durmus E; Kivrak T; Besiroglu F; Gerin F; Sari I; Mutlu B
    Ther Adv Cardiovasc Dis; 2013 Aug; 7(4):224-7. PubMed ID: 23868674
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Immunoglobulin light chain amyloidosis: 2013 update on diagnosis, prognosis, and treatment.
    Gertz MA
    Am J Hematol; 2013 May; 88(5):416-25. PubMed ID: 23605846
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diagnostic and prognostic utility of the serum free light chain assay in patients with AL amyloidosis.
    Morris KL; Tate JR; Gill D; Kennedy G; Wellwood J; Marlton P; Bird R; Mills AK; Mollee P
    Intern Med J; 2007 Jul; 37(7):456-63. PubMed ID: 17547724
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Light-chain (AL) amyloidosis: diagnosis and treatment.
    Sanchorawala V
    Clin J Am Soc Nephrol; 2006 Nov; 1(6):1331-41. PubMed ID: 17699366
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pathogenesis, diagnosis and treatment of systemic amyloidosis.
    Pepys MB
    Philos Trans R Soc Lond B Biol Sci; 2001 Feb; 356(1406):203-10; discussion 210-1. PubMed ID: 11260801
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Complete remission of nephrotic syndrome and improvement of renal function in a patient with light chain deposition disease following high dose chemotherapy with transplantation of autologous haematopoietic stem cells. A case study and review of literature].
    Adam Z; Krejcí M; Pour L; Stepánková S; Cermáková Z; Voska L; Teplan V; Krivanová A; Hájek R; Mayer J
    Vnitr Lek; 2009 Nov; 55(11):1089-96. PubMed ID: 20017442
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of primary immunoglobulin light chain amyloidosis with a delayed appearance of Bence Jones protein in urine.
    Kurusu A; Yamada T; Yamaji K; Nishitani M; Tashiro K; Maeda K; Horikoshi S; Shirato I; Rinno H; Tomino Y
    Nephrology (Carlton); 2004 Jun; 9(3):122-5. PubMed ID: 15189172
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A patient with AL amyloidosis and severe factor X deficiency has been in complete haematological remission with normal factor X activity for 7 years following high-dose chemotherapy. A case study and literature review].
    Adam Z; Matýková M; Krejcí M; Pour L; Kissová J; Slechtová M; Chlupová G; Stavarová Y; Simonides J; Penka M; Mayer J; Hájek R
    Vnitr Lek; 2010 Jan; 56(1):67-78. PubMed ID: 20184115
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of clinical and pathological characteristics of 28 cases with renal amyloidosis.
    Zhu X; Liu F; Liu Y; Liu H; Xu X; Peng Y; Sun L; Yuan S
    Clin Lab; 2011; 57(11-12):947-52. PubMed ID: 22239026
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Primary amyloidosis (AL) as a cause of nephrotic syndrome.
    Bataille Y; Bovy C; Lancellotti P; Melchior V; Delbecque K; Beguin Y; Krzesinski JM
    Acta Clin Belg; 2005; 60(2):94-7. PubMed ID: 16082995
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Immunoglobulin light and heavy chain amyloidosis AL/AH: renal pathology and differential diagnosis.
    Picken MM
    Contrib Nephrol; 2007; 153():135-55. PubMed ID: 17075228
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Immunoglobulin amyloidosis].
    Hermine O; Bourquelot P; Buzyn A; Aucouturier P
    Rev Prat; 1997 Oct; 47(16):1787-91. PubMed ID: 9453204
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Current and emerging views and treatments of systemic immunoglobulin light-chain (Al) amyloidosis.
    Comenzo RL
    Contrib Nephrol; 2007; 153():195-210. PubMed ID: 17075231
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Current methods of systemic amyloidosis diagnosis and monitoring of its course].
    Rameev VV; Kozlovskaia LV; Malinina EA; Serova AG; Kogarko IN; Kogarko BS; Liubimova NV
    Ter Arkh; 2011; 83(8):48-54. PubMed ID: 21961333
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.