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 *

138 related articles for article (PubMed ID: 20406438)

  • 21. Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation.
    Chograni M; Chaabouni M; Mâazoul F; Bouzid H; Kraiem A; Chaabouni HB
    BMC Ophthalmol; 2011 Nov; 11():35. PubMed ID: 22103961
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mal de Meleda in a taiwanese.
    Chao SC; Lai FJ; Yang MH; Lee JY
    J Formos Med Assoc; 2005 Apr; 104(4):276-8. PubMed ID: 15909066
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mal de Meleda without mutations in the ARS coding sequence.
    van Steensel MA; van Geel MV; Steijlen PM
    Eur J Dermatol; 2002; 12(2):129-32. PubMed ID: 11872406
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A Different Presentation of Mal De Meleda: New Skin Lesions in a Residual Limb after Traumatic Amputation.
    Adıgüzel E; Yüksel E; Safaz İ; Kenan Tan A
    Acta Dermatovenerol Croat; 2016 Jun; 24(2):137-9. PubMed ID: 27477174
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family.
    Charfeddine C; Dallali H; Abdessalem G; Ghedira K; Hamdi Y; Elouej S; Landoulsi Z; Delague V; Lagarde A; Levy N; El-Amraoui A; Boubaker MS; Abdelhak S; Mokni M
    J Hum Genet; 2020 Apr; 65(4):397-410. PubMed ID: 31911611
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Abnormal keratinization and cutaneous inflammation in Mal de Meleda.
    Kudo M; Ishiura N; Tamura-Nakano M; Shimizu T; Kamata M; Akasaka E; Nakano H; Okuma Y; Tada Y; Okochi H; Tamaki T
    J Dermatol; 2020 May; 47(5):554-558. PubMed ID: 32157724
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates.
    Eckl KM; Stevens HP; Lestringant GG; Westenberger-Treumann M; Traupe H; Hinz B; Frossard PM; Stadler R; Leigh IM; Nürnberg P; Reis A; Hennies HC
    Hum Genet; 2003 Jan; 112(1):50-6. PubMed ID: 12483299
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical and molecular investigation of Buschke-Fischer-Brauer in consanguineous Tunisian families.
    Charfeddine C; Ktaifi C; Laroussi N; Hammami H; Jmel H; Landoulsi Z; Badri T; Benmously R; Bchetnia M; Boubaker MS; Fenniche S; Abdelhak S; Mokni M
    J Eur Acad Dermatol Venereol; 2016 Dec; 30(12):2122-2130. PubMed ID: 27400994
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Clinical and genetic studies of 3 large, consanguineous, Algerian families with Mal de Meleda.
    Bouadjar B; Benmazouzia S; Prud'homme JF; Cure S; Fischer J
    Arch Dermatol; 2000 Oct; 136(10):1247-52. PubMed ID: 11030771
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutations in the gene encoding SLURP-1 in Mal de Meleda.
    Fischer J; Bouadjar B; Heilig R; Huber M; Lefèvre C; Jobard F; Macari F; Bakija-Konsuo A; Ait-Belkacem F; Weissenbach J; Lathrop M; Hohl D; Prud'homme JF
    Hum Mol Genet; 2001 Apr; 10(8):875-80. PubMed ID: 11285253
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mal de Meleda in Indonesia: Mutations in the SLURP1 gene appear to be ubiquitous.
    Taylor JA; Bondavalli D; Monif M; Yap LM; Winship I
    Australas J Dermatol; 2016 Feb; 57(1):e11-3. PubMed ID: 25557416
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Transgradient Variant of Mal De Meleda Presenting As Palmoplantar Keratoderma: A Case Report.
    Khan A; Singh A; Madke B; Gupta K; Sree Ramya T
    Cureus; 2024 May; 16(5):e60717. PubMed ID: 38903266
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic linkage of Meleda disease to chromosome 8qter.
    Fischer J; Bouadjar B; Heilig R; Fizames C; Prud'homme JF; Weissenbach J
    Eur J Hum Genet; 1998; 6(6):542-7. PubMed ID: 9887370
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A recurrent mutation in the ARS (component B) gene encoding SLURP-1 in Turkish families with mal de Meleda: evidence of a founder effect.
    Hu G; Yildirim M; Baysal V; Yerebakan O; Yilmaz E; Inaloz HS; Martinez-Mir A; Christiano AM; Celebi JT
    J Invest Dermatol; 2003 Jun; 120(6):967-9. PubMed ID: 12787122
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mutations in the SLURP-1 gene underlie Mal de Meleda in three Pakistani families.
    Wajid M; Kurban M; Shimomura Y; Christiano AM
    J Dermatol Sci; 2009 Oct; 56(1):27-32. PubMed ID: 19692209
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract.
    Behnam M; Imagawa E; Chaleshtori AR; Ronasian F; Salehi M; Miyake N; Matsumoto N
    J Hum Genet; 2016 Feb; 61(2):177-9. PubMed ID: 26490182
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mal De Meleda with Flexural Involvement.
    Sethy M; Chatterjee S; Srinivas CR; Sachan S
    Indian Dermatol Online J; 2022; 13(5):636-639. PubMed ID: 36304642
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Malignant melanoma developing in an area of hereditary palmoplantar keratoderma (Mal de Meleda).
    Mozzillo N; Nunziata CA; Caracò C; Fazioli F; Botti G;
    J Surg Oncol; 2003 Dec; 84(4):229-33. PubMed ID: 14756434
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mal de Meleda: a report of two cases of familial occurrence.
    Morais e Silva FA; Cunha TV; Boeno Edos S; Steiner D
    An Bras Dermatol; 2011; 86(4 Suppl 1):S100-3. PubMed ID: 22068784
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mal de Meleda: genetic haplotype analysis and clinicopathological findings in cases originating from the island of Mljet (Meleda), Croatia.
    Bakija-Konsuo A; Basta-Juzbasic A; Rudan I; Situm M; Nardelli-Kovacic M; Levanat S; Fischer J; Hohl D; Loncaric D; Seiwert S; Campbell H
    Dermatology; 2002; 205(1):32-9. PubMed ID: 12145432
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.