Progeria (Turkish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Progeria" in Turkish language version.

refsWebsite

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6nih.gov

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11^th place

4web.archive.org

1^st place

4doi.org

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2fda.gov

447^th place

858^th place

1archive.org

6^th place

1rarediseases.org

5,181^st place

5,723^rd place

1sciencebasedmedicine.org

5,063^rd place

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1handle.net

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archive.org

James W, Berger T, Elston D (2005). Andrews' Diseases of the Skin: Clinical Dermatology (10. bas.). Saunders. s. 574. ISBN 978-0-7216-2921-6.

doi.org

Olive M, Harten I, Mitchell R, Beers JK, Djabali K, Cao K, Erdos MR, Blair C, Funke B, Smoot L, Gerhard-Herman M, Machan JT, Kutys R, Virmani R, Collins FS, Wight TN, Nabel EG, Gordon LB (November 2010). "Cardiovascular pathology in Hutchinson-Gilford progeria: correlation with the vascular pathology of aging". Arteriosclerosis, Thrombosis, and Vascular Biology. 30 (11): 2301-2309. doi:10.1161/ATVBAHA.110.209460. PMC 2965471 $2. PMID 20798379.
Merideth MA, Gordon LB, Clauss S, Sachdev V, Smith AC, Perry MB, Brewer CC, Zalewski C, Kim HJ, Solomon B, Brooks BP, Gerber LH, Turner ML, Domingo DL, Hart TC, Graf J, Reynolds JC, Gropman A, Yanovski JA, Gerhard-Herman M, Collins FS, Nabel EG, Cannon RO, Gahl WA, Introne WJ (2008). "Phenotype and course of Hutchinson-Gilford progeria syndrome". The New England Journal of Medicine. 358 (6): 592-604. doi:10.1056/NEJMoa0706898. PMID 18256394.
De Sandre-Giovannoli A, Bernard R, Cau P, Navarro C, Amiel J, Boccaccio I, Lyonnet S, Stewart CL, Munnich A, Le Merrer M, Lévy N (June 2003). "Lamin a truncation in Hutchinson-Gilford progeria". Science. 300 (5628): 2055. doi:10.1126/science.1084125. PMID 12702809.
Arancio W, Pizzolanti G, Genovese SI, Pitrone M, Giordano C (2014). "Epigenetic involvement in Hutchinson-Gilford progeria syndrome: a mini-review". Gerontology. 60 (3): 197-203. doi:10.1159/000357206. hdl:10447/93705. PMID 24603298.

fda.gov

"FDA Approves First Treatment for Hutchinson-Gilford Progeria Syndrome and Some Progeroid Laminopathies". U.S Food and Drug Administration (FDA) (Basın açıklaması). 20 Kasım 2020. 28 Kasım 2020 tarihinde kaynağından arşivlendi. Erişim tarihi: 20 Kasım 2020. Bu madde, bu kaynaktan alınan kamu malı olan bir metni içermektedir.
"Drug Trials Snapshots: Zokinvy". U.S. Food and Drug Administration. 20 Kasım 2020. 12 Aralık 2020 tarihinde kaynağından arşivlendi. Erişim tarihi: 11 Aralık 2020. Bu madde, bu kaynaktan alınan kamu malı olan bir metni içermektedir.

handle.net

hdl.handle.net

Arancio W, Pizzolanti G, Genovese SI, Pitrone M, Giordano C (2014). "Epigenetic involvement in Hutchinson-Gilford progeria syndrome: a mini-review". Gerontology. 60 (3): 197-203. doi:10.1159/000357206. hdl:10447/93705. PMID 24603298.

nih.gov

ncbi.nlm.nih.gov

Olive M, Harten I, Mitchell R, Beers JK, Djabali K, Cao K, Erdos MR, Blair C, Funke B, Smoot L, Gerhard-Herman M, Machan JT, Kutys R, Virmani R, Collins FS, Wight TN, Nabel EG, Gordon LB (November 2010). "Cardiovascular pathology in Hutchinson-Gilford progeria: correlation with the vascular pathology of aging". Arteriosclerosis, Thrombosis, and Vascular Biology. 30 (11): 2301-2309. doi:10.1161/ATVBAHA.110.209460. PMC 2965471 $2. PMID 20798379.
Sinha JK, Ghosh S, Raghunath M (May 2014). "Progeria: a rare genetic premature ageing disorder". The Indian Journal of Medical Research. 139 (5): 667-674. PMC 4140030 $2. PMID 25027075.
Merideth MA, Gordon LB, Clauss S, Sachdev V, Smith AC, Perry MB, Brewer CC, Zalewski C, Kim HJ, Solomon B, Brooks BP, Gerber LH, Turner ML, Domingo DL, Hart TC, Graf J, Reynolds JC, Gropman A, Yanovski JA, Gerhard-Herman M, Collins FS, Nabel EG, Cannon RO, Gahl WA, Introne WJ (2008). "Phenotype and course of Hutchinson-Gilford progeria syndrome". The New England Journal of Medicine. 358 (6): 592-604. doi:10.1056/NEJMoa0706898. PMID 18256394.
Hutchinson J (1888). "Congenital absence of hair and mammary glands with atrophic condition of the skin and its appendages, in a boy whose mother had been almost wholly bald from alopecia areata from the age of six". Medico-Chirurgical Transactions. 71: 473-477. PMC 2032088 $2. PMID 20896682.
De Sandre-Giovannoli A, Bernard R, Cau P, Navarro C, Amiel J, Boccaccio I, Lyonnet S, Stewart CL, Munnich A, Le Merrer M, Lévy N (June 2003). "Lamin a truncation in Hutchinson-Gilford progeria". Science. 300 (5628): 2055. doi:10.1126/science.1084125. PMID 12702809.
Arancio W, Pizzolanti G, Genovese SI, Pitrone M, Giordano C (2014). "Epigenetic involvement in Hutchinson-Gilford progeria syndrome: a mini-review". Gerontology. 60 (3): 197-203. doi:10.1159/000357206. hdl:10447/93705. PMID 24603298.

rarediseases.org

"Hutchinson-Gilford Progeria - NORD (National Organization for Rare Disorders)". NORD (National Organization for Rare Disorders). 2014. 13 Nisan 2020 tarihinde kaynağından arşivlendi. Erişim tarihi: 21 Nisan 2017.

sciencebasedmedicine.org

Hall H (8 Aralık 2020). "Progeria". Science-Based Medicine. 23 Nisan 2021 tarihinde kaynağından arşivlendi. Erişim tarihi: 23 Nisan 2021.

web.archive.org

"Hutchinson-Gilford Progeria - NORD (National Organization for Rare Disorders)". NORD (National Organization for Rare Disorders). 2014. 13 Nisan 2020 tarihinde kaynağından arşivlendi. Erişim tarihi: 21 Nisan 2017.
"FDA Approves First Treatment for Hutchinson-Gilford Progeria Syndrome and Some Progeroid Laminopathies". U.S Food and Drug Administration (FDA) (Basın açıklaması). 20 Kasım 2020. 28 Kasım 2020 tarihinde kaynağından arşivlendi. Erişim tarihi: 20 Kasım 2020. Bu madde, bu kaynaktan alınan kamu malı olan bir metni içermektedir.
"Drug Trials Snapshots: Zokinvy". U.S. Food and Drug Administration. 20 Kasım 2020. 12 Aralık 2020 tarihinde kaynağından arşivlendi. Erişim tarihi: 11 Aralık 2020. Bu madde, bu kaynaktan alınan kamu malı olan bir metni içermektedir.
Hall H (8 Aralık 2020). "Progeria". Science-Based Medicine. 23 Nisan 2021 tarihinde kaynağından arşivlendi. Erişim tarihi: 23 Nisan 2021.