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 *

116 related articles for article (PubMed ID: 22099209)

  • 1. [Osteopoikilosis complicated by short stature: a case report and a family survey].
    Wang LB; Ma HW; Wang L; Hu M; Ren S
    Zhongguo Dang Dai Er Ke Za Zhi; 2011 Nov; 13(11):929-30. PubMed ID: 22099209
    [No Abstract]   [Full Text] [Related]  

  • 2. Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14.
    Menten B; Buysse K; Zahir F; Hellemans J; Hamilton SJ; Costa T; Fagerstrom C; Anadiotis G; Kingsbury D; McGillivray BC; Marra MA; Friedman JM; Speleman F; Mortier G
    J Med Genet; 2007 Apr; 44(4):264-8. PubMed ID: 17220210
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Osteopoikilosis - a family with five cases].
    Zhou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):404-5. PubMed ID: 24928029
    [No Abstract]   [Full Text] [Related]  

  • 4. LEMD3: the gene responsible for bone density disorders (osteopoikilosis).
    Ben-Asher E; Zelzer E; Lancet D
    Isr Med Assoc J; 2005 Apr; 7(4):273-4. PubMed ID: 15847215
    [No Abstract]   [Full Text] [Related]  

  • 5. A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis.
    Couto AR; Bruges-Armas J; Peach CA; Chapman K; Brown MA; Wordsworth BP; Zhang Y
    Calcif Tissue Int; 2007 Aug; 81(2):81-4. PubMed ID: 17622481
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of a novel LEMD3 Y871X mutation in a three-generation family with osteopoikilosis and review of the literature.
    Zhang Q; Mo ZH; Dong CS; Yang F; Xie YH; Jin P
    J Endocrinol Invest; 2016 Jun; 39(6):679-85. PubMed ID: 26694706
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Novel 4-bp Intronic Deletion (c.1560+5_1560+8del) [corrected] in LEMD3 in a Korean Patient With Osteopoikilosis.
    Yoo IY; Song JS; Ki CS; Kim JW; Cha HS; Min YK
    Ann Lab Med; 2017 Nov; 37(6):540-543. PubMed ID: 28840995
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel and recurrent germline LEMD3 mutations causing Buschke-Ollendorff syndrome and osteopoikilosis but not isolated melorheostosis.
    Zhang Y; Castori M; Ferranti G; Paradisi M; Wordsworth BP
    Clin Genet; 2009 Jun; 75(6):556-61. PubMed ID: 19438932
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.
    Hellemans J; Preobrazhenska O; Willaert A; Debeer P; Verdonk PC; Costa T; Janssens K; Menten B; Van Roy N; Vermeulen SJ; Savarirayan R; Van Hul W; Vanhoenacker F; Huylebroeck D; De Paepe A; Naeyaert JM; Vandesompele J; Speleman F; Verschueren K; Coucke PJ; Mortier GR
    Nat Genet; 2004 Nov; 36(11):1213-8. PubMed ID: 15489854
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Osteopoikilosis in a patient with rheumatoid arthritis complicated with dry eyes.
    Ureten K
    Rheumatol Int; 2007 Sep; 27(11):1079-82. PubMed ID: 17393171
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel Somatic Mutation in LEMD3 Splice Site Results in Buschke-Ollendorff Syndrome with Polyostotic Melorheostosis and Osteopoikilosis.
    Gutierrez D; Cooper KD; Mitchell AL; Cohn HI
    Pediatr Dermatol; 2015; 32(5):e219-20. PubMed ID: 26135202
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Buschke-Ollendorff syndrome due to a novel LEMD3 mutation - an unusual case of alopecia.
    Darr-Foit S; Schliemann S; Schulz S; Elsner P
    J Dtsch Dermatol Ges; 2018 Mar; 16(3):348-349. PubMed ID: 29465813
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Germline LEMD3 mutations are rare in sporadic patients with isolated melorheostosis.
    Hellemans J; Debeer P; Wright M; Janecke A; Kjaer KW; Verdonk PC; Savarirayan R; Basel L; Moss C; Roth J; David A; De Paepe A; Coucke P; Mortier GR
    Hum Mutat; 2006 Mar; 27(3):290. PubMed ID: 16470551
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Buschke-Ollendorff syndrome.
    Hassikou H; Tabache F; Safi S; Baaj M; Hadri L
    Joint Bone Spine; 2008 Mar; 75(2):212-4. PubMed ID: 18313966
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Juvenile elastoma without germline mutations in LEMD3 gene: A case of Buschke-Ollendorff syndrome?
    Condorelli A; Musso N; Scuderi L; Condorelli DF; Barresi V; De Pasquale R
    Pediatr Dermatol; 2017 Nov; 34(6):e345-e346. PubMed ID: 29023873
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.