These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 7205902)

  • 1. A family with diaphyseal aclasis and peripheral dysostosis.
    Brooks AP; Wynne-Davies R
    J Med Genet; 1980 Aug; 17(4):277-80. PubMed ID: 7205902
    [TBL] [Abstract][Full Text] [Related]  

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

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

  • 4. Tumoral calcinosis and Engelmann disease.
    Thurmon TF; Jackson J
    Birth Defects Orig Artic Ser; 1976; 12(5):321-5. PubMed ID: 953237
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dominantly inherited craniodiaphyseal dysplasia: a new craniotubular dysplasia.
    Schaefer B; Stein S; Oshman D; Rennert O; Thurnau G; Wall J; Bodensteiner J; Brown O
    Clin Genet; 1986 Nov; 30(5):381-91. PubMed ID: 3802557
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Marked phenotypic variability in progressive diaphyseal dysplasia (Camurati-Engelmann disease): report of a four-generation pedigree, identification of a mutation in TGFB1, and review.
    Wallace SE; Lachman RS; Mekikian PB; Bui KK; Wilcox WR
    Am J Med Genet A; 2004 Sep; 129A(3):235-47. PubMed ID: 15326622
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Craniofacial dysostosis with diaphyseal hyperplasia].
    Maximilian C; Dumitriu L; Ioanitiu D; Ispas I; Firu P; Ciovirnache M; Duca D
    J Genet Hum; 1981 Jun; 29(2):129-39. PubMed ID: 7328407
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Case report 202. Engelmann disease of bone (diaphyseal dysplasia) with bilateral shortened fibulae.
    Crisp AJ; Brenton DP; Shaw DG
    Skeletal Radiol; 1982; 8(3):239-40. PubMed ID: 7112156
    [No Abstract]   [Full Text] [Related]  

  • 9. Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13.
    Janssens K; Gershoni-Baruch R; Van Hul E; Brik R; GuaƱabens N; Migone N; Verbruggen LA; Ralston SH; Bonduelle M; Van Maldergem L; Vanhoenacker F; Van Hul W
    J Med Genet; 2000 Apr; 37(4):245-9. PubMed ID: 10745041
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Progressive diaphyseal dysplasia: a three-generation family with markedly variable expressivity.
    Saraiva JM
    Am J Med Genet; 1997 Aug; 71(3):348-52. PubMed ID: 9268107
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Case of progressive diaphyseal dysplasia (Engelmann) presenting with trigeminal neuropathy and hearing disorder].
    Mineta Y; Kakigi R; Oda K; Okue A; Shibasaki H
    Rinsho Shinkeigaku; 1983 Aug; 23(8):700-5. PubMed ID: 6661872
    [No Abstract]   [Full Text] [Related]  

  • 12. [Observations on Camurati-Engelmann's disease (author's transl)].
    Grossmann I; Grossmann P; Trzenschik K; Wolf S; Nitz I
    Radiol Diagn (Berl); 1980; 21(2):221-6. PubMed ID: 7444033
    [No Abstract]   [Full Text] [Related]  

  • 13. Radiology of the autosomal dominant form of craniometaphyseal dysplasia.
    Spiro PC; Hamersma H; Beighton P
    S Afr Med J; 1975 May; 49(21):839-42. PubMed ID: 1135718
    [TBL] [Abstract][Full Text] [Related]  

  • 14. New skeletal dysplasia with unique brachydactyly.
    Mononen TK; Karnes PS; Senac MO; Falk RE
    Am J Med Genet; 1992 Mar; 42(5):706-13. PubMed ID: 1632443
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial occurrence of a syndrome with mental retardation, nasal hypoplasia, peripheral dysostosis, and blue eyes in Japanese siblings.
    Niikawa N; Matsuda I; Ohsawa T; Kajii T
    Hum Genet; 1978 Jun; 42(2):227-32. PubMed ID: 669707
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Progressive diaphyseal dysplasia (Engelmann disease(: scintigraphic-radiographic-clinical correlations.
    Kumar B; Murphy WA; Whyte MP
    Radiology; 1981 Jul; 140(1):87-92. PubMed ID: 6454165
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Anticipation in progressive diaphyseal dysplasia.
    Saraiva JM
    J Med Genet; 2000 May; 37(5):394-5. PubMed ID: 10905898
    [No Abstract]   [Full Text] [Related]  

  • 18. [Familial progressive diaphyseal dysplasia (Engelmann's disease)].
    Qu H
    Zhonghua Fang She Xue Za Zhi; 1985 Feb; 19(1):25-7. PubMed ID: 3158492
    [No Abstract]   [Full Text] [Related]  

  • 19. 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; 66(2):93-9. PubMed ID: 6630143
    [No Abstract]   [Full Text] [Related]  

  • 20. Engelmann--Camurati disease.
    Dharmadasa K; Mendis BL; Karunanayake R; de Silva SP
    Ceylon Med J; 1981 Dec; 26(4):178-9. PubMed ID: 7348614
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.