PRENATAL DIAGNOSIS OF FARBER'S DISEASE

Author:

Fensom A.H.,Neville B.R.G.,Moser AnnE.,Benson P.F.,Moser H.W.,Dulaney J.T.

Publisher

Elsevier BV

Subject

General Medicine

Reference14 articles.

Cited by 36 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. Farber Disease Mimicking Juvenile Idiopathic Arthritis: The First Reported Case in Qatar and Review of the Literature;Case Reports in Genetics;2022-02-10

2. Rare Diseases in Glycosphingolipid Metabolism;Sphingolipid Metabolism and Metabolic Disease;2022

3. Prenatal Diagnosis of Disorders of Lipid Metabolism;Genetic Disorders and the Fetus;2021-04-20

4. Acid ceramidase deficiency: Farber lipogranulomatosis, spinal muscular atrophy associated with progressive myoclonic epilepsy and peripheral osteolysis;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020

5. Acid Sphingomyelinase Deficiency Ameliorates Farber Disease;International Journal of Molecular Sciences;2019-12-11

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