PubMed for id: 91010

Year	Number of Results
1993	1
1995	1
1997	1
1998	1
1999	1
2000	1
2002	1
2006	1
2007	1
2008	1
2011	1
2013	1
2014	1
2015	1
2019	1
2023	1

1

Naegeli-Franceschetti-Jadassohn syndrome: A rare case.

Shah BJ, Jagati AK, Gupta NP, Dhamale SS. Shah BJ, et al. Indian Dermatol Online J. 2015 Nov-Dec;6(6):403-6. doi: 10.4103/2229-5178.169712. Indian Dermatol Online J. 2015. PMID: 26753140 Free PMC article.

2

Naegeli-Franceschetti-Jadassohn syndrome in a Saudi Arabian family.

Tubaigy SM, Hassan HM. Tubaigy SM, et al. J Forensic Sci. 2014 Mar;59(2):555-8. doi: 10.1111/1556-4029.12316. Epub 2013 Nov 21. J Forensic Sci. 2014. PMID: 24261749 Review.

3

Prenatal and postnatal growth retardation, microcephaly, developmental delay, and pigmentation abnormalities: Naegeli syndrome, dyskeratosis congenita, poikiloderma Clericuzio type, or separate entity?

Belligni EF, Dokal I, Hennekam RC. Belligni EF, et al. Eur J Med Genet. 2011 May-Jun;54(3):231-5. doi: 10.1016/j.ejmg.2011.01.001. Epub 2011 Jan 18. Eur J Med Genet. 2011. PMID: 21252004

4

KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome.

Lugassy J, McGrath JA, Itin P, Shemer R, Verbov J, Murphy HR, Ishida-Yamamoto A, Digiovanna JJ, Bercovich D, Karin N, Vitenshtein A, Uitto J, Bergman R, Richard G, Sprecher E. Lugassy J, et al. J Invest Dermatol. 2008 Jun;128(6):1517-24. doi: 10.1038/sj.jid.5701187. Epub 2007 Nov 29. J Invest Dermatol. 2008. PMID: 18049449 Free article.

5

Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14.

Lugassy J, Itin P, Ishida-Yamamoto A, Holland K, Huson S, Geiger D, Hennies HC, Indelman M, Bercovich D, Uitto J, Bergman R, McGrath JA, Richard G, Sprecher E. Lugassy J, et al. Am J Hum Genet. 2006 Oct;79(4):724-30. doi: 10.1086/507792. Epub 2006 Aug 25. Am J Hum Genet. 2006. PMID: 16960809 Free PMC article.

6

Refined mapping of Naegeli-Franceschetti- Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genes.

Sprecher E, Itin P, Whittock NV, McGrath JA, Meyer R, DiGiovanna JJ, Bale SJ, Uitto J, Richard G. Sprecher E, et al. J Invest Dermatol. 2002 Sep;119(3):692-8. doi: 10.1046/j.1523-1747.2002.01855.x. J Invest Dermatol. 2002. PMID: 12230514 Free article.

7

The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21.

Whittock NV, Coleman CM, McLean WH, Ashton GH, Acland KM, Eady RA, McGrath JA. Whittock NV, et al. J Invest Dermatol. 2000 Oct;115(4):694-8. doi: 10.1046/j.1523-1747.2000.00097.x. J Invest Dermatol. 2000. PMID: 10998145 Free article.

8

Reticular pigmented genodermatosis with milia--a special form of Naegeli-Franceschetti-Jadassohn syndrome or a new entity?

Tzermias C, Zioga A, Hatzis I. Tzermias C, et al. Clin Exp Dermatol. 1995 Jul;20(4):331-5. doi: 10.1111/j.1365-2230.1995.tb01336.x. Clin Exp Dermatol. 1995. PMID: 8548993

9

Natural history of the Naegeli-Franceschetti-Jadassohn syndrome and further delineation of its clinical manifestations.

Itin PH, Lautenschlager S, Meyer R, Mevorah B, Rufli T. Itin PH, et al. J Am Acad Dermatol. 1993 Jun;28(6):942-50. doi: 10.1016/0190-9622(93)70135-g. J Am Acad Dermatol. 1993. PMID: 8496458

10

Segmental forms of autosomal dominant skin disorders: the puzzle of mosaicism.

Itin PH, Buechner SA. Itin PH, et al. Am J Med Genet. 1999 Aug 6;85(4):351-4. Am J Med Genet. 1999. PMID: 10398258 Review.

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