BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 22000878)

  • 1. JAAD Grand Rounds quiz. Palmoplantar keratoderma, hypodontia, hypotrichosis, nail dystrophy, and multiple eyelid cysts.
    DiGiorgio CM; Bohlke AK; Oswald BJ; Wang AR; Boh EE
    J Am Acad Dermatol; 2011 Nov; 65(5):1066-9. PubMed ID: 22000878
    [No Abstract]   [Full Text] [Related]  

  • 2. A case of Schöpf-Schulz-Passarge syndrome.
    Hampton PJ; Angus B; Carmichael AJ
    Clin Exp Dermatol; 2005 Sep; 30(5):528-30. PubMed ID: 16045686
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Late diagnosis of ectodermal dysplasia syndrome.
    Granger RH; Marshman G; Liu L; McGrath JA
    Australas J Dermatol; 2013 Feb; 54(1):46-8. PubMed ID: 22670871
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Schöpf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations.
    Castori M; Ruggieri S; Giannetti L; Annessi G; Zambruno G
    Acta Derm Venereol; 2008; 88(6):607-12. PubMed ID: 19002348
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Apocrine hidrocystomas of the lids, hypodontia, palmar-plantar hyperkeratosis, and onychodystrophy. A new variant of ectodermal dysplasia.
    Font RL; Stone MS; Schanzer MC; Lewis RA
    Arch Ophthalmol; 1986 Dec; 104(12):1811-3. PubMed ID: 2947556
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Well-Differentiated Syringofibrocarcinoma in a Patient With Clouston Syndrome.
    Odell ID; Lilly E; Reeve K; Bosenberg MW; Milstone LM
    JAMA Dermatol; 2016 Apr; 152(4):484-6. PubMed ID: 26792110
    [No Abstract]   [Full Text] [Related]  

  • 7. Syndrome of cystic eyelids, palmo-plantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive trait.
    Schöpf E; Schulz HJ; Passarge E
    Birth Defects Orig Artic Ser; 1971 Jun; 7(8):219-21. PubMed ID: 4281327
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Multiple eccrine hydrocystomas of the eyelids in the framework of Schöpf syndrome. A case report].
    Dot C; Dordain M; Boucher E; Metge F; Millet P; Maille M; Maurin J
    J Fr Ophtalmol; 2000 Oct; 23(8):809-16. PubMed ID: 11033504
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Ectodermal dysplasia: multiple manifestations of a hereditary disease].
    Ouellet B; Agha-Amiri M; Dubé-Baril C; Mascrès C
    J Can Dent Assoc; 1997 May; 63(5):377-81. PubMed ID: 9182019
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Schöpf-Schulz-Passarge syndrome associated with two new missense mutations in WNT10A.
    Pauly KJ; Balakirski G; Megahed M; Rübben A; Schmitt L
    J Dtsch Dermatol Ges; 2018 Jan; 16(1):66-69. PubMed ID: 29314690
    [No Abstract]   [Full Text] [Related]  

  • 11. Eccrine syringofibroadenoma as a clue for the diagnosis of Schöpf-Schulz-Passarge syndrome in acquired palmoplantar keratoderma.
    Riera-Monroig J; Martínez-Romero MDC; Alós L; Guillén-Navarro E; Mascaró JM
    J Cutan Pathol; 2020 Oct; 47(10):987-989. PubMed ID: 32406069
    [No Abstract]   [Full Text] [Related]  

  • 12. Eccrine syringofibroadenoma of the eyelid in association with eye prosthesis.
    Guerin M; Droney T; Keohane C; Fenton S
    Eye (Lond); 2011 Aug; 25(8):1102-3. PubMed ID: 21587277
    [No Abstract]   [Full Text] [Related]  

  • 13. Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations.
    Kantaputra P; Kaewgahya M; Jotikasthira D; Kantaputra W
    Am J Med Genet A; 2014 Apr; 164A(4):1041-8. PubMed ID: 24458874
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Schöpf-Schulz-Passarge syndrome with an unusual pattern of inheritance.
    Craigen WJ; Levy ML; Lewis RA
    Am J Med Genet; 1997 Aug; 71(2):186-8. PubMed ID: 9217219
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Multiple eyelid cysts with palmoplantar hyperkeratosis--quiz case.
    Gira AK; Robertson D; Swerlick RA
    Arch Dermatol; 2004 Feb; 140(2):231-6. PubMed ID: 14967804
    [No Abstract]   [Full Text] [Related]  

  • 16. [Schopf-Schulz-Passarge syndrome: 2 cases].
    Gkolfinopoulos T; Ingen-Housz-Oro S; Cavelier-Balloy B; Blanchet-Bardon C
    Ann Dermatol Venereol; 2001 Dec; 128(12):1330-3. PubMed ID: 11908136
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Hypohidrotic ectodermal dysplasia in the female].
    Bonora G; Gelmetti C; Acerbi L; Case L; Luciani L
    Minerva Pediatr; 1981 Sep; 33(18):911-6. PubMed ID: 6895543
    [No Abstract]   [Full Text] [Related]  

  • 18. Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A.
    Nagy N; Wedgeworth E; Hamada T; White JM; Hashimoto T; McGrath JA
    J Dermatol Sci; 2010 Jun; 58(3):220-2. PubMed ID: 20418069
    [No Abstract]   [Full Text] [Related]  

  • 19. Schöpf-Schulz-Passarge syndrome with pili torti: A new association?
    SZEPETIUK G; VANHOOTEGHEM O; MULLER G; STENE JJ; NIKKELS AF
    Eur J Dermatol; 2009; 19(5):517-8. PubMed ID: 19527991
    [No Abstract]   [Full Text] [Related]  

  • 20. Schopf-Schulz-Passarge syndrome: a rare ectodermal dysplasia with a delayed diagnosis.
    Ismail FF; McGrath J; Sinclair R
    Int J Dermatol; 2020 Feb; 59(2):257-258. PubMed ID: 31468502
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.