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Journal Abstract Search

118 related items for PubMed ID: 5360577

  • 21. [Case of Van der Hoeve syndrome complicated by a defect of the primary ostium of the auricular septum].
    Niki T, Yokoyama Y, Kawamata K, Izumi K.
    Nihon Rinsho; 1967 Nov; 25(11):2611-6. PubMed ID: 5628392
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
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  • 23. [Van der Hoeve's syndrome].
    Lur'e IV, Aleĭnik VN.
    Klin Med (Mosk); 1969 Mar; 47(3):143-6. PubMed ID: 5406817
    [No Abstract] [Full Text] [Related]

  • 24. [Van der Hoeve's syndrome].
    Kalmykov IF.
    Klin Med (Mosk); 1975 Mar; 53(3):141-2. PubMed ID: 1117677
    [No Abstract] [Full Text] [Related]

  • 25. [Heredity in the Van der Hoeve syndrome].
    Constantin C.
    Rev Chir Oncol Radiol O R L Oftalmol Stomatol Ser Oftalmol; 1980 Mar; 24(4):279-80. PubMed ID: 6454922
    [No Abstract] [Full Text] [Related]

  • 26.
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  • 27. [Case of van der Hoeve's syndrome].
    Aluffi E, Gandolfi G, Ferrari F, Actis G.
    Ann Osp Maria Vittoria Torino; 1981 Mar; 24(1-6):3-12. PubMed ID: 7340667
    [No Abstract] [Full Text] [Related]

  • 28. Osteogenesis imperfecta and hearing loss.
    Verstreken M, Claes J, Van de Heyning PH.
    Acta Otorhinolaryngol Belg; 1996 Mar; 50(2):91-8. PubMed ID: 8767251
    [Abstract] [Full Text] [Related]

  • 29. [van der Hoeve's syndrome].
    Komatsuzaki A.
    Nihon Rinsho; 1977 Mar; 35 Suppl 1():1286-7. PubMed ID: 612822
    [No Abstract] [Full Text] [Related]

  • 30.
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  • 32. Osteogenesis imperfecta of the temporal bone: CT and MR imaging in Van der Hoeve-de Kleyn syndrome.
    Alkadhi H, Rissmann D, Kollias SS.
    AJNR Am J Neuroradiol; 2004 Mar; 25(6):1106-9. PubMed ID: 15205159
    [Abstract] [Full Text] [Related]

  • 33. Identification of two recurrent mutations of COL1A1 gene in Chinese Van der Hoeve syndrome patients.
    Duan H, Yan Z, Lu Y, Cheng J, Zhang D, Yuan H, Han D.
    Acta Otolaryngol; 2016 Aug; 136(8):786-91. PubMed ID: 27044453
    [Abstract] [Full Text] [Related]

  • 34. [A case of Ekman-Eddowes-van der Hoeve syndrome with coexistent pigmented nevus of the choroid].
    Goryszewska-Maciochowa H, Kornacki B.
    Klin Oczna; 1985 Jan; 87(1):17-9. PubMed ID: 4046466
    [No Abstract] [Full Text] [Related]

  • 35. Surgical and histological findings of the stapes associated with Van der Hoeve syndrome in a Japanese boy.
    Morimitsu T, Hayashida K.
    ORL J Otorhinolaryngol Relat Spec; 1973 Jan; 35(6):342-9. PubMed ID: 4797685
    [No Abstract] [Full Text] [Related]

  • 36. Cochlear implantation in a patient with osteogenesis imperfecta and otospongiosis.
    Huang TS, Yen PT, Liu SY.
    Am J Otolaryngol; 1998 Jan; 19(3):209-12. PubMed ID: 9617935
    [Abstract] [Full Text] [Related]

  • 37. [Chromosomal study in otosclerosis and in van der Hoeve de Kleyn's syndrome].
    Cada K, Soudek D.
    Cesk Otolaryngol; 1968 Oct; 17(5):285-7. PubMed ID: 5727172
    [No Abstract] [Full Text] [Related]

  • 38. [The experience in surgical treatment of hearing loss in Van der Hoeve patients].
    Anikin IA, Astashchenko SV, Sugarova SB, Kaliapin DD.
    Vestn Otorinolaringol; 2021 Oct; 86(1):6-10. PubMed ID: 33720643
    [Abstract] [Full Text] [Related]

  • 39. [Deafness in osteogenesis imperfecta (author's transl)].
    Müller E.
    Laryngol Rhinol Otol (Stuttg); 1974 Nov; 53(11):805-9. PubMed ID: 4456086
    [No Abstract] [Full Text] [Related]

  • 40. [The blue sclera syndrome (Van der Heave syndrome)].
    Alikadić-Husović A, Merhemić Z.
    Med Arh; 2000 Nov; 54(5-6):325-6. PubMed ID: 11219919
    [Abstract] [Full Text] [Related]

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