Galactosemia, a Single Gene Disorder With Epigenetic Consequences-Reference-Cited by-同舟云学术

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Galactosemia, a Single Gene Disorder With Epigenetic Consequences

Published:2010-03 Issue:3 Volume:67 Page:286-292
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Coman David J,Murray David W,Byrne Jennifer C,Rudd Pauline M,Bagaglia Paola M,Doran Peter D,Treacy Eileen P

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference34 articles.

1. Long-term prognosis in galactosaemia: Results of a survey of 350 cases

2. Long-term outcome in 134 patients with galactosaemia

3. Outcomes of Siblings with Classical Galactosemia

4. Carbohydrate-deficient transferrin in galactosaemia

Cited by 64 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. Galactokinase 1 is the source of elevated galactose‐1‐phosphate and cerebrosides are modestly reduced in a mouse model of classic galactosemia;JIMD Reports;2024-06-23

2. Brain function in classic galactosemia, a galactosemia network (GalNet) members review;Frontiers in Genetics;2024-02-15

3. Biomarker discovery in galactosemia: Metabolomics with UPLC/HRMS in dried blood spots;Frontiers in Molecular Biosciences;2023-04-04

4. The hypergonadotropic hypogonadism conundrum of classic galactosemia;Human Reproduction Update;2022-12-13

5. Early postnatal alterations in follicular stress response and survival in a mouse model of Classic Galactosemia;Journal of Ovarian Research;2022-11-21

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