BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 31990479)

  • 21. Osteopoikilosis: report of a familial case and review of the literature.
    Korkmaz MF; Elli M; Özkan MB; Bilgici MC; Dağdemir A; Korkmaz M; Tosun FC
    Rheumatol Int; 2015 May; 35(5):921-4. PubMed ID: 25352085
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Buschke-Ollendorff syndrome with striking phenotypic variation resulting from a novel c.2203C>T nonsense mutation in LEMD3.
    Yuste-Chaves M; Cañueto J; Santos-Briz Á; Ciria S; González-Sarmiento R; Unamuno P
    Pediatr Dermatol; 2011; 28(4):447-50. PubMed ID: 20678097
    [TBL] [Abstract][Full Text] [Related]  

  • 23. RNA recognition motif of LEMD3 as a key player in the pathogenesis of Buschke-Ollendorff syndrome.
    Takashima S; Fujita Y; Suzuki S; Saito N; Shinkuma S; Nomura T; Shimizu H
    J Dermatol Sci; 2016 Mar; 81(3):205-8. PubMed ID: 26711937
    [No Abstract]   [Full Text] [Related]  

  • 24. Osteopoikilosis: A rare cause of bone pain.
    Mahbouba J; Mondher G; Amira M; Walid M; Naceur B
    Caspian J Intern Med; 2015; 6(3):177-9. PubMed ID: 26644888
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mutation in LEMD3 (Man1) Associated with Osteopoikilosis and Late-Onset Generalized Morphea: A New Buschke-Ollendorf Syndrome Variant.
    Korman B; Wei J; Laumann A; Ferguson P; Varga J
    Case Rep Dermatol Med; 2016; 2016():2483041. PubMed ID: 27382493
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Buschke-Ollendorff syndrome with LEMD3 germline stopgain mutation p.R678* presenting as multiple subcutaneous nodules with mucin deposition.
    Xu Z; Yang C; Xue R
    J Cutan Pathol; 2021 Jan; 48(1):77-80. PubMed ID: 32519343
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Modeling-based bone formation transforms trabeculae to cortical bone in the sclerotic areas in Buschke-Ollendorff syndrome. A case study of two females with LEMD3 variants.
    Frost M; Rahbek ET; Ejersted C; Høilund-Carlsen PF; Bygum A; Thomsen JS; Andreasen CM; Andersen TL; Frederiksen AL
    Bone; 2020 Jun; 135():115313. PubMed ID: 32151766
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Familial osteopoikilosis.
    Boyaci A; Boyaci N; Tutoglu A
    J Back Musculoskelet Rehabil; 2013; 26(3):247-50. PubMed ID: 23893138
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Buschke-Ollendorff syndrome in a three-generation family: influence of a novel LEMD3 mutation to tropoelastin expression.
    Burger B; Hershkovitz D; Indelman M; Kovac M; Galambos J; Haeusermann P; Sprecher E; Itin PH
    Eur J Dermatol; 2010; 20(6):693-7. PubMed ID: 20732851
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification of a Novel Point Mutation in the LEMD3 Gene in an Infant With Buschke-Ollendorff Syndrome.
    Kratzsch J; Mitter D; Ziemer M; Kohlhase J; Voth H
    JAMA Dermatol; 2016 Jul; 152(7):844-5. PubMed ID: 27007781
    [No Abstract]   [Full Text] [Related]  

  • 31. Buschke-Ollendorff syndrome: a manifestation of a heterozygous nonsense mutation in the LEMD3 gene.
    Gass JK; Hellemans J; Mortier G; Griffiths M; Burrows NP
    J Am Acad Dermatol; 2008 May; 58(5 Suppl 1):S103-4. PubMed ID: 18489034
    [No Abstract]   [Full Text] [Related]  

  • 32. Buschke-Ollendorff syndrome associated with hypertrophic scar formation: a possible role for LEMD3 mutation.
    Korekawa A; Nakano H; Toyomaki Y; Takiyoshi N; Rokunohe D; Akasaka E; Nakajima K; Sawamura D
    Br J Dermatol; 2012 Apr; 166(4):900-3. PubMed ID: 21985280
    [No Abstract]   [Full Text] [Related]  

  • 33. [Buschke-Ollendorff syndrome: inactivating mutation of the LEMD3 gene].
    Dereure O
    Ann Dermatol Venereol; 2005; 132(6-7 Pt 1):593. PubMed ID: 16142115
    [No Abstract]   [Full Text] [Related]  

  • 34. [Osteopoikilosis--case report].
    Vukić D; Janjić D; Ercegan G; Bojat V
    Med Pregl; 1993; 46(7-8):261-3. PubMed ID: 7968821
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A rare benign disorder mimicking metastasis on radiographic examination: a case report of osteopoikilosis.
    Ozdemirel AE; Cakit BD; Erdem HR; Koc B
    Rheumatol Int; 2011 Aug; 31(8):1113-6. PubMed ID: 21120491
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Melorheostosis in a family with autosomal dominant osteopoikilosis.
    Nevin NC; Thomas PS; Davis RI; Cowie GH
    Am J Med Genet; 1999 Feb; 82(5):409-14. PubMed ID: 10069713
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Osteopoikilosis: a case with osteopenia.
    Kaya E; Zinnuroglu M; Zeki Kiralp M
    J Back Musculoskelet Rehabil; 2009; 22(4):231-4. PubMed ID: 20023356
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Buschke-Ollendorff syndrome presenting with asymptomatic yellowish papules and leg length discrepancy: A case report.
    Hung WK; Shen MH; Chen KY; Chung WH; Shih IH; Chang CH; Yang CY
    J Musculoskelet Neuronal Interact; 2022 Jun; 22(2):292-295. PubMed ID: 35642708
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Osteopoikilosis: 2 clinical cases].
    Cravo AR; Villacreses C; da Silva JC
    Acta Reumatol Port; 2006; 31(3):255-60. PubMed ID: 17094337
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Osteopoikilosis: what does the rheumatologist must know about it?
    Woyciechowsky TG; Monticielo MR; Keiserman B; Monticielo OA
    Clin Rheumatol; 2012 Apr; 31(4):745-8. PubMed ID: 22246417
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.