BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

333 related articles for article (PubMed ID: 19002348)

  • 1. 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]  

  • 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. [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]  

  • 4. 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]  

  • 5. 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]  

  • 6. [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]  

  • 7. Case report of Schöpf-Schulz-Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A.
    Hsu TC; Lee JY; Hsu MM; Chao SC
    J Dermatol; 2018 Apr; 45(4):475-478. PubMed ID: 29271000
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Schopf-Schulz-Passarge Syndrome.
    Rambhia KD; Kharkar V; Mahajan S; Khopkar US
    Indian Dermatol Online J; 2018; 9(6):448-451. PubMed ID: 30505790
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. The Schöpf-Schulz-Passarge syndrome.
    Verplancke P; Driessen L; Wynants P; Naeyaert JM
    Dermatology; 1998; 196(4):463-6. PubMed ID: 9669133
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.
    Tziotzios C; Petrof G; Liu L; Verma A; Wedgeworth EK; Mellerio JE; McGrath JA
    Br J Dermatol; 2014 Nov; 171(5):1211-4. PubMed ID: 24902757
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Schöpf syndrome. Clinical, genetic and lipid biochemical studies].
    Küster W; Hammerstein W
    Hautarzt; 1992 Dec; 43(12):763-6. PubMed ID: 1473970
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic study in a suspected case of Schöpf-Schulz-Passarge syndrome.
    Vilas-Sueiro A; Monteagudo B; González-Vilas D; Varela-Veiga A; De las Heras C
    Indian J Dermatol Venereol Leprol; 2015; 81(4):408-10. PubMed ID: 26087098
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Schöpf-Schulz-Passarge Syndrome: Previously Unreported WNT10A Genotype and Phenotypes in 9 Family Members.
    Zimmermann CE; Soufi M; Ruppert V; Schaefer JR; von Domarus H
    Acta Derm Venereol; 2019 Jan; 99(1):113-114. PubMed ID: 30265373
    [No Abstract]   [Full Text] [Related]  

  • 17. Long-term dental management of a patient with features of Schöpf-Schulz-Passarge syndrome.
    Manchanda N; Anthonappa R; Al-Mulla H; King N
    Spec Care Dentist; 2017 Jul; 37(4):204-208. PubMed ID: 28598512
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A.
    Petrof G; Fong K; Lai-Cheong JE; Cockayne SE; McGrath JA
    Australas J Dermatol; 2011 Aug; 52(3):224-6. PubMed ID: 21834823
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 17.