These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 7896482)

  • 1. Reticulate pigmentary dermatosis associated with hypohydrosis and short stature: a variant of Naegeli-Franceschetti-Jadassohn syndrome?
    Kudo Y; Fujiwara S; Takayasu S; Ooki H; Ogawa A
    Int J Dermatol; 1995 Jan; 34(1):30-1. PubMed ID: 7896482
    [No Abstract]   [Full Text] [Related]  

  • 2. 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
    Eur J Med Genet; 2011; 54(3):231-5. PubMed ID: 21252004
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Natural history of the Naegeli-Franceschetti-Jadassohn syndrome.
    Papini M
    J Am Acad Dermatol; 1994 Nov; 31(5 Pt 1):830. PubMed ID: 7929942
    [No Abstract]   [Full Text] [Related]  

  • 4. Naegeli-Franceschetti-Jadassohn Syndrome: A Rare Reticulate Pigmentary Disorder.
    Sanodia G; Hulmani M; Kumar VJ
    Indian J Dermatol; 2019; 64(3):235-238. PubMed ID: 31148864
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    J Invest Dermatol; 2002 Sep; 119(3):692-8. PubMed ID: 12230514
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spontaneous fading of reticular pigmentation in Naegeli-Franceschetti-Jadassohn syndrome.
    Itin PH; Burger B
    Dermatology; 2010; 221(2):135-6. PubMed ID: 20587992
    [No Abstract]   [Full Text] [Related]  

  • 7. Naegeli-Franceschetti-Jadassohn syndrome in a Saudi Arabian family.
    Tubaigy SM; Hassan HM
    J Forensic Sci; 2014 Mar; 59(2):555-8. PubMed ID: 24261749
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    J Am Acad Dermatol; 1993 Jun; 28(6):942-50. PubMed ID: 8496458
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: intrafamilial overlap of phenotypes in patients with the same KRT14 frameshift variant.
    Burger B; Spoerri I; Imahorn E; Wariwoda H; Leeb T; Itin PH
    Br J Dermatol; 2019 Oct; 181(4):864-866. PubMed ID: 30968399
    [No Abstract]   [Full Text] [Related]  

  • 10. Naegeli-Franceschetti-Jadassohn syndrome: A rare case.
    Shah BJ; Jagati AK; Gupta NP; Dhamale SS
    Indian Dermatol Online J; 2015; 6(6):403-6. PubMed ID: 26753140
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Reticular pigmented genodermatosis with milia--a special form of Naegeli-Franceschetti-Jadassohn syndrome or a new entity?
    Tzermias C; Zioga A; Hatzis I
    Clin Exp Dermatol; 1995 Jul; 20(4):331-5. PubMed ID: 8548993
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hyperpigmentation and hypohidrosis. (The Naegeli-Franceschetti-Jadassohn syndrome): report of a family and review of the literature.
    Sparrow GP; Samman PD; Wells RS
    Clin Exp Dermatol; 1976 Jun; 1(2):127-40. PubMed ID: 939040
    [No Abstract]   [Full Text] [Related]  

  • 13. Image Gallery: Periorbital and temporal dermal melanocytosis of hypohidrotic ectodermal dysplasia.
    Namiki T; Tokoro S; Hanafusa T; Yokozeki H
    Br J Dermatol; 2016 Dec; 175(6):e146-e147. PubMed ID: 27996143
    [No Abstract]   [Full Text] [Related]  

  • 14. Genodermatosis with reticulate, patchy and mottled pigmentation of the neck--a clue to rare dermatologic disorders.
    Itin PH; Lautenschlager S
    Dermatology; 1998; 197(3):281-90. PubMed ID: 9812038
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of a founder mutation in KRT14 associated with Naegeli-Franceschetti-Jadassohn syndrome.
    Ralser DJ; Kumar S; Borisov O; Sarig O; Richard G; Wolf S; Krawitz PM; Sprecher E; Kreiß M; Betz RC
    Br J Dermatol; 2020 Oct; 183(4):756-757. PubMed ID: 32282935
    [No Abstract]   [Full Text] [Related]  

  • 16. [Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis. Two allelic ectodermal dysplasias related to mutations of dominant gene coding for keratin 14].
    Dereure O
    Ann Dermatol Venereol; 2007; 134(6-7):595. PubMed ID: 17657198
    [No Abstract]   [Full Text] [Related]  

  • 17. A new case of keratin 14 functional knockout causes severe recessive EBS and questions the haploinsufficiency model of Naegeli-Franceschetti-Jadassohn syndrome.
    Titeux M; Décha A; Pironon N; Tonasso L; Gasc G; Mejía JE; Prost-Squarcioni C; Hovnanian A
    J Invest Dermatol; 2011 Oct; 131(10):2131-3. PubMed ID: 21734713
    [No Abstract]   [Full Text] [Related]  

  • 18. A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signs.
    Freire-Maia N; Fortes VA; Pereira LC; Opitz JM; Marcalle FA; Cavalli IJ
    J Med Genet; 1975 Sep; 12(3):308-10. PubMed ID: 1177286
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Classification and pigmentary characteristics in ectodermal dysplasia.
    Solomon LM
    J Clin Dysmorphol; 1983; 1(2):28-9. PubMed ID: 6580393
    [No Abstract]   [Full Text] [Related]  

  • 20. Pigmentary characteristics of the ectodermal dysplasias.
    Elejalde BR; de Elejalde MM
    J Clin Dysmorphol; 1983; 1(1):2-8. PubMed ID: 6580384
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.