- ►nejm.org JL Moake - New England Journal of Medicine, 2002 - content.nejm.org The thrombotic microangiopathies are microvascular occlusive disorders
characterized by systemic or intrarenal aggregation of platelets,
thrombocytopenia, and mechanical injury to erythrocytes. In thrombotic ... Cited by 583 - Related articles - BL Direct - All 13 versions
- ►hematologylibrary.org JN George - Blood, 2000 - bloodjournal.hematologylibrary.org Adults who have the defining diagnostic features of TTP (Table 1) but in whom
acute renal failure is a prominent abnormality, with or without a diarrhea
prodrome, have been described as having adult HUS, and some consider this ... Cited by 297 - Related articles - BL Direct - All 12 versions
- ►uiuc.edu [PDF] JN George - N Engl J Med, 2006 - nejm.org A 40-year-old obese black woman has had weakness and epigastric pain for several
weeks and diarrhea and vomiting for four days. She does not appear acutely ill;
physi- cal examination is normal except for abdominal tenderness. Her ... Cited by 168 - Related articles - BL Direct - All 16 versions
- ►hematologylibrary.org JE Sadler, JL Moake, T Miyata, JN George - Hematology, 2004 - asheducationbook.hematologylibrary.org Thrombotic thrombocytopenic purpura (TTP) is characterized by microangiopathic
hemolytic anemia and thrombocytopenia, accompanied by microvascular thrombosis
that causes variable degrees of tissue ischemia and infarction. ... Cited by 163 - Related articles - All 4 versions
M Furlan, B Lämmle - Best Practice & Research Clinical Haematology, 2001 - Elsevier Thrombotic thrombocytopenic purpura (TTP) and haemolytic uraemic syndrome (HUS)
are today often regarded as variants of one syndrome denoted as TTP/HUS,
characterized by thrombocytopenia caused by intravascular platelet ... Cited by 121 - Related articles - BL Direct - All 8 versions
- ►hematologylibrary.org F Fakhouri, JP Vernant, A Veyradier, M Wolf, … - Blood, 2005 - bloodjournal.hematologylibrary.org From the Service de Néphrologie, Hôpital Necker, Université Paris V-René
Descartes, Paris, France; Service d'Hématologie, Hôpital de la
Pitié-Salpêtrière, Paris, France; Service d'Hématologie biologique, ... Cited by 117 - Related articles - BL Direct - All 4 versions
MA Elliott, WL Nichols - Mayo Clinic Proceedings, 2001 - mayoclinicproceedings.com Thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS)
are multisystemic disorders that are characterized by thrombocytopenia,
microangiopathic hemolytic anemia, and ischemic manifestations, resulting ... Cited by 83 - Related articles - BL Direct - All 9 versions
B Lammle, JA Kremer Hovinga, L Alberio - Journal of Thrombosis and Haemostasis, 2005 - interscience.wiley.com Summary. This overview summarizes the history of thrombotic thrombocytopenic
purpura (TTP) from its initial recognition in 1924 as a most often fatal disease
to the discovery in 1997 of ADAMTS-13 deficiency as a major risk factor for ... Cited by 82 - Related articles - BL Direct - All 4 versions
C Arnal, J Piette, J Léone, B Taillan, E … - J Rheumatol, 2002 - jrheum.org From the Service de Médecine Interne, Hôpital Henri Mondor, Assistance
Publique Hôpitaux de Paris, Creteil; Groupe Hospitalier Pitié Salpétrière,
Paris; CHU de Reims, Reims; CHU de Nice, Nice; Hôpital Claude Huriez, CHU ... Cited by 52 - Related articles - All 7 versions
JL MOAKE, TW CHOW - The American journal of the medical sciences, 1998 - journals.lww.com Serial studies of plasma samples from patients during episodes of thrombotic
thrombocytopenic purpura (TTP) have often shown either the presence of unusually
large (UL) von Willebrand factor (vWf) multimers or, alternatively, absence ... Cited by 51 - Related articles - BL Direct - All 3 versions
