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 *

111 related articles for article (PubMed ID: 14828625)

  • 21. Patient with dyschromatosis symmetrica hereditaria treated with miniature punch grafting, followed by excimer light therapy.
    Kawakami T; Otaguchi R; Kyoya M; Soma Y; Suzuki T
    J Dermatol; 2013 Sep; 40(9):771-2. PubMed ID: 23803141
    [No Abstract]   [Full Text] [Related]  

  • 22. Acral dyschromatosis with developmental regression and dystonia in a seven-year-old child: dyschromatosis symmetrica hereditaria variant or a new syndrome?
    Kaliyadan F; Vinayan KP; Fernandes B; Jayasree MG
    Indian J Dermatol Venereol Leprol; 2009; 75(4):412-4. PubMed ID: 19584476
    [No Abstract]   [Full Text] [Related]  

  • 23. [Xeroderma pigmentosum and pigmented xerodermoid. Clinical and molecular biological studies].
    Jung EG; Schnyder UW
    Schweiz Med Wochenschr; 1970 Oct; 100(41):1718-26. PubMed ID: 5480540
    [No Abstract]   [Full Text] [Related]  

  • 24. Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis.
    Suzuki N; Suzuki T; Inagaki K; Ito S; Kono M; Fukai K; Takama H; Sato K; Ishikawa O; Abe M; Shimizu H; Kawai M; Horikawa T; Yoshida K; Matsumoto K; Terui T; Tsujioka K; Tomita Y
    J Invest Dermatol; 2005 Jun; 124(6):1186-92. PubMed ID: 15955093
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Dyschromias: A Series of Five Interesting Cases from India.
    Namitha P; Sacchidanand S
    Indian J Dermatol; 2015; 60(6):636. PubMed ID: 26677297
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Immune function, mutant frequency, and cancer risk in the DNA repair defective genodermatoses xeroderma pigmentosum, Cockayne's syndrome, and trichothiodystrophy.
    Norris PG; Limb GA; Hamblin AS; Lehmann AR; Arlett CF; Cole J; Waugh AP; Hawk JL
    J Invest Dermatol; 1990 Jan; 94(1):94-100. PubMed ID: 2295840
    [TBL] [Abstract][Full Text] [Related]  

  • 27. What is the novel clinical finding in dyschromatosis symmetrica hereditaria?
    Tomita Y
    J Dermatol; 2013 Jan; 40(1):84-5. PubMed ID: 22974199
    [No Abstract]   [Full Text] [Related]  

  • 28. [THE CUTANEOUS LESIONS OF XERODERMA PIGMENTOSUM].
    BOUISSOU H; SADEGHI N; CATAGNOL R
    Toulouse Med; 1964 Feb; 65():281-93. PubMed ID: 14146592
    [No Abstract]   [Full Text] [Related]  

  • 29. [ANATOMOCLINICAL STUDY OF SKIN LESIONS OF XERODERMA PIGMENTOSUM (APROPOS OF 21 CASES)].
    BOUISSOU H; SADEGHI N; CASTAGNOL
    Ann Pediatr (Paris); 1964 Nov; 11():568-81. PubMed ID: 14226012
    [No Abstract]   [Full Text] [Related]  

  • 30. [Universal dyschromatosis: a familial case].
    Schoenlaub P; Leroy JP; Dupré D; Chaboche C; Plantin P
    Ann Dermatol Venereol; 1998 Oct; 125(10):700-4. PubMed ID: 9835959
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Generalized pigmentation with linear atrophy; xeroderma pigmentosum?
    SAMMAN PD
    Proc R Soc Med; 1949 Mar; 42(3):136. PubMed ID: 18126970
    [No Abstract]   [Full Text] [Related]  

  • 32. A suggested mode of pigment transfer into the dermis.
    Guerrier C
    Acta Derm Venereol; 1973; 53(3):173-7. PubMed ID: 4124006
    [No Abstract]   [Full Text] [Related]  

  • 33. A novel mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.
    Li M; Jiang YX; Liu JB; Yang S; He PP; Gao M; Wei SC; Yan KL; Huang W; Zhang XJ
    Clin Exp Dermatol; 2004 Sep; 29(5):533-5. PubMed ID: 15347341
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel nonsense mutation of the DSRAD gene in a Taiwanese family with dyschromatosis symmetrica hereditaria.
    Chao SC; Huang CY; Yang MH
    Eur J Dermatol; 2006; 16(4):449-50. PubMed ID: 16935814
    [No Abstract]   [Full Text] [Related]  

  • 35. Dyschromatosis symmetrica in a Chinese with 47-XYY syndrome.
    Tay CH; Tock EP; Ong BH
    Int J Dermatol; 1972; 11(3):134-9. PubMed ID: 5039896
    [No Abstract]   [Full Text] [Related]  

  • 36. Dyschromatosis symmetrica hereditaria with acral hypertrophy.
    Murata T; Yagi Y; Tanioka M; Suzuki T; Miyachi Y; Morita K; Utani A
    Eur J Dermatol; 2011; 21(4):649-50. PubMed ID: 21840790
    [No Abstract]   [Full Text] [Related]  

  • 37. Novel frameshift mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.
    Ren JW; Luo SJ; Peng ZH; Liu Y; Pan M; Xiao SX
    J Eur Acad Dermatol Venereol; 2008 Nov; 22(11):1375-6. PubMed ID: 18331298
    [No Abstract]   [Full Text] [Related]  

  • 38. Dermoscopic features in a case of dyschromatosis symmetrica hereditaria.
    Oiso N; Murata I; Hayashi M; Amatsu A; Yoshida M; Suzuki T; Kawada A
    J Dermatol; 2011 Jan; 38(1):91-3. PubMed ID: 21175763
    [No Abstract]   [Full Text] [Related]  

  • 39. Malignant melanoma of the iris in xeroderma pigmentosum.
    Johnson MW; Skuta GL; Kincaid MC; Nelson CC; Wolter JR
    Arch Ophthalmol; 1989 Mar; 107(3):402-7. PubMed ID: 2923565
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?
    Kono M; Akiyama M; Suganuma M; Tomita Y; Sanchez-Valle A
    Int J Dermatol; 2013 Dec; 52(12):1582-4. PubMed ID: 24261734
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.