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Rehabilitation of Patients with Diabetes

Die Rehabilitation, 2018-12, Vol.57 (6), p.388

2018

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Supporting Patients with Diabetes mellitus type 2 and Obesity in Transfer of Medically Indicated Lifestyle Changes into Everyday Life by a Planning Competence Training in a Randomized Controlled Trial

Die Rehabilitation, 2020-04, Vol.59 (2), p.104

2020

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Telephone-Delivered Lifestyle Support With Action Planning and Motivational Interviewing Techniques to Improve Rehabilitation Outcomes

Rehabilitation psychology, 2018-05, Vol.63 (2), p.170-181

2018

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DGRW-Update: Rehabilitation in Diabetes Mellitus

Die Rehabilitation, 2013-08, Vol.52 (4), p.234

2013

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Online Rehab-Need Test (OREST): Effectiveness of an Invitation to Proactive Screening (self-test) for the Need for Medical Rehabilitation Among Individuals Covered by the German Statutory Pension Insurance Agencies in Baden-Württemberg and the Rhine Region

Die Rehabilitation, 2021-08, Vol.60 (4), p.243

2021

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Prophylaxis and quality of life in patients with hemophilia A during routine treatment with ADVATE [antihemophilic factor (recombinant), plasma/albumin-free method] in Germany: a subgroup analysis of the ADVATE PASS post-approval, non-interventional study

Annals of hematology, 2013-05, Vol.92 (5), p.689-698

2013

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Mutational analysis of ectopic factor VIII transcripts from hemophilia A patients : identification of cryptic splice site, exon skipping and novel point mutations

Human genetics, 1997-10, Vol.100 (5-6), p.508-511

1997

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Real-world outcomes with recombinant factor VIIa treatment of acute bleeds in haemophilia patients with inhibitors: results from the international ONE registry

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-07, Vol.19 (4), p.571-577

2013

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Erratum to: Prophylaxis and quality of life in patients with hemophilia A during routine treatment with ADVATE [antihemophilic factor (recombinant), plasma/albumin-free method] in Germany: a subgroup analysis of the ADVATE PASS post-approval, non-interventional study

Annals of hematology, 2013-07, Vol.92 (7), p.1005-1005

2013

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Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A

Human mutation, 2007-01, Vol.28 (1), p.54-60

2007

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Need for Prophylactic Treatment in Adult Haemophilia A Patients

Transfusion medicine and hemotherapy, 2009-08, Vol.36 (4), p.283-288

2009

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A systematic overview of the first pasteurised VWF/FVIII medicinal product, Haemate®P/ Humate®-P: History and clinical performance

European journal of haematology, 2008-05, Vol.80 (s70), p.3-35

2008

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Symposium in Honor of Professor Heimburger on His 70th Birthday

Seminars in thrombosis and hemostasis, 2002, Vol.28 (S1), p.005-006

Pollmann, Hartmut

2002

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Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A

Human mutation, 2005-09, Vol.26 (3), p.249-254

2005

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Status of infection in young hemophilia patients in Münster: Virus Safety of Hemophilia Treatment in Germany and Austria. A Tribute to Norbert Heimburger, Ph.D

Seminars in thrombosis and hemostasis, 2002, Vol.28, p.47-50

2002

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Preliminary Observations from the European Study on Orthopedic Status (ESOS) in Hemophilia Patients with Inhibitors

Blood, 2006-11, Vol.108 (11), p.1037-1037

2006

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Virus Safety of Hemophilia Treatment in Germany and Austria: A Tribute to Norbert Heimburger, Ph.D

Seminars in thrombosis and hemostasis, 2002, Vol.28 (S1), p.001-004

Mammen, Eberhard F.

2002

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Factor V G1691A and Factor II G20210A Mutations and Clinical Expression of Severe Hemophilia A (< 2%) in Children: Impact on Bleeding Episodes and Joint Damage

Blood, 2004-11, Vol.104 (11), p.3095-3095

2004

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Status of Infection in Young Hemophilia Patients in Münster

Seminars in thrombosis and hemostasis, 2002-04, Vol.28 (S1), p.047-050

2002

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Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A

Human mutation, 2002-09, Vol.20 (3), p.236-237

2002

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Platelet dysfunction as the cause of spontaneous bleeding in two haemophilic patients taking HIV protease inhibitors

Thrombosis and haemostasis, 1998-06, Vol.79 (6), p.1213

1998

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Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A: MUTATIONS IN BRIEF

Human mutation, 2002-09, Vol.20 (3), p.236-237

2002

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Molecular diagnostics of 15 hemophilia A patients: Characterization of eight novel mutations in the factor VIII gene, two of which result in exon skipping

Human mutation, 1998, Vol.12 (5), p.301-303

1998

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Addressing current challenges in haemophilia care: consensus recommendations of a European Interdisciplinary Working Group

Haemophilia : the official journal of the World Federation of Hemophilia, 2005-09, Vol.11 (5), p.433-437

2005

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Seven novel and four recurrent point mutations in the factor VIII (F8C) gene

Human mutation, 2002-01, Vol.19 (1), p.84-84

2002

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Rehabilitation of Patients with Diabetes

Supporting Patients with Diabetes mellitus type 2 and Obesity in Transfer of Medically Indicated Lifestyle Changes into Everyday Life by a Planning Competence Training in a Randomized Controlled Trial

Telephone-Delivered Lifestyle Support With Action Planning and Motivational Interviewing Techniques to Improve Rehabilitation Outcomes

DGRW-Update: Rehabilitation in Diabetes Mellitus

Online Rehab-Need Test (OREST): Effectiveness of an Invitation to Proactive Screening (self-test) for the Need for Medical Rehabilitation Among Individuals Covered by the German Statutory Pension Insurance Agencies in Baden-Württemberg and the Rhine Region

Prophylaxis and quality of life in patients with hemophilia A during routine treatment with ADVATE [antihemophilic factor (recombinant), plasma/albumin-free method] in Germany: a subgroup analysis of the ADVATE PASS post-approval, non-interventional study

Mutational analysis of ectopic factor VIII transcripts from hemophilia A patients : identification of cryptic splice site, exon skipping and novel point mutations

Real-world outcomes with recombinant factor VIIa treatment of acute bleeds in haemophilia patients with inhibitors: results from the international ONE registry

Erratum to: Prophylaxis and quality of life in patients with hemophilia A during routine treatment with ADVATE [antihemophilic factor (recombinant), plasma/albumin-free method] in Germany: a subgroup analysis of the ADVATE PASS post-approval, non-interventional study

Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A

Need for Prophylactic Treatment in Adult Haemophilia A Patients

A systematic overview of the first pasteurised VWF/FVIII medicinal product, Haemate®P/ Humate®-P: History and clinical performance

Symposium in Honor of Professor Heimburger on His 70th Birthday

Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A

Status of infection in young hemophilia patients in Münster: Virus Safety of Hemophilia Treatment in Germany and Austria. A Tribute to Norbert Heimburger, Ph.D

Preliminary Observations from the European Study on Orthopedic Status (ESOS) in Hemophilia Patients with Inhibitors

Virus Safety of Hemophilia Treatment in Germany and Austria: A Tribute to Norbert Heimburger, Ph.D

Factor V G1691A and Factor II G20210A Mutations and Clinical Expression of Severe Hemophilia A (< 2%) in Children: Impact on Bleeding Episodes and Joint Damage

Status of Infection in Young Hemophilia Patients in Münster

Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A

Platelet dysfunction as the cause of spontaneous bleeding in two haemophilic patients taking HIV protease inhibitors

Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A: MUTATIONS IN BRIEF

Molecular diagnostics of 15 hemophilia A patients: Characterization of eight novel mutations in the factor VIII gene, two of which result in exon skipping

Addressing current challenges in haemophilia care: consensus recommendations of a European Interdisciplinary Working Group

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene

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