BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 22068768)

  • 1. Keratosis pilaris and ulerythema ophryogenes in a woman with monosomy of the short arm of chromosome 18.
    Carvalho CA; Carvalho AV; Kiss A; Paskulin G; Götze FM
    An Bras Dermatol; 2011; 86(4 Suppl 1):S42-5. PubMed ID: 22068768
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome.
    Liakou AI; Esteves de Carvalho AV; Nazarenko LP
    J Dermatol; 2014 May; 41(5):371-6. PubMed ID: 24801913
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Keratosis pilaris and ulerythema ophryogenes associated with an 18p deletion caused by a Y/18 translocation.
    Nazarenko SA; Ostroverkhova NV; Vasiljeva EO; Nazarenko LP; Puzyrev VP; Malet P; Nemtseva TA
    Am J Med Genet; 1999 Jul; 85(2):179-82. PubMed ID: 10406673
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ulerythema ophryogenes and keratosis pilaris in a child with monosomy 18p.
    Zouboulis CC; Stratakis CA; Rinck G; Wegner RD; Gollnick H; Orfanos CE
    Pediatr Dermatol; 1994 Jun; 11(2):172-5. PubMed ID: 8041661
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Ulerythema ophryogenes as an entity associated with 18p- syndrome in a pediatric patient].
    Couselo-Rodríguez C; Batalla-Cebey A; Álvarez-Álvarez C; Flórez Á
    Arch Argent Pediatr; 2021 Dec; 119(6):e636-e638. PubMed ID: 34813246
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ulerythema ophryogenes, a rare and often misdiagnosed syndrome: analysis of an idiopathic case.
    Dianzani C; Pizzuti A; Gaspardini F; Bernardini L; Rizzo B; Degener AM
    Int J Immunopathol Pharmacol; 2011; 24(2):523-7. PubMed ID: 21658329
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ulerythema ophryogenes, a rarely reported cutaneous manifestation of noonan syndrome: case report and review of the literature.
    Li K; Ann Thomas M; Haber RM
    J Cutan Med Surg; 2013; 17(3):212-8. PubMed ID: 23673306
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Keratosis pilaris and keratosis pilaris atrophicans faciei].
    Arnold AW; Buechner SA
    J Dtsch Dermatol Ges; 2006 Apr; 4(4):319-23. PubMed ID: 16638061
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical characteristics in patients with interstitial deletions of chromosome region 12q21-q22 and identification of a critical region associated with keratosis pilaris.
    Al-Maawali A; Marshall CR; Scherer SW; Dupuis L; Mendoza-Londono R; Stavropoulos DJ
    Am J Med Genet A; 2014 Mar; 164A(3):796-800. PubMed ID: 24375972
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Keratosis pilaris (ulerythema ophryogenes).
    GROSS P
    AMA Arch Derm Syphilol; 1952 Nov; 66(5):642-3. PubMed ID: 12996047
    [No Abstract]   [Full Text] [Related]  

  • 11. And next… Adnexa: Ulerythema ophryogenes and keratosis pilaris.
    Coelho De Sousa V; Pinheiro R; Cunha N; Lencastre A; Cabete J
    Eur J Dermatol; 2018 Aug; 28(4):566-567. PubMed ID: 30396871
    [No Abstract]   [Full Text] [Related]  

  • 12. Keratosis pilaris/ulerythema ophryogenes and 18p deletion: is it possible that the LAMA1 gene is involved?
    Zouboulis CC; Stratakis CA; Gollnick HP; Orfanos CE
    J Med Genet; 2001 Feb; 38(2):127-8. PubMed ID: 11288714
    [No Abstract]   [Full Text] [Related]  

  • 13. [Tuberous xanthomatosis, ulerythema ophryogenes and keratosis pilaris; pathogenic considerations].
    ZELCER I
    Sem Med; 1949 Nov; 56(45):876-8. PubMed ID: 15401650
    [No Abstract]   [Full Text] [Related]  

  • 14. A mosaic intragenic microduplication of LAMA1 and a constitutional 18p11.32 microduplication in a patient with keratosis pilaris and intellectual disability.
    Kashevarova AA; Nazarenko LP; Skryabin NA; Nikitina TV; Vasilyev SA; Tolmacheva EN; Lopatkina ME; Salyukova OA; Chechetkina NN; Vorotelyak EA; Kalabusheva EP; Fishman VS; Kzhyshkowska J; Graziano C; Magini P; Romeo G; Lebedev IN
    Am J Med Genet A; 2018 Nov; 176(11):2395-2403. PubMed ID: 30244536
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ulerythema ophryogenes and keratosis pilaris.
    Patrizi A; Bianchi T; Orlandi C; Mazzanti L
    Eur J Dermatol; 2002; 12(6):572. PubMed ID: 12503583
    [No Abstract]   [Full Text] [Related]  

  • 16. [REPORT OF A CASE AND THERAPY OF ULERYTHEMA OPHRYOGENES].
    ANTONEV AA; LOPUKHOVA KA; RABEN AS
    Vestn Dermatol Venerol; 1964 Sep; 38():76-7. PubMed ID: 14248119
    [No Abstract]   [Full Text] [Related]  

  • 17. A Case of Noonan Syndrome and Kyrle Disease: Casualty or Causality?
    Brusasco M; Kalaja A; Satolli F; Feliciani C; De Felici Del Giudice MB
    Acta Dermatovenerol Croat; 2023 Dec; 31(3):160-161. PubMed ID: 38439730
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rubinstein--Taybi syndrome and ulerythema ophryogenes in a 9-year-old boy.
    Gómez Centeno P; Rosón E; Peteiro C; Mercedes Pereiro M; Toribio J
    Pediatr Dermatol; 1999; 16(2):134-6. PubMed ID: 10337678
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ulerythema ophryogenes (Unna-Taenzer).
    ZAKON SJ; GOLDBERG AL
    AMA Arch Derm Syphilol; 1951 Dec; 64(6):785-7. PubMed ID: 14867921
    [No Abstract]   [Full Text] [Related]  

  • 20. [Atrophic red keratosis pilaris of the face in sclerodermiform areas with banal keratosis pilaris; hereditary case].
    COSTE F; PIGUET B
    Bull Soc Fr Dermatol Syphiligr; 1948; 55(2):135. PubMed ID: 18892029
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.