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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

183 related items for PubMed ID: 4617749

  • 1. [Erythrodermia ichthyosiformis congenita with hypotrichosis, anhidrosis, deaf-mutism and decreased elimination of various amino acids in the urine].
    Salamon T, Budai V, Lazović O, Macanović K, Volić N.
    Hautarzt; 1974 Sep; 25(9):448-53. PubMed ID: 4617749
    [No Abstract] [Full Text] [Related]

  • 2. [Erythrodermia congenitalis ichthyosiformis bullosa].
    Jacobi H, Heidelbach U.
    Dermatol Monatsschr; 1977 Oct; 163(10):840-3. PubMed ID: 336425
    [No Abstract] [Full Text] [Related]

  • 3. [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
    Spiegl B, Hundeiker M.
    Fortschr Med; 1979 Nov 22; 97(44):2018-22. PubMed ID: 511082
    [Abstract] [Full Text] [Related]

  • 4. A congenital ichthyosiform syndrome with deafness and keratitis.
    Cram DL, Resneck JS, Jackson WB.
    Arch Dermatol; 1979 Apr 22; 115(4):467-71. PubMed ID: 434873
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Congenital ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis: a new genodermatosis?
    Lestringant GG, Küster W, Frossard PM, Happle R.
    Am J Med Genet; 1998 Jan 13; 75(2):186-9. PubMed ID: 9450882
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. [Hypotrichosis congenita hereditaria Marie Unna with Ehlers-Danlos syndrome and atopy].
    Mende B, Kreysel HW.
    Hautarzt; 1987 Sep 13; 38(9):532-5. PubMed ID: 3692855
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [Collodion baby with development of erythroderma ichthyosiforme].
    Duperrat B, Deroubaix P, Noury-Duperrat G, Delanoe-Michel J.
    Ann Dermatol Venereol; 1977 Jan 13; 104(1):58-9. PubMed ID: 320933
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Congenital ichthyosiform erythroderma, bullous type [proceedings].
    Starink TM, Wachters DH.
    Dermatologica; 1978 Jan 13; 156(5):309. PubMed ID: 346399
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. [Hereditary keratinization disorders and deafness].
    Voigtländer V.
    Z Hautkr; 1977 Oct 15; 52(20):1017-25. PubMed ID: 144374
    [No Abstract] [Full Text] [Related]

  • 17. [Erythrodermia ichthyosiformis congenita bullosa brocq. on the so-called granular degeneration. I. Introduction and report of cases].
    Ishibashi Y, Klingmüller G.
    Arch Klin Exp Dermatol; 1968 May 09; 231(4):424-36. PubMed ID: 5696861
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. [Hereditary congenital hypotrichosis, Marie Unna type].
    Chlebarov S.
    Z Hautkr; 1985 Apr 01; 60(7):583-96. PubMed ID: 4002769
    [Abstract] [Full Text] [Related]

  • 20. [Aggressive eyelid basalioma with erythroderma ichthyosiforme congenita sicca].
    Strempel I.
    Ophthalmologica; 1978 Apr 01; 176(1):53-8. PubMed ID: 343031
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.