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Journal Abstract Search
221 related items for PubMed ID: 2823332
21. Camurati-Engelmann disease-a rare cause of tetany identified on bone scintigraphy: A case report. Xie P, Huang JM, Li HL, Huang XJ, Wei LG. Medicine (Baltimore); 2017 Jul; 96(27):e7141. PubMed ID: 28682867 [Abstract] [Full Text] [Related]
22. Cranio-meta-diaphyseal dysplasia: 25 year follow-up and review of literature. Dhar SU, Taylor T, Trinh C, Sutton VR. Am J Med Genet A; 2010 Sep; 152A(9):2335-8. PubMed ID: 20684007 [Abstract] [Full Text] [Related]
27. 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 Sep; 66(2):93-9. PubMed ID: 6630143 [No Abstract] [Full Text] [Related]
28. Camurati-Engelmann disease: contribution of bone scintigraphy to genetic counseling. Clybouw C, Desmyttere S, Bonduelle M, Piepsz A. Genet Couns; 1994 Sep; 5(2):195-8. PubMed ID: 7917133 [Abstract] [Full Text] [Related]
29. Camurati-Engelmann disease. Effects of corticosteroids. Heymans O, Gebhart M, Alexiou J, Sokolow Y. Acta Clin Belg; 1998 Jun; 53(3):189-92. PubMed ID: 9701854 [Abstract] [Full Text] [Related]
30. [A case of craniodiaphyseal dysplasia]. Itagaki Y, Sakamoto M, Nishitani H. No To Hattatsu; 1989 Jan; 21(1):69-73. PubMed ID: 2910334 [No Abstract] [Full Text] [Related]
31. MR of multiple cranial neuropathies in a patient with camurati-engelmann disease: case report. Applegate LJ, Applegate GR, Kemp SS. AJNR Am J Neuroradiol; 1991 Jan; 12(3):557-9. PubMed ID: 2058515 [No Abstract] [Full Text] [Related]
32. [Hyperostosis cranialis interna; a new syndrome with autosomal dominant inheritance]. Manni JJ, Scaf JJ, Huygen PL, Cruysberg JR, Verhagen WI. Ned Tijdschr Geneeskd; 1990 Sep 01; 134(35):1697-701. PubMed ID: 2215719 [Abstract] [Full Text] [Related]
34. Camurati-Engelmann Disease. Van Hul W, Boudin E, Vanhoenacker FM, Mortier G. Calcif Tissue Int; 2019 May 01; 104(5):554-560. PubMed ID: 30721323 [Abstract] [Full Text] [Related]
35. 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 01; 10(12):133-6. PubMed ID: 4376705 [No Abstract] [Full Text] [Related]
36. Neurotologic manifestations of the osteopetroses. Miyamoto RT, House WF, Brackmann DE. Arch Otolaryngol; 1980 Apr 01; 106(4):210-4. PubMed ID: 6244810 [Abstract] [Full Text] [Related]
37. [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 01; 34(1):71-3. PubMed ID: 2018262 [No Abstract] [Full Text] [Related]
38. [Otolaryngological aspects of Camurati-Engelmann disease (progressive diaphyseal dysplasia): review of literature and report of one case]. Paludetti G, Galli A, Lombardi R, Almadori G, Pujolas FX, Maurizi M. Acta Otorrinolaringol Esp; 1994 Jan 01; 45(3):207-13. PubMed ID: 8068367 [Abstract] [Full Text] [Related]