G20210A prothrombin gene mutation in two siblings with cerebral venous thrombosis

Artificial intelligence applied to electroencephalography in epilepsy.

Revue neurologique·2025

French National Diagnostic and Care Protocol for antiphospholipid syndrome in adults and children.

La Revue de medecine interne·2023

Airo® navigation versus freehand fluoroscopy technique: A comparative study of accuracy and radiological exposure for thoracolumbar screws placement.

Neuro-Chirurgie·2023

A case of intramuscular lumbar myxoma: Uncertainty in the preoperative diagnosis of a spinal soft tissue tumour.

Neuro-Chirurgie·2021

Evaluation of Thin Film Microextraction for trace elemental analysis of liquid samples using LIBS detection.

Talanta·2020

Anticoagulant activity and pleiotropic effects of heparin.

Journal de medecine vasculaire·2020

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

The dynamics of ciliogenesis in prepubertal mouse meiosis reveals new clues about testis maturation.

Frontiers in cell and developmental biology·2026

Somatic Cells in the Anuran Testis.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation·2026

Mixed evidence that dosage sensitive genes drive global dosage compensation in flour beetles.

Genome biology and evolution·2026

[Genetic analysis of a fetus with Short-rib thoracic dysplasia 8 with or without polydactyly due to variants of DYNC2I1 gene].

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

NR5A1 gene variants: variable phenotypes, new variants, and genotype-phenotype correlations.

Frontiers in endocrinology·2026

[Genetic Dystonias].

Medicina·2026

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G20210A prothrombin gene mutation in two siblings with cerebral venous thrombosis

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Artificial intelligence applied to electroencephalography in epilepsy.

French National Diagnostic and Care Protocol for antiphospholipid syndrome in adults and children.

Airo® navigation versus freehand fluoroscopy technique: A comparative study of accuracy and radiological exposure for thoracolumbar screws placement.

A case of intramuscular lumbar myxoma: Uncertainty in the preoperative diagnosis of a spinal soft tissue tumour.

Evaluation of Thin Film Microextraction for trace elemental analysis of liquid samples using LIBS detection.

Anticoagulant activity and pleiotropic effects of heparin.

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.

The dynamics of ciliogenesis in prepubertal mouse meiosis reveals new clues about testis maturation.

Somatic Cells in the Anuran Testis.

Mixed evidence that dosage sensitive genes drive global dosage compensation in flour beetles.

[Genetic analysis of a fetus with Short-rib thoracic dysplasia 8 with or without polydactyly due to variants of DYNC2I1 gene].

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G20210A prothrombin gene mutation in two siblings with cerebral venous thrombosis

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