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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

160 related items for PubMed ID: 26708699

  • 1. Buschke-Ollendorff syndrome: a novel case series and systematic review.
    Pope V, Dupuis L, Kannu P, Mendoza-Londono R, Sajic D, So J, Yoon G, Lara-Corrales I.
    Br J Dermatol; 2016 Apr; 174(4):723-9. PubMed ID: 26708699
    [Abstract] [Full Text] [Related]

  • 2. Deactivating germline mutations in LEMD3 cause osteopoikilosis and Buschke-Ollendorff syndrome, but not sporadic melorheostosis.
    Mumm S, Wenkert D, Zhang X, McAlister WH, Mier RJ, Whyte MP.
    J Bone Miner Res; 2007 Feb; 22(2):243-50. PubMed ID: 17087626
    [Abstract] [Full Text] [Related]

  • 3. Buschke-Ollendorff syndrome in a 6-year-old patient: clinical and histopathological aspects of a rare disease.
    Diotallevi F, Simonetti O, Radi G, Martina E, Paolinelli M, Sapigni C, Guanciarossa F, Bianchelli T, Brancorsini D, Offidani A.
    Acta Dermatovenerol Alp Pannonica Adriat; 2020 Mar; 29(1):31-33. PubMed ID: 32206820
    [Abstract] [Full Text] [Related]

  • 4. Depressed indurated plaque with elastorrhexis as a distinctive lesion in Buschke-Ollendorff syndrome.
    Velasco Huici R, Martín JM, Vázquez B, Silva E, Estébanez A, Cuesta A, Ramón D, Monteagudo C.
    Pediatr Dermatol; 2020 Mar; 37(2):385-387. PubMed ID: 31943321
    [Abstract] [Full Text] [Related]

  • 5. The Buschke-Ollendorff syndrome: a case report of simultaneous osteo-cutaneous malformations in the hand.
    Brodbeck M, Yousif Q, Diener PA, Zweier M, Gruenert J.
    BMC Res Notes; 2016 Jun 07; 9():294. PubMed ID: 27267960
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Buschke-Ollendorff syndrome: sparing unnecessary investigations.
    Surrenti T, Callea F, De Horatio LT, Diociaiuti A, El Hachem M.
    Cutis; 2014 Aug 07; 94(2):97-100. PubMed ID: 25184645
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Buschke-Ollendorff syndrome: absence of LEMD3 mutation in an affected family.
    Yadegari M, Whyte MP, Mumm S, Phelps RG, Shanske A, Totty WG, Cohen SR.
    Arch Dermatol; 2010 Jan 07; 146(1):63-8. PubMed ID: 20083694
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [Buschke-Ollendorff syndrome. Connective tissue nevi in osteopoikilosis].
    Bonde CT, Vielfreund L.
    Ugeskr Laeger; 2001 Jan 08; 163(2):170-1. PubMed ID: 11379244
    [Abstract] [Full Text] [Related]

  • 19. 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 Jan 08; 28(4):447-50. PubMed ID: 20678097
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.