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Journal Abstract Search

241 related items for PubMed ID: 619016

  • 1. Camurati-Engelmann disease (progressive hereditary craniodiaphyseal dysplasia). Case report.
    Yen JK, Bourke RS, Popp AJ, Wirth CR.
    J Neurosurg; 1978 Jan; 48(1):138-42. PubMed ID: 619016
    [Abstract] [Full Text] [Related]

  • 2. Engelmann's disease.
    Krohel GB, Wirth CR.
    Am J Ophthalmol; 1977 Oct; 84(4):520-5. PubMed ID: 910856
    [Abstract] [Full Text] [Related]

  • 3. Papilledema Treated by Cranial Expansion in a 5-Year-Old Boy with Camurati-Engelmann Syndrome.
    Chang MY, Borchert MS.
    Ophthalmology; 2019 Nov; 126(11):1579. PubMed ID: 31635703
    [No Abstract] [Full Text] [Related]

  • 4. [Diaphyseal dysplasia (Camurati-Engelmann syndrome) with progressive loss of vision: 30-year observations and the effect of prednisolone treatment (author's transl)].
    Kuhlencordt F, Kruse HP, Hellner KA, Montz R.
    Dtsch Med Wochenschr; 1981 May 08; 106(19):617-21. PubMed ID: 7215191
    [Abstract] [Full Text] [Related]

  • 5. [Value of various radiological study results in the follow-up of Camurati-Engelmann disease].
    Wilhelm KR, Lenarz T, Weise D, Baldauf G, Fritz P, Bihl H.
    Rofo; 1987 Sep 08; 147(3):278-82. PubMed ID: 2823332
    [Abstract] [Full Text] [Related]

  • 6. [Course of diaphyseal dysplasia. Camurati-Engelmann disease followed for 14 years].
    Marchal AL, Bretagne MC, Fourchy E, Olive D, Hoeffel JC.
    J Radiol; 1983 Dec 08; 64(12):675-9. PubMed ID: 6663565
    [Abstract] [Full Text] [Related]

  • 7. [Progressive diaphyseal dysplasia (report of 4 cases)].
    Cao LB.
    Zhonghua Fang She Xue Za Zhi; 1982 Aug 08; 16(3):175-7. PubMed ID: 6217043
    [No Abstract] [Full Text] [Related]

  • 8. [Camurati-Engelmann disease: description of a case in a child].
    Calandi C, Pacciani G, Silenzi M, Mannori C, Aulisi A, Adami-Lami Conti C.
    Radiol Med; 1980 Oct 08; 66(10):711-2. PubMed ID: 7221031
    [No Abstract] [Full Text] [Related]

  • 9. Unusual association between enchondroma and Camurati-Engelmann disease: a case report.
    Nagasawa H, Okada K, Nanjo H, Sasaki H, Chida S, Shimada Y.
    Ups J Med Sci; 2010 May 08; 115(2):157-60. PubMed ID: 19943817
    [Abstract] [Full Text] [Related]

  • 10. A generalized disorders of the connective tissues with progeria, choanal atresia, symphalangism, hypoplasia of dentine and craniodiaphyseal hypostosis.
    Lenz WD, Majewski F.
    Birth Defects Orig Artic Ser; 1974 May 08; 10(12):133-6. PubMed ID: 4376705
    [No Abstract] [Full Text] [Related]

  • 11. [Progressive diaphyseal dysplasia with unusual bone involvement (Camurati-Engelmann disease)].
    González Espinosa C, Pérez Albelo T, Cerrudo Hernández RC, Hernández González JR, Fernández J, Toledo Trujillo F.
    An Esp Pediatr; 1991 Jan 08; 34(1):71-3. PubMed ID: 2018262
    [No Abstract] [Full Text] [Related]

  • 12. [Camurati-Engelmann disease (progressive diaphyseal dysplasia). Differential diagnostic problems].
    Mastragelopulos N, Bähr R, Pfister U.
    Unfallchirurgie; 1989 Apr 08; 15(2):104-7. PubMed ID: 2734958
    [Abstract] [Full Text] [Related]

  • 13. Diaphyseal dysplasia (Engelmann) treated with corticosteroids.
    Lindstrom JA.
    Birth Defects Orig Artic Ser; 1974 Apr 08; 10(12):504-7. PubMed ID: 4461085
    [No Abstract] [Full Text] [Related]

  • 14. Progressive diaphyseal dysplasia: genetics and clinical and radiologic manifestations.
    Naveh Y, Kaftori JK, Alon U, Ben-David J, Berant M.
    Pediatrics; 1984 Sep 08; 74(3):399-405. PubMed ID: 6472973
    [Abstract] [Full Text] [Related]

  • 15. [Unusual case of hyperostosis of the type "cranio-diaphyseal dysplasia"].
    Menichini G, Scarfò GB, Cantore GP, Marchetti PG, Tomaccini D.
    Minerva Pediatr; 1977 Jul 14; 29(23):1485-97. PubMed ID: 895688
    [No Abstract] [Full Text] [Related]

  • 16. Cochlear implantation for auditory rehabilitation in Camurati-Engelmann disease.
    Friedland DR, Wackym PA, Rhee JS, Finn MS.
    Ann Otol Rhinol Laryngol; 2000 Feb 14; 109(2):160-2. PubMed ID: 10685567
    [Abstract] [Full Text] [Related]

  • 17. Diaphyseal dysplasia (englemann's syndrome). A case report demonstrating a deficiency in cortical haversian system formation.
    Wirth CR, Kay J, Bourke R.
    Clin Orthop Relat Res; 1982 Feb 14; (171):186-95. PubMed ID: 7140069
    [No Abstract] [Full Text] [Related]

  • 18. [Camurati-Engelmann disease (clinico-radiological contribution and chromosome study)].
    Di Gruttola G.
    Pediatria (Napoli); 1975 Mar 31; 83(1):1-19. PubMed ID: 1223730
    [No Abstract] [Full Text] [Related]

  • 19. [Diaphyseal dysplasia (Camurati-Engelmann)].
    Weickert H, Lehr H, Braun HS.
    Z Orthop Ihre Grenzgeb; 1983 Mar 31; 121(6):744-8. PubMed ID: 6421022
    [Abstract] [Full Text] [Related]

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