1. Updated Approach to Patients with Multiple Café au Lait Macules
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  3. Diagnostic difficulties and possibilities of NF1-like syndromes in childhood
    Eva Pinti et al, 2021, BMC Pediatrics CrossRef
  4. Genetic Evaluation of Common Neurocutaneous Syndromes
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  5. Genetic evaluation of 50 Turkish patients with neurofibromatosis type 1: 2 years experience of a single center
    Mehmet Kocabey et al, 2023, International Journal of Developmental Neuroscience CrossRef
  6. Perspective in Pigmentation Disorders
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  7. Q-switch Laser (755 nm) Therapy for Pigmentation Within a Solitary Neurofibroma: A Case Report With 20 Years of Follow-up
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  8. Pigmentierte Flecken als mögliche Frühzeichen genetischer Syndrome
    H. Hamm et al, 2019, Der Hautarzt CrossRef
  9. Multiple café-au-lait macules and movement disorder: think beyond neurofibromatosis
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  10. Value of a café‐au‐lait macules screening clinic: Experience from The Hospital for Sick Children in Toronto
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  11. Craniofacial findings in syndromes associated with cafe-au-lait spots: a literature review
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  12. A pigmentary manifestation associated with PPP2R5D-related neurodevelopmental disorder: a case report and review of literature
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  13. Biomarker Landscape in RASopathies
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  14. Case report: Gene mutation analysis and skin imaging of isolated café-au-lait macules
    Zhenyu Zhong et al, 2023, Frontiers in Genetics CrossRef
  15. Treatment of Café‐Au‐Lait Spots Using Q‐Switched Alexandrite Laser: Analysis of Clinical Characteristics of 471 Children in Mainland China
    Bin Zhang et al, 2019, Lasers in Surgery and Medicine CrossRef