Hereditary Hyperekplexia Latest Advances

Role of the Glycine Transporter GlyT2 in the Neuronal Differentiation of PC12 Cells.

Journal: International journal of molecular sciences

Published: January 21, 2026

Case report: Thymoma-associated GAD65 autoimmunity: a unifying mechanism for multi-organ injury involving nervous, endocrine, and renal systems.

Journal: Frontiers in immunology

Published: January 18, 2026

Immunobiology and immunotherapies in stiff-person syndrome and glutamic acid decarboxylase antibody-spectrum disorders: Present and future therapeutic prospects.

Journal: Handbook of clinical neurology

Published: January 12, 2026

Understanding stiff-person syndrome: Epidemiological trends, diagnostic challenges, and treatment advances.

Journal: Journal of neuroimmunology

Published: November 18, 2025

Promising Effects of CAR T-Cell Therapy in Refractory Stiff Person Syndrome and a Hopeful Future for All Neuroautoimmunities.

Journal: Neurology(R) neuroimmunology & neuroinflammation

Published: November 17, 2025

A fatal infantile case with suspected hyperekplexia.

Journal: The journal of medical investigation : JMI

Published: November 03, 2025

Anti-CD19 CAR T-Cell Therapy in Advanced Stiff-Person Syndrome and Concomitant Myasthenia Gravis.

Journal: Neurology(R) neuroimmunology & neuroinflammation

Published: October 06, 2025

A Novel Variant in GLRA1 Associated With Emotional Stimulus-Sensitive Hemichoreic Movements.

Journal: American journal of medical genetics. Part A

Published: August 30, 2025

A case of childhood hyperekplexia due to a novel nonsense variant in the GLRA1 gene.

Journal: Medicine

Published: August 06, 2025

Case Report: A case of influenza A infection-associated stiff person spectrum disorder with favorable outcome.

Journal: Frontiers in immunology

Published: July 26, 2025

Polycythemia vera and stiff-person syndrome: a case report.

Journal: BMC neurology

Published: July 22, 2025

Deciphering the molecular mechanisms of startle disease: The role of the Asn46Lys mutation in the glycine receptor.

Journal: The Journal of chemical physics

Published: June 30, 2025

Hereditary Hyperekplexia Latest Advances

Find the Latest Research About Hereditary Hyperekplexia

Role of the Glycine Transporter GlyT2 in the Neuronal Differentiation of PC12 Cells.

Role of the Glycine Transporter GlyT2 in the Neuronal Differentiation of PC12 Cells.

Case report: Thymoma-associated GAD65 autoimmunity: a unifying mechanism for multi-organ injury involving nervous, endocrine, and renal systems.

Case report: Thymoma-associated GAD65 autoimmunity: a unifying mechanism for multi-organ injury involving nervous, endocrine, and renal systems.

Immunobiology and immunotherapies in stiff-person syndrome and glutamic acid decarboxylase antibody-spectrum disorders: Present and future therapeutic prospects.

Immunobiology and immunotherapies in stiff-person syndrome and glutamic acid decarboxylase antibody-spectrum disorders: Present and future therapeutic prospects.

Understanding stiff-person syndrome: Epidemiological trends, diagnostic challenges, and treatment advances.

Understanding stiff-person syndrome: Epidemiological trends, diagnostic challenges, and treatment advances.

Promising Effects of CAR T-Cell Therapy in Refractory Stiff Person Syndrome and a Hopeful Future for All Neuroautoimmunities.

Promising Effects of CAR T-Cell Therapy in Refractory Stiff Person Syndrome and a Hopeful Future for All Neuroautoimmunities.

A fatal infantile case with suspected hyperekplexia.

A fatal infantile case with suspected hyperekplexia.

Anti-CD19 CAR T-Cell Therapy in Advanced Stiff-Person Syndrome and Concomitant Myasthenia Gravis.

Anti-CD19 CAR T-Cell Therapy in Advanced Stiff-Person Syndrome and Concomitant Myasthenia Gravis.

A Novel Variant in GLRA1 Associated With Emotional Stimulus-Sensitive Hemichoreic Movements.

A Novel Variant in GLRA1 Associated With Emotional Stimulus-Sensitive Hemichoreic Movements.

A case of childhood hyperekplexia due to a novel nonsense variant in the GLRA1 gene.

A case of childhood hyperekplexia due to a novel nonsense variant in the GLRA1 gene.

Case Report: A case of influenza A infection-associated stiff person spectrum disorder with favorable outcome.

Case Report: A case of influenza A infection-associated stiff person spectrum disorder with favorable outcome.

Polycythemia vera and stiff-person syndrome: a case report.

Polycythemia vera and stiff-person syndrome: a case report.

Deciphering the molecular mechanisms of startle disease: The role of the Asn46Lys mutation in the glycine receptor.

Deciphering the molecular mechanisms of startle disease: The role of the Asn46Lys mutation in the glycine receptor.