129 related articles for article (PubMed ID: 7023758)
41. Infantile cortical hyperostosis.
Ho KK
P N G Med J; 1976 Sep; 18(3):183-5. PubMed ID: 779336
[TBL] [Abstract][Full Text] [Related]
42. Idiopathic cortical hyperostosis.
Jones ET; Hensinger RN; Holt JF
Clin Orthop Relat Res; 1982 Mar; (163):210-3. PubMed ID: 7039916
[TBL] [Abstract][Full Text] [Related]
43. [Familial facial paralysis. Generalised cortical hyperostosis (author's transl)].
Forest H; Mardel C; Goujard P; Blum F; Diehly A
Ann Otolaryngol Chir Cervicofac; 1979 Dec; 96(12):919-23. PubMed ID: 394647
[TBL] [Abstract][Full Text] [Related]
44. [Generalized hyperostosis corticalis (dominant transmission) (Worth's type)].
Maroteaux P; Fontaine G; Scharfman W; Farriaux JP
Arch Fr Pediatr; 1971; 28(7):685-98. PubMed ID: 4942110
[No Abstract] [Full Text] [Related]
45. Caffey disease: an unlikely collagenopathy.
Glorieux FH
J Clin Invest; 2005 May; 115(5):1142-4. PubMed ID: 15864344
[TBL] [Abstract][Full Text] [Related]
46. INFANTILE CORTICAL HYPEROSTOSIS (CAFFEY-SMYTH SYNDROME).
CYPRESS GC
J Natl Med Assoc; 1964 Mar; 56(2):124-6. PubMed ID: 14129745
[No Abstract] [Full Text] [Related]
47. Neurological involvement in Worth type endosteal hyperostosis: report of a family.
Adès LC; Morris LL; Burns R; Haan EA
Am J Med Genet; 1994 May; 51(1):46-50. PubMed ID: 8030669
[TBL] [Abstract][Full Text] [Related]
48. [Infantile cortical hyperostosis].
Mitsui T; Tanaka H; Nishida M
Seikei Geka; 1967 Nov; 18(13):1165-73. PubMed ID: 4872520
[No Abstract] [Full Text] [Related]
49. Infantile cortical hyperostosis with raised immunoglobulins.
Mainardi PC
Arch Dis Child; 1979 Dec; 54(12):985. PubMed ID: 394687
[No Abstract] [Full Text] [Related]
50. [INFANTILE CORTICAL HYPEROSTOSIS OR CAFFEY-DE TONI DISEASE. PRESENTATION OF 2 CASES SEEN IN COLOMBIA AND REVIEW OF THE LITERATURE].
MORILLO G; SABOGAL E; MELO D
Rev Soc Colomb Pediatr Pueric; 1964 Apr; 6():287-316. PubMed ID: 14153057
[No Abstract] [Full Text] [Related]
51. Infantile cortical hyperostosis.
Dutta S; Jain N; Bhattacharya A; Mukhopadhyay K
Indian Pediatr; 2005 Jan; 42(1):64-6. PubMed ID: 15695863
[TBL] [Abstract][Full Text] [Related]
52. A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2.
Isojima T; Doi K; Mitsui J; Oda Y; Tokuhiro E; Yasoda A; Yorifuji T; Horikawa R; Yoshimura J; Ishiura H; Morishita S; Tsuji S; Kitanaka S
J Bone Miner Res; 2014 Apr; 29(4):992-8. PubMed ID: 23996431
[TBL] [Abstract][Full Text] [Related]
53. Letter: Infantile cortical hyperostosis--familial occurrence in a mother and daughter.
Langewisch WH
J Pediatr; 1975 Aug; 87(2):323-4. PubMed ID: 1097622
[No Abstract] [Full Text] [Related]
54. [Infantile cortical hyperostosis (Caffey-Silverman syndrome): report of 5 new cases].
Snobl O; Tláskal P; Lisá L
Cesk Pediatr; 1978 Apr; 33(4):215-8. PubMed ID: 357026
[No Abstract] [Full Text] [Related]
55. [Familial infantile cortical hyperostosis with prenatal beginning].
Schärer K; Szabó J
Fortschr Geb Rontgenstr Nuklearmed; 1966 Aug; 105(2):154-63. PubMed ID: 4891339
[No Abstract] [Full Text] [Related]
56. Van Buchem's disease (hyperostosis corticalis generalisata).
Owen RH
Br J Radiol; 1976 Feb; 49(578):126-32. PubMed ID: 181111
[TBL] [Abstract][Full Text] [Related]
57. Infantile cortical hyperostosis (Caffey-Smyth syndrome): report of four cases.
BOGERT J
J Oral Surg Anesth Hosp Dent Serv; 1962 Jan; 20():67-71. PubMed ID: 13870578
[No Abstract] [Full Text] [Related]
58. [Infantile cortical hyperostosis (Caffey-de Toni-Silverman disease)].
Mensi E
Minerva Nipiol; 1968; 18():Suppl 6:247+. PubMed ID: 4910413
[No Abstract] [Full Text] [Related]
59. [Caffey disease. A case report].
Alvear-Pineda JA; Cortés-Gómez J
Acta Ortop Mex; 2013; 27(2):114-8. PubMed ID: 24701763
[TBL] [Abstract][Full Text] [Related]
60. Prenatal cortical hyperostosis (Caffey disease) with Down syndrome.
Kroon ND; Smith F; Sanghavi R; Sarkar P
J Obstet Gynaecol; 2009 Jan; 29(1):57-8. PubMed ID: 19280500
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
