Mining the genome for causes and cures of neurological disease

[Progressive myoclonic epilepsy in the department of neurology of the University Teaching hospital Point "G"].

Le Mali medical·2023

Mifepristone-inducible transgene expression in neural progenitor cells in vitro and in vivo.

Gene therapy·2016

Spinal and bulbar muscular atrophy: pathogenesis and clinical management.

Oral diseases·2013

Association study of polymorphisms in leptin and leptin receptor genes with antipsychotic-induced body weight gain.

Progress in neuro-psychopharmacology & biological psychiatry·2012

Dominant GDAP1 mutations cause predominantly mild CMT phenotypes.

Neurology·2011

Clinical and genetic analysis of spinocerebellar ataxia in Mali.

European journal of neurology·2011

AI virtual cells for drug discovery and pharmacology.

Trends in pharmacological sciences·2026

Pyroptotic pores reopen the case for caspase inhibitors.

Trends in pharmacological sciences·2026

Nitroxyl (HNO) therapeutics: exposure control and target engagement.

Trends in pharmacological sciences·2026

Emerging STAT1 post-translational modifications: mechanisms and translational perspectives.

Trends in pharmacological sciences·2026

The expanding role of Cav3 channels in glioblastoma.

Trends in pharmacological sciences·2026

Why pharmacological concepts survive despite scientific progress.

Trends in pharmacological sciences·2026

A meta-analysis of periodic and aperiodic electrophysiological features in Parkinson's disease.

Brain communications·2026

RBPMS::NTRK3-rearranged sacral malignant spindle cell tumor in neurofibromatosis diagnosed by RNA sequencing: a case report and literature review.

Frontiers in medicine·2026

Gut Microbiota, Neuroinflammation, and Autonomic Dysfunction in Neurodegenerative Diseases: A Systematic Review of Mechanistic and Translational Evidence.

Cureus·2026

The metastatic spectrum in functional and non-functional NENs: mechanistic insights from multi-omics.

Frontiers in endocrinology·2026

"Internal carotid artery-type cervical spondylosis" is not supported as an independent subtype: a perspective on diagnostic classification and clinical differentiation.

Frontiers in neurology·2026

POEMS syndrome presenting as presumed chronic glomerulonephritis with a 1-year delay in diagnosis: a case report.

Frontiers in medicine·2026

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Mining the genome for causes and cures of neurological disease

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[Progressive myoclonic epilepsy in the department of neurology of the University Teaching hospital Point "G"].

Mifepristone-inducible transgene expression in neural progenitor cells in vitro and in vivo.

Spinal and bulbar muscular atrophy: pathogenesis and clinical management.

Association study of polymorphisms in leptin and leptin receptor genes with antipsychotic-induced body weight gain.

Dominant GDAP1 mutations cause predominantly mild CMT phenotypes.

Clinical and genetic analysis of spinocerebellar ataxia in Mali.

AI virtual cells for drug discovery and pharmacology.

Pyroptotic pores reopen the case for caspase inhibitors.

Nitroxyl (HNO) therapeutics: exposure control and target engagement.

Emerging STAT1 post-translational modifications: mechanisms and translational perspectives.

The expanding role of Cav3 channels in glioblastoma.

Why pharmacological concepts survive despite scientific progress.

A meta-analysis of periodic and aperiodic electrophysiological features in Parkinson's disease.

RBPMS::NTRK3-rearranged sacral malignant spindle cell tumor in neurofibromatosis diagnosed by RNA sequencing: a case report and literature review.

Gut Microbiota, Neuroinflammation, and Autonomic Dysfunction in Neurodegenerative Diseases: A Systematic Review of Mechanistic and Translational Evidence.

The metastatic spectrum in functional and non-functional NENs: mechanistic insights from multi-omics.

"Internal carotid artery-type cervical spondylosis" is not supported as an independent subtype: a perspective on diagnostic classification and clinical differentiation.

POEMS syndrome presenting as presumed chronic glomerulonephritis with a 1-year delay in diagnosis: a case report.

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Mining the genome for causes and cures of neurological disease

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