Autosomal dominant cerebellar phenotypes: the genotype has settled the issue

Prion proteins: a biological role beyond prion diseases.

Acta neurologica Scandinavica·2007

Category fluency in mild cognitive impairment: reduced effect of practice in test-retest conditions.

Alzheimer disease and associated disorders·2004

Correlation of statin-increased platelet APP ratios and reduced blood lipids in AD patients.

Neurology·2003

Reporting clinical trials: full access to all the data.

Journal of neurology, neurosurgery, and psychiatry·2002

Effects of practice on category fluency in Alzheimer's disease.

The Clinical neuropsychologist·2002

Comparison of the hopkins verbal learning test-revised to the California verbal learning test in Alzheimer's disease.

Applied neuropsychology·2001

Analysis of Interindividual Lesion Progression Variability in Adult Cerebral Adrenoleukodystrophy.

Neurology·2026

Prediction of Long-Term Postsurgical Seizure Recurrence From MRI Brain Hub Disruption in Patients With Temporal Lobe Epilepsy.

Neurology·2026

Association Between Menopausal Hormone Therapy and Alzheimer Disease Neuropathology.

Neurology·2026

Blood-Based Biomarkers for Alzheimer Disease in Primary Care: The Gap Between Biology and Clinical Utility.

Neurology·2026

Intervention or Conservative Management for Symptomatic Cerebral Cavernous Malformations: A Prospective, Population-Based Cohort Study.

Neurology·2026

Individualized vs Standard Blood Pressure Control During Thrombectomy for Ischemic Stroke: The DETERMINE Randomized Clinical Trial.

Neurology·2026

Hyperexcitability in hippocampal CA1 pyramidal cells OF Fmr1 knockout mice emerges during late postnatal development.

Neuroscience·2026

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

American journal of medical genetics. Part A·2026

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

International journal of molecular sciences·2026

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

International journal of molecular sciences·2026

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

Cells·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Related Experiment Videos

Autosomal dominant cerebellar phenotypes: the genotype has settled the issue

Related Concept Videos

Prion proteins: a biological role beyond prion diseases.

Category fluency in mild cognitive impairment: reduced effect of practice in test-retest conditions.

Correlation of statin-increased platelet APP ratios and reduced blood lipids in AD patients.

Reporting clinical trials: full access to all the data.

Effects of practice on category fluency in Alzheimer's disease.

Comparison of the hopkins verbal learning test-revised to the California verbal learning test in Alzheimer's disease.

Analysis of Interindividual Lesion Progression Variability in Adult Cerebral Adrenoleukodystrophy.

Prediction of Long-Term Postsurgical Seizure Recurrence From MRI Brain Hub Disruption in Patients With Temporal Lobe Epilepsy.

Association Between Menopausal Hormone Therapy and Alzheimer Disease Neuropathology.

Blood-Based Biomarkers for Alzheimer Disease in Primary Care: The Gap Between Biology and Clinical Utility.

Intervention or Conservative Management for Symptomatic Cerebral Cavernous Malformations: A Prospective, Population-Based Cohort Study.

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Hyperexcitability in hippocampal CA1 pyramidal cells OF Fmr1 knockout mice emerges during late postnatal development.

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

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Autosomal dominant cerebellar phenotypes: the genotype has settled the issue

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