Junlan Lv

Beijing, China

Last Updated: 09/26/2026

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Found 14 publications

Pragmatic Phenotype-Electrophysiology-Genomics Integration in Pediatric Congenital Myasthenic Syndromes: Insights From 36 Patients in a Single-Center Study in China.

Pragmatic Phenotype-Electrophysiology-Genomics Integration in Pediatric Congenital Myasthenic Syndromes: Insights From 36 Patients in a Single-Center Study in China.

Journal: CNS neuroscience & therapeutics

Published: June 21, 2026

Clinical characteristics of anti-neurofascin 155 antibody-positive autoimmune nodopathy in children.

Clinical characteristics of anti-neurofascin 155 antibody-positive autoimmune nodopathy in children.

Journal: Pediatric investigation

Published: December 23, 2024

A 1-year analysis from a natural history study in Chinese individuals with Duchenne muscular dystrophy.

A 1-year analysis from a natural history study in Chinese individuals with Duchenne muscular dystrophy.

Journal: The Lancet regional health. Western Pacific

Published: April 18, 2023

HyperCKemia: An early sign of childhood-onset neutral lipid storage disease with myopathy.

HyperCKemia: An early sign of childhood-onset neutral lipid storage disease with myopathy.

Journal: Neuromuscular disorders : NMD

Published: March 24, 2023

The phenotypic spectrum of COX20-associated mitochondrial disorder.

The phenotypic spectrum of COX20-associated mitochondrial disorder.

Journal: Brain : a journal of neurology

Published: August 25, 2022

Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese children.

Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese children.

Journal: Developmental medicine and child neurology

Published: April 22, 2022

Functional connectivity differences in speech production networks in Chinese children with Rolandic epilepsy.

Functional connectivity differences in speech production networks in Chinese children with Rolandic epilepsy.

Journal: Epilepsy & behavior : E&B

Published: February 18, 2022

Collaborative studies of U.S.-China neurologists on acute motor axonal neuropathy.

Collaborative studies of U.S.-China neurologists on acute motor axonal neuropathy.

Journal: Pediatric investigation

Published: February 10, 2022

Phenotypic and Genotypic Characteristics of SCN1A Associated Seizure Diseases.

Phenotypic and Genotypic Characteristics of SCN1A Associated Seizure Diseases.

Journal: Frontiers in molecular neuroscience

Published: November 23, 2021

Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center study.

Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center study.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: March 04, 2021

Whole exome sequencing identifies a novel homozygous MECR mutation in a Chinese patient with childhood-onset dystonia and basal ganglia abnormalities, without optic atrophy.

Whole exome sequencing identifies a novel homozygous MECR mutation in a Chinese patient with childhood-onset dystonia and basal ganglia abnormalities, without optic atrophy.

Journal: Mitochondrion

Published: September 12, 2020

Erratum to: The clinical and genetic characteristics in children with mitochondrial disease in China.

Erratum to: The clinical and genetic characteristics in children with mitochondrial disease in China.

Journal: Science China. Life sciences

Published: July 22, 2017

Showing 1-12 of 14

Last Updated: 09/26/2026