Association of WKL1/MLC1 with catatonic schizophrenia

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[Alexander disease as an explanation for long-term unexplained psychiatric symptoms in a young girl].

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Severe PTSD symptoms magnify episodic memory-encoding deficits and amygdala-ACC attenuation during unpredictable threat in male combat veterans.

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Developmental and cellular vulnerabilities underlie genetic architecture of schizophrenia.

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Advanced glycation end products drive blood-brain barrier lipid dysregulation via RAGE-ABCA1 signaling to promote neurovascular dysfunction in Alzheimer's disease.

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Heterogeneous structural brain signatures of methamphetamine and ketamine use disorders revealed by normative modeling.

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Dysregulated phosphatidylglycerol metabolism in dorsal root ganglia contributes to pain hypersensitivity in a mouse model of Fabry disease.

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Related Experiment Videos

Association of WKL1/MLC1 with catatonic schizophrenia

Related Concept Videos

Patient and Family Perspectives on Clinical Outcomes in Therapy Trials in Megalencephalic Leukoencephalopathy with Subcortical Cysts: An Open Inventory.

Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory services.

Translation initiation factor eIF2Bε promotes Wnt-mediated clonogenicity and global translation in intestinal epithelial cells.

Imaging Patterns Characterizing Mitochondrial Leukodystrophies.

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Pharmacological and non-pharmacological modulation of striatal dopamine release: a meta-analysis of [11C]raclopride PET studies.

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Association of WKL1/MLC1 with catatonic schizophrenia

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