Clinical, pathological and genetic evaluations of Chinese patients with autosomal-dominant hypophosphatasia-Reference-Cited by-同舟云学术

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Clinical, pathological and genetic evaluations of Chinese patients with autosomal-dominant hypophosphatasia

Published:2010-12 Issue:12 Volume:55 Page:1017-1023
ISSN:0003-9969
Container-title:Archives of Oral Biology
language:en
Short-container-title:Archives of Oral Biology

Author:

Wei Ke-wen,Xuan Kun,Liu Yan-li,Fang Jun,Ji Kun,Wang Xi,Jin Yan,Watanabe Shigeru,Watanabe Koji,Ojihara Takashi

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Cell Biology,General Dentistry,General Medicine,Otorhinolaryngology

Reference39 articles.

1. Hypophosphatasia;Mornet;Orphanet J Rare Dis,2007

2. Novel human pathological mutations. Gene symbol: ALPL. Disease: hypophosphatasia;Bertola;Hum Genet,2009

3. Developmental biology and genetics of dental malformations;Hu;Orthod Craniofac Res,2007

4. Orodental phenotype and genotype findings in all subtypes of hypophosphatasia;Reibel;Orphanet J Rare Dis,2009

5. Hypophosphatasia: the mutations in the tissue-nonspecific alkaline phosphatase gene;Mornet;Hum Mutat,2000

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1. Skeletal indicators of pathology in the context of early tooth loss in children: A systematic literature review;International Journal of Paleopathology;2024-09

2. Diagnosis and initial management of children presenting with premature loss of primary teeth associated with a systemic condition: A scoping review and development of clinical aid;International Journal of Paediatric Dentistry;2024-04-12

3. Clinical and molecular description of the first Italian cohort of 33 subjects with hypophosphatasia;Frontiers in Endocrinology;2023-08-01

4. Presentation of a Case of Short Root Anomaly in an 11-Year-Old Child;Case Reports in Dentistry;2023-01-04

5. Clinical and genetic characteristics of hypophosphatasia in Chinese children;Orphanet Journal of Rare Diseases;2021-04-07

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