Results 1 to 10 of about 548 (179)
Developmental Medicine &Child Neurology, Volume 67, Issue 8, Page 1004-1025, August 2025.Why does infantile epileptic spasms syndrome (IESS) occur with a variety of underlying conditions and why does it respond to adrenocorticotrophin hormone (ACTH)/corticosteroids? Our scoping review summarizes five hypotheses from the literature: gene/epigenetic regulation, stress/HPA axis activation, neuroinflammation/immune function, altered neuronal ...
Emily A. Innes +6 more
wiley +1 more source
Revista da Sociedade Brasileira de Fonoaudiologia, 2010 Este trabalho teve como objetivo apresentar os resultados obtidos na avaliação do processamento auditivo de um paciente com Neurofibromatose tipo 1.
Pollyanna Barros Batista +4 more
doaj +1 more source
Diagnostic Importance of Cutaneous Manifestations of Neurofibromatosis—A Systematic Review
Neurology and Clinical Neuroscience, Volume 13, Issue 3, Page 165-173, May 2025.ABSTRACT A class of hereditary diseases known as neurofibromatoses results in tumor growth on tissue from nerves. The spinal cord, nerves, and brain are among the parts of the nervous framework where these tumors can form. Similar to other genetic disorders, neurofibromatosis discloses complicated phenotypes, exhibiting varying benign and malignant ...
Hina Aslam +11 more
wiley +1 more source
Developmental Medicine &Child Neurology, Volume 67, Issue 4, Page 537-549, April 2025.Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16157 In this double‐blind, placebo‐controlled, randomized clinical trial, 31 adolescents with neurofibromatosis type 1 (NF1) were enrolled to test the effects of lamotrigine on cognitive functioning.
Myrthe J. Ottenhoff +21 more
wiley +1 more source
Implicações para o cuidar de enfermagem a partir de percepções do ser portador de neurofibromatose
Aquichan, 2009 A neurofibromatose tipo 1 é uma síndrome genética autossômica muito freqüente no ser humano com crescimento de tumores benignos nos nervos; pode acontecer em qualquer parte do corpo.
Claudia de Carvalho-Dantas +4 more
doaj
The Pan African Medical Journal, 2016 Le syndrome de Usher est défini par l'association d''une surdité de perception congénitale de sévérité variable évolutive ou non et d'une rétinopathie pigmentaire progressivement cécitante. La Neurofibromatose de Von Recklinghausen ou Neurofibromatose de
Pépin-Williams Atipo-Tsiba
doaj +1 more source
FEOCROMOCITOMA E NEUROFIBROMATOSE 1
Revista da Sociedade Portuguesa de Dermatologia e Venereologia, 2014 Introdução: Feocromocitomas são tumores originários de células cromafins do sistema simpato-adrenal. As suas manifestações clínicas são múltiplas e diversificadas, função do perfil secretório variável de múltiplos compostos, incluindo catecolaminas ...
Rui Tavares-Bello +5 more
doaj +1 more source
An Unexplored Diversity for Adaptation of Germination to High Temperatures in Brassica Species
Evolutionary Applications, Volume 18, Issue 3, March 2025.ABSTRACT Elevated temperatures inhibit the germination of a concerning number of crop species. One strategy to mitigate the impact of warming temperatures is to identify and introgress adaptive genes into elite germplasm. Diversity must be sought in wild populations, coupled with an understanding of the complex pattern of adaptation across a broad ...
M. Tiret +10 more
wiley +1 more source
Neurofibromatosis: part 2 – clinical management
Arquivos de Neuro-Psiquiatria, 2015 Part 1 of this guideline addressed the differential diagnosis of the neurofibromatoses (NF): neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2) and schwannomatosis (SCH). NF shares some features such as the genetic origin of the neural tumors
Pollyanna Barros Batista +27 more
doaj +1 more source
Skin Research and Technology, Volume 30, Issue 9, September 2024.Abstract Background Cutaneous neurofibromas (cNFs) are a major cause of disfigurement in patients with Neurofibromatosis Type 1 (NF1). However, clinical trials investigating cNF treatments lack standardised outcome measures to objectively evaluate changes in cNF size and appearance.
Jonathan C. L. Lau +12 more
wiley +1 more source