Suchergebnisse - "Lv, Junlan"

PubPharm (21)

1

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

enthalten in: The Lancet regional health. Western Pacific | 2024

von Li, X. | Lv, J. | Zhu, W. | +8

2

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

enthalten in: Neuromuscular disorders : NMD | 2023

von Fu, X. | Yang, X. | Wang, X. | +6

3

Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese children

enthalten in: Developmental medicine and child neurology | 2023

von Wang, J. | Fang, F. | Ding, C. | +10

CommentIn: Dev Med Child Neurol. 2023 Mar;65(3):307-308. - PMID 36168202

4

Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese children

enthalten in: Developmental Medicine & Child Neurology | 2023

von Wang, J. | Fang, F. | Ding, C. | +7

5

The phenotypic spectrum of COX20-associated mitochondrial disorder

enthalten in: Brain : a journal of neurology | 2022

von Ban, R. | Kopajtich, R. | Lv, J. | +12

CommentOn: Brain. 2021 Sep 4;144(8):2457-2470. - PMID 33751098

6

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

enthalten in: Epilepsy & behavior : E&B | 2022

von Wu, Y. | Fang, F. | Li, K. | +9

7

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

enthalten in: Pediatric investigation | 2022

von Lv, J. | Zhaori, G.

8

Phenotypic and Genotypic Characteristics of SCN1A Associated Seizure Diseases

enthalten in: Frontiers in molecular neuroscience | 2022

von Chen, C. | Fang, F. | Wang, X. | +3

9

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

enthalten in: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society | 2021

von Zhang, W. | Ren, C. | Wang, X. | +16

10

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

enthalten in: Mitochondrion | 2021

von Liu, Z. | Shimura, M. | Zhang, L. | +10