BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 6370402)

  • 1. Familial infantile cortical hyperostosis in a large Canadian family.
    Maclachlan AK; Gerrard JW; Houston CS; Ives EJ
    Can Med Assoc J; 1984 May; 130(9):1172-4. PubMed ID: 6370402
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Familial childhood cortical hyperostosis].
    Lacasa A; Vera F; Marzo L; Díaz N; Marco E; Ajada NT; Oliván MJ; Gonzalvo N; Buñuel C
    An Esp Pediatr; 1987 Jan; 26(1):44-6. PubMed ID: 3548517
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Endosteal hyperostosis with dominant transmission. Description of 8 cases in 3 generations of the same nuclear family].
    Moretti C; D'Osualdo F; Modesto A; Benedetti A; Corsi M
    Radiol Med; 1982; 68(3):151-8. PubMed ID: 7048438
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial infantile cortical hyperostosis: an update.
    Newberg AH; Tampas JP
    AJR Am J Roentgenol; 1981 Jul; 137(1):93-6. PubMed ID: 6787897
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial infantile cortical hyperostosis.
    Emmery L; Timmermans J; Christens J; Fryns JP
    Eur J Pediatr; 1983 Oct; 141(1):56-8. PubMed ID: 6357801
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Infantile cortical hyperostosis.
    Frána L; Sekanina M
    Arch Dis Child; 1976 Aug; 51(8):589-95. PubMed ID: 786183
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dominant mesomelic dysplasia, ankle, carpal, and tarsal synostosis type: a new autosomal dominant bone disorder.
    Kantaputra PN; Gorlin RJ; Langer LO
    Am J Med Genet; 1992 Dec; 44(6):730-7. PubMed ID: 1481840
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial congenital bowing of the tibia with pseudarthrosis and pectus excavatum: report of a kindred.
    Beals RK; Fraser W
    J Bone Joint Surg Am; 1976 Jun; 58(4):545-8. PubMed ID: 1270474
    [No Abstract]   [Full Text] [Related]  

  • 9. [Familial mesomelial dwarfism (Nievergelt syndrome)].
    Hess OM; Goebel NH; Streuli R
    Schweiz Med Wochenschr; 1978 Aug; 108(31):1202-6. PubMed ID: 675214
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Familial occurrence of infantile cortical hyperostosis. (Caffey-de Toni-Silvermann syndrome)].
    Pelikán L; Doubravský J; Mikes K; Cerný M
    Acta Chir Orthop Traumatol Cech; 1967 Oct; 34(5):430-4. PubMed ID: 4874755
    [No Abstract]   [Full Text] [Related]  

  • 11. Familial neonatal and infantile seizures: an autosomal-dominant disorder.
    Zonana J; Silvey K; Strimling B
    Am J Med Genet; 1984 Jul; 18(3):455-9. PubMed ID: 6476007
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial microtia in four generations with variable expressivity and incomplete penetrance in association with type I syndactyly.
    Balci S; Boduroğlu K; Kaya S
    Turk J Pediatr; 2001; 43(4):362-5. PubMed ID: 11765172
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Familial infantile cortical hyperostosis (author's transl)].
    Baldellou Vázquez A; Gomá Brufau A; Carreras Calvete A; Used Aznar MD; Gómez Beltrán JL
    An Esp Pediatr; 1979 Feb; 12(2):155-8. PubMed ID: 371475
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Absent tibiae--polydactyly--triphalangeal thumbs with fibular dimelia: variable expression of the Werner (McKusick 188770) syndrome?
    Vargas FR; Pontes RL; Llerena Júnior JC; de Almeida JC
    Am J Med Genet; 1995 Jan; 55(3):261-4. PubMed ID: 7726219
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recurrence of infantile cortical hyperostosis: a case report and review of the literature.
    Navarre P; Pehlivanov I; Morin B
    J Pediatr Orthop; 2013 Mar; 33(2):e10-7. PubMed ID: 23389580
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.
    Gensure RC; Mäkitie O; Barclay C; Chan C; Depalma SR; Bastepe M; Abuzahra H; Couper R; Mundlos S; Sillence D; Ala Kokko L; Seidman JG; Cole WG; Jüppner H
    J Clin Invest; 2005 May; 115(5):1250-7. PubMed ID: 15864348
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Recurrent familial neuropathy: report of one family].
    Hinault P; Menault F; Le Marec B; Sabouraud O
    J Genet Hum; 1981 Dec; 29(4):409-17. PubMed ID: 7328415
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neurological involvement in Worth type endosteal hyperostosis: report of a family.
    Adès LC; Morris LL; Burns R; Haan EA
    Am J Med Genet; 1994 May; 51(1):46-50. PubMed ID: 8030669
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal dominant inheritance with incomplete penetrance of Caffey disease (infantile cortical hyperostosis).
    Fried K; Manor A; Pajewski M; Starinsky R; Vure E
    Clin Genet; 1981 Apr; 19(4):271-4. PubMed ID: 7023758
    [No Abstract]   [Full Text] [Related]  

  • 20. Familial total anomalous pulmonary venous return: a large Utah-Idaho family.
    Bleyl S; Ruttenberg HD; Carey JC; Ward K
    Am J Med Genet; 1994 Oct; 52(4):462-6. PubMed ID: 7747759
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.