Alkaptonuria. Report of a family with seven cases appearing in four successive generations, with metabolic studies in one patient-Reference-Cited by-同舟云学术

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Alkaptonuria. Report of a family with seven cases appearing in four successive generations, with metabolic studies in one patient

Published:1958-06 Issue:6 Volume:7 Page:455-465
ISSN:0021-9681
Container-title:Journal of Chronic Diseases
language:en
Short-container-title:Journal of Chronic Diseases

Author:

Khachadurian A.,Feisal K.Abu

Publisher

Elsevier BV

Subject

Epidemiology

Reference58 articles.

1. Inborn Errors of Metabolism;Garrod,1923

2. Ueber das alkapton;Boedeker;Ztschr. f. rat. Med.,1859

3. Inborn Errors of Metabolism;Wolkow,1923

4. Ein Fall von allgemeiner Ochronose der Knorpel und knorpelähnlichen Teile;Virchow;Virchows Arch. path. Anat.,1866

5. Ueber Ochronose;Albrecht;Ztschr. Heilk,1902

Cited by 27 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. Homogentisate 1,2-dioxygenase (HGD) gene variants in young Egyptian patients with alkaptonuria;Scientific Reports;2023-09-01

2. Surgical Management in Cervical Spondylotic Myelopathy Due to Alkaptonuria;World Neurosurgery;2018-05

3. A Case Report of Chronic Low Back Pain with Ochronosis;Türkiye Fiziksel Tip ve Rehabilitasyon Dergisi;2014-07-09

4. Mutation Screening of theHGDGene Identifies a Novel Alkaptonuria Mutation with Significant Founder Effect and High Prevalence;Annals of Human Genetics;2014-02-12

5. Molecular Genetics of Alkaptonuria;eLS;2013-01-15

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