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Publications by Stephan vom Dahl

Long-Term Clinical Outcomes in Type 1 Gaucher Disease Following 10 Years of Imiglucerase Treatment

Journal of Inherited Metabolic Disease

Genetics

2012

English

Gaucher Disease and Malignancy: A Model for Cancer Pathogenesis in an Inborn Error of Metabolism

Critical Reviews in Oncogenesis

2013

English

Related publications

Russian Pediatric Experience on Assessing the Effectiveness of Imiglucerase for Long-Term Enzyme Replacement Therapy of Gaucher Disease Type 1 in Children

Vestnik Rossiiskoi Akademii Meditsinskikh Nauk

Medicine

2017

English

Review of the Safety and Efficacy of Imiglucerase Treatment of Gaucher Disease

Biologics: Targets and Therapy

English

Impact of Imiglucerase Supply Constraint on the Therapeutic Management and Course of Disease in French Patients With Gaucher Disease Type 1

Orphanet Journal of Rare Diseases

English

High Incidence of Cholesterol Gallstone Disease in Type 1 Gaucher Disease: Characterizing the Biliary Phenotype of Type 1 Gaucher Disease

Journal of Inherited Metabolic Disease

Genetics

2010

English

Long-Term Adverse Event Profile From Four Completed Trials of Oral Eliglustat in Adults With Gaucher Disease Type 1

Orphanet Journal of Rare Diseases

English

The Clinical Management of Type 2 Gaucher Disease

Molecular Genetics and Metabolism

English

Long-Term Follow Up and Sudden Unexpected Death in Gaucher Disease Type 3 in Egypt

Molecular Genetics and Metabolism

English

Surgical Treatment of Bronchiectasis: Clinical Characteristics and Long-Term Outcomes

Turkish Journal of Thoracic and Cardiovascular Surgery

Respiratory Medicine

Pulmonary

Cardiovascular Medicine

Surgery

Cardiology

2014

English

Long-Term Outcomes of Prenatally Diagnosed Ventriculomegaly — 10 Years of Polish Tertiary Centre Experience

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Stephan vom Dahl

Long-Term Clinical Outcomes in Type 1 Gaucher Disease Following 10 Years of Imiglucerase Treatment

Gaucher Disease and Malignancy: A Model for Cancer Pathogenesis in an Inborn Error of Metabolism

Related publications

Russian Pediatric Experience on Assessing the Effectiveness of Imiglucerase for Long-Term Enzyme Replacement Therapy of Gaucher Disease Type 1 in Children

Review of the Safety and Efficacy of Imiglucerase Treatment of Gaucher Disease

Impact of Imiglucerase Supply Constraint on the Therapeutic Management and Course of Disease in French Patients With Gaucher Disease Type 1

High Incidence of Cholesterol Gallstone Disease in Type 1 Gaucher Disease: Characterizing the Biliary Phenotype of Type 1 Gaucher Disease

Long-Term Adverse Event Profile From Four Completed Trials of Oral Eliglustat in Adults With Gaucher Disease Type 1

The Clinical Management of Type 2 Gaucher Disease

Long-Term Follow Up and Sudden Unexpected Death in Gaucher Disease Type 3 in Egypt

Surgical Treatment of Bronchiectasis: Clinical Characteristics and Long-Term Outcomes

Long-Term Outcomes of Prenatally Diagnosed Ventriculomegaly — 10 Years of Polish Tertiary Centre Experience