Works by de Vries, Juna M.
Results: 8
HLA and KIR genetic association and NK cells in anti-NMDAR encephalitis.
- Published in:
- Frontiers in Immunology, 2024, p. 1, doi. 10.3389/fimmu.2024.1423149
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- Article
Distinct movement disorders in contactin-associated-protein-like-2 antibody-associated autoimmune encephalitis.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 2, p. 657, doi. 10.1093/brain/awac276
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- Article
Phenotypical variation within 22 families with Pompe disease.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-182
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- Article
Phenotypical variation within 22 families with Pompe disease.
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- 2013
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- Publication type:
- journal article
Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study.
- Published in:
- Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 88, doi. 10.1186/1750-1172-7-88
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- Publication type:
- Article
Effect of enzyme therapy and prognostic factors in 69 adults with Pompe disease: an open-label single-center study.
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- Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 73, doi. 10.1186/1750-1172-7-73
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- Article
Survival and associated factors in 268 adults with Pompe disease prior to treatment with enzyme replacement therapy.
- Published in:
- 2011
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- Publication type:
- journal article
Rapid Ultraperformance Liquid Chromatography--Tandem Mass Spectrometry Assay for a Characteristic Glycogen-Derived Tetrasaccharide in Pompe Disease and Other Glycogen Storage Diseases.
- Published in:
- Clinical Chemistry, 2012, v. 58, n. 7, p. 1139, doi. 10.1373/clinchem.2011.178319
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- Publication type:
- Article