Osteopetrosis (English Wikipedia)

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

refsWebsite

Global rank English rank

14nih.gov

4^th place

8doi.org

2^nd place

3web.archive.org

1^st place

2cda-adc.ca

low place

2worldcat.org

5^th place

1checkorphan.org

low place

1semanticscholar.org

11^th place

8^th place

1radiopaedia.org

4,968^th place

3,180^th place

1bmj.com

1,226^th place

1,421^st place

1rarediseases.org

5,181^st place

3,260^th place

1medlineplus.gov

1,581^st place

1,299^th place

1dnalab.ru

low place

1cap.ru

7,671^st place

low place

1sfgate.com

166^th place

121^st place

bmj.com

jmg.bmj.com

Memet, Aker; Rouvinski, Alex; Hshavia, Saar; Ta-Shma, Asaf; Shaag, Avraham; Zenvirt, Shamir; Israel, Shoshana; Weintraub, Michael; Taraboulos, Albert; Bar-Shavit, Zvi; Elpeleg, Orly (April 2012). "An SNX10 mutation causes malignant osteoporosis of infancy". Journal of Medical Genetics. 49 (4): 221–6. doi:10.1136/jmedgenet-2011-100520. PMID 22499339. Retrieved August 19, 2016.

cap.ru

genetik.med.cap.ru

Медицинская генетика Чувашии Archived February 1, 2016, at the Wayback Machine

cda-adc.ca

"Marble Bone Disease: A Review of Osteopetrosis and Its Oral Health Implications for Dentists". Cda-adc.ca. Retrieved 2013-10-17.
Lam DK, Sándor GK, Holmes HI, Carmichael RP, Clokie CM (2007). "Marble bone disease: a review of osteopetrosis and its oral health implications for dentists". J Can Dent Assoc. 73 (9): 839–43. PMID 18028760.

checkorphan.org

"Albers-Schonberg disease — CheckOrphan". www.checkorphan.org. 31 December 2014. Retrieved 2017-12-13.

dnalab.ru

"Остеопетроз рецессивный (мраморная болезнь костей) - ДНК-диагностика - Центр Молекулярной Генетики". www.dnalab.ru.

doi.org

Stark, Zornitza; Savarirayan, Ravi (2009-02-20). "Osteopetrosis". Orphanet Journal of Rare Diseases. 4: 5. doi:10.1186/1750-1172-4-5. ISSN 1750-1172. PMC 2654865. PMID 19232111.
Elsobky TA, Elsobky E, Sadek I, Elsayed SM, Khattab MF (2016). "A case of infantile osteopetrosis: The radioclinical features with literature update". Bone Rep. 4: 11–16. doi:10.1016/j.bonr.2015.11.002. PMC 4926827. PMID 28326337.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Orchard PJ, Fasth AL, Le Rademacher J, He W, Boelens JJ, Horwitz EM; et al. (2015). "Hematopoietic stem cell transplantation for infantile osteopetrosis". Blood. 126 (2): 270–6. doi:10.1182/blood-2015-01-625541. PMC 4497967. PMID 26012570.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Elsobky TA, El-Haddad A, Elsobky E, Elsayed SM, Sakr HM (2017). "Reversal of skeletal radiographic pathology in a case of malignant infantile osteopetrosis following hematopoietic stem cell transplantation". Egypt J Radiol Nucl Med. 48 (1): 237–43. doi:10.1016/j.ejrnm.2016.12.013.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Hashemi Taheri AP, Radmard AR, Kooraki S, Behfar M, Pak N, Hamidieh AA; et al. (2015). "Radiologic resolution of malignant infantile osteopetrosis skeletal changes following hematopoietic stem cell transplantation". Pediatr Blood Cancer. 62 (9): 1645–9. doi:10.1002/pbc.25524. PMID 25820806. S2CID 11287381.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Memet, Aker; Rouvinski, Alex; Hshavia, Saar; Ta-Shma, Asaf; Shaag, Avraham; Zenvirt, Shamir; Israel, Shoshana; Weintraub, Michael; Taraboulos, Albert; Bar-Shavit, Zvi; Elpeleg, Orly (April 2012). "An SNX10 mutation causes malignant osteoporosis of infancy". Journal of Medical Genetics. 49 (4): 221–6. doi:10.1136/jmedgenet-2011-100520. PMID 22499339. Retrieved August 19, 2016.
Ihde LL, Forrester DM, Gottsegen CJ, Masih S, Patel DB, Vachon LA; et al. (2011). "Sclerosing bone dysplasias: Review and differentiation from other causes of osteosclerosis". RadioGraphics. 31 (7): 1865–82. doi:10.1148/rg.317115093. PMID 22084176.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Lo Iacono, Nadia; Blair, Harry C.; Poliani, Pietro L.; Marrella, Veronica; Ficara, Francesca; Cassani, Barbara; Facchetti, Fabio; Fontana, Elena; Guerrini, Matteo M. (December 2012). "Osteopetrosis rescue upon RANKL administration to Rankl(-/-) mice: a new therapy for human RANKL-dependent ARO". Journal of Bone and Mineral Research. 27 (12): 2501–2510. doi:10.1002/jbmr.1712. ISSN 1523-4681. PMID 22836362.

medlineplus.gov

"Osteopetrosis: MedlinePlus Genetics". medlineplus.gov.

nih.gov

pubmed.ncbi.nlm.nih.gov

Lam DK, Sándor GK, Holmes HI, Carmichael RP, Clokie CM (2007). "Marble bone disease: a review of osteopetrosis and its oral health implications for dentists". J Can Dent Assoc. 73 (9): 839–43. PMID 18028760.
Stark, Zornitza; Savarirayan, Ravi (2009-02-20). "Osteopetrosis". Orphanet Journal of Rare Diseases. 4: 5. doi:10.1186/1750-1172-4-5. ISSN 1750-1172. PMC 2654865. PMID 19232111.
Elsobky TA, Elsobky E, Sadek I, Elsayed SM, Khattab MF (2016). "A case of infantile osteopetrosis: The radioclinical features with literature update". Bone Rep. 4: 11–16. doi:10.1016/j.bonr.2015.11.002. PMC 4926827. PMID 28326337.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Orchard PJ, Fasth AL, Le Rademacher J, He W, Boelens JJ, Horwitz EM; et al. (2015). "Hematopoietic stem cell transplantation for infantile osteopetrosis". Blood. 126 (2): 270–6. doi:10.1182/blood-2015-01-625541. PMC 4497967. PMID 26012570.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Hashemi Taheri AP, Radmard AR, Kooraki S, Behfar M, Pak N, Hamidieh AA; et al. (2015). "Radiologic resolution of malignant infantile osteopetrosis skeletal changes following hematopoietic stem cell transplantation". Pediatr Blood Cancer. 62 (9): 1645–9. doi:10.1002/pbc.25524. PMID 25820806. S2CID 11287381.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Memet, Aker; Rouvinski, Alex; Hshavia, Saar; Ta-Shma, Asaf; Shaag, Avraham; Zenvirt, Shamir; Israel, Shoshana; Weintraub, Michael; Taraboulos, Albert; Bar-Shavit, Zvi; Elpeleg, Orly (April 2012). "An SNX10 mutation causes malignant osteoporosis of infancy". Journal of Medical Genetics. 49 (4): 221–6. doi:10.1136/jmedgenet-2011-100520. PMID 22499339. Retrieved August 19, 2016.
Ihde LL, Forrester DM, Gottsegen CJ, Masih S, Patel DB, Vachon LA; et al. (2011). "Sclerosing bone dysplasias: Review and differentiation from other causes of osteosclerosis". RadioGraphics. 31 (7): 1865–82. doi:10.1148/rg.317115093. PMID 22084176.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Lo Iacono, Nadia; Blair, Harry C.; Poliani, Pietro L.; Marrella, Veronica; Ficara, Francesca; Cassani, Barbara; Facchetti, Fabio; Fontana, Elena; Guerrini, Matteo M. (December 2012). "Osteopetrosis rescue upon RANKL administration to Rankl(-/-) mice: a new therapy for human RANKL-dependent ARO". Journal of Bone and Mineral Research. 27 (12): 2501–2510. doi:10.1002/jbmr.1712. ISSN 1523-4681. PMID 22836362.

ncbi.nlm.nih.gov

Stark, Zornitza; Savarirayan, Ravi (2009-02-20). "Osteopetrosis". Orphanet Journal of Rare Diseases. 4: 5. doi:10.1186/1750-1172-4-5. ISSN 1750-1172. PMC 2654865. PMID 19232111.
Elsobky TA, Elsobky E, Sadek I, Elsayed SM, Khattab MF (2016). "A case of infantile osteopetrosis: The radioclinical features with literature update". Bone Rep. 4: 11–16. doi:10.1016/j.bonr.2015.11.002. PMC 4926827. PMID 28326337.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Orchard PJ, Fasth AL, Le Rademacher J, He W, Boelens JJ, Horwitz EM; et al. (2015). "Hematopoietic stem cell transplantation for infantile osteopetrosis". Blood. 126 (2): 270–6. doi:10.1182/blood-2015-01-625541. PMC 4497967. PMID 26012570.{{cite journal}}: CS1 maint: multiple names: authors list (link)

rarediseases.info.nih.gov

"Osteopetrosis | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 2017-12-13. Retrieved 2017-12-13.
"List of FDA Orphan Drugs | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". Archived from the original on 2021-11-23. Retrieved 2021-09-01.

ghr.nlm.nih.gov

Reference, Genetics Home. "osteopetrosis". Genetics Home Reference. Retrieved 2017-12-13.

radiopaedia.org

Niknejad, Mohammadtaghi. "Sandwich vertebral body | Radiology Reference Article | Radiopaedia.org". Radiopaedia.

rarediseases.org

"Osteopetrosis - NORD (National Organization for Rare Disorders)". NORD (National Organization for Rare Disorders). Retrieved 2017-12-13.

semanticscholar.org

api.semanticscholar.org

Hashemi Taheri AP, Radmard AR, Kooraki S, Behfar M, Pak N, Hamidieh AA; et al. (2015). "Radiologic resolution of malignant infantile osteopetrosis skeletal changes following hematopoietic stem cell transplantation". Pediatr Blood Cancer. 62 (9): 1645–9. doi:10.1002/pbc.25524. PMID 25820806. S2CID 11287381.{{cite journal}}: CS1 maint: multiple names: authors list (link)

sfgate.com

Maddan, Heather (2007-09-23). "Marin County artist Laurel Burch dead at 61 of rare bone disease". The San Francisco Chronicle. Retrieved 2007-12-23.

web.archive.org

"Osteopetrosis | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 2017-12-13. Retrieved 2017-12-13.
Медицинская генетика Чувашии Archived February 1, 2016, at the Wayback Machine
"List of FDA Orphan Drugs | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". Archived from the original on 2021-11-23. Retrieved 2021-09-01.

worldcat.org

Stark, Zornitza; Savarirayan, Ravi (2009-02-20). "Osteopetrosis". Orphanet Journal of Rare Diseases. 4: 5. doi:10.1186/1750-1172-4-5. ISSN 1750-1172. PMC 2654865. PMID 19232111.
Lo Iacono, Nadia; Blair, Harry C.; Poliani, Pietro L.; Marrella, Veronica; Ficara, Francesca; Cassani, Barbara; Facchetti, Fabio; Fontana, Elena; Guerrini, Matteo M. (December 2012). "Osteopetrosis rescue upon RANKL administration to Rankl(-/-) mice: a new therapy for human RANKL-dependent ARO". Journal of Bone and Mineral Research. 27 (12): 2501–2510. doi:10.1002/jbmr.1712. ISSN 1523-4681. PMID 22836362.