Албрајтова наследна остеодистрофија (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Албрајтова наследна остеодистрофија" in Serbian language version.

refsWebsite

Global rank Serbian rank

4^th place

8^th place

2^nd place

4^th place

6^th place

5^th place

1^st place

3,537^th place

low place

1,581^st place

1,760^th place

5^th place

12^th place

archive.org

MACGREGOR, M. E.; WHITEHEAD, T. P. (октобар 1954). „Pseudo-hypoparathyroidism; a description of three cases and a critical appraisal of earlier accounts of the disease”. Arch Dis Child. 29 (147): 398—418. .
Wilson, L. C.; Trembath, R. C. (октобар 1994). „Albright's hereditary osteodystrophy”. J Med Genet. 31 (10): 779—84. .
Patten, J. L.; Johns, D. R.; Valle, D; Eil, C.; Gruppuso, P. A.; Steele G, Smallwood PM, Levine MA (мај 1990). „Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy”. New England Journal of Medicine. 322 (20): 1412—9. .

Mantovani, G.; Elli, F. M. (2019). „Inactivating PTH/PTHRP Signaling Disorders”. Front Horm Res. Frontiers of Hormone Research. 51: 147—159. ISBN 978-3-318-06408-7. PMID 30641531. doi:10.1159/000491045.
Nakamura Y, Matsumoto T, Tamakoshi A, Kawamura T, Seino Y, Kasuga M, Yanagawa H, Ohno Y (јануар 2000). „Prevalence of idiopathic hypoparathyroidism and pseudohypoparathyroidism in Japan”. J Epidemiol. 10 (1): 29—33. PMID 10695258. doi:10.2188/jea.10.29.
Underbjerg L, Sikjaer T, Mosekilde L, Rejnmark L (јун 2016). „Pseudohypoparathyroidism - epidemiology, mortality and risk of complications”. Clin Endocrinol (Oxf). 84 (6): 904—11. PMID 26387561. doi:10.1111/cen.12948.
Pereda, Arrate; Garin, Intza; Garcia-Barcina, Maria; Gener, Blanca; Beristain, Elena; Ibañez, Ane Miren; Perez de Nanclares, Guiomar (2013-09-12). „Brachydactyly E: isolated or as a feature of a syndrome”. Orphanet Journal of Rare Diseases. 8 (1). ISSN 1750-1172. doi:10.1186/1750-1172-8-141.

Pereda, Arrate; Garin, Intza; Garcia-Barcina, Maria; Gener, Blanca; Beristain, Elena; Ibañez, Ane Miren; Perez de Nanclares, Guiomar (2013-09-12). „Brachydactyly E: isolated or as a feature of a syndrome”. Orphanet Journal of Rare Diseases. 8 (1). ISSN 1750-1172. doi:10.1186/1750-1172-8-141.

„Pseudohypoparathyroidism: MedlinePlus Medical Encyclopedia”. medlineplus.gov (на језику: енглески). Приступљено 12. 2. 2017.

Mantovani, G.; Elli, F. M. (2019). „Inactivating PTH/PTHRP Signaling Disorders”. Front Horm Res. Frontiers of Hormone Research. 51: 147—159. ISBN 978-3-318-06408-7. PMID 30641531. doi:10.1159/000491045.
Nakamura Y, Matsumoto T, Tamakoshi A, Kawamura T, Seino Y, Kasuga M, Yanagawa H, Ohno Y (јануар 2000). „Prevalence of idiopathic hypoparathyroidism and pseudohypoparathyroidism in Japan”. J Epidemiol. 10 (1): 29—33. PMID 10695258. doi:10.2188/jea.10.29.
Underbjerg L, Sikjaer T, Mosekilde L, Rejnmark L (јун 2016). „Pseudohypoparathyroidism - epidemiology, mortality and risk of complications”. Clin Endocrinol (Oxf). 84 (6): 904—11. PMID 26387561. doi:10.1111/cen.12948.
Garavelli, L.; Pedori, S.; Zanacca, C.; et al. (април 2005). „Albright's hereditary osteodystrophy (pseudohypoparathyroidism type Ia): clinical case with a novel mutation of GNAS1”. Acta Biomedica. 76 (1): 45—8. PMID 16116826.

„Albright's hereditary osteodystrophy” (на језику: енглески). Genetic and Rare Diseases Information Center (GARD) – an NCATS Program. Архивирано из оригинала 11. 02. 2017. г. Приступљено 9. 2. 2017.
„Albright's hereditary osteodystrophy | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program”. rarediseases.info.nih.gov. Архивирано из оригинала 11. 02. 2017. г. Приступљено 2022-01-28.

„Albright's hereditary osteodystrophy” (на језику: енглески). Genetic and Rare Diseases Information Center (GARD) – an NCATS Program. Архивирано из оригинала 11. 02. 2017. г. Приступљено 9. 2. 2017.
„Albright's hereditary osteodystrophy | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program”. rarediseases.info.nih.gov. Архивирано из оригинала 11. 02. 2017. г. Приступљено 2022-01-28.

Pereda, Arrate; Garin, Intza; Garcia-Barcina, Maria; Gener, Blanca; Beristain, Elena; Ibañez, Ane Miren; Perez de Nanclares, Guiomar (2013-09-12). „Brachydactyly E: isolated or as a feature of a syndrome”. Orphanet Journal of Rare Diseases. 8 (1). ISSN 1750-1172. doi:10.1186/1750-1172-8-141.