Natural History of CLN2 Disease: Quantitative Assessment of Disease Characteristics and Rate of Progression-Reference-Cited by-同舟云学术

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Natural History of CLN2 Disease: Quantitative Assessment of Disease Characteristics and Rate of Progression

Published:2016-04-20 Issue:S 01 Volume:47 Page:
ISSN:0174-304X
Container-title:Neuropediatrics
language:en
Short-container-title:Neuropediatrics

Author:

Nickel M.,Jacoby D.,Lezius S.,Down M.,Simonati A.,Genter F.,Wittes J.,Kohlschütter A.,Schulz A.

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The neuronal ceroid lipofuscinosis type 2 – associated variants: An analysis of alterations in the TPP1 gene and genotype–phenotype correlation in Ukraine;JIMD Reports;2024-05-14

2. The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy;Molecular Neurobiology;2023-12-28

3. TPP1 Variants in Iranian patients: A Novel Pathogenic Homozygous Variant Causing Neuronal Ceroid Lipofuscinosis 2;Molecular Syndromology;2023-10-16

4. Buffy Coat Score as a Biomarker of Treatment Response in Neuronal Ceroid Lipofuscinosis Type 2;Brain Sciences;2023-01-27

5. Whole Exome Sequencing for the Diagnosis of Rare Genetic Neurodevelopmental Disorders Associated with Cerebellar Atrophy;2023-01-19

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