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22. Osteogenesis imperfecta and hearing loss--description of three case reports. Pereira da Silva A; Feliciano T; Figueirinhas R; Almeida E Sousa C Acta Otorrinolaringol Esp; 2013; 64(6):423-7. PubMed ID: 24139453 [TBL] [Abstract][Full Text] [Related]
23. [Van der Hoeve's syndrome. Observation of a case]. Labayle J; Fleury P; Hamel S; Leclerc H Ann Otolaryngol Chir Cervicofac; 1971 Mar; 88(3):189-90. PubMed ID: 5552334 [No Abstract] [Full Text] [Related]
24. [Autosomal dominant keratoconus as the chief ocular symptom in Lobstein osteogenesis imperfecta tarda]. Beckh U; Schönherr U; Naumann GO Klin Monbl Augenheilkd; 1995 Apr; 206(4):268-72. PubMed ID: 7791289 [TBL] [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; 24(4):279-80. PubMed ID: 6454922 [No Abstract] [Full Text] [Related]
26. Blue sclerae in monozygotic twins: a family study of osteogenesis imperfecta in three generations. Jain SC; Shrivastva DK Eye Ear Nose Throat Mon; 1975 Oct; 54(10):385-6. PubMed ID: 1183547 [No Abstract] [Full Text] [Related]
27. [Familial occurrence of Ekman-Lebstein-van der Hoeve syndrome]. Pecoldowa K; Warchalewska-Pykalowa U Klin Oczna; 1970; 40(2):227-32. PubMed ID: 5446659 [No Abstract] [Full Text] [Related]
28. Low ocular rigidity in patients with osteogenesis imperfecta. Kaiser-Kupfer MI; McCain L; Shapiro JR; Podgor MJ; Kupfer C; Rowe D Invest Ophthalmol Vis Sci; 1981 Jun; 20(6):807-9. PubMed ID: 7239850 [TBL] [Abstract][Full Text] [Related]
29. A distinct dominant form of microtia and conductive hearing loss. Sánchez-Corona J; García-Cruz D; Ruenes R; Cantú JM Birth Defects Orig Artic Ser; 1982; 18(3B):211-6. PubMed ID: 7139104 [No Abstract] [Full Text] [Related]
30. Stapedectomy in Van der Hoeve's syndrome. Patterson CN; Stone HB Laryngoscope; 1970 Apr; 80(4):544-58. PubMed ID: 5440715 [No Abstract] [Full Text] [Related]
31. [The Van der Hoeve syndrome. (Clinical case report)]. Mensi E Minerva Nipiol; 1968; 18():Suppl 6:325+. PubMed ID: 5745334 [No Abstract] [Full Text] [Related]
32. [On the blue sclera syndrome]. Niurenberg OIu Vestn Oftalmol; 1966; 79(1):85-8. PubMed ID: 5982238 [No Abstract] [Full Text] [Related]
33. [A case of Lobstein's osteopsathyrosis]. Iordănescu C; Dogan D; Nicolae S; Burnei D; Cioablă D Oftalmologia; 1995; 39(3):235-8. PubMed ID: 7654677 [TBL] [Abstract][Full Text] [Related]
34. [Clinical and radiological considerations on 12 cases, belonging to 2 families, of osteogenesis imperfecta, delayed type]. Cometa F; Scaglioso C; Scianaro L; Cassone L; Loiodice G Minerva Pediatr; 1981 Feb; 33(3):135-40. PubMed ID: 7017371 [No Abstract] [Full Text] [Related]
35. [Case of Ekman-Lobstein-van der Hoeve syndrome with bilateral glaucoma and right-sided thrombosis of the central retinal vein]. Smolińska K; Olbromska W Pol Tyg Lek; 1977 May; 32(22):843-4. PubMed ID: 887490 [No Abstract] [Full Text] [Related]
36. [Van der Hoeve (Lobstein) and Marfan syndrome in brother and sister]. Felsch G; Neumann W; Neumann M Z Arztl Fortbild (Jena); 1972 Mar; 66(5):280-3. PubMed ID: 5039035 [No Abstract] [Full Text] [Related]
37. [Osteogenesis imperfecta and blue sclera. Presentation of 2 cases]. GURFINKEL M; NISKIER M; DAIHA FA; SANTOS DG; NACHEF JN Med Cir Farm; 1961; 292():96-108. PubMed ID: 13709862 [No Abstract] [Full Text] [Related]
38. [Syndrome of the blue sclera (Van der Hoeve-Lobstein)]. Kojić M Med Pregl; 1976; 29(3-4):143-5. PubMed ID: 1272201 [No Abstract] [Full Text] [Related]
39. Blue sclerae and keratoconus: key features of a distinct heritable disorder of connective tissue. Greenfield G; Stein R; Romano A; Goodman RM Clin Genet; 1973; 4(1):8-16. PubMed ID: 4691558 [No Abstract] [Full Text] [Related]
40. Audiometric, surgical, and genetic findings in 15 ears of patients with osteogenesis imperfecta. Swinnen FK; De Leenheer EM; Coucke PJ; Cremers CW; Dhooge IJ Laryngoscope; 2009 Jun; 119(6):1171-9. PubMed ID: 19358256 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]