Results 171 to 180 of about 61,384 (225)

Thrombotic Microangiopathy Secondary to Capnocytophaga Sepsis: A Case Report. [PDF]

Cureus
Abdelsalam M, Alayyan AH, Elamin A, Goh ES, Bin Tariq A.   +4 more
europepmc   +1 more source

[Thrombotic microangiopathy].

Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, 2003
C, Chiurchiu, G, Remuzzi
openaire   +1 more source

Thrombotic Microangiopathy Presenting With Multisystem Involvement and Acute Neurologic Deficits in a 61-Year-Old Female: A Case of Acquired Thrombotic Thrombocytopenic Purpura. [PDF]

Cureus
Verhaegh T, Panossian A, Michael F, Rahman T, Namavar AA, Ilyas Z.   +5 more
europepmc   +1 more source

Eculizumab for ATCR-associated <i>de novo</i> thrombotic microangiopathy in a Chinese kidney transplant recipient with type 2 diabetes: a case report. [PDF]

Front Med (Lausanne)
Su S, Zhu Y, Han G, Zhang Z, Liang L, Gao Y.   +5 more
europepmc   +1 more source

Thrombotic microangiopathy after kidney transplantation: diagnosis and management strategies. [PDF]

Clin Kidney J
Mirioglu S, Morelle J, Efe O, Hurdogan O, Dirim AB, Kumru G, Lentine KL, Caliskan Y.   +7 more
europepmc   +1 more source

[Thrombotic microangiopathy].

Polish journal of pathology : official journal of the Polish Society of Pathologists, 2012
openaire   +1 more source

Thrombotic microangiopathy

Transfusion and Apheresis Science, 2011
Thrombotic microangiopathy (TMA) is a histopathological feature of various diseases including thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS). There are many secondary causes of TMA, many of them could mimic TTP or HUS. This article presents a short overview on TMA.
M, Mörtzell, G, Berlin, T, Nilsson, C G, Axelsson, M, Efvergren, J, Audzijoni, A, Griskevicius, J, Ptak, M, Blaha, H, Tomsova, G M, Liumbruno, P, Centoni, E, Newman, S, Eloot, A, Dhondt, J, Tomaz, V, Witt, G, Rock, B, Stegmayr   +18 more
openaire   +3 more sources

Thrombotic Microangiopathy in the Cancer Patient

Acta Haematologica, 2001
Thrombotic microangiopathy, manifesting as thrombotic thrombocytopenic purpura (TTP) or hemolytic uremic syndrome, is a common complication in cancer patients. It shares the pathogenic microvascular occlusive lesion and many clinical manifestations as the classical TTP, but the spectrum of complications varies widely.
H C, Kwaan, L I, Gordon
openaire   +3 more sources

[Thrombotic microangiopathy].

Der Internist, 2013
Thrombotic microangiopathy should be suspected every time the combination of microangiopathic hemolytic anemia without a coexisting cause, thrombocytopenia as well as renal and/or neurologic abnormalities occurs. The general term thrombotic microangiopathy includes different subtypes of the disease leading to abnormalities in multiple organ systems by ...
Ganser, A., Kielstein, J. T., Beutel, G.
openaire   +4 more sources