BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 36317216)

  • 21. Predicting neurofibromatosis type 1 risk among children with isolated café-au-lait macules.
    Ben-Shachar S; Dubov T; Toledano-Alhadef H; Mashiah J; Sprecher E; Constantini S; Leshno M; Messiaen LM
    J Am Acad Dermatol; 2017 Jun; 76(6):1077-1083.e3. PubMed ID: 28318682
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mutational spectrum by phenotype: panel-based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café-au-lait macules.
    Castellanos E; Rosas I; Negro A; Gel B; Alibés A; Baena N; Pineda M; Pi G; Pintos G; Salvador H; Lázaro C; Blanco I; Vilageliu L; Brems H; Grinberg D; Legius E; Serra E
    Clin Genet; 2020 Feb; 97(2):264-275. PubMed ID: 31573083
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Phenotypic variability among café-au-lait macules in neurofibromatosis type 1.
    Boyd KP; Gao L; Feng R; Beasley M; Messiaen L; Korf BR; Theos A
    J Am Acad Dermatol; 2010 Sep; 63(3):440-7. PubMed ID: 20605257
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis.
    Burkitt Wright EM; Sach E; Sharif S; Quarrell O; Carroll T; Whitehouse RW; Upadhyaya M; Huson SM; Evans DG
    J Med Genet; 2013 Sep; 50(9):606-13. PubMed ID: 23812910
    [TBL] [Abstract][Full Text] [Related]  

  • 25. An Update on Neurofibromatosis Type 1: Not Just Café-au-Lait Spots and Freckling. Part II. Other Skin Manifestations Characteristic of NF1. NF1 and Cancer.
    Hernández-Martín A; Duat-Rodríguez A
    Actas Dermosifiliogr; 2016; 107(6):465-73. PubMed ID: 26956402
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic and clinical considerations in six cases with neurofibromatosis type 1.
    Buteică E; Stoicescu I; Burada F; Stănoiu B
    Rom J Morphol Embryol; 2007; 48(3):243-8. PubMed ID: 17914490
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Multiple café au lait macules and Crowe sign.
    López Aventín D; Gilaberte M; Pujol RM
    Arch Dermatol; 2011 Jun; 147(6):735-40. PubMed ID: 21690543
    [No Abstract]   [Full Text] [Related]  

  • 28. Familial café au lait spots: a variant of neurofibromatosis type 1.
    Abeliovich D; Gelman-Kohan Z; Silverstein S; Lerer I; Chemke J; Merin S; Zlotogora J
    J Med Genet; 1995 Dec; 32(12):985-6. PubMed ID: 8825931
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Updated Approach to Patients with Multiple Café au Lait Macules.
    Albaghdadi M; Thibodeau ML; Lara-Corrales I
    Dermatol Clin; 2022 Jan; 40(1):9-23. PubMed ID: 34799039
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Atypical hematologic and renal manifestations in neurofibromatosis type I: coincidence or pathophysiological link?
    Van-Gils J; Harambat J; Jubert C; Vidaud D; Llanas B; Perel Y; Lacombe D; Goizet C
    Eur J Med Genet; 2014; 57(11-12):639-42. PubMed ID: 25234363
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular screening strategies for NF1-like syndromes with café-au-lait macules (Review).
    Zhang J; Li M; Yao Z
    Mol Med Rep; 2016 Nov; 14(5):4023-4029. PubMed ID: 27666661
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The diagnostic and clinical significance of café-au-lait macules.
    Shah KN
    Pediatr Clin North Am; 2010 Oct; 57(5):1131-53. PubMed ID: 20888463
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identification of a Novel
    Xu G; Li M; Niu Y; Huang X; Li Y; Tang G; Long S; Zhao H; Jiang H
    Biomed Res Int; 2019; 2019():2721357. PubMed ID: 31886188
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Jaffe-Campanacci syndrome or neurofibromatosis type 1: a case report of phenotypic overlap with detection of NF1 gene mutation in non-ossifying fibroma.
    Vannelli S; Buganza R; Runfola F; Mussinatto I; Andreacchio A; de Sanctis L
    Ital J Pediatr; 2020 May; 46(1):58. PubMed ID: 32393377
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Piebaldism with café-au-lait macules resulting from a novel mutation of KIT gene in a three-generation Chinese family.
    Li X; Xing X; Liang X; Song C; Yang J; Ren D; Zhou Y
    Skin Res Technol; 2023 Jun; 29(6):e13352. PubMed ID: 37357653
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Analysis of neurofibromatosis 1 (NF1) lesions by body segment.
    Palmer C; Szudek J; Joe H; Riccardi VM; Friedman JM
    Am J Med Genet A; 2004 Mar; 125A(2):157-61. PubMed ID: 14981716
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Rhabdomyosarcoma as the first presentation in Neurofibromatosis Type 1: case series and review of the literature.
    Castle AMR; Empringham B; Pinto LM; Villani A; Kanwar N; Abbott LS; Sawyer SL
    Pediatr Hematol Oncol; 2023; 40(5):506-515. PubMed ID: 36625737
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Retinal cafe-au-lait macules: A rare retinal finding in a patient with neurofibromatosis type 1.
    Venkatesh R; Jain K; Pereira A; Jain SD; Aseem A; Mahendradas P; Yadav NK
    Indian J Ophthalmol; 2019 Dec; 67(12):2101-2103. PubMed ID: 31755475
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hereditary spinal neurofibromatosis: a rare form of NF1?
    Poyhonen M; Leisti EL; Kytölä S; Leisti J
    J Med Genet; 1997 Mar; 34(3):184-7. PubMed ID: 9132486
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic evaluation of 50 Turkish patients with neurofibromatosis type 1: 2 years experience of a single center.
    Kocabey M; Özkalaycı H; Çankaya T; Yılmaz Uzman C; Çağlayan AO; Ülgenalp A; Erçal MD
    Int J Dev Neurosci; 2023 Aug; 83(5):456-465. PubMed ID: 37280783
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.