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Journal Abstract Search

180 related items for PubMed ID: 20693940

  • 21. Giant café au lait spot in a patient with neurofibromatosis.
    Erdi H, Boyvat A, Calikoglu E.
    Acta Derm Venereol; 1999 Nov; 79(6):496. PubMed ID: 10598783
    [No Abstract] [Full Text] [Related]

  • 22. Spontaneous dislocation of a vertebra in a patient who had neurofibromatosis. Report of a case with dural ectasia.
    Winter RB.
    J Bone Joint Surg Am; 1991 Oct; 73(9):1402-4. PubMed ID: 1918125
    [No Abstract] [Full Text] [Related]

  • 23. MRI diagnosis of NF-1 in children without café-au-lait skin lesions.
    Curless RG, Siatkowski M, Glaser JS, Shatz NJ.
    Pediatr Neurol; 1998 Mar; 18(3):269-71. PubMed ID: 9568928
    [Abstract] [Full Text] [Related]

  • 24. Concomitant meningioma and glioma within the same optic nerve in neurofibromatosis type 1.
    Büyükkapu-Bay S, Akça A, Karadoğan M, Çorapçioğlu F, Anik Y.
    J Child Neurol; 2014 Mar; 29(3):385-8. PubMed ID: 23420652
    [Abstract] [Full Text] [Related]

  • 25. Café au lait spots: the pediatrician's perspective.
    Tekin M, Bodurtha JN, Riccardi VM.
    Pediatr Rev; 2001 Mar; 22(3):82-90. PubMed ID: 11230626
    [No Abstract] [Full Text] [Related]

  • 26. Association of urticaria pigmentosa with café-au-lait spots, neurofibromas and neurofibroma-like neoplasms: a mere coincidence?
    Möhrenschlager M, Engst R, Müller-Weihrich S, Spiessl W, Rüdisser K, Weigl LB, Jessberger B, Braun-Falco M, Abeck D, Ring J.
    Dermatology; 2003 Mar; 206(4):297-302. PubMed ID: 12771469
    [Abstract] [Full Text] [Related]

  • 27. JAAD Grand Rounds quiz. Café-au-lait macules and enlarging papules on the face.
    Mallory M, Bryer BM, Wilson BB.
    J Am Acad Dermatol; 2013 Feb; 68(2):348-50. PubMed ID: 23317978
    [No Abstract] [Full Text] [Related]

  • 28. Café au lait spots: When and how to pursue their genetic origins.
    Lalor L, Davies OMT, Basel D, Siegel DH.
    Clin Dermatol; 2020 Feb; 38(4):421-431. PubMed ID: 32972601
    [Abstract] [Full Text] [Related]

  • 29. Choroidal abnormalities in café-au-lait syndromes: a new differential diagnostic tool?
    Cassiman C, Casteels I, Jacob J, Plasschaert E, Brems H, Dubron K, Keer KV, Legius E.
    Clin Genet; 2017 Apr; 91(4):529-535. PubMed ID: 27716896
    [Abstract] [Full Text] [Related]

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  • 31. Partial unilateral lentiginosis with ipsilateral Lisch nodules and axillary freckling.
    Chen W, Fan PC, Happle R.
    Dermatology; 2004 Apr; 209(4):321-4. PubMed ID: 15539896
    [Abstract] [Full Text] [Related]

  • 32. Congenital glaucoma and neurofibromatosis in a monozygotic twin: case report and review of the literature.
    Payne MS, Nadell JM, Lacassie Y, Tilton AH.
    J Child Neurol; 2003 Jul; 18(7):504-8. PubMed ID: 12940659
    [Abstract] [Full Text] [Related]

  • 33. A 13-year-old girl with neurofibromatosis-1, scoliosis.
    Listernick R.
    Pediatr Ann; 2004 Nov; 33(11):736-9. PubMed ID: 15559699
    [No Abstract] [Full Text] [Related]

  • 34. Neurofibromatosis type 1 with overlap Turner syndrome and Klinefelter syndrome.
    Hatipoglu N, Kurtoglu S, Kendirci M, Keskin M, Per H.
    J Trop Pediatr; 2010 Feb; 56(1):69-72. PubMed ID: 19578129
    [Abstract] [Full Text] [Related]

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  • 37. [Neurofibromatosis type 1 initially presented with glaucoma in the Department of Ophthalmology: a case report].
    Yan HX, Fei F, Hu D, Zhou J, Li MH, Zhang ZF, Wang YS.
    Zhonghua Yan Ke Za Zhi; 2022 May 11; 58(5):373-375. PubMed ID: 35511664
    [Abstract] [Full Text] [Related]

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  • 40. An unusual case of pediatric embryonal rhabdomyosarcoma with subsequent diagnosis of neurofibromatosis type 1.
    Spurr A, DeBiasio C, El Demellawy D, Gavigan G.
    Pediatr Dermatol; 2022 Jul 11; 39(4):664-666. PubMed ID: 35504621
    [Abstract] [Full Text] [Related]

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