维罗妮卡. 金斯勒医生是世界闻名的儿童皮肤科专家医师,也是英国伦敦大奥蒙德儿童医院儿童皮肤科的学术主任临床医师。她的专业领域包括儿科色素失调和皮肤遗传学,包括镶嵌障碍。此外,她在伦敦大学学院 (UCL) 大奥蒙德街儿童健康研究所的遗传学和基因组医学项目中开设了一个研究实验室,对罕见儿童皮肤病的病因和潜在治疗方法进行了突破性研究。
专长领域 Areas of expertise
罕见的小儿皮肤科疾病
小儿色素紊乱
皮肤遗传学,包括镶嵌障碍
胎记
神经营养障碍
教育和资质背景 Education and Qualification
教育背景 Training:
皇家儿科和儿童健康学院院士
伦敦大学学院 (UCL) 分子遗传学博士
剑桥大学艺术硕士,神经生理学硕士
剑桥大学医学和外科学士
研究兴趣 Research Interests
罕见小儿皮肤科疾病的遗传学
治疗罕见小儿皮肤病的新疗法
论文发表 Publications
Fuggle, N. R., Bragoli, W., Glover, M., Martinez, A. E., & Kinsler, V. A. 2015. The adverse effect profile of oral azathioprine in pediatric atopic dermatitis, and recommendations for monitoring. Journal of the American Academy of Dermatology. 72(1). pp 108-114.
Kinsler, V. A., Krengel, S., Riviere, J. -. B., Waelchli, R., Chapusot, C., Al-Olabi, L., . . . Vabres, P. 2014. Next-generation sequencing of nevus spilus-type congenital melanocytic nevus: exquisite genotype-phenotype correlation in mosaic RASopathies. J Invest Dermatol. 134(10) pp. 2658-2660.
Kinsler, V. A., Anderson, G., Latimer, B., Natarajan, D., Healy, E., Moore, G. E., & Sebire, N. J. 2013. Immunohistochemical and ultrastructural features of congenital melanocytic naevus cells support a stem-cell phenotype. Br J Dermatol. 169(2). pp. 374-383.
Kinsler, V. A., Thomas, A. C., Ishida, M., Bulstrode, N. W., Loughlin, S., Hing, S., . . . Moore, G. E. 2013. Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS. J Invest Dermatol. 133(9). pp. 2229-2236.
Kinsler, V. A., Abu-Amero, S., Budd, P., Jackson, I. J., Ring, S. M., Northstone, K., . . . Healy, E. 2012. Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development. Journal of Investigative Dermatology.
Kinsler, V. A., Paine, S. M. L., Anderson, G. W., Wijesekara, D. S., Sebire, N. J., Chong, W. K., . . . Jacques, T. S. 2012. Neuropathology of neurocutaneous melanosis: histological foci of melanotic neurones and glia may be undetectable on MRI. Acta Neuropathol. 123(3). pp. 453-456.
Kinsler, V., Shaw, A. C., Merks, J. H., & Hennekam, R. C. 2012. The face in congenital melanocytic nevus syndrome. Am J Med Genet A.158A(5). pp. 1014-1019
Kinsler, V., & Bulstrode, N. 2009. The role of surgery in the management of congenital melanocytic naevi in children: a perspective from Great Ormond Street Hospital. J Plast Reconstr Aesthet Surg. 62(5). pp. 595-601.
图片来源:大奥蒙德儿童医院(GOSH)