Ngā hua rapu - Marjo S. van der Knaap
- E whakaatu ana i te 1 - 20 hua o te 106
- Haere ki te Whārangi Whai Ake
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Treatment of leukodystrophies: Advances and challenges mā Nicole I. Wolf, Marjo S. van der Knaap, Marc Engelen
I whakaputaina 2025Revisão -
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Quantitative MRI in leukodystrophies mā Menno D. Stellingwerff, Petra J. W. Pouwels, Stefan D. Roosendaal, Frederik Barkhof, Marjo S. van der Knaap
I whakaputaina 2023Revisão -
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Ribose-5-Phosphate Isomerase Deficiency: New Inborn Error in the Pentose Phosphate Pathway Associated with a Slowly Progressive Leukoencephalopathy mā Jojanneke H.J. Huck, Nanda M. Verhoeven, Eduard A. Struys, Gajja S. Salomons, Cornelis Jakobs, Marjo S. van der Knaap
I whakaputaina 2004Artigo -
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Bergmann glia translocation: a new disease marker for vanishing white matter identifies therapeutic effects of Guanabenz treatment mā Stephanie Dooves, Marianna Bugiani, Lisanne E. Wisse, Truus E. M. Abbink, Marjo S. van der Knaap, Vivi M. Heine
I whakaputaina 2017Artigo -
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Hyaluronan accumulation and arrested oligodendrocyte progenitor maturation in vanishing white matter disease mā Marianna Bugiani, Nienke L. Postma, Emiel Polder, Nikki Dieleman, P Scheffer, Fraser J. Sim, Marjo S. van der Knaap, Ilja Boor
I whakaputaina 2013Artigo -
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Glia-Specific Activation of All Pathways of the Unfolded Protein Response in Vanishing White Matter Disease mā Barbara van Kollenburg, Jantine van Dijk, James Garbern, Adri A.M. Thomas, Gert C. Scheper, James M. Powers, Marjo S. van der Knaap
I whakaputaina 2006Artigo -
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Transaldolase Deficiency: Liver Cirrhosis Associated with a New Inborn Error in the Pentose Phosphate Pathway mā Nanda M. Verhoeven, Jojanneke H.J. Huck, Birthe Roos, Eduard A. Struys, Gajja S. Salomons, A. C. Douwes, Marjo S. van der Knaap, Cornelis Jakobs
I whakaputaina 2001Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Medicine
Biology
Pathology
Genetics
Disease
Gene
Magnetic resonance imaging
Radiology
Neuroscience
White matter
Mutation
Leukodystrophy
Internal medicine
Leukoencephalopathy
Central nervous system
Phenotype
Cell biology
Myelin
Missense mutation
Biochemistry
Pediatrics
Immunology
Oligodendrocyte
Astrocyte
Compound heterozygosity
Psychology
Atrophy
Molecular biology
Psychiatry
Ataxia