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Scholar Results 1 - 10 of about 87 citing Hoeper: Pulmonary hypertension after splenectomy?. (0.12 sec) 

Clinical classification of pulmonary hypertension

- onlinejacc.org
G Simonneau, N Galiè, LJ Rubin, D Langleben … - Journal of the American College of Cardiology, 2004 - Elsevier
In 1998, during the Second World Symposium on Pulmonary Hypertension (PH) held
in Evian, France, a clinical classification of PH was proposed. The aim of the
Evian classification was to individualize different categories sharing ...
Cited by 974 - Related articles - BL Direct - All 16 versions

Splenectomy for adult patients with idiopathic thrombocytopenic purpura: a systematic review …

- hematologylibrary.org
K Kojouri, SK Vesely, DR Terrell, JN George - Blood, 2004 - bloodjournal.hematologylibrary.org
Splenectomy was the primary treatment for idiopathic (immune) thrombocytopenic
purpura (ITP) prior to the introduction of glucocorticoids more than 50 years
ago. 1 For the past 50 years, splenectomy has remained a standard treatment ...
Cited by 145 - Related articles - BL Direct - All 9 versions

Chronic thromboembolic pulmonary hypertension


MM Hoeper, E Mayer, G Simonneau, LJ … - Circulation, 2006 - Am Heart Assoc
Chronic thromboembolic pulmonary hypertension (CTEPH) has emerged as one of the
leading causes of severe pulmonary hypertension. The disease is notoriously
underdiagnosed, and the true prevalence is still unclear. CTEPH is ...
Cited by 125 - Related articles - All 6 versions

Unexplained Pulmonary Hypertension in Chronic Myeloproliferative Disorders*

- chestpubs.org
D Dingli, JP Utz, MJ Krowka, AL Oberg, A … - Chest, 2001 - chestjournal.chestpubs.org
Results: Twenty-six patients satisfied the criteria for both a CMD and PH.
Twelve patients had myeloid metaplasia with myelofibrosis (MMM), 5 patients had
essential thrombocythemia (ET), 6 patients had polycythemia vera, 2 ...
Cited by 89 - Related articles - BL Direct - All 5 versions

Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development …

- nih.gov
GJ Kato, MT Gladwin, MH Steinberg - Blood reviews, 2007 - Elsevier
Hemolysis, long discounted as a critical measure of sickle cell disease severity
when compared with sickle vaso-occlusion, may be the proximate cause of some
disease complications. New mechanistic information about hemolysis and its ...
Cited by 86 - Related articles - All 10 versions

Long term follow-up after splenectomy performed for immune thrombocytopenic purpura (ITP …


J Schwartz, MD Leber, S Gillis, A Giunta, A … - American journal of hematology, 2003 - interscience.wiley.com
Splenectomy is the only treatment of ITP known to have curative effects in a
substantial fraction of patients. However, the true long-term outcome is
uncertain and controversial because published series have not adjusted for ...
Cited by 69 - Related articles - BL Direct - All 3 versions

Long-term evaluation of the beneficial effect of subtotal splenectomy for management of …

- hematologylibrary.org - Free from Publisher
B Bader-Meunier, F Gauthier, F Archambaud, … - Blood, 2001 - bloodjournal.hematologylibrary.org
Hereditary spherocytosis (HS) is a relatively common inherited hemolytic anemia,
with an estimated incidence in Northern Europe of 1 to 2 in 5000 individuals.
Spherocytic red cells, precociously trapped in the spleen, are phagocytosed ...
Cited by 66 - Related articles - BL Direct - All 5 versions

Chronic sickle cell lung disease: new insights into the diagnosis, pathogenesis and …

- critcaremed.org
RF Machado, MT Gladwin - British journal of haematology, 2005 - ccmjournal.org
Pulmonary hypertension is a common complication of sickle cell disease (SCD). In
spite of the mild elevations in pulmonary artery pressures in these patients,
the associated morbidity and mortality is high. In fact, in adult patients ...
Cited by 66 - Related articles - All 7 versions

Guidelines for the diagnosis and management of hereditary spherocytosis


PHB Bolton-Maggs, RF Stevens, NJ Dodd, G … - British journal of haematology, 2004 - cat.inist.fr
Hereditary spherocytosis(HS) is a heterogeneous group of disorders with regard
to clinical severity, protein defects and mode of inheritance. It is relatively
common in Caucasian populations; most affected individuals have mild or ...
Cited by 62 - Related articles - BL Direct - All 2 versions

[PDF] Medical conditions increasing the risk of chronic thromboembolic pulmonary hypertension


D Bonderman, J Jakowitsch, C Adlbrecht, M … - THROMBOSIS AND HAEMOSTASIS-STUTTGART-, 2005 - lungenhochdruck.at
Summary Chronic thromboembolic pulmonary hypertension (CTEPH) is characterized
by organized thromboemboli that obstruct the pulmonary vascular bed.Although
CTEPH is a serious compli- cation of acute symptomatic pulmonary embolism ...
Cited by 60 - Related articles - BL Direct - All 4 versions


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