List of works - Bernhard Lämmle

A common origin of the 4143insA ADAMTS13 mutation

scientific article

A first case of congenital TTP on the African continent due to a new homozygous mutation in the catalytic domain of ADAMTS13.

scientific article

ADAMTS13 activity in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: relation to presenting features and clinical outcomes in a prospective cohort of 142 patients

scientific article

ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases

scientific article

ADAMTS13 gene defects in two brothers with constitutional thrombotic thrombocytopenic purpura and normalization of von Willebrand factor-cleaving protease activity by recombinant human ADAMTS13.

scientific article

Assays of von Willebrand factor-cleaving protease: a test for diagnosis of familial and acquired thrombotic thrombocytopenic purpura

scientific article

Blood group O and black race are independent risk factors for thrombotic thrombocytopenic purpura associated with severe ADAMTS13 deficiency

scientific article

Circulating DNA and myeloperoxidase indicate disease activity in patients with thrombotic microangiopathies

scientific article

Clinical outcomes after platelet transfusions in patients with thrombotic thrombocytopenic purpura

scientific article

Cloning, expression, and functional characterization of the von Willebrand factor-cleaving protease (ADAMTS13).

scientific article

Cognitive deficits after recovery from thrombotic thrombocytopenic purpura

scientific article

Congenital thrombotic thrombocytopenic purpura caused by new compound heterozygous mutations of the ADAMTS13 gene

scientific article

Contact system activation in human sepsis - 47kD HK, a marker of sepsis severity?

scientific article

Current insights into thrombotic microangiopathies: Thrombotic thrombocytopenic purpura and pregnancy

scientific article

Decreasing frequency of plasma exchange complications in patients treated for thrombotic thrombocytopenic purpura-hemolytic uremic syndrome, 1996 to 2011.

scientific article

Depression and cognitive deficits as long-term consequences of thrombotic thrombocytopenic purpura

scientific article

Depressive symptoms as a novel risk factor for recurrent venous thromboembolism: a longitudinal observational study in patients referred for thrombophilia investigation

scientific article published on 4 May 2015

Design and establishment of a biobank in a multicenter prospective cohort study of elderly patients with venous thromboembolism (SWITCO65+).

scientific article

Diagnostic criteria for hematopoietic stem cell transplant-associated microangiopathy: results of a consensus process by an International Working Group

scientific article

Different disparities of gender and race among the thrombotic thrombocytopenic purpura and hemolytic-uremic syndromes

scientific article

Dosing lepirudin in patients with heparin-induced thrombocytopenia and normal or impaired renal function: a single-center experience with 68 patients

scientific article

Elevated nucleosome levels in systemic inflammation and sepsis

scientific article published on July 2003

Epitope mapping of ADAMTS13 autoantibodies in acquired thrombotic thrombocytopenic purpura

scientific article

Evaluation of a Platelet Function Analyser (PFA-100) in patients with a bleeding tendency

scientific article (publication date: 10 August 2002)

Evidence for a role of anti-ADAMTS13 autoantibodies despite normal ADAMTS13 activity in recurrent thrombotic thrombocytopenic purpura

scientific article

Familial acquired thrombotic thrombocytopenic purpura: ADAMTS13 inhibitory autoantibodies in identical twins

scientific article

Fatal congenital thrombotic thrombocytopenic purpura with apparent ADAMTS13 inhibitor: in vitro inhibition of ADAMTS13 activity by hemoglobin

scientific article

Frequency and significance of HIV infection among patients diagnosed with thrombotic thrombocytopenic purpura

scientific article

Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency

scientific article

Hemophilia A pseudoaneurysm in a patient with high responding inhibitors complicating total knee arthroplasty: embolization: a cost-reducing alternative to medical therapy

scientific article

Is factor V Leiden a risk factor for thrombotic microangiopathies without severe ADAMTS 13 deficiency?

scientific article

Multiple major morbidities and increased mortality during long-term follow-up after recovery from thrombotic thrombocytopenic purpura

scientific article

Pancreatitis preceding acute episodes of thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: report of five patients with a systematic review of published reports

scientific article

Plasma therapy in thrombotic thrombocytopenic purpura: review of the literature and the Bern experience in a subgroup of patients with severe acquired ADAMTS-13 deficiency

scientific article

Platelets: thrombotic thrombocytopenic purpura

scientific article

Rapid determination of anti-heparin/platelet factor 4 antibody titers in the diagnosis of heparin-induced thrombocytopenia

scientific article

Rapid exclusion or confirmation of heparin-induced thrombocytopenia: a single-center experience with 1,291 patients

scientific article

Ribosomal and immune transcripts associate with relapse in acquired ADAMTS13-deficient thrombotic thrombocytopenic purpura

scientific article

Rituximab for acute plasma-refractory thrombotic thrombocytopenic purpura. A case report and concise review of the literature

scientific article

Role of ADAMTS13 in the pathogenesis, diagnosis, and treatment of thrombotic thrombocytopenic purpura

scientific article

Rumpel-Leede sign in thrombocytopenia due to Epstein-Barr virus-induced mononucleosis

scientific article

Sporadic bloody diarrhoea-associated thrombotic thrombocytopenic purpura-haemolytic uraemic syndrome: an adult and paediatric comparison

scientific article

Survival and relapse in patients with thrombotic thrombocytopenic purpura

scientific article

The Oklahoma Thrombotic Thrombocytopenic Purpura-Hemolytic Uremic Syndrome Registry: the Swiss connection

scientific article

The von Willebrand factor-cleaving protease (ADAMTS-13) and the diagnosis of thrombotic thrombocytopenic purpura (TTP)

scientific article

Thromboembolism in patients with congenital afibrinogenaemia. Long-term observational data and systematic review

scientific article

Thrombotic microangiopathic syndromes associated with drugs, HIV infection, hematopoietic stem cell transplantation and cancer

scientific article

Thrombotic microangiopathy: Caplacizumab accelerates resolution of acute acquired TTP.

scientific article

Thrombotic thrombocytopenic purpura: advances in pathophysiology, diagnosis, and treatment--introduction

scientific article

Titre of anti-heparin/PF4-antibodies and extent of in vivo activation of the coagulation and fibrinolytic systems

scientific article

Von Willebrand factor-cleaving protease (ADAMTS13) in thrombocytopenic disorders: a severely deficient activity is specific for thrombotic thrombocytopenic purpura

scientific article

von Willebrand factor-cleaving protease (ADAMTS-13) activity determination in the diagnosis of thrombotic microangiopathies: the Swiss experience

scientific article

von Willebrand factor-mediated platelet adhesion is critical for deep vein thrombosis in mouse models

scientific article

List of works by Bernhard Lämmle

A common origin of the 4143insA ADAMTS13 mutation

A first case of congenital TTP on the African continent due to a new homozygous mutation in the catalytic domain of ADAMTS13.

ADAMTS13 activity in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: relation to presenting features and clinical outcomes in a prospective cohort of 142 patients

ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases

ADAMTS13 gene defects in two brothers with constitutional thrombotic thrombocytopenic purpura and normalization of von Willebrand factor-cleaving protease activity by recombinant human ADAMTS13.

Assays of von Willebrand factor-cleaving protease: a test for diagnosis of familial and acquired thrombotic thrombocytopenic purpura

Blood group O and black race are independent risk factors for thrombotic thrombocytopenic purpura associated with severe ADAMTS13 deficiency

Circulating DNA and myeloperoxidase indicate disease activity in patients with thrombotic microangiopathies

Clinical outcomes after platelet transfusions in patients with thrombotic thrombocytopenic purpura

Cloning, expression, and functional characterization of the von Willebrand factor-cleaving protease (ADAMTS13).

Cognitive deficits after recovery from thrombotic thrombocytopenic purpura

Congenital thrombotic thrombocytopenic purpura caused by new compound heterozygous mutations of the ADAMTS13 gene

Contact system activation in human sepsis - 47kD HK, a marker of sepsis severity?

Current insights into thrombotic microangiopathies: Thrombotic thrombocytopenic purpura and pregnancy

Decreasing frequency of plasma exchange complications in patients treated for thrombotic thrombocytopenic purpura-hemolytic uremic syndrome, 1996 to 2011.

Depression and cognitive deficits as long-term consequences of thrombotic thrombocytopenic purpura

Depressive symptoms as a novel risk factor for recurrent venous thromboembolism: a longitudinal observational study in patients referred for thrombophilia investigation

Design and establishment of a biobank in a multicenter prospective cohort study of elderly patients with venous thromboembolism (SWITCO65+).

Diagnostic criteria for hematopoietic stem cell transplant-associated microangiopathy: results of a consensus process by an International Working Group

Different disparities of gender and race among the thrombotic thrombocytopenic purpura and hemolytic-uremic syndromes

Dosing lepirudin in patients with heparin-induced thrombocytopenia and normal or impaired renal function: a single-center experience with 68 patients

Elevated nucleosome levels in systemic inflammation and sepsis

Epitope mapping of ADAMTS13 autoantibodies in acquired thrombotic thrombocytopenic purpura

Evaluation of a Platelet Function Analyser (PFA-100) in patients with a bleeding tendency

Evidence for a role of anti-ADAMTS13 autoantibodies despite normal ADAMTS13 activity in recurrent thrombotic thrombocytopenic purpura

Familial acquired thrombotic thrombocytopenic purpura: ADAMTS13 inhibitory autoantibodies in identical twins

Fatal congenital thrombotic thrombocytopenic purpura with apparent ADAMTS13 inhibitor: in vitro inhibition of ADAMTS13 activity by hemoglobin

Frequency and significance of HIV infection among patients diagnosed with thrombotic thrombocytopenic purpura

Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency

Hemophilia A pseudoaneurysm in a patient with high responding inhibitors complicating total knee arthroplasty: embolization: a cost-reducing alternative to medical therapy

Is factor V Leiden a risk factor for thrombotic microangiopathies without severe ADAMTS 13 deficiency?

Multiple major morbidities and increased mortality during long-term follow-up after recovery from thrombotic thrombocytopenic purpura

Pancreatitis preceding acute episodes of thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: report of five patients with a systematic review of published reports

Plasma therapy in thrombotic thrombocytopenic purpura: review of the literature and the Bern experience in a subgroup of patients with severe acquired ADAMTS-13 deficiency

Platelets: thrombotic thrombocytopenic purpura

Rapid determination of anti-heparin/platelet factor 4 antibody titers in the diagnosis of heparin-induced thrombocytopenia

Rapid exclusion or confirmation of heparin-induced thrombocytopenia: a single-center experience with 1,291 patients

Ribosomal and immune transcripts associate with relapse in acquired ADAMTS13-deficient thrombotic thrombocytopenic purpura

Rituximab for acute plasma-refractory thrombotic thrombocytopenic purpura. A case report and concise review of the literature

Role of ADAMTS13 in the pathogenesis, diagnosis, and treatment of thrombotic thrombocytopenic purpura

Rumpel-Leede sign in thrombocytopenia due to Epstein-Barr virus-induced mononucleosis

Sporadic bloody diarrhoea-associated thrombotic thrombocytopenic purpura-haemolytic uraemic syndrome: an adult and paediatric comparison

Survival and relapse in patients with thrombotic thrombocytopenic purpura

The Oklahoma Thrombotic Thrombocytopenic Purpura-Hemolytic Uremic Syndrome Registry: the Swiss connection

The von Willebrand factor-cleaving protease (ADAMTS-13) and the diagnosis of thrombotic thrombocytopenic purpura (TTP)

Thromboembolism in patients with congenital afibrinogenaemia. Long-term observational data and systematic review

Thrombotic microangiopathic syndromes associated with drugs, HIV infection, hematopoietic stem cell transplantation and cancer

Thrombotic microangiopathy: Caplacizumab accelerates resolution of acute acquired TTP.

Thrombotic thrombocytopenic purpura: advances in pathophysiology, diagnosis, and treatment--introduction

Titre of anti-heparin/PF4-antibodies and extent of in vivo activation of the coagulation and fibrinolytic systems

Von Willebrand factor-cleaving protease (ADAMTS13) in thrombocytopenic disorders: a severely deficient activity is specific for thrombotic thrombocytopenic purpura

von Willebrand factor-cleaving protease (ADAMTS-13) activity determination in the diagnosis of thrombotic microangiopathies: the Swiss experience

von Willebrand factor-mediated platelet adhesion is critical for deep vein thrombosis in mouse models