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Journal Abstract Search
178 related items for PubMed ID: 4376705
1. 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; 10(12):133-6. PubMed ID: 4376705 [No Abstract] [Full Text] [Related]
2. [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; 64(12):675-9. PubMed ID: 6663565 [Abstract] [Full Text] [Related]
5. [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]
6. Symphalangism and brachydactyly syndrome: report of the WL symphalangism-brachydactyly syndrome: review of literature and classification. Herrmann J. Birth Defects Orig Artic Ser; 1974 Mar 31; 10(5):23-53. PubMed ID: 4469994 [No Abstract] [Full Text] [Related]
7. [A case of craniodiaphyseal dysplasia]. Itagaki Y, Sakamoto M, Nishitani H. No To Hattatsu; 1989 Jan 31; 21(1):69-73. PubMed ID: 2910334 [No Abstract] [Full Text] [Related]
8. [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]
9. [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 14; 147(3):278-82. PubMed ID: 2823332 [Abstract] [Full Text] [Related]
10. [Camurati-Engelmann syndrome in a 10-year-old girl]. Kubicz S. Pediatr Pol; 1981 Sep 14; 56(4):437-41. PubMed ID: 7267215 [No Abstract] [Full Text] [Related]
11. [Camurati-Engelmann disease. Review of the literature and a case contribution]. Gulino G, Gulino F, Grasso G. Chir Organi Mov; 1985 Sep 14; 70(1):81-9. PubMed ID: 4064808 [No Abstract] [Full Text] [Related]
12. [Transitory myelofibrosis in a case of diaphyseal dysplasia (Camurati-Engelmann's disease) (author's transl)]. Emons D, Hussel D, Bechrakis G, Födisch HJ. Rofo; 1978 Jan 14; 128(1):70-4. PubMed ID: 146665 [Abstract] [Full Text] [Related]
13. [Progressive diaphyseal dysplasia (report of 4 cases)]. Cao LB. Zhonghua Fang She Xue Za Zhi; 1982 Aug 14; 16(3):175-7. PubMed ID: 6217043 [No Abstract] [Full Text] [Related]
14. [Progressive diaphyseal dysplasia (Camurati-Engelmann syndrome). Early diagnosis in a 2-year-old child]. Orazi C, Barbuti D, Lembo A, Toniolo R, Vecchioli Scaldazza A. Radiol Med; 1994 Dec 14; 88(6):871-4. PubMed ID: 7878251 [No Abstract] [Full Text] [Related]
15. [Clinico-hematological and radiological aspects of Camurati-Engelmann disease]. Esposito L, Ferrara M, Pescatore L. Pediatria (Napoli); 1978 Mar 31; 86(1):89-101. PubMed ID: 683797 [No Abstract] [Full Text] [Related]
16. 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 Mar 31; (171):186-95. PubMed ID: 7140069 [No Abstract] [Full Text] [Related]
17. Radiology of the autosomal dominant form of craniometaphyseal dysplasia. Spiro PC, Hamersma H, Beighton P. S Afr Med J; 1975 May 17; 49(21):839-42. PubMed ID: 1135718 [Abstract] [Full Text] [Related]
18. Diaphyseal dysplasia. Late radiological discovery of 3 familial cases. Schollaert E, Pouders E, Matton P, Claessens H, Van de Velde E. J Belge Radiol; 1983 May 17; 66(2):93-9. PubMed ID: 6630143 [No Abstract] [Full Text] [Related]
19. Diaphyseal dysplasia [corrected] with anemia and thrombocytopenia. Bagga A, Choudhry VP. Indian Pediatr; 1989 Nov 17; 26(11):1162-3. PubMed ID: 2630482 [No Abstract] [Full Text] [Related]
20. Frontometaphyseal dysplasia: a progressive disease of bone and connective tissue. Danks DM, Mayne V. Birth Defects Orig Artic Ser; 1974 Nov 17; 10(12):57-60. PubMed ID: 4282264 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]