Metaphyseal chondrodysplasia, Schmid type Clinical and radiographic deliniation with a review of the literature-Reference-Cited by-同舟云学术

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Metaphyseal chondrodysplasia, Schmid type Clinical and radiographic deliniation with a review of the literature

Published:1988-02 Issue:2 Volume:18 Page:93-102
ISSN:0301-0449
Container-title:Pediatric Radiology
language:en
Short-container-title:Pediatr Radiol

Author:

Lachman R. S.,Rimoin D. L.,Spranger J.

Publisher

Springer Science and Business Media LLC

Subject

Radiology, Nuclear Medicine and imaging,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF02387549.pdf

Reference60 articles.

1. Schmid F (1949) Beitrag zur Dysostosis enchondralis metaphysaria. Monatsschr Kinderheilk 97: 393

2. Huhne T, Schonfeld H (1929) Eine eigenartige symmetrische Erkrankung Epi- und Metaphysen eines 5jährigen Knaben. Chirurgie 213: 73

3. Hassler E (1936) Das Krankheitsbild der Dysostosis enchondralis. Monatsschr Kinderheilk 67: 254

4. Jacobsen AW (1939) Hereditary osteochondrodystrophia deformans. JAMA 113: 121

5. Müller GM, Sissons HA (1951) A case of Renal rickets simulating “metaphyseal dysostosis”. JBJS 33 B: 231

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1. A rare case of SCHMID metaphyseal chondrodysplasia associated with hypothyroidism,growth hormone deficiency and celiac disease: case report;Annals of Medicine & Surgery;2023-06-28

2. Interventions for improving clinical outcomes and health-related quality-of-life for people living with skeletal dysplasias: an evidence gap map;Quality of Life Research;2023-06-09

3. Natural history and genetic spectrum of the Turkish metaphyseal dysplasia cohort, including rare types caused by biallelic COL10A1, COL2A1, and LBR variants;Bone;2023-02

4. Schmid metaphyseal chondrodysplasia: an example of radiology guidance to molecular diagnosis;Radiology Case Reports;2020-12

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