Results 201 to 210 of about 38,064 (238)
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Ulnar hypoplasia and neurofibromatosis type I
The Journal of Pediatrics, 2004Euthymia, Vargiami +2 more
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Neurofibromatosis Type I: case report
Introduction: neurofibromatosis comprises three dominant inherited disorders, type I being the most common, relatively frequent, with a prevalence of 1 in 3500, with defining features and diverse manifestations, including a 5-10 times increased risk of cancer, with a cumulative risk of 40% at 50 years of age.León Bermeo, Cristina Martha +2 more
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Lisch nodules in neurofibromatosis type I
Medicina Clínica (English Edition), 2019Antonio, Ramos Suárez +2 more
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Type 2 chronic inflammatory diseases: targets, therapies and unmet needs
Nature Reviews Drug Discovery, 2023P V Kolkhir +2 more
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Type VII secretion systems: structure, functions and transport models
Nature Reviews Microbiology, 2021Angel Rivera-Calzada +2 more
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Neurofibromatosis type I and Arnold–Chiari malformation
Journal of the European Academy of Dermatology and Venereology, 2002GIUSTINI, Sandra +7 more
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Neurofibromatosis Type I and Neurofibromatosis Type II
Rebecca Ronsley +2 moreopenaire +1 more source
Neurofibromatosis Type I Learning Disabilities
2008C. Shilyansky, B.J. Wiltgen, A.J. Silva
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