BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 198847)

  • 21. [A case of diffuse hyperostosis].
    du Lac Y; Bassi M; Mundler B; Tuot H
    Rev Rhum Mal Osteoartic; 1977 Mar; 44(3):175-81. PubMed ID: 191904
    [No Abstract]   [Full Text] [Related]  

  • 22. Clinical heterogeneity in the tricho-dento-osseous syndrome.
    Quattromani F; Shapiro SD; Young RS; Jorgenson RJ; Parker JW; Blumhardt R; Reece RR
    Hum Genet; 1983; 64(2):116-21. PubMed ID: 6885044
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Autosomal dominant inheritance of Caffey disease.
    Bull MJ; Feingold M
    Birth Defects Orig Artic Ser; 1974; 10(9):139-46. PubMed ID: 4609117
    [No Abstract]   [Full Text] [Related]  

  • 24. [Infanitle cortical hyperostosis. Apropos of a congenital chronic case].
    Corda R; Scano V
    Minerva Pediatr; 1968 Apr; 20(16):861-70. PubMed ID: 4906165
    [No Abstract]   [Full Text] [Related]  

  • 25. [Axial osteosclerosis with autosomal dominant transmission: a new entity?].
    Simon D; Cazalis P; Dryll A; Roland R; Bordier P; de Vernejoul MC; Ryckewaert A
    Rev Rhum Mal Osteoartic; 1979 Jun; 46(6):375-82. PubMed ID: 504945
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Facial paralysis at the age of 2 months as a first clinical sign of van Buchem disease (endosteal hyperostosis).
    Fryns JP; Van den Berghe H
    Eur J Pediatr; 1988 Jan; 147(1):99-100. PubMed ID: 3276528
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Osseous changes of osteopathia striata associated with cranial sclerosis. An autosomal dominant entity.
    Schnyder PA
    Skeletal Radiol; 1980 Feb; 5(1):19-22. PubMed ID: 7361120
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Osteomesopycnosis. A new case.
    Schmidt H; Mannkopf H; Ullrich K; von Lengerke HJ
    Pediatr Radiol; 1989; 19(6-7):489-92. PubMed ID: 2771500
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Acrodysostosis in two generations: an autosomal dominant syndrome.
    Hernández RM; Miranda A; Kofman-Alfaro S
    Clin Genet; 1991 May; 39(5):376-82. PubMed ID: 1860254
    [TBL] [Abstract][Full Text] [Related]  

  • 30. LRP5 high bone mass (Worth-type autosomal dominant endosteal hyperostosis): case report and historical review of the literature.
    De Mattia G; Maffi M; Mosca M; Mazzantini M
    Arch Osteoporos; 2023 Sep; 18(1):112. PubMed ID: 37659026
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Dentine dysplasia with sclerotic bone and skeletal anomalies inherited as an autosomal dominant trait. A new syndrome.
    Morris ME; Augsburger RH
    Oral Surg Oral Med Oral Pathol; 1977 Feb; 43(2):267-83. PubMed ID: 264650
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. [Pachydermoperiostosis (author's transl)].
    Fournier AM; Mourou M
    J Radiol Electrol Med Nucl; 1973 May; 54(5):417-23. PubMed ID: 4200551
    [No Abstract]   [Full Text] [Related]  

  • 34. Radiology of the autosomal dominant form of craniometaphyseal dysplasia.
    Spiro PC; Hamersma H; Beighton P
    S Afr Med J; 1975 May; 49(21):839-42. PubMed ID: 1135718
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hereditary hypophosphataemic rickets with autosomal recessive inheritance and severe osteosclerosis. A report of two cases.
    Perry W; Stamp TC
    J Bone Joint Surg Br; 1978 Aug; 60-B(3):430-4. PubMed ID: 681423
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Camurati-Engelmann disease. Genetics and clinical manifestations with a review of the literature.
    Sparkes RS; Graham CB
    J Med Genet; 1972 Mar; 9(1):73-85. PubMed ID: 5025487
    [No Abstract]   [Full Text] [Related]  

  • 37. [New cases of familial generalized cortical hyperostosis with dominant transmission (Worth's type) (author's transl)].
    Vayssairat M; Prier A; Meisel C; Camus JP; Grellet J
    J Radiol Electrol Med Nucl; 1976 Oct; 10(57):719-24. PubMed ID: 794463
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Differential diagnosis of an obscure bone disease in an infant rhesus monkey.
    Chesney CF; Hanlon GF; Scheffler G; Houser WD
    Lab Anim Sci; 1973 Jun; 23(3):414-22. PubMed ID: 4351482
    [No Abstract]   [Full Text] [Related]  

  • 39. Tricho-dento-osseous syndrome: a scanning electron microscopic analysis.
    Melnick M; Shields ED; El-Kafrawy AH
    Clin Genet; 1977 Jul; 12(1):17-27. PubMed ID: 891005
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Hyperostosis cranialis interna; a new syndrome with autosomal dominant inheritance].
    Manni JJ; Scaf JJ; Huygen PL; Cruysberg JR; Verhagen WI
    Ned Tijdschr Geneeskd; 1990 Sep; 134(35):1697-701. PubMed ID: 2215719
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.