BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 9268107)

  • 1. 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]  

  • 2. 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]  

  • 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. [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]  

  • 5. Camurati-Engelmann disease: contribution of bone scintigraphy to genetic counseling.
    Clybouw C; Desmyttere S; Bonduelle M; Piepsz A
    Genet Couns; 1994; 5(2):195-8. PubMed ID: 7917133
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. [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]  

  • 8. 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]  

  • 9. Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family.
    Simsek S; Janssens K; Kwee ML; Van Hul W; Veenstra J; Netelenbos JC
    Osteoporos Int; 2005 Sep; 16(9):1167-70. PubMed ID: 15959620
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Camurati-Engelmann disease type II: progressive diaphyseal dysplasia with striations of the bones.
    Nishimura G; Nishimura H; Tanaka Y; Makita Y; Ikegawa S; Ghadami M; Kinoshita A; Niikawa N
    Am J Med Genet; 2002 Jan; 107(1):5-11. PubMed ID: 11807860
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13.
    Janssens K; Gershoni-Baruch R; Van Hul E; Brik R; Guañabens 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]  

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

  • 13. Scintigraphic evaluation of pamidronate and corticosteroid therapy in a patient with progressive diaphyseal dysplasia (Camurati-Engelmann disease).
    Inaoka T; Shuke N; Sato J; Ishikawa Y; Takahashi K; Aburano T; Makita Y
    Clin Nucl Med; 2001 Aug; 26(8):680-2. PubMed ID: 11452173
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1-q13.3.
    Ghadami M; Makita Y; Yoshida K; Nishimura G; Fukushima Y; Wakui K; Ikegawa S; Yamada K; Kondo S; Niikawa N; Tomita Ha
    Am J Hum Genet; 2000 Jan; 66(1):143-7. PubMed ID: 10631145
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Camurati-Engelmann disease--a rare cause of bone pain.
    Mundra V; Taxel P
    Conn Med; 2012 Jan; 76(1):33-7. PubMed ID: 22372177
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Camurati-Engelmann disease (progressive diaphyseal dysplasia): reports of an Indian kindred.
    Bhadada SK; Sridhar S; Steenackers E; Dhiman V; Mortier G; Bhansali A; Van Hul W
    Calcif Tissue Int; 2014 Feb; 94(2):240-7. PubMed ID: 24154985
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Progressive diaphyseal dysplasia mimicking childhood myopathy: clinical and biochemical response to prednisolone.
    Low LC; Stephenson JB; Stuart-Smith DA
    Aust Paediatr J; 1985 Aug; 21(3):193-6. PubMed ID: 4062720
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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; 106(19):617-21. PubMed ID: 7215191
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The first Korean case of Camurati-Engelmann disease (progressive diaphyseal dysplasia) confirmed by TGFB1 gene mutation analysis.
    Park SJ; Yoon CS; Park HW; Choi JR; Chung JS; Lee KA
    J Korean Med Sci; 2009 Aug; 24(4):737-40. PubMed ID: 19654961
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 8.