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 *

182 related articles for article (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; 97(44):2018-22. PubMed ID: 511082
    [TBL] [Abstract][Full Text] [Related]  

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

  • 5. [Congenital bullous ichthyosiform erythroderma (case 20)].
    Schnyder UW; Gloor M
    Z Hautkr; 1977 Aug; 52(15):809-11. PubMed ID: 331703
    [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; 75(2):186-9. PubMed ID: 9450882
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Hypotrichosis congenita hereditaria Maria Unna].
    Wirth G; Bindewald I; Küster W; Goerz G
    Hautarzt; 1985 Oct; 36(10):577-80. PubMed ID: 4066319
    [TBL] [Abstract][Full Text] [Related]  

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

  • 9. Hereditary hypotrichosis (Marie-Unna type) (two cases).
    Hutchinson PE; Wells RS
    Proc R Soc Med; 1975 Aug; 68(8):534-5. PubMed ID: 1202498
    [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; 104(1):58-9. PubMed ID: 320933
    [No Abstract]   [Full Text] [Related]  

  • 11. [On a case of clinical nonbullous form of erythrodermia ichthyosiformis congenita].
    Salamon T; Bogdanović B
    Z Haut Geschlechtskr; 1966 Aug; 41(4):125-31. PubMed ID: 5992174
    [No Abstract]   [Full Text] [Related]  

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

  • 13. Novel p.Glu519Gln missense mutation in ST14 in a patient with ichthyosis, follicular atrophoderma and hypotrichosis and review of the literature.
    Neri I; Virdi A; Tortora G; Baldassari S; Seri M; Patrizi A
    J Dermatol Sci; 2016 Jan; 81(1):63-6. PubMed ID: 26596219
    [No Abstract]   [Full Text] [Related]  

  • 14. [Ultrastructural characteristics of lamellar exfoliation of the newborn. Report of 2 cases].
    Iafusco F; Cuccurullo L; D'Avanzo M; Manocchio G
    Pediatria (Napoli); 1974 Oct; 82(3):447-56. PubMed ID: 4615293
    [No Abstract]   [Full Text] [Related]  

  • 15. Hereditary hypotrichosis. A previously undescribed syndrome.
    Bentley-Phillips B; Grace HJ
    Br J Dermatol; 1979 Sep; 101(3):331-9. PubMed ID: 508598
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Hereditary keratinization disorders and deafness].
    Voigtländer V
    Z Hautkr; 1977 Oct; 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; 231(4):424-36. PubMed ID: 5696861
    [No Abstract]   [Full Text] [Related]  

  • 18. Hair shaft abnormalities in localized autosomal recessive hypotrichosis 2 and a review of other non-syndromic human alopecias.
    Suga H; Tsunemi Y; Sugaya M; Shinkuma S; Akiyama M; Shimizu H; Sato S
    Acta Derm Venereol; 2011 Jun; 91(4):486-8. PubMed ID: 21537821
    [No Abstract]   [Full Text] [Related]  

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

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

    [Next]    [New Search]
    of 10.