Progeria (Italian Wikipedia)

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

refsWebsite

Global rank Italian rank

13doi.org

2^nd place

7^th place

13nih.gov

4^th place

9^th place

5oadoi.org

799^th place

22^nd place

4web.archive.org

1^st place

2corriere.it

161^st place

3^rd place

1archive.org

6^th place

8^th place

1plosone.org

4,730^th place

2,208^th place

1nejm.org

2,374^th place

1,283^rd place

1cnr.it

6,667^th place

487^th place

1bbc.co.uk

8^th place

23^rd place

1flanderstoday.eu

low place

1msn.com

117^th place

266^th place

1ucsf.edu

5,479^th place

low place

1nature.com

234^th place

226^th place

1benbest.com

low place

1fanpage.it

1,405^th place

50^th place

1omim.org

4,380^th place

4,368^th place

1mirror.co.uk

245^th place

309^th place

1dailymail.co.uk

219^th place

74^th place

archive.org (Global: 6^th place; Italian: 8^th place)

Ewell Steve Roach & Van S. Miller, Neurocutaneous Disorders, Cambridge University Press, 2004, p. 150, ISBN 978-0-521-78153-4.

bbc.co.uk (Global: 8^th place; Italian: 23^rd place)

news.bbc.co.uk

Grant, Matthew (22 February 2005). "Family tormented by ageing disease". BBC News. Retrieved on 3 May 2009.

benbest.com (Global: low place; Italian: low place)

Best,BP, Nuclear DNA damage as a direct cause of aging (PDF), in Rejuvenation Research, vol. 12, n. 3, 2009, pp. 199-208, DOI:10.1089/rej.2009.0847, PMID 19594328.

cnr.it (Global: 6,667^th place; Italian: 487^th place)

igm.cnr.it

Laminopatie, su igm.cnr.it.

corriere.it (Global: 161^st place; Italian: 3^rd place)

corriere.it

Progeria: è morta in Sudafrica Ontlametse Phalatse, era soprannominata «la first lady», su Corriere della Sera, 14 aprile 2017. URL consultato il 5 dicembre 2025.

corrieredelveneto.corriere.it

Sammy Basso, l'università di Padova premiata per lo studio sulla progeria: «La sua storia ci ha ispirati», su Corriere della Sera, 11 novembre 2025. URL consultato il 12 novembre 2025.

dailymail.co.uk (Global: 219^th place; Italian: 74^th place)

(EN) A sad farewell for teenager with the body of a 150-year-old: Philippines mourns 19-year-old with disorder that caused her to age rapidly, Daily Mail

doi.org (Global: 2^nd place; Italian: 7^th place)

dx.doi.org

McClintock D, Ratner D, Lokuge M et al., The Mutant Form of Lamin A that Causes Hutchinson-Gilford Progeria Is a Biomarker of Cellular Aging in Human Skin, in Alfred Lewin (a cura di), PLoS ONE, vol. 2, n. 12, 2007, pp. e1269, DOI:10.1371/journal.pone.0001269, PMC 2092390, PMID 18060063.
Korf B, Hutchinson-Gilford progeria syndrome, aging, and the nuclear lamina, in N. Engl. J. Med., vol. 358, n. 6, 2008, pp. 552-5, DOI:10.1056/NEJMp0800071, PMID 18256390. URL consultato il 30 gennaio 2015 (archiviato dall'url originale il 7 marzo 2009).
Merideth MA, Gordon LB, Clauss S et al., Phenotype and course of Hutchinson-Gilford progeria syndrome^{[collegamento interrotto]}, in N. Engl. J. Med., vol. 358, n. 6, 2008, pp. 592-604, DOI:10.1056/NEJMoa0706898, PMC 2940940, PMID 18256394.
Hennekam RC, Hutchinson-Gilford progeria syndrome: review of the phenotype, in Am. J. Med. Genet. A, vol. 140, n. 23, 2006, pp. 2603-24, DOI:10.1002/ajmg.a.31346, PMID 16838330.
A. De Sandre-Giovannoli, R. Bernard, P. Cau, C. Navarro, J. Amiel, I. Boccaccio, S. Lyonnet, CL. Stewart, A. Munnich, M Le Merrer e N Lévy, Lamin a truncation in Hutchinson-Gilford progeria, in Science, vol. 300, n. 5628, Jun 2003, p. 2055, DOI:10.1126/science.1084125, PMID 12702809.
K. Cao e Collins, F. S., Rapamycin Reverses Cellular Phenotypes and Enhances Mutant Protein Clearance in Hutchinson-Gilford Progeria Syndrome Cells, in Science Translational Medicine, vol. 3, n. 89, giugno 2011, pp. 89ra58, DOI:10.1126/scitranslmed.3002346, PMID 21715679. URL consultato il 30 gennaio 2015 (archiviato dall'url originale il 1º dicembre 2016).
Zirn B, Kress W, Grimm T, Berthold LD et al., Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy, in Am J Med Genet A, 146A, n. 8, 2008, pp. 1049-1054, DOI:10.1002/ajmg.a.32259, PMID 18348272.
Cao H, Hegele RA e Hegele, Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy, in Hum. Molec. Genet., vol. 9, n. 1, 2002, pp. 109-12, DOI:10.1093/hmg/9.1.109, PMID 10587585.
Al-Haggar M, Madej-Pilarczyk A, Kozlowski L, Bujnicki JM, Yahia S, Abdel-Hadi D, Shams A, Ahmad N, Hamed S, Puzianowska-Kuznicka M, Madej-Pilarczyk, Kozlowski, Bujnicki, Yahia, Abdel-Hadi, Shams, Ahmad, Hamed e Puzianowska-Kuznicka, A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome, in Eur J Hum Genet., vol. 20, n. 11, 2012, pp. 1134-40, DOI:10.1038/ejhg.2012.77, PMC 3476705, PMID 22549407.
Garg A, Cogulu O, Ozkinay F, Onay H, Agarwal AK, Cogulu, Ozkinay, Onay e Agarwal, A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia, in J. Clin. Endocrinol. Metab., vol. 90, n. 9, 2005, pp. 5259-64, DOI:10.1210/jc.2004-2560, PMID 15998779.
Best,BP, Nuclear DNA damage as a direct cause of aging (PDF), in Rejuvenation Research, vol. 12, n. 3, 2009, pp. 199-208, DOI:10.1089/rej.2009.0847, PMID 19594328.
(EN) Yuhui Wang, Nan Wu e Donglin Sun, NUBPL, a novel metastasis‐related gene, promotes colorectal carcinoma cell motility by inducing epithelial–mesenchymal transition, in Cancer Science, vol. 108, n. 6, 2017-06, pp. 1169-1176, DOI:10.1111/cas.13243. URL consultato il 9 febbraio 2025 (archiviato dall'url originale il 9 febbraio 2025).
Margherita Protasoni, Claudio Bruno e Maria Alice Donati, Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement, in Molecular Genetics and Metabolism, vol. 129, n. 1, 2020-01, pp. 26-34, DOI:10.1016/j.ymgme.2019.11.003. URL consultato il 9 febbraio 2025.

fanpage.it (Global: 1,405^th place; Italian: 50^th place)

Elena a 14 anni è affetta da una malattia rara: “Solo 10 persone come lei nel mondo, aiutateci”, su Fanpage, 11 settembre 2020. URL consultato il 9 febbraio 2025.

flanderstoday.eu (Global: low place; Italian: low place)

Face of Flanders – Michiel Vandeweert, su www.flanderstoday.eu. URL consultato il 5 dicembre 2025.

mirror.co.uk (Global: 245^th place; Italian: 309^th place)

(EN) I'm only 18 - but I have the body of a 144-year-old, Daily Mirror

msn.com (Global: 117^th place; Italian: 266^th place)

msnbc.msn.com

(EN) Black child with aging disease hopes for future, in msnbc.com, 12 settembre 2011. URL consultato il 5 dicembre 2025.

nature.com (Global: 234^th place; Italian: 226^th place)

Al-Haggar M, Madej-Pilarczyk A, Kozlowski L, Bujnicki JM, Yahia S, Abdel-Hadi D, Shams A, Ahmad N, Hamed S, Puzianowska-Kuznicka M, Madej-Pilarczyk, Kozlowski, Bujnicki, Yahia, Abdel-Hadi, Shams, Ahmad, Hamed e Puzianowska-Kuznicka, A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome, in Eur J Hum Genet., vol. 20, n. 11, 2012, pp. 1134-40, DOI:10.1038/ejhg.2012.77, PMC 3476705, PMID 22549407.

nejm.org (Global: 2,374^th place; Italian: 1,283^rd place)

content.nejm.org

Merideth MA, Gordon LB, Clauss S et al., Phenotype and course of Hutchinson-Gilford progeria syndrome^{[collegamento interrotto]}, in N. Engl. J. Med., vol. 358, n. 6, 2008, pp. 592-604, DOI:10.1056/NEJMoa0706898, PMC 2940940, PMID 18256394.

nih.gov (Global: 4^th place; Italian: 9^th place)

ncbi.nlm.nih.gov

McClintock D, Ratner D, Lokuge M et al., The Mutant Form of Lamin A that Causes Hutchinson-Gilford Progeria Is a Biomarker of Cellular Aging in Human Skin, in Alfred Lewin (a cura di), PLoS ONE, vol. 2, n. 12, 2007, pp. e1269, DOI:10.1371/journal.pone.0001269, PMC 2092390, PMID 18060063.
Korf B, Hutchinson-Gilford progeria syndrome, aging, and the nuclear lamina, in N. Engl. J. Med., vol. 358, n. 6, 2008, pp. 552-5, DOI:10.1056/NEJMp0800071, PMID 18256390. URL consultato il 30 gennaio 2015 (archiviato dall'url originale il 7 marzo 2009).
Merideth MA, Gordon LB, Clauss S et al., Phenotype and course of Hutchinson-Gilford progeria syndrome^{[collegamento interrotto]}, in N. Engl. J. Med., vol. 358, n. 6, 2008, pp. 592-604, DOI:10.1056/NEJMoa0706898, PMC 2940940, PMID 18256394.
Hennekam RC, Hutchinson-Gilford progeria syndrome: review of the phenotype, in Am. J. Med. Genet. A, vol. 140, n. 23, 2006, pp. 2603-24, DOI:10.1002/ajmg.a.31346, PMID 16838330.
A. De Sandre-Giovannoli, R. Bernard, P. Cau, C. Navarro, J. Amiel, I. Boccaccio, S. Lyonnet, CL. Stewart, A. Munnich, M Le Merrer e N Lévy, Lamin a truncation in Hutchinson-Gilford progeria, in Science, vol. 300, n. 5628, Jun 2003, p. 2055, DOI:10.1126/science.1084125, PMID 12702809.
K. Cao e Collins, F. S., Rapamycin Reverses Cellular Phenotypes and Enhances Mutant Protein Clearance in Hutchinson-Gilford Progeria Syndrome Cells, in Science Translational Medicine, vol. 3, n. 89, giugno 2011, pp. 89ra58, DOI:10.1126/scitranslmed.3002346, PMID 21715679. URL consultato il 30 gennaio 2015 (archiviato dall'url originale il 1º dicembre 2016).
Zirn B, Kress W, Grimm T, Berthold LD et al., Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy, in Am J Med Genet A, 146A, n. 8, 2008, pp. 1049-1054, DOI:10.1002/ajmg.a.32259, PMID 18348272.
Cao H, Hegele RA e Hegele, Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy, in Hum. Molec. Genet., vol. 9, n. 1, 2002, pp. 109-12, DOI:10.1093/hmg/9.1.109, PMID 10587585.
Al-Haggar M, Madej-Pilarczyk A, Kozlowski L, Bujnicki JM, Yahia S, Abdel-Hadi D, Shams A, Ahmad N, Hamed S, Puzianowska-Kuznicka M, Madej-Pilarczyk, Kozlowski, Bujnicki, Yahia, Abdel-Hadi, Shams, Ahmad, Hamed e Puzianowska-Kuznicka, A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome, in Eur J Hum Genet., vol. 20, n. 11, 2012, pp. 1134-40, DOI:10.1038/ejhg.2012.77, PMC 3476705, PMID 22549407.
Garg A, Cogulu O, Ozkinay F, Onay H, Agarwal AK, Cogulu, Ozkinay, Onay e Agarwal, A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia, in J. Clin. Endocrinol. Metab., vol. 90, n. 9, 2005, pp. 5259-64, DOI:10.1210/jc.2004-2560, PMID 15998779.
Best,BP, Nuclear DNA damage as a direct cause of aging (PDF), in Rejuvenation Research, vol. 12, n. 3, 2009, pp. 199-208, DOI:10.1089/rej.2009.0847, PMID 19594328.
Nubpl nucleotide binding protein-like [Mus musculus (house mouse)] - Gene - NCBI, su www.ncbi.nlm.nih.gov. URL consultato il 9 febbraio 2025.

pubmed.ncbi.nlm.nih.gov

Margherita Protasoni, Claudio Bruno e Maria Alice Donati, Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement, in Molecular Genetics and Metabolism, vol. 129, n. 1, 2020-01, pp. 26-34, DOI:10.1016/j.ymgme.2019.11.003. URL consultato il 9 febbraio 2025.

oadoi.org (Global: 799^th place; Italian: 22^nd place)

Hennekam RC, Hutchinson-Gilford progeria syndrome: review of the phenotype, in Am. J. Med. Genet. A, vol. 140, n. 23, 2006, pp. 2603-24, DOI:10.1002/ajmg.a.31346, PMID 16838330.
A. De Sandre-Giovannoli, R. Bernard, P. Cau, C. Navarro, J. Amiel, I. Boccaccio, S. Lyonnet, CL. Stewart, A. Munnich, M Le Merrer e N Lévy, Lamin a truncation in Hutchinson-Gilford progeria, in Science, vol. 300, n. 5628, Jun 2003, p. 2055, DOI:10.1126/science.1084125, PMID 12702809.
Zirn B, Kress W, Grimm T, Berthold LD et al., Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy, in Am J Med Genet A, 146A, n. 8, 2008, pp. 1049-1054, DOI:10.1002/ajmg.a.32259, PMID 18348272.
Cao H, Hegele RA e Hegele, Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy, in Hum. Molec. Genet., vol. 9, n. 1, 2002, pp. 109-12, DOI:10.1093/hmg/9.1.109, PMID 10587585.
Garg A, Cogulu O, Ozkinay F, Onay H, Agarwal AK, Cogulu, Ozkinay, Onay e Agarwal, A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia, in J. Clin. Endocrinol. Metab., vol. 90, n. 9, 2005, pp. 5259-64, DOI:10.1210/jc.2004-2560, PMID 15998779.

omim.org (Global: 4,380^th place; Italian: 4,368^th place)

(EN) NUCLEOTIDE-BINDING PROTEIN-LIKE PROTEIN; NUBPL, su www.omim.org. URL consultato il 9 febbraio 2025.

plosone.org (Global: 4,730^th place; Italian: 2,208^th place)

McClintock D, Ratner D, Lokuge M et al., The Mutant Form of Lamin A that Causes Hutchinson-Gilford Progeria Is a Biomarker of Cellular Aging in Human Skin, in Alfred Lewin (a cura di), PLoS ONE, vol. 2, n. 12, 2007, pp. e1269, DOI:10.1371/journal.pone.0001269, PMC 2092390, PMID 18060063.

ucsf.edu (Global: 5,479^th place; Italian: low place)

J. Norris, Aging Disease in Children Sheds Light on Normal Aging, su UCSF web site, UCSF, 21 ottobre 2011. URL consultato il 25 ottobre 2011.

web.archive.org (Global: 1^st place; Italian: 1^st place)

Korf B, Hutchinson-Gilford progeria syndrome, aging, and the nuclear lamina, in N. Engl. J. Med., vol. 358, n. 6, 2008, pp. 552-5, DOI:10.1056/NEJMp0800071, PMID 18256390. URL consultato il 30 gennaio 2015 (archiviato dall'url originale il 7 marzo 2009).
Progeria Info, su progeria.be. URL consultato il 28 novembre 2013 (archiviato dall'url originale il 2 dicembre 2013).
K. Cao e Collins, F. S., Rapamycin Reverses Cellular Phenotypes and Enhances Mutant Protein Clearance in Hutchinson-Gilford Progeria Syndrome Cells, in Science Translational Medicine, vol. 3, n. 89, giugno 2011, pp. 89ra58, DOI:10.1126/scitranslmed.3002346, PMID 21715679. URL consultato il 30 gennaio 2015 (archiviato dall'url originale il 1º dicembre 2016).
(EN) Yuhui Wang, Nan Wu e Donglin Sun, NUBPL, a novel metastasis‐related gene, promotes colorectal carcinoma cell motility by inducing epithelial–mesenchymal transition, in Cancer Science, vol. 108, n. 6, 2017-06, pp. 1169-1176, DOI:10.1111/cas.13243. URL consultato il 9 febbraio 2025 (archiviato dall'url originale il 9 febbraio 2025).

Progeria (Italian Wikipedia)

archive.org (Global: 6th place; Italian: 8th place)

bbc.co.uk (Global: 8th place; Italian: 23rd place)

news.bbc.co.uk

benbest.com (Global: low place; Italian: low place)

cnr.it (Global: 6,667th place; Italian: 487th place)

igm.cnr.it

corriere.it (Global: 161st place; Italian: 3rd place)

corriere.it

corrieredelveneto.corriere.it

dailymail.co.uk (Global: 219th place; Italian: 74th place)

doi.org (Global: 2nd place; Italian: 7th place)

dx.doi.org

fanpage.it (Global: 1,405th place; Italian: 50th place)

flanderstoday.eu (Global: low place; Italian: low place)

mirror.co.uk (Global: 245th place; Italian: 309th place)

msn.com (Global: 117th place; Italian: 266th place)

msnbc.msn.com

nature.com (Global: 234th place; Italian: 226th place)

nejm.org (Global: 2,374th place; Italian: 1,283rd place)

content.nejm.org

nih.gov (Global: 4th place; Italian: 9th place)

ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov

oadoi.org (Global: 799th place; Italian: 22nd place)

omim.org (Global: 4,380th place; Italian: 4,368th place)

plosone.org (Global: 4,730th place; Italian: 2,208th place)

ucsf.edu (Global: 5,479th place; Italian: low place)

web.archive.org (Global: 1st place; Italian: 1st place)

archive.org (Global: 6^th place; Italian: 8^th place)

bbc.co.uk (Global: 8^th place; Italian: 23^rd place)

cnr.it (Global: 6,667^th place; Italian: 487^th place)

corriere.it (Global: 161^st place; Italian: 3^rd place)

dailymail.co.uk (Global: 219^th place; Italian: 74^th place)

doi.org (Global: 2^nd place; Italian: 7^th place)

fanpage.it (Global: 1,405^th place; Italian: 50^th place)

mirror.co.uk (Global: 245^th place; Italian: 309^th place)

msn.com (Global: 117^th place; Italian: 266^th place)

nature.com (Global: 234^th place; Italian: 226^th place)

nejm.org (Global: 2,374^th place; Italian: 1,283^rd place)

nih.gov (Global: 4^th place; Italian: 9^th place)

oadoi.org (Global: 799^th place; Italian: 22^nd place)

omim.org (Global: 4,380^th place; Italian: 4,368^th place)

plosone.org (Global: 4,730^th place; Italian: 2,208^th place)

ucsf.edu (Global: 5,479^th place; Italian: low place)

web.archive.org (Global: 1^st place; Italian: 1^st place)