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Journal Abstract Search

265 related items for PubMed ID: 32972601

  • 1. Café au lait spots: When and how to pursue their genetic origins.
    Lalor L, Davies OMT, Basel D, Siegel DH.
    Clin Dermatol; 2020; 38(4):421-431. PubMed ID: 32972601
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  • 2. Genetic analyses of mosaic neurofibromatosis type 1 with giant café-au-lait macule, plexiform neurofibroma and multiple melanocytic nevi.
    Hida T, Idogawa M, Okura M, Sugita S, Sugawara T, Sasaki Y, Tokino T, Yamashita T, Uhara H.
    J Dermatol; 2020 Jun; 47(6):658-662. PubMed ID: 32246533
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  • 5. Diagnostic value of multiple café-au-lait macules for neurofibromatosis 1 in Chinese children.
    Yao R, Wang L, Yu Y, Wang J, Shen Y.
    J Dermatol; 2016 May; 43(5):537-42. PubMed ID: 26458495
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  • 6. Legius Syndrome and its Relationship with Neurofibromatosis Type 1.
    Denayer E, Legius E.
    Acta Derm Venereol; 2020 Mar 25; 100(7):adv00093. PubMed ID: 32147744
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  • 7. Café-au-lait spots.
    Cohen JB, Janniger CK, Schwartz RA.
    Cutis; 2000 Jul 25; 66(1):22-4. PubMed ID: 10916686
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  • 8. Neurofibromatosis type 1 without cutaneous neurofibromas: a rare genotype-phenotype correlation?
    Hida T, Idogawa M, Ishikawa A, Mizukami M, Kato J, Sumikawa Y, Okura M, Tokino T, Uhara H.
    Eur J Dermatol; 2020 Oct 01; 30(5):608-609. PubMed ID: 33185534
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  • 11. Multiple café au lait macules and Crowe sign.
    López Aventín D, Gilaberte M, Pujol RM.
    Arch Dermatol; 2011 Jun 01; 147(6):735-40. PubMed ID: 21690543
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  • 14. Multiple or familial café-au-lait spots is neurofibromatosis type 6: clarification of a diagnosis.
    Madson JG.
    Dermatol Online J; 2012 May 15; 18(5):4. PubMed ID: 22630574
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  • 15. An Update on Neurofibromatosis Type 1: Not Just Café-au-Lait Spots, Freckling, and Neurofibromas. An Update. Part I. Dermatological Clinical Criteria Diagnostic of the Disease.
    Hernández-Martín A, Duat-Rodríguez A.
    Actas Dermosifiliogr; 2016 May 15; 107(6):454-64. PubMed ID: 26979265
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  • 16. Café-au-lait Macules and Neurofibromatosis Type 1: A Review of the Literature.
    Bernier A, Larbrisseau A, Perreault S.
    Pediatr Neurol; 2016 Jul 15; 60():24-29.e1. PubMed ID: 27212418
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  • 17. [Café-au-lait spots].
    Lacour JP.
    Ann Dermatol Venereol; 1999 Oct 15; 126(10):749-54. PubMed ID: 10604023
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  • 20. Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders.
    Giugliano T, Santoro C, Torella A, Del Vecchio Blanco F, Grandone A, Onore ME, Melone MAB, Straccia G, Melis D, Piccolo V, Limongelli G, Buono S, Perrotta S, Nigro V, Piluso G.
    Genes (Basel); 2019 Jul 31; 10(8):. PubMed ID: 31370276
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