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 *

133 related articles for article (PubMed ID: 5772388)

  • 1. [On monilethrix].
    Rodermund OE
    Z Haut Geschlechtskr; 1969 May; 44(9):291-6. PubMed ID: 5772388
    [No Abstract]   [Full Text] [Related]  

  • 2. [Monilethrix].
    Bartosová L; Jorda V
    Cesk Dermatol; 1973 Aug; 48(4):232-7. PubMed ID: 4727827
    [No Abstract]   [Full Text] [Related]  

  • 3. [Monilethrix. A study apropos of 2 familial cases].
    Marqués Llagará E; Calap Calatayud J; Torres Peris V
    Actas Dermosifiliogr; 1973; 64(3-4):203-12. PubMed ID: 4805249
    [No Abstract]   [Full Text] [Related]  

  • 4. [2 cases of familial monilethrix].
    Peirone F; Spada A
    Minerva Med; 1972 Jan; 63(4):272-8. PubMed ID: 5058300
    [No Abstract]   [Full Text] [Related]  

  • 5. [Monilethrix: exclusive involvement of body hair].
    Hamm H; Echternacht-Happle K; Happle R
    Z Hautkr; 1984 Sep; 59(17):1177-8. PubMed ID: 6485460
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Special hyperpigmentation of the hair roots in a case of parakeratosis psoriasiformis].
    Janiszewska M; Kostanecki W
    Z Haut Geschlechtskr; 1970 Sep; 45(18):643-5. PubMed ID: 5455467
    [No Abstract]   [Full Text] [Related]  

  • 7. [Hereditary skin diseases related to sex].
    Desmons F; Walbaum R
    Lille Med; 1972 Mar; 17(3):447-70. PubMed ID: 4340312
    [No Abstract]   [Full Text] [Related]  

  • 8. Hypoplastic enamel, onycholysis, and hypohidrosis inherited as an autosomal dominant trait. A review of ectodermal dysplasia syndromes.
    Witkop CJ; Brearley LJ; Gentry WC
    Oral Surg Oral Med Oral Pathol; 1975 Jan; 39(1):71-86. PubMed ID: 122795
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Hereditary dermatoses and syndromes in pediatric dermatologic practice].
    Vedrova IN; Kriazheva SS; Mikhaĭlova MB
    Vestn Dermatol Venerol; 1981 Nov; (11):20-4. PubMed ID: 7314886
    [No Abstract]   [Full Text] [Related]  

  • 10. [Cytogenetic studies on some rarer dermatoses].
    Back F; Maestri D
    Hautarzt; 1966 Jan; 17(1):35-6. PubMed ID: 4963733
    [No Abstract]   [Full Text] [Related]  

  • 11. [Genetic counseling in dermatology].
    Stoll C; Grosshans EM
    Minerva Med; 1972 Dec; 63(90):4961-8. PubMed ID: 4345325
    [No Abstract]   [Full Text] [Related]  

  • 12. [Monilethrix and arginine succinuria].
    Sobolewska G; Wilmańska J
    Przegl Dermatol; 1968; 55(2):157-63. PubMed ID: 5677746
    [No Abstract]   [Full Text] [Related]  

  • 13. [Darier disease in children. Eight case-reports (author's transl)].
    Larregue M; Bonnetblanc P; Prigent F; Lorette G; Laresche MC; Ramdenne P; Titi A
    Ann Pediatr (Paris); 1982 Jan; 29(1):35-9. PubMed ID: 7055356
    [No Abstract]   [Full Text] [Related]  

  • 14. Severe monilethrix associated with intractable scalp pruritus, posterior subcapsular cataract, brachiocephaly, and distinct facial features: a new variant of monilethrix syndrome?
    Erbagci Z; Erbagci I; Erbagci H; Erkilic S; Tuncel AA
    Pediatr Dermatol; 2004; 21(4):486-90. PubMed ID: 15283798
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Jadassohn-Lewandowski syndrome with microphthalmos].
    Vogt HJ; Calap J
    Hautarzt; 1971 Jul; 22(7):294-9. PubMed ID: 5570028
    [No Abstract]   [Full Text] [Related]  

  • 16. [Studies on monilethrix].
    Lubach D; Triantos N
    Hautarzt; 1979 May; 30(5):253-6. PubMed ID: 447529
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Follicular atrophoderma, basocellular proliferations and hypotrichosis].
    Pierard J; Dhondt F; Geerts ML; Kriekemans J
    Arch Belg Dermatol Syphiligr; 1971; 27(1):55-68. PubMed ID: 5126848
    [No Abstract]   [Full Text] [Related]  

  • 18. Inherited diseases--the genodermatoses.
    Harper J
    Br J Hosp Med; 1982 Jun; 27(6):647-52. PubMed ID: 7116040
    [No Abstract]   [Full Text] [Related]  

  • 19. Graham Little-Piccardi-Lassueur syndrome in a patient with androgen insensitivity syndrome.
    Donovan JC
    Int J Dermatol; 2016 Apr; 55(4):e211-2. PubMed ID: 26566966
    [No Abstract]   [Full Text] [Related]  

  • 20. Familial Netherton's disease.
    Kassis V; Nielsen JM; Klem-Thomsen H; Dahl-Christensen J; Wadskov S
    Cutis; 1986 Sep; 38(3):175-8. PubMed ID: 3769553
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.