A family with benign sex-linked muscular dystrophy: a clinicopathologic study

Near infrared spectroscopy (NIRS) distinguishes seizure types.

Seizure·2000

Health-related quality of life outcome in medically refractory epilepsy treated with anterior temporal lobectomy.

Epilepsia·2000

Hyphal forms in the central nervous system of patients with coccidioidomycosis.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America·2000

The contribution of life events to pseudoseizure occurrence in adults.

Bulletin of the Menninger Clinic·1999

Foreign bodies in small arteries after use of an infusion microcatheter.

AJNR. American journal of neuroradiology·1997

Spheroid body myopathy revisited.

Muscle & nerve·1997

Severe Parsonage-Turner Syndrome and Surgically Managed Traumatic Brachial Plexopathy: Motor-Unit Reinnervation and Functional Recovery.

Neurology·2026

Centrally Acting Medications, Chronic Pain, and Orthopedic Surgical History Among Former American Football Players.

Neurology·2026

Bridging the Gap: Translating Microemboli-Induced Spreading Depolarization Into Clinical Practice.

Neurology·2026

Lesion-Level Subtypes of White Matter Hyperintensity Evolution Beyond Spatial Location.

Neurology·2026

Child Neurology: Radiologic Evolution and Developmental Correlates in Fetal Cerebral Sinovenous Thrombosis: A Case Report.

Neurology·2026

De-Escalating and Discontinuing Immunotherapies in Patients With NMOSD and MOGAD.

Neurology·2026

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Science (New York, N.Y.)·2026

Related Experiment Videos

A family with benign sex-linked muscular dystrophy: a clinicopathologic study

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Near infrared spectroscopy (NIRS) distinguishes seizure types.

Health-related quality of life outcome in medically refractory epilepsy treated with anterior temporal lobectomy.

Hyphal forms in the central nervous system of patients with coccidioidomycosis.

The contribution of life events to pseudoseizure occurrence in adults.

Foreign bodies in small arteries after use of an infusion microcatheter.

Spheroid body myopathy revisited.

Severe Parsonage-Turner Syndrome and Surgically Managed Traumatic Brachial Plexopathy: Motor-Unit Reinnervation and Functional Recovery.

Centrally Acting Medications, Chronic Pain, and Orthopedic Surgical History Among Former American Football Players.

Bridging the Gap: Translating Microemboli-Induced Spreading Depolarization Into Clinical Practice.

Lesion-Level Subtypes of White Matter Hyperintensity Evolution Beyond Spatial Location.

Child Neurology: Radiologic Evolution and Developmental Correlates in Fetal Cerebral Sinovenous Thrombosis: A Case Report.

De-Escalating and Discontinuing Immunotherapies in Patients With NMOSD and MOGAD.

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Related Experiment Videos

A family with benign sex-linked muscular dystrophy: a clinicopathologic study

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