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 *

159 related articles for article (PubMed ID: 418998)

  • 1. [Additional comments on the differential diagnosis of rare bone diseases (author's transl)].
    Engels M; Höger AM
    Padiatr Padol; 1979; 14(1):75-81. PubMed ID: 418998
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Chondrodystrophia calcificans congenita (Conradi-Hünermann syndrome). A case report (author's transl)].
    Vanĕk J; Losan F
    Acta Chir Orthop Traumatol Cech; 1978 Feb; 45(1):6-9. PubMed ID: 654821
    [No Abstract]   [Full Text] [Related]  

  • 3. [Localized stippled epiphyses and dysmorphia of the nose (minor form of Conradi Hünermann disease). (author's transl)].
    BETOULIERES P; Ferran JL; Bassini P; Del Socorro P; Bonnet H; Jean R
    J Radiol Electrol Med Nucl; 1974 Dec; 55(12):877-81. PubMed ID: 4455873
    [No Abstract]   [Full Text] [Related]  

  • 4. [Chondrodysplasia punctata (the Conradi-Hünermann syndrome). A clinical case report and review of the literature].
    Omobono E; Goetsch W
    Minerva Pediatr; 1993 Mar; 45(3):117-21. PubMed ID: 8341225
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Rhizomelic type of chondrodysplasia punctata in 2 sisters. Evidence for hereditary transmission of a recessive autosomic type].
    Fabris C; Licata D; Martano C; Silengo M; Franceschini P
    Minerva Pediatr; 1981 Jan; 33(2):81-5. PubMed ID: 7242481
    [No Abstract]   [Full Text] [Related]  

  • 6. Serum lipid analysis confirms the diagnosis of X-linked dominant chondrodysplasia punctata - Conradi-Hünermann-Happle syndrome.
    Lindenthal B; Repgen R; Emons D; Lentze MJ; von Bergmann K; Lütjohann D
    Klin Padiatr; 2004; 216(2):67-9. PubMed ID: 15106076
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Infantile thoracic dystrophy.
    Say B; Balci S; Tunçbilek E; Pirnar T
    Turk J Pediatr; 1969 Jul; 11(3):120-6. PubMed ID: 5392658
    [No Abstract]   [Full Text] [Related]  

  • 8. [Cataract in chondrodystrophia calcificans congenita (Conradi-Hünermann syndrome)].
    Thiel HJ; Manzke H; Gunschera H
    Klin Monbl Augenheilkd; 1969 Apr; 154(4):536-45. PubMed ID: 5354428
    [No Abstract]   [Full Text] [Related]  

  • 9. [Description of a case of the Conradi-Hunermann syndrome (congenital calcifying dystrophy)].
    Verrengia D; Coppola V; Lilli C; Gatta T; Rossi R; Scozia P
    Minerva Pediatr; 1982 May; 34(9):421-6. PubMed ID: 7121440
    [No Abstract]   [Full Text] [Related]  

  • 10. Guess what! X-linked dominant chondrodysplasia punctata (Conradi-Hünermann-Happle Syndrome).
    Krisp A; König A; Hoffmann R; Happle R
    Eur J Dermatol; 2001; 11(4):389-91. PubMed ID: 11458930
    [No Abstract]   [Full Text] [Related]  

  • 11. [Conradi-Hünermann-Happle syndrome].
    Bukkems SF; Ijspeert WJ; Vreenurg M; van Rhijn LW; Schrander JJ; van Steensel MA
    Ned Tijdschr Geneeskd; 2012; 156(10):A4105. PubMed ID: 22394443
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Normal peroxisomal function and absent skeletal manifestations in Conradi-Hünermann syndrome.
    Prendiville JS; Zaparackas ZG; Esterly NB
    Arch Dermatol; 1991 Apr; 127(4):539-42. PubMed ID: 2006879
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chondrodystrophia calcificans congenita (the conradi-hunermann syndrome). Report of a case recognized antenatally.
    Hyndman WB; Alexander DS; Mackie KW
    Clin Pediatr (Phila); 1976 Apr; 15(4):311-21. PubMed ID: 1253511
    [No Abstract]   [Full Text] [Related]  

  • 14. Chondrodysplasia punctata--Conradi Hunermann syndrome.
    Reddeppa T; Rao KS; Ramachandra S; Gurunadh VS; Datta V
    Indian Pediatr; 1991 Aug; 28(8):934-6. PubMed ID: 1808084
    [No Abstract]   [Full Text] [Related]  

  • 15. [Congenital epiphyseal chondrodysplasia punctata. Study of 9 cases].
    Frontera Izquierdo P; Cabezuelo Huerta G; Malo Concepción P
    An Esp Pediatr; 1985 Sep; 23(3):175-82. PubMed ID: 4073686
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Chondrodystrophia calcificans congenita observed during six years (author's transl)].
    Scheibenreiter S; Melzer E
    Padiatr Padol; 1982; 17(2):521-8. PubMed ID: 7099698
    [No Abstract]   [Full Text] [Related]  

  • 17. [Conradi-Hünermann syndrome in a newborn infant].
    Maszkiewicz W; Kagan-Sypula I; Ginczewska T
    Pediatr Pol; 1978 Jul; 53(7):889-92. PubMed ID: 693139
    [No Abstract]   [Full Text] [Related]  

  • 18. [A contribution to chondrodystrophia calcificans congenita].
    Kaufmann J
    Monatsschr Kinderheilkd (1902); 1965 Oct; 113(10):589-91. PubMed ID: 5881764
    [No Abstract]   [Full Text] [Related]  

  • 19. Metaphyseal chondrodysplasia calcificans. A report on two cases.
    van Creveld S; Kozlowski K; Pietron K; van der Valk A
    Br J Radiol; 1971 Oct; 44(526):773-9. PubMed ID: 4256065
    [No Abstract]   [Full Text] [Related]  

  • 20. [Histological ocular findings in chondrodystrophia calcificans congenita (Conradi-Hünermann syndrome)].
    Heimann K
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1968; 68():444-51. PubMed ID: 5756820
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.