Metaphyseal dysplasia (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Metaphyseal dysplasia" in English language version.

refsWebsite

Global rank English rank

4^th place

2^nd place

1^st place

low place

2,888^th place

2,730^th place

3,537^th place

7,177^th place

11^th place

8^th place

doi.org

Heselson NG, Raad MS, Hamersma H, Cremin BJ, Beighton P (June 1979). "The radiological manifestations of metaphyseal dysplasia (Pyle disease)". The British Journal of Radiology. 52 (618): 431–40. doi:10.1259/0007-1285-52-618-431. PMID 465917.
Kiper PO, Saito H, Gori F, Unger S, Hesse E, Yamana K, et al. (June 2016). "Cortical-Bone Fragility--Insights from sFRP4 Deficiency in Pyle's Disease". The New England Journal of Medicine. 374 (26): 2553–2562. doi:10.1056/NEJMoa1509342. PMC 5070790. PMID 27355534.
Galada C, Shah H, Shukla A, Girisha KM (April 2017). "A novel sequence variant in SFRP4 causing Pyle disease". Journal of Human Genetics. 62 (5): 575–576. doi:10.1038/jhg.2016.166. PMID 28100910. S2CID 1740656.

Pyle E (Oct 1, 1931). "A Case of unusual bone development". Journal of Bone and Joint Surgery. 13 (4). Needham, Massachusetts: 874–876. Archived from the original on March 17, 2010. Retrieved Aug 18, 2009.

Heselson NG, Raad MS, Hamersma H, Cremin BJ, Beighton P (June 1979). "The radiological manifestations of metaphyseal dysplasia (Pyle disease)". The British Journal of Radiology. 52 (618): 431–40. doi:10.1259/0007-1285-52-618-431. PMID 465917.
Kiper PO, Saito H, Gori F, Unger S, Hesse E, Yamana K, et al. (June 2016). "Cortical-Bone Fragility--Insights from sFRP4 Deficiency in Pyle's Disease". The New England Journal of Medicine. 374 (26): 2553–2562. doi:10.1056/NEJMoa1509342. PMC 5070790. PMID 27355534.
Galada C, Shah H, Shukla A, Girisha KM (April 2017). "A novel sequence variant in SFRP4 causing Pyle disease". Journal of Human Genetics. 62 (5): 575–576. doi:10.1038/jhg.2016.166. PMID 28100910. S2CID 1740656.

"Pyle metaphyseal dysplasia - Conditions - GTR - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2019-12-11.
Kiper PO, Saito H, Gori F, Unger S, Hesse E, Yamana K, et al. (June 2016). "Cortical-Bone Fragility--Insights from sFRP4 Deficiency in Pyle's Disease". The New England Journal of Medicine. 374 (26): 2553–2562. doi:10.1056/NEJMoa1509342. PMC 5070790. PMID 27355534.

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Metaphyseal dysplasia, Braun Tinschert type". www.orpha.net. Retrieved 2019-12-12.{{cite web}}: CS1 maint: numeric names: authors list (link)

Galada C, Shah H, Shukla A, Girisha KM (April 2017). "A novel sequence variant in SFRP4 causing Pyle disease". Journal of Human Genetics. 62 (5): 575–576. doi:10.1038/jhg.2016.166. PMID 28100910. S2CID 1740656.

Pyle E (Oct 1, 1931). "A Case of unusual bone development". Journal of Bone and Joint Surgery. 13 (4). Needham, Massachusetts: 874–876. Archived from the original on March 17, 2010. Retrieved Aug 18, 2009.