Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome-Reference-Cited by-同舟云学术

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Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

Published:2001-09-11 Issue:5 Volume:57 Page:911-914
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Salvi S.,Santorelli F. M.,Bertini E.,Boldrini R.,Meli C.,Donati A.,Burlina A. B.,Rizzo C.,Di Capua M.,Fariello G.,Dionisi-Vici C.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 57 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. Hyperornithinemia-hyperammonemia-homocitrullinuria: a rare neurometabolic disorder in two siblings;Metabolic Brain Disease;2024-06-04

2. Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 gene;Frontiers in Genetics;2022-11-24

3. Systematic impacts of fluoride exposure on the metabolomics of rats;Ecotoxicology and Environmental Safety;2022-09

4. A Novel Mutation of ORNT1 Detected in a Hyperornithinemia–Hyperammonemia–Homocitrullinuria Syndrome Child by Clinical Whole-Exome Sequencing;Journal of Pediatric Genetics;2022-02-10

5. Childhood-onset hereditary spastic paraplegia and its treatable mimics;Molecular Genetics and Metabolism;2021-06

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