M.S. van der Knaap

prof. dr.

19972019
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Research Output 1997 2019

2019

Biallelic variants in LARS2 and KARS cause deafness and (ovario)leukodystrophy

Van Der Knaap, M. S., Bugiani, M., Mendes, M. I., Riley, L. G., Smith, D. E. C., Rudinger-Thirion, J., Frugier, M., Breur, M., Crawford, J., Van Gaalen, J., Schouten, M., Willems, M., Waisfisz, Q., Mau-Them, F. T., Rodenburg, R. J., Taft, R. J., Keren, B., Christodoulou, J., Depienne, C., Simons, C. & 2 othersSalomons, G. S. & Mochel, F., 12 Mar 2019, In : Neurology. 92, 11, p. E1225-E1237 13 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Deafness
Aminoacylation
Transfer RNA
Brain
Fibroblasts

Cell Replacement Therapy Improves Pathological Hallmarks in a Mouse Model of Leukodystrophy Vanishing White Matter

Dooves, S., Leferink, P. S., Krabbenborg, S., Breeuwsma, N., Bots, S., Hillen, A. E. J., Jacobs, G., van der Knaap, M. S. & Heine, V. M., 5 Mar 2019, In : Stem cell reports. 12, 3, p. 441-450 10 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Leukoencephalopathies
Cell- and Tissue-Based Therapy
Neuroglia
Stem Cells
Stem cells

Induced pluripotent stem cell research for Vanishing White Matter: From in vitro disease modeling to in vivo cell replacement therapy

Leferink, P. S., 2019, 285 p.

Research output: PhD ThesisPhD Thesis - Research VU, graduation VUAcademic

Open Access
File

Leukodystrophies: Contributions of clinical phenotyping

Hamilton, E. M. C., 2019, 253 p.

Research output: PhD ThesisPhD Thesis - Research VU, graduation VUAcademic

Open Access
File

Leukoencephalopathy due to variants in GFPT1-associated congenital myasthenic syndrome

Helman, G., Sharma, S., Crawford, J., Patra, B., Jain, P., Bent, S. J., Urtizberea, J. A., Saran, R. K., Taft, R. J., van der Knaap, M. S. & Simons, C., 5 Feb 2019, In : Neurology. 92, 6, p. e587-e593 7 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Congenital Myasthenic Syndromes
Leukoencephalopathies
Mitochondrial Diseases
Muscle Weakness
Genome

Severe leukoencephalopathy with clinical recovery caused by recessive BOLA3 mutations

Stutterd, C. A., Lake, N. J., Peters, H., Lockhart, P. J., Taft, R. J., van der Knaap, M. S., Vanderver, A., Thorburn, D. R., Simons, C. & Leventer, R. J., 2019, JIMD Reports. Morava, E. (ed.). Springer, p. 63-70 8 p. (JIMD Reports; vol. 43).

Research output: Chapter in Book / Report / Conference proceedingChapterAcademicpeer-review

Leukoencephalopathies
Fibroblasts
Magnetic resonance imaging
Recovery
Mutation
2018

Adult mouse eIF2Bϵ Arg191His astrocytes display a normal integrated stress response in vitro

Wisse, L. E., Ter Braak, T. J., Van De Beek, M. C., Van Berkel, C. G. M., Wortel, J., Heine, V. M., Proud, C. G., Van Der Knaap, M. S. & Abbink, T. E. M., 28 Feb 2018, In : Scientific Reports. 8, 1, p. 1-9 9 p., 3773.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Eukaryotic Initiation Factor-2B
Astrocytes
Mutation
White Matter
In Vitro Techniques

Affected astrocytes in the spinal cord of the leukodystrophy vanishing white matter

Leferink, P. S., Breeuwsma, N., Bugiani, M., van der Knaap, M. S. & Heine, V. M., Apr 2018, In : Glia. 66, 4, p. 862-873 12 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Leukoencephalopathies
Astrocytes
Spinal Cord
Pathology
Oligodendroglia

Axonal abnormalities in vanishing white matter

Klok, M. D., Bugiani, M., de Vries, S. I., Gerritsen, W., Breur, M., van der Sluis, S., Heine, V. M., Kole, M. H. P., Baron, W. & van der Knaap, M. S., 1 Apr 2018, In : Annals of Clinical and Translational Neurology. 5, 4, p. 429-444 16 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Astrocytes
Axons
Myelin Sheath
Prosencephalon
Coculture Techniques

Bergmann glia translocation: a new disease marker for vanishing white matter identifies therapeutic effects of Guanabenz treatment

Dooves, S., Bugiani, M., Wisse, L. E., Abbink, T. E. M., van der Knaap, M. S. & Heine, V. M., Jun 2018, In : Neuropathology and Applied Neurobiology. 44, 4, p. 391-403 13 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Guanabenz
Therapeutic Uses
Neuroglia
Pathology
Therapeutics

Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy

Mendes, M. I., Gutierrez Salazar, M., Guerrero, K., Thiffault, I., Salomons, G. S., Gauquelin, L., Tran, L. T., Forget, D., Gauthier, M. S., Waisfisz, Q., Smith, D. E. C., Simons, C., van der Knaap, M. S., Marquardt, I., Lemes, A., Mierzewska, H., Weschke, B., Koehler, W., Coulombe, B., Wolf, N. I. & 1 othersBernard, G., 5 Apr 2018, In : American Journal of Human Genetics. 102, 4, p. 676-684 9 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Amino Acyl-tRNA Synthetases
Mutation
Aminoacylation
Myelin Sheath
Inborn Genetic Diseases

Diffusion tensor imaging in metachromatic leukodystrophy

van Rappard, D. F., Königs, M., Steenweg, M. E., Boelens, J. J., Oosterlaan, J., van der Knaap, M. S., Wolf, N. I. & Pouwels, P. J. W., Mar 2018, In : Journal of Neurology. 265, 3, p. 659-668 10 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Metachromatic Leukodystrophy
Diffusion Tensor Imaging
Cell Transplantation
Anisotropy
Sulfoglycosphingolipids

Genetic defects disrupting glial ion and water homeostasis in the brain

Min, R. & van der Knaap, M. S., May 2018, In : Brain Pathology. 28, 3, p. 372-387 16 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Neuroglia
Homeostasis
Ions
Water
Brain

Hypomyelination with tooth and bone involvement: New insights: Brain MR imaging and in vitro models

Cayami, F. K., 2018, 194 p.

Research output: PhD ThesisPhD Thesis - Research VU, graduation VUAcademic

Open Access
File

Leukodystrophies — much more than just diseases of myelin

van der Knaap, M. S. & Bugiani, M., Dec 2018, In : Nature Reviews Neurology. 14, 12, p. 747-748 2 p.

Research output: Contribution to JournalLetterAcademicpeer-review

Metachromatic leukodystrophy: Natural evolution and treatment effects

van Rappard, D. F., 2018, 183 p.

Research output: PhD ThesisPhD Thesis - Research VU, graduation VUAcademic

Open Access
File

Natural History of Vanishing White Matter

Hamilton, E. M. C., van der Lei, H. D. W., Vermeulen, G., Gerver, J. A. M., Lourenço, C. M., Naidu, S., Mierzewska, H., Gemke, R. J. B. J., de Vet, H. C. W., Uitdehaag, B. M. J., Lissenberg-Witte, B. I., Research Group, V. W. M. & van der Knaap, M. S., Aug 2018, In : Annals of Neurology. 84, 2, p. 274-288 15 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Natural History
Age of Onset
Leukoencephalopathies
Absence Epilepsy
Sex Characteristics

Ovarioleukodystrophy: Vanishing white matter versus AARS2-related ovarioleukodystrophy

van der Knaap, M. S. & Abbink, T. E. M., Aug 2018, In : Clinical Neurology and Neurosurgery. 171, 1 p.

Research output: Contribution to JournalLetterAcademicpeer-review

Reply: The recurrent mutation in TMEM106B also causes hypomyelinating leukodystrophy in China and is a CpG hotspot

Simons, C., Dyment, D., van der Knaap, M. S. & Wolf, N. I., 1 May 2018, In : Brain. 141, 5, p. 1-2 2 p., e37.

Research output: Contribution to JournalLetterAcademicpeer-review

Report from the Edge of Neuroscience: Investigating an RNA Polymerase III related leukodystrophy using patient-derived iPSCs, neural cells, and mini-brains

Holmes, D. B., 2018, 158 p.

Research output: PhD ThesisPhD Thesis - Research VU, graduation VUAcademic

Open Access
File

Seizures and disturbed brain potassium dynamics in the leukodystrophy megalencephalic leukoencephalopathy with subcortical cysts

Dubey, M., Brouwers, E., Hamilton, E. M. C., Stiedl, O., Bugiani, M., Koch, H., Kole, M. H. P., Boschert, U., Wykes, R. C., Mansvelder, H. D., van der Knaap, M. S. & Min, R., Mar 2018, In : Annals of Neurology. 83, 3, p. 636-649 14 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Potassium
Seizures
Brain
Astrocytes
Epilepsy

Slowly Progressive Psychiatric Symptoms: Think Metachromatic Leukodystrophy

van Rappard, D. F., de Vries, A. L. C., Oostrom, K. J., Boelens, J. J., Hollak, C. E. M., van der Knaap, M. S. & Wolf, N. I., 1 Feb 2018, In : Journal of the American Academy of Child and Adolescent Psychiatry. 57, 2, p. 86-95 10 p.

Research output: Contribution to JournalEditorialAcademicpeer-review

Towards the molecular mechanism of vanishing white matter

Wisse, L. E., 2018, 214 p.

Research output: PhD ThesisPhD Thesis - Research VU, graduation VUAcademic

Open Access
File
2017

Leukodystrophies: a proposed classification system based on pathological changes and pathogenetic mechanisms

van der Knaap, M. S. & Bugiani, M., 1 Sep 2017, In : Acta Neuropathologica. 134, 3, p. 351-382 32 p.

Research output: Contribution to JournalReview articleAcademicpeer-review

Open Access
Myelin Sheath
Oligodendroglia
Pathology
Microglia
Astrocytes

Megalencephalic leukoencephalopathy with cysts: the Glialcam-null mouse model

Bugiani, M., Dubey, M., Breur, M., Postma, N. L., Dekker, M. P., Ter Braak, T., Boschert, U., Abbink, T. E. M., Mansvelder, H. D., Min, R., van Weering, J. R. T. & van der Knaap, M. S., Jul 2017, In : Annals of Clinical and Translational Neurology. 4, 7, p. 450-465 16 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Leukoencephalopathies
Cysts
Megalencephaly
Edema
Astrocytes

UFM1 founder mutation in the Roma population causes recessive variant of H-ABC

Hamilton, E. M. C., Bertini, E., Kalaydjieva, L., Morar, B., Dojčáková, D., Liu, J., Vanderver, A., Curiel, J., Persoon, C. M., Diodato, D., Pinelli, L., Van Der Meij, N. L., Plecko, B., Blaser, S., Wolf, N. I., Waisfisz, Q., Abbink, T. E. M. & Van Der Knaap, M. S., 24 Oct 2017, In : Neurology. 89, 17, p. 1821-1828 8 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Roma
Mutation
Population
Exome
Founder Effect
Open Access
File
2016

Astrocytes are central in the pathomechanisms of vanishing white matter

Dooves, S., Bugiani, M., Postma, N. L., Polder, E., Land, N., Horan, S. T., van Deijk, A. L. F., van de Kreeke, A., Jacobs, J. G., Vuong, C., Klooster, J., Kamermans, M., Wortel, J., Loos, M., Wisse, L. E., Scheper, G. C., Abbink, G. E. M., Heine, V. M. & Knaap, M., 2016, In : Journal of Clinical Investigation. 126, p. 1512-1524 4.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access

Leukodystrophies: Five new things.

Knaap, M., Wolf, N. & Heine, V. M., 2016, In : Neurology: Clinical Practice. 6, 6, p. 506-514 9 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Novel brain white matter disorders and their genetic causes

Kevelam, S. H. G., 2016

Research output: PhD ThesisPhD Thesis - Research VU, graduation VUAcademic

Open Access
File
Inborn Genetic Diseases
Brain
White Matter

Stem cell therapy for white matter disorders: don't forget the microenvironment!

Dooves, S., Knaap, M. & Heine, V. M., 2016, In : Journal of Inherited Metabolic Disease. 39, p. 513-518 4.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
2015

A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies

Parikh, S., Bernard, G., Leventer, R. J., van der Knaap, M. S., ten Hove, J., Pizzino, A., McNeill, N. H., Helman, G., Simons, C., Schmidt, J. L., Rizzo, W. B., Patterson, M. C., Taft, R. J. & Vanderver, A., 2015, In : Molecular Genetics and Metabolism. 114, 4, p. 501-515

Research output: Contribution to JournalArticleAcademicpeer-review

Leukoencephalopathies
Testing
Genes
Anodontia
Adrenoleukodystrophy

Altered PLP1 splicing causes hypomyelination of early myelinating structures

Kevelam, S. H., Taube, J. R., van Spaendonk, R. M. L., Bertini, E., Sperle, K., Tarnopolsky, M., Tonduti, D., Valente, E. M., Travaglini, L., Sistermans, E. A., Bernard, G., Catsman-Berrevoets, C. E., van Karnebeek, C. D. M., Ostergaard, J. R., Friederich, R. L., Elsaid, M. F., Schieving, J. H., Tarailo-Graovac, M., Orcesi, S., Steenweg, M. E. & 6 othersvan Berkel, C. G. M., Waisfisz, Q., Abbink, G. E. M., Knaap, M., Hobson, G. M. & Wolf, N. I., 2015, In : Annals of Clinical and Translational Neurology. 2, 6, p. 648-661

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access

Berardinelli-Seip syndrome and achalasia: a shared pathomechanism?

van der Pol, R. J., Benninga, M., Magre, J., van Maldergem, L., Rotteveel, J., van der Knaap, M. S. & de Meij, T. G. J., 2015, In : European Journal of Pediatrics. 174, 7, p. 975-980

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Congenital Generalized Lipodystrophy
Esophageal Achalasia
Esophageal Motility Disorders
Acanthosis Nigricans
Hirsutism

Case definition and classification of leukodystrophies and leukoencephalopathies

Vanderver, A., Prust, M., Tonduti, D., Mochel, F., Hussey, H. M., Helman, G., Garbern, J., Eichler, F., Labauge, P., Aubourg, P., Rodriguez, D., Patterson, M. C., van Hove, J. LK., Schmidt, J., Wolf, N. I., Boespflug-Tanguy, O., Schiffmann, R. & van der Knaap, M. S., 2015, In : Molecular Genetics and Metabolism. 114, 4, p. 494-500

Research output: Contribution to JournalArticleAcademicpeer-review

Leukoencephalopathies
Epidemiology
Public health
Molecular Epidemiology
Epidemiologic Studies

Characterization of Human Disease Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

Crow, Y. J., Chase, D. S., Schmidt, J. L., Szynkiewicz, M., Forte, G. M. A., Gornall, H. L., Oojageer, A., Anderson, B., Pizzino, A., Helman, G., Abdel-Hamid, M. S., Abdel-Salam, G. M., Ackroyd, S., Aeby, A., Agosta, G., Albin, C., Allon-Shalev, S., Arellano, M., Ariaudo, G., Aswani, V. & 82 othersBabul-Hirji, R., Baildam, E. M., Bahi-Buisson, N., Bailey, K. M., Barnerias, C., Barth, M., Battini, R., Beresford, M. W., Bernard, G., Bianchi, M., de Villemeur, T. B., Blair, E. M., Bloom, M., Burlina, A. B., Carpanelli, M. L., Carvalho, D. R., Castro-Gago, M., Cavallini, A., Cereda, C., Chandler, K. E., Chitayat, D. A., Collins, A. E., Corcoles, C. S., Cordeiro, N. J. V., Crichiutti, G., Dabydeen, L., Dale, R. C., D'Arrigo, S., De Goede, C. G. E. L., de Laet, C., De Waele, L. M. H., Denzler, I., Desguerre, I., Devriendt, K., Di Rocco, M., Fahey, M. C., Fazzi, E., Ferrie, C. D., Figueiredo, A., Gener, B., Goizet, C., Gowrinathan, N. R., Gowrishankar, K., Hanrahan, D., Isidor, B., Kara, L., Khan, N., King, M. D., Kirk, E. P., Kumar, R., Lagae, L., Landrieu, P., Lauffer, H., Laugel, V., La Piana, R., Lim, M. J., Lin, J. P. S. M., Linnankivi, T., Mackay, M. T., Marom, D. R., Lourenco, C. M., McKee, S. A., Moroni, I., Morton, J. E. V., Moutard, M. L., Murray, K., Nabbout, R., Nampoothiri, S., Nunez-Enamorado, N., Oades, P. J., Olivieri, I., Ostergaard, J. R., Perez-Duenas, B., Prendiville, J. S., Ramesh, V., Rasmussen, M., Regal, L., Ricci, F., Rio, M., Knaap, M., Orcesi, S. & Rice, G. I., 2015, In : American Journal of Medical Genetics Part A. 167, 2, p. 296-312

Research output: Contribution to JournalArticleAcademicpeer-review

Phenotype
Mutation
Aicardi Syndrome
Interferons
Interferon Type I

Childhood white matter disorders: Research at the interface of MRI, clinical phenotype and genetics

Steenweg, M. E., 2015

Research output: PhD ThesisPhD Thesis - Research VU, graduation VUAcademic

CLCN2-Related Leukoencephalopathy

Knaap, M., Depienne, C., Sedel, F. & Abbink, T. E. M., 2015, GeneReviews® [internet]. Pagon, R. A., Adam, M. P. & Ardinger, H. H. (eds.). Seattle (WA): University of Washington

Research output: Chapter in Book / Report / Conference proceedingChapterAcademic

Comparing and contrasting white matter disorders: a neuropathological approach to pathophysiology

Bugiani, M., 2015

Research output: PhD ThesisPhD Thesis - Research VU, graduation VUAcademic

Open Access
File

CSF and Blood Levels of GFAP in Alexander Disease

Jany, P. L., Agosta, G. E., Benko, W. S., Eickhoff, J. C., Keller, S. R., Koehler, W., Koeller, D., Mar, S., Naidu, S., Marie Ness, J., Pareyson, D., Renaud, D. L., Salsano, E., Schiffmann, R., Simon, J., Vanderver, A., Eichler, F., van der Knaap, M. S. & Messing, A., 2015, In : eNeuro. 2, 5

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access

DARS-associated leukoencephalopathy can mimic a steroid-responsive neuroinflammatory disorder

Wolf, N. I., Toro, C., Kister, I., Abd Latif, K., Leventer, R., Pizzino, A., Simons, C., Abbink, G. E. M., Taft, R. J., van der Knaap, M. S. & Vanderver, A., 2015, In : Neurology. 84, 3, p. 226-230

Research output: Contribution to JournalArticleAcademicpeer-review

Leukoencephalopathies
Steroids
Spinal Cord
Paraplegia
Mutation

Disease specific therapies in leukodystrophies and leukoencephalopathies

Helman, G., van Haren, K., Bonkowsky, J. L., Bernard, G., Pizzino, A., Braverman, N., Suhr, D., Patterson, M. C., Fatemi, S. A., Leonard, J., van der Knaap, M. S., Back, S. A., Damiani, S., Goldman, S. A., Takanohashi, A., Petryniak, M., Rowitch, D., Messing, A., Wrabetz, L., Schiffmann, R. & 3 othersEichler, F., Escolar, M. L. & Vanderver, A., 2015, In : Molecular Genetics and Metabolism. 114, 4, p. 527-536

Research output: Contribution to JournalArticleAcademicpeer-review

Leukoencephalopathies
Patient Care Management
Therapeutics
Phase II Clinical Trials
Clinical Trials, Phase I

Early-Onset Aicardi-Goutieres Syndrome: Magnetic Resonance Imaging (MRI) Pattern Recognition

Vanderver, A., Prust, M., Kadom, N., Demarest, S., Crow, Y. J., Helman, G., Orcesi, S., La Piana, R., Uggetti, C., Wang, J. C., Gordisch-Dressman, H., van der Knaap, M. S. & Livingston, J. H., 2015, In : Journal of Child Neurology. 30, 10, p. 1343-1348

Research output: Contribution to JournalArticleAcademicpeer-review

Aicardi Syndrome
Magnetic Resonance Imaging
Temporal Lobe
Atrophy
Leukoencephalopathies

Early-Onset Severe Encephalopathy with Epilepsy: The BRAT1 Gene Should Be Added to the List of Causes

van de Pol, L. A., Wolf, N. I., van Weissenbruch, M. M., Stam, C. J., Weiss, M. M., Waisfisz, Q., Kevelam, S. H., Bugiani, M., van de Kamp, J. M. & Knaap, M., 2015, In : Neuropediatrics. 46, 6, p. 392-400

Research output: Contribution to JournalArticleAcademicpeer-review

Brain Diseases
Epilepsy
Exome
Genes
Frameshift Mutation

Eight novel mutations in MLC1 from 18 Iranian patients with megalencephalic leukoencephalopathy with subcortical cysts

Kariminejad, A., Rajaee, A., Ashrafi, M. R., Alizadeh, H., Tonekaboni, S. H., Malamiri, R. A., Ghofrani, M., Karimzadeh, P., Mohammadi, M. M., Baghalshooshtari, A., Bozorgmehr, B., Kariminejad, M. H., Postma, N., Abbink, G. E. M. & van der Knaap, M. S., 2015, In : European Journal of Medical Genetics. 58, 2, p. 71-74

Research output: Contribution to JournalArticleAcademicpeer-review

Mutation
Megalencephaly
Seizures
Magnetic Resonance Imaging
Inbreeding

Hypomyelination and Congenital Cataract

Biancheri, R., Zara, F., Bruno, C., Gazzerro, E., Rossi, A., Knaap, M. & Minetti, C., 4 Jun 2015, GeneReviews® [internet]. Pagon, R. A., Adam, M. P. & Ardinger, H. H. (eds.). Seattle, WA: University of Washington, 1 p.

Research output: Chapter in Book / Report / Conference proceedingChapterAcademic

Interferon-alpha and the calcifying microangiopathy in Aicardi-Goutieres syndrome

Klok, M. D., Bakels, H. S., Postma, N. L., van Spaendonk, R. M. L., van der Knaap, M. S. & Bugiani, M., 2015, In : Annals of Clinical and Translational Neurology. 2, 7, p. 774-779

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access

Large exonic deletions in POLR3B gene cause POLR3-related leukodystrophy

Gutierrez, M., Thiffault, I., Guerrero, K., Martos-Moreno, G. A., Tran, L. T., Benko, W., Knaap, M., van Spaendonk, R. M. L., Wolf, N. I. & Bernard, G., 2015, In : Orphanet journal of rare diseases. 10, 69.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Mutation
Exons
Genes
Complementary DNA
Phenotype

Mice with megalencephalic leukoencephalopathy with cysts: a developmental angle

Dubey, M., Bugiani, M., Ridder, M. C., Postma, N. L., Brouwers, E., Polder, E., Jacobs, J. G., Baaijen, J. C., Klooster, J., Kamermans, M., Aardse, R., de Kock, C. P. J., Dekker, M. P., van Weering, J. R. T., Heine, V. M., Abbink, T. E. M., Scheper, G. C., Boor, P. K. I., Lodder, J. C., Mansvelder, H. D. & 1 othersKnaap, M., 2015, In : Annals of Neurology. 77, 11, p. 114-131

Research output: Contribution to JournalArticleAcademicpeer-review

Leukoencephalopathies
Cysts
Astrocytes
Edema
Brain