van Geel, Björn M.

X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management

Engelen, M., Kemp, S., de Visser, M., van Geel, B. M., Wanders, R. J., Aubourg, P., & Poll-The, B. (2012) · Orphanet Journal of Rare Diseases

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 562

X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy

van Geel, B. M., Assies, J., Wanders, R. J. A., & Barth, P. G. (1997) · Journal of Neurology, Neurosurgery & Psychiatry

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 162

Progression of abnormalities in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy despite treatment with "Lorenzo's oil"

van Geel, B. M., Assies, J., Haverkort, E. B., Koelman, J. H. T. M., Verbeeten, B., Wanders, R. J. A., & Barth, P. G. (1999) · Journal of Neurology, Neurosurgery & Psychiatry

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 131

Presence of diarrhea and absence of tendon xanthomas in patients with cerebrotendinous xanthomatosis

Verrips, A., van Engelen, B. G. M., Wevers, R. A., van Geel, B. M., Cruysberg, J. R. M., van den Heuvel, L. P. W. J., Keyser, A., & Gabreëls, F. J. M. (2000) · Archives of Neurology

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 104

Disease progression in women with X-linked adrenoleukodystrophy is slow

Huffnagel, I. C., Dijkgraaf, M. G. W., Janssens, G. E., van Weeghel, M., van Geel, B. M., Poll-The, B. T., Kemp, S., & Engelen, M. (2019) · Orphanet Journal of Rare Diseases

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 100

Frequent occurrence of cerebral demyelination in adrenomyeloneuropathy

de Beer, M., Engelen, M., & van Geel, B. M. (2014) · Neurology

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 97

Hematopoietic cell transplantation does not prevent myelopathy in X-linked adrenoleukodystrophy: A retrospective study

van Geel, B. M., Poll‐The, B. T., Verrips, A., Boelens, J., Kemp, S., & Engelen, M. (2015) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 78

ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy

Kemp, S., Mooyer, P. A. W., Bolhuis, P. A., van Geel, B. M., Mandel, J. L., Barth, P. G., Aubourg, P., & Wanders, R. J. A. (1996) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 37

Delay in diagnosis of X-linked adrenoleukodystrophy

van Geel, B. M., Assies, J., Haverkort, E. B., Barth, P. G., Wanders, R. J. A., Schutgens, R. B. H., Keyser, A., & Zwetsloot, C. P. (1993) · Clinical Neurology and Neurosurgery

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 26

X-linked adrenomyeloneuropathy due to a novel missense mutation in the ABCD1 start codon presenting as demyelinating neuropathy

Engelen, M., van der Kooi, A. J., Kemp, S., Wanders, R. J. A., Sistermans, E. A., Waterham, H. R., Koelman, J. T. M., van Geel, B. M., & de Visser, M. (2011) · Journal of the Peripheral Nervous System

Hereditary Neurological DisordersMetabolism and Genetic Disorders

Cited by 12