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 *

177 related articles for article (PubMed ID: 19527991)

  • 1. 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]  

  • 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. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. [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]  

  • 10. 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]  

  • 11. 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]  

  • 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-Schulz-Passarge syndrome.
    Monk BE; Pieris S; Soni V
    Br J Dermatol; 1992 Jul; 127(1):33-5. PubMed ID: 1637691
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Eccrine porocarcinoma in a patient with Schöpf-Schulz-Passarge syndrome.
    Howard L; Davis R; Bhatt N; Khan U; Keith D
    Clin Exp Dermatol; 2019 Dec; 44(8):938-939. PubMed ID: 30689236
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 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. Pili torti and onychodysplasia. Report of a previously undescribed hidrotic ectodermal dysplasia.
    Calzavara-Pinton P; Carlino A; Benetti A; De Panfilis G
    Dermatologica; 1991; 182(3):184-7. PubMed ID: 1879585
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Rapp-Hodgkin syndrome with palmoplantar keratoderma, glossy tongue, congenital absence of lingual frenum and of sublingual caruncles: newly recognized findings.
    Kantaputra PN; Pruksachatkunakorn C; Vanittanakom P
    Am J Med Genet; 1998 Oct; 79(5):343-6. PubMed ID: 9779799
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.