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  1. 981
    “…A large intrathoracic meningocele, a saccular protrusion of the meninges through a dilated intervertebral foramen or a bony defect of the vertebral column, was diagnosed in a 41-year-old female patient showing clinical features of neurofibromatosis-1 (NF-1), including café-au-lait spots, cutaneous neurofibromas, and axillary frecklings and Lisch nodules on the iris. …”
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    A Large Intrathoracic Meningocele in a Patient with Neurofibromatosis-1
  2. 982
    “…Physical examination revealed the presence of café au lait macules, freckling in the axillary region and multiple neurofibromas over the trunk. …”
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    Facial plexiform neurofibromatosis: A surgical challenge
  3. 983
    “…At the age of 9 years, café-au-lait spots and axillary freckling were apparent. …”
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    Bilateral and Symmetrical Anteromedial Bowing of the Lower Limbs in a Patient with Neurofibromatosis Type-I
  4. 984
    “…Around one-fifth had reduced contacts with general practitioners in the previous 6 months due to stigma and discrimination and the leisure activity most affected was visiting pubs/restaurants/café. CONCLUSIONS: In conclusion, stigma and discrimination result in reduced use of services and reduced engagement in leisure activities. …”
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    Measuring the economic costs of discrimination experienced by people with mental health problems: development of the Costs of Discrimination Assessment (CODA)
  5. 985
    “…Neurofibromatosis (von Recklinghausen’s disease) is a neuroectodermal disorder characterized by pigmentary changes of the skin (café-au-lait spots), cutaneous and visceral tumors (neurofibromas) and systemic abnormalities. …”
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    Intestinal Neurofibromatosis in von Recklinghausen’s Disease: Presenting as Chronic Anemia due to Recurrent Intestinal Hemorrhage
  6. 986
    “…The patient had multiple café-au-lait macules and a pilomatricoma mimicking the clinical phenotype of constitutional mismatch repair deficiency. …”
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    A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency
  7. 987
    por Mann, Nolan, Ma, Truong, Dalton, Arthur
    Publicado 2017
    “…Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder characterized by the appearance of cafe au lait spots, neurofibromas and Lisch nodules. …”
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    Neurofibromatosis type 1 and male breast cancer: emerging risk factor?
  8. 988
    “…METHODS: The FRAM was used to synthesise data which were: routine monitoring of fluoride varnish application in 2015/16; a longitudinal survey with practitioners (n = 1090); in-depth practitioner and key informant interviews (n = 43); and a ‘world café’ workshop (n = 56). RESULTS: We describe a detailed model of functions linked to application, and use this to make recommendations for system-wide intervention. …”
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    A systems approach using the functional resonance analysis method to support fluoride varnish application for children attending general dental practice
  9. 989
    “…Twenty-eight delegates from the 2017 All Together Better Health Conference in Oxford, UK participated in a World Café to discuss the how teamwork in sports can inform IPCP in healthcare and sports medicine. …”
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    Health Care as a Team Sport?—Studying Athletics to Improve Interprofessional Collaboration
  10. 990
    “…The present article highlights a case of a 12-year-old male child with additional clinical findings of café-au-late pigmentation and ocular lipodermoid. …”
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    Classical oral manifestations of Dyke-Davidoff-Masson syndrome: a case report with review of the literature
  11. 991
    “…McCune-Albright syndrome (MAS) is a rare disease characterised by triad of monostotic or polyostotic fibrous dysplasia, café au-lait skin spots and a variety of endocrine disorders; precocious puberty (PP) being the most common presenting symptom in female patients. …”
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    Short stature and growth hormone deficiency: unexpected manifestations of McCune-Albright syndrome
  12. 992
    “…McCune-Albright syndrome (MAS) is characterized by the triad of precocious puberty, café au lait pigmentation, and polyostotic fibrous dysplasia (FD) of bone, and is caused by post-zygotic somatic mutations—R201H or R201C—in the guanine nucleotide binding protein, alpha stimulating (GNAS) gene. …”
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    Detection of Rare Somatic GNAS Mutation in McCune-Albright Syndrome Using a Novel Peptide Nucleic Acid Probe in a Single Tube
  13. 993
    “…Systemic evaluation revealed café-au-lait spots on the chest and back. A diagnosis of Neurofibromatosis Type I with congenital ectropion uveae and glaucoma was arrived at and neuroimaging failed to detect any optic pathway gliomas. …”
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    A rare case of neurofibromatosis type I with unilateral congenital ectropion uveae and glaucoma
  14. 994
    “…Three high-school classes students participated in a World Café event. A thematic analysis was performed. Participants showed lack of knowledge on diseases prevention. …”
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    Engaging adolescents in developing health education interventions: a multidisciplinary pilot project
  15. 995
    “…Although the patient had café au lait spots on the skin, neurofibromatosis was not suspected due to lack of symptoms. …”
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    Schwannoma and Neurofibroma, Originating from the Ulnar Nerve in Neurofibromatosis: A Case Report and Review of the Literature
  16. 996
    “…In this review the main features of café-au-lait macules, freckling, neurofibromas, juvenile xanthogranuloma, nevus anemicus and other cutaneous findings will be discussed.…”
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    Cutaneous Findings in Neurofibromatosis Type 1
  17. 997
    “…Participants walked across four flat floors, each comprising of a visual illusion: two patterns perceived as alternating 3D “furrows and ridges,” the Primrose Field illusion, and a variant of the Cafe Wall illusion as a control pattern without perceived 3D effects. …”
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    Walking on Visual Illusions
  18. 998
    “…The lesions were non-tender, non-pruritic, and did not bleed when lightly scraped. A café-au-lait macule was incidentally found in the mid-back of the patient. …”
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    A Case Study and Review of Literature of Eruptive Syringoma in a Six-Year-Old
  19. 999
    “…Its clinical manifestations include multiple cafe´‐au lait (CAL) spots, skinfold freckling, neurofibroma, bone dysplasia, learning disabilities, and an increased risk of malignancy. …”
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    A novel mutation in NF1 gene of patient with Neurofibromatosis type 1: A case report and functional study
  20. 1000
    “…CASE PRESENTATION: We present the case of a 12-year-old patient referred by his pediatrician for intermittent dysphagia and a sensation of food attachment, in whom several café-au-lait spots on the body had been found, and a case of type 1 neurofibromatosis in the patient's siblings. …”
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    Intermittent dysphagia revealing a lateropharyngeal neurofibroma in a child: Case report: A case report
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