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Kozlovskaya N.L.

Department of Nephrology and Hemodialysis, I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia;
Research Department of Nephrology, Research Center, I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia, Moscow, Russia

Chebotareva N.V.

Medical University «Russian University of Friendship of Peoples» Ministry of Health of the Russian Federation, Moscow, Russia, 117198

Nikogosova A.D.

I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia, Moscow, Russia

Dem'ianova K.A.

Kafedra nefrologii i gemodializa instituta professional'nogo obrazovaniia GBOU VPO "Pervyĭ MGMU im. I.M. Sechenova" Minzdrava Rossii

Varshavskiĭ V.A.

Kafedra patologicheskoĭ anatomii im. A.I. Strukova GBOU VPO "Pervyĭ Moskovskiĭ gosudarstvennyĭ meditsinskiĭ universitet im. I.M. Sechenova" Minzdrava Rossii

Roshchupkina S.V.

UKB #3, Klinika nefrologii, vnutrennikh i professional'nykh bolezneĭ im. E.M. Tareeva GBOU VPO "Pervyĭ MGMU im. I.M. Sechenova" Minzdrava Rossii

Incomplete thrombotic microangiopathy as a variant of hemolytic-uremic syndrome

Authors:

Kozlovskaya N.L., Chebotareva N.V., Nikogosova A.D., Dem'ianova K.A., Varshavskiĭ V.A., Roshchupkina S.V.

More about the authors

Journal: Therapeutic Archive. 2016;88(6): 77‑79

Read: 2506 times


To cite this article:

Kozlovskaya NL, Chebotareva NV, Nikogosova AD, Dem'ianova KA, Varshavskiĭ VA, Roshchupkina SV. Incomplete thrombotic microangiopathy as a variant of hemolytic-uremic syndrome. Therapeutic Archive. 2016;88(6):77‑79. (In Russ.)
https://doi.org/10.17116/terarkh201688677-79

References:

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  2. Noris M, Remuzzi G. Atypical haemolytic-uremic syndrome. N Engl J Med. 2009;361:1676-1687. doi:10.1056/NEJMra0902814
  3. Kaplan BS, Meyers KE, Schulman SL. The pathogenesis and treatment of hemolytic uremic syndrome. J Am Soc Nephrol. 1998;9(6):1126-1133. doi:10.5582/irdr.2014.01001.
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  5. Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA, Macher MA, Niaudet P, Guest G, Boudailliez B, Bouissou F, Deschenes G, Gie S, Tsimaratos M, Fischbach M, Morin D, Nivet H., Alberti C, Loirat C. Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome. J Am Soc Nephrol. 2007;18(8):2392-2400. doi:10.1681/ASN.2006080811.
  6. Fremeaux-Bacchi V, Fakhouri F, Garnier A, Bienaime F, Dragon-Durey MA, Ngo S. Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide french series comparing children and adults. Clin J Am Soc Nephrol. 2013;8:554-562.  doi:10.2215/CJN.04760512.
  7. Veyradier A, Obert B, Houllier A, Meyer D, Girma JP. Specific von Willebrand factor — cleaving protease in thrombotic microangiopathies: a study of 111 cases. Blood. 2001;98(6):1765-1772. doi:10.1182/blood.V98.6.1765.
  8. Fakhouri F, Roumenina L, Provot F, Sallee M, Caillard S, Couzi L, Essig M, Ribes D, Dragon-Durey MA, Bridoux F, Rondeau E, Frémeaux-Bacchi V. Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations. J Am Soc Nephrol. 2010;21:859-867.  doi:10.1681/ASN.2009070706.
  9. De Serres SA, Isenring P. Athrombocytopenic thrombotic microangiopathy, a condition that could be overlooked based on current diagnostic criteria. Nephrol Dial Transplant. 2009;24:1048-1050. doi:10.1093/ndt/gfn687.
  10. Sallee M, Ismail K, Fakhouri F, Vacher-Coponat H, Moussi-Frances J, Fremaux-Bacchi V, Burtey S. Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome. BMC Nephrology. 2013;14(3):1471-2369. doi:10.1186/1471-2369-14-3. 
  11. Kozlovskaya N, Demyanova K, Kuznetsov D, Kuchieva A, Bobrova L, Stolyarevich E. Atypical haemolytic uremic syndrome with «subclinical» thrombotic microangiopathy: a single case or regularity? Nefrologiay i Dialis. 2014;16(2):280-287. (In Russ.)

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