Spasmus Nutans Latest Advances

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Last Updated: 09/26/2026

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Found 5260 publications

From Metabolic Crises to Epileptic Encephalopathy: TANGO2 Deficiency Disorder due to Homozygous Multi-exon Deletion.

From Metabolic Crises to Epileptic Encephalopathy: TANGO2 Deficiency Disorder due to Homozygous Multi-exon Deletion.

Journal: Journal of child neurology
Published: August 18, 2026

Early hand preference and infantile spasms: A case of left-sided cerebral palsy.

Early hand preference and infantile spasms: A case of left-sided cerebral palsy.

Journal: Australian journal of general practice
Published: August 06, 2026

Time-frequency characteristics of scalp high-frequency oscillations provide complementary biomarkers in infantile epileptic spasms syndrome.

Time-frequency characteristics of scalp high-frequency oscillations provide complementary biomarkers in infantile epileptic spasms syndrome.

Journal: Experimental physiology
Published: July 21, 2026

Clinical characteristics of six cases of neurofibromatosis type 1-associated infantile epileptic spasms syndrome

Clinical characteristics of six cases of neurofibromatosis type 1-associated infantile epileptic spasms syndrome

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: July 15, 2026

RFX3 Pathogenic Variants as a Rare Cause of Infantile Epileptic Spasms Syndrome.

RFX3 Pathogenic Variants as a Rare Cause of Infantile Epileptic Spasms Syndrome.

Journal: International journal of molecular sciences
Published: July 06, 2026

Electrophysiological readout of ACTH-related neuroendocrine-immunomodulatory treatment response in infantile epileptic spasms syndrome: suppression of scalp ripple propagation networks.

Electrophysiological readout of ACTH-related neuroendocrine-immunomodulatory treatment response in infantile epileptic spasms syndrome: suppression of scalp ripple propagation networks.

Journal: Frontiers in immunology
Published: June 29, 2026

Early infantile developmental and epileptic encephalopathy: clinical spectrum, diagnosis, outcomes, and evolving treatment strategies.

Early infantile developmental and epileptic encephalopathy: clinical spectrum, diagnosis, outcomes, and evolving treatment strategies.

Journal: Brain & development
Published: June 17, 2026

From Hypsarrhythmia to Hyperkinesia: ACTH-Induced Status Dystonicus in Infantile Epileptic Spasms Syndrome.

From Hypsarrhythmia to Hyperkinesia: ACTH-Induced Status Dystonicus in Infantile Epileptic Spasms Syndrome.

Journal: Indian journal of pediatrics
Published: June 14, 2026

Pharmacokinetics, Pharmacodynamics and Immunogenicity of AC02, a Novel Synthetic Derivate Peptide of Human Adrenocorticotropic Hormone for Infantile Spasms.

Pharmacokinetics, Pharmacodynamics and Immunogenicity of AC02, a Novel Synthetic Derivate Peptide of Human Adrenocorticotropic Hormone for Infantile Spasms.

Journal: Pharmaceutics
Published: June 01, 2026

Primary concomitant horizontal strabismus as a clinical biomarker of severity in West Syndrome.

Primary concomitant horizontal strabismus as a clinical biomarker of severity in West Syndrome.

Journal: Strabismus
Published: June 01, 2026

Burst-Suppression EEG in Early Infantile Developmental and Epileptic Encephalopathies: Phenotype, Genotype, and Outcome.

Burst-Suppression EEG in Early Infantile Developmental and Epileptic Encephalopathies: Phenotype, Genotype, and Outcome.

Journal: Neurology
Published: May 26, 2026

Vigabatrin-Associated Brain Abnormalities on MRI in a Patient with PCDH19-Clustering Epilepsy.

Vigabatrin-Associated Brain Abnormalities on MRI in a Patient with PCDH19-Clustering Epilepsy.

Journal: Journal of clinical medicine
Published: May 18, 2026
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Last Updated: 09/26/2026