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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1995 2
2006 1
2012 1
2014 1
2015 2
2016 1
2018 1
2019 1
2021 1
2023 0

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PubMed for id: 91006

11 results

Results by year

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Page 1
Hereditary sclerosing poikiloderma.
Lee HJ, Shin DH, Choi JS, Kim KH. Lee HJ, et al. J Korean Med Sci. 2012 Feb;27(2):225-7. doi: 10.3346/jkms.2012.27.2.225. Epub 2012 Jan 27. J Korean Med Sci. 2012. PMID: 22323875 Free PMC article.
[Weary hereditary sclerosing poikiloderma].
Fazio M, Lisi S, Amantea A, Maini A, Menaguale G, Sacerdoti G, Balus L. Fazio M, et al. Ann Dermatol Venereol. 1995;122(9):618-20. Ann Dermatol Venereol. 1995. PMID: 8745690 French.
Hereditary sclerosing poikiloderma.
Greer KE, Weary PE, Nagy R, Robinow M. Greer KE, et al. Int J Dermatol. 1978 May;17(4):316-22. doi: 10.1111/j.1365-4362.1978.tb06085.x. Int J Dermatol. 1978. PMID: 659034
Search for ReCQL4 mutations in 39 patients genotyped for suspected Rothmund-Thomson/Baller-Gerold syndromes.
Piard J, Aral B, Vabres P, Holder-Espinasse M, Mégarbané A, Gauthier S, Capra V, Pierquin G, Callier P, Baumann C, Pasquier L, Baujat G, Martorell L, Rodriguez A, Brady AF, Boralevi F, González-Enseñat MA, Rio M, Bodemer C, Philip N, Cordier MP, Goldenberg A, Demeer B, Wright M, Blair E, Puzenat E, Parent P, Sznajer Y, Francannet C, DiDonato N, Boute O, Barlogis V, Moldovan O, Bessis D, Coubes C, Tardieu M, Cormier-Daire V, Sousa AB, Franques J, Toutain A, Tajir M, Elalaoui SC, Geneviève D, Thevenon J, Courcet JB, Rivière JB, Collet C, Gigot N, Faivre L, Thauvin-Robinet C. Piard J, et al. Clin Genet. 2015 Mar;87(3):244-51. doi: 10.1111/cge.12361. Epub 2014 Mar 26. Clin Genet. 2015. PMID: 24635570
Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.
Mercier S, Küry S, Salort-Campana E, Magot A, Agbim U, Besnard T, Bodak N, Bou-Hanna C, Bréhéret F, Brunelle P, Caillon F, Chabrol B, Cormier-Daire V, David A, Eymard B, Faivre L, Figarella-Branger D, Fleurence E, Ganapathi M, Gherardi R, Goldenberg A, Hamel A, Igual J, Irvine AD, Israël-Biet D, Kannengiesser C, Laboisse C, Le Caignec C, Mahé JY, Mallet S, MacGowan S, McAleer MA, McLean I, Méni C, Munnich A, Mussini JM, Nagy PL, Odel J, O'Regan GM, Péréon Y, Perrier J, Piard J, Puzenat E, Sampson JB, Smith F, Soufir N, Tanji K, Thauvin C, Ulane C, Watson RM, Khumalo NP, Mayosi BM, Barbarot S, Bézieau S. Mercier S, et al. Orphanet J Rare Dis. 2015 Oct 15;10:135. doi: 10.1186/s13023-015-0352-4. Orphanet J Rare Dis. 2015. PMID: 26471370 Free PMC article.
11 results