by jlohrconsulting | Sep 15, 2025 | Uncategorized
Front Pediatr. 2025 Aug 29;13:1634704. doi: 10.3389/fped.2025.1634704. eCollection 2025. ABSTRACT A mutation rendering microtubulin and microtubule-associated proteins ineffective leads to a tubulinopathy known as complex cortical dysplasia (CCD), characterized by...
by jlohrconsulting | Sep 15, 2025 | Uncategorized
Front Immunol. 2025 Aug 29;16:1611748. doi: 10.3389/fimmu.2025.1611748. eCollection 2025. ABSTRACT BACKGROUND: X-linked agammaglobulinemia (XLA) is a rare disorder associated with defective B-lymphocyte differentiation, also known as circulating B-cell deletion or...
by jlohrconsulting | Sep 15, 2025 | Uncategorized
Front Pharmacol. 2025 Aug 29;16:1656301. doi: 10.3389/fphar.2025.1656301. eCollection 2025. ABSTRACT INTRODUCTION: Epilepsy is a chronic neurological disorder marked by recurrent seizures. Neuroinflammation and mammalian target of rapamycin (mTOR) signaling are...
by jlohrconsulting | Sep 15, 2025 | Uncategorized
Front Pharmacol. 2025 Aug 29;16:1649543. doi: 10.3389/fphar.2025.1649543. eCollection 2025. ABSTRACT Migraine and epilepsy are two common, chronic, disabling, paroxysmal neurological disorders. A growing body of evidence from epidemiological, genetic,...
by jlohrconsulting | Sep 15, 2025 | Uncategorized
Noro Psikiyatr Ars. 2025 Jun 28;62(3):279-285. doi: 10.29399/npa.29110. eCollection 2025. ABSTRACT INTRODUCTION: Childhood Absence Epilepsy, a subtype of genetic generealised epilepsy, is characterised by sudden and brief episodes of impaired consciousness. The...
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