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Biallelic variants in SLC35B2 cause a novel chondrodysplasia with hypomyelinating leukodystrophy.
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Brain. 2022Pmid / DOI:
35325049 -
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency
Sven KRACKER, Romane THOUENON
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Science ImmunologyPmid / DOI:
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Cajal-retzius cells: Recent advances in identity and function
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Curr Opin NeurobiolPmid / DOI:
36774666 -
DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity
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BloodPmid / DOI:
36952639 -
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Brain Commun.Pmid / DOI:
36324869 -
New PublicationArterial Spin-Labeling Perfusion Imaging in the Early Stage of Sturge-Weber Syndrome
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AJNR Am J NeuroradiolPmid / DOI:
36137664 -
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NeuropediatricsPmid / DOI:
36223876 -
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Dev Med Child Neurol
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31050360 -
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Acta Neuropathol
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36121478 -
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Eur Radiol.Pmid / DOI:
34003354 -
CT and Multimodal MR Imaging Features of Embryonal Tumors with Multilayered Rosettes in Children
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AJNR Am J Neuroradiol.Pmid / DOI:
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Neuro Oncol.Pmid / DOI:
29244086 -
Neuroimaging evidence of brain abnormalities in mastocytosis
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Transl PsychiatryPmid / DOI:
28786975 -
Arterial Spin-Labeling in Children with Brain Tumor: A Meta-Analysis
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AJNR Am J NeuroradiolPmid / DOI:
30072368