Stephan Kemp

Associate Professor & AMC Principal Investigator

Amsterdam UMC, University of Amsterdam

Netherlands

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Stephan Kemp is an Associate Professor and Principal Investigator at Amsterdam UMC - University of Amsterdam, Netherlands. His research primarily focuses on adrenoleukodystrophy, with recent articles exploring health-economic modeling for newborn screening, effects of gene therapy, and lipidomics profiling. Dr. Kemp's work aims to enhance the understanding of neurological disorders and the therapeutic potential surrounding them.

Stephan Kemp

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Articles (20)

Cost–Effectiveness of Newborn Screening for X-Linked Adrenoleukodystrophy in the Netherlands: A Health-Economic Modelling Study

Newborn Screening for Adrenoleukodystrophy.

Altered lipid profile and reduced neuronal support in human induced pluripotent stem cell‐derived astrocytes from adrenoleukodystrophy patients

Targeting VEGF-mediated blood-brain barrier disruption in advanced cerebral leukodystrophy

Disruption of polyunsaturated fatty acid biosynthesis drives STING-dependent acute myeloid leukemia cell maturation and death.

An in vitro and in vivo efficacy evaluation of gene therapy candidate SBT101 in mouse models of adrenomyeloneuropathy and in NHPs

Stearoyl-CoA desaturase-1: a potential therapeutic target for neurological disorders.

Lipidomic biomarkers in plasma correlate with disease severity in adrenoleukodystrophy.

Four-dimensional lipidomics profiling in X-linked adrenoleukodystrophy using trapped ion mobility mass spectrometry.

Adrenoleukodystrophy.

Attitudes of Patients with Adrenoleukodystrophy towards Sex-Specific Newborn Screening

ABCD1 Transporter Deficiency Results in Altered Cholesterol Homeostasis

ABCD subfamily of peroxisomal ABC transporters in GtoPdb v.2023.1

Treatment of cerebral adrenoleukodystrophy: allogeneic transplantation and lentiviral gene therapy

Peroxisomal very long-chain fatty acid transport is targeted by herpesviruses and the antiviral host response

Sex-specific newborn screening for X-linked adrenoleukodystrophy.

International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy: A Consensus-Based Approach.

Parents' views on accepting, declining, and expanding newborn bloodspot screening.

Peroxisome Metabolism Contributes to PIEZO2-Mediated Mechanical Allodynia

Structure and Function of the ABCD1 Variant Database: 20 Years, 940 Pathogenic Variants, and 3400 Cases of Adrenoleukodystrophy

Collaborators (12)

Vivi Heine

Elizabeth Pierpont

Lidewij Henneman

David Nascene

Annemieke C Heijboer

Paul J Orchard

Assumpció Bosch

Johannes Berger

Bradley Miller

Sergi Verdés-Franquesa

Marc Engelen

Aaron Goldman

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