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Journal Abstract Search

164 related items for PubMed ID: 822473

  • 21. Genetic skeletal dysplasia in Thailand: the Siriraj experience.
    Wasant P, Waeteekul S, Rimoin DL, Lachman RS.
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():59-67. PubMed ID: 8629144
    [Abstract] [Full Text] [Related]

  • 22. [Study of congenital osteodystrophies. Considerations on 4 cases of Rathbun's hypophosphatasia and 7 unusual cases of rachitic osteodystrophy].
    Tirnoveanu G, Georgescu MI, Mitescu G.
    Rev Med Chir Soc Med Nat Iasi; 1972; 16(3):667-72. PubMed ID: 5080559
    [No Abstract] [Full Text] [Related]

  • 23. Cardiovascular manifestations of heritable disorders of connective tissue.
    Pyeritz RE.
    Prog Med Genet; 1983; 5():191-302. PubMed ID: 6407064
    [No Abstract] [Full Text] [Related]

  • 24. Biochemical abnormalities in osteogenesis imperfecta.
    Brown DM.
    Clin Orthop Relat Res; 1981 Sep; (159):75-9. PubMed ID: 7285472
    [Abstract] [Full Text] [Related]

  • 25. Eye signs of hypophosphatasia.
    Brenner RL, Smith JL, Cleveland WW, Bejar RL, Lockhart WS.
    Arch Ophthalmol; 1969 May; 81(5):614-7. PubMed ID: 4305610
    [No Abstract] [Full Text] [Related]

  • 26. Prenatal abnormal bone growth: a perspective.
    Rimoin DL.
    Prog Clin Biol Res; 1985 May; 187():131-40. PubMed ID: 3903758
    [No Abstract] [Full Text] [Related]

  • 27. [A syndrome of osteogenesis imperfecta, macrocephaly, wormian bones, frontal bossing, brachytelephalangy, hyperextensible joints, congenital blindness and oligophrenia in 3 sibs (author's transl)].
    Heide T.
    Klin Padiatr; 1981 Jul; 193(4):334-40. PubMed ID: 7265806
    [Abstract] [Full Text] [Related]

  • 28. [The establishment of osteogenesis imperfecta for personal identification].
    Osipenkova TK, Mikhaĭlova LN.
    Sud Med Ekspert; 1996 Jul; 39(2):21-6. PubMed ID: 8754511
    [Abstract] [Full Text] [Related]

  • 29. Craniofacial defects in the human skeletal dysplasias.
    Eteson DJ, Stewart RE.
    Birth Defects Orig Artic Ser; 1984 Jul; 20(3):19-45. PubMed ID: 6391575
    [Abstract] [Full Text] [Related]

  • 30. [Collagen metabolism in osteogenesis imperfecta].
    Balaba TIa, Furtseva LN, Nefed'eva NN.
    Vopr Med Khim; 1974 Jul; 20(5):471-6. PubMed ID: 4456796
    [No Abstract] [Full Text] [Related]

  • 31. Genetic skeletal dysplasias in the Museum of Pathological Anatomy, Vienna.
    Beighton P, Sujansky E, Patzak B, Portele KA.
    Am J Med Genet; 1993 Nov 01; 47(6):843-7. PubMed ID: 8279481
    [Abstract] [Full Text] [Related]

  • 32. [Pathologic anatomy of osteogenesis imperfecta. Light and electron microscopic studies of supportive tissue and skin].
    Stöss H.
    Veroff Pathol; 1990 Nov 01; 134():1-88. PubMed ID: 2385955
    [Abstract] [Full Text] [Related]

  • 33. [Genetic basis for skeletal disease. Dental management of patients with bone diseases].
    Shintani S, Ooshima T.
    Clin Calcium; 2010 Aug 01; 20(8):1259-65. PubMed ID: 20675938
    [Abstract] [Full Text] [Related]

  • 34. Histochemical, immunohistochemical, and lectin studies in undecalcified iliac crest growth plate in skeletal dysplasias.
    Horton WA.
    Prog Clin Biol Res; 1982 Aug 01; 104():401-10. PubMed ID: 6298816
    [No Abstract] [Full Text] [Related]

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  • 37. A new lethal brittle bone syndrome with increased amount of type V collagen in a patient.
    Bonaventure J, Zylberberg L, Cohen-Solal L, Allain JC, Lasselin C, Maroteaux P.
    Am J Med Genet; 1989 Jul 01; 33(3):299-310. PubMed ID: 2478018
    [Abstract] [Full Text] [Related]

  • 38. [Metabolic determined skeletal diseases].
    Swoboda W.
    Fortschr Geb Rontgenstrahlen Nuklearmed Erganzungsbd; 1969 Jul 01; 78():141-64. PubMed ID: 4393880
    [No Abstract] [Full Text] [Related]

  • 39. [Hereditary connective tissue diseases and arthropathy].
    Iizuka K, Murata K.
    Nihon Rinsho; 1975 Feb 10; 33(2):398-403. PubMed ID: 806718
    [No Abstract] [Full Text] [Related]

  • 40. [Effect of iron-deficient diets on the formation of bone tissue].
    Smoliar VI.
    Vopr Pitan; 1984 Feb 10; (5):55-9. PubMed ID: 6516286
    [Abstract] [Full Text] [Related]

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