个人简介

      高峰，主任医师、教授，硕士生导师，浙江大学医学院附属儿童医院 神经内科科主任。

      中华医学会儿科学分会精准医学专业委员会副主任委员、中华医学会儿科分会小儿神经学组成员、中国出生缺陷干预救助基金会儿童遗传代谢病专家委员会委员、浙江省医学会儿科学分会小儿神经学组组长、浙江省抗癫痫协会常务理事、浙江省医师协会儿科分会委员，浙江省预防医学会免疫规划专业委员会委员。

      从事儿科神经系统疾病临床和科研工作30年，对儿童癫痫及难治性癫痫、神经遗传性疾病、中枢神经系统感染等疾病的诊治有较深入的研究。国内率先报道儿童急性坏死性脑病病例；对儿童难治性癫痫应用包括药物治疗、免疫治疗、生酮饮食治疗、迷走神经刺激术等个体化治疗方案，使患者的无发作率居国内前列，并参与相关疾病的临床指南制定2项。

       先后主持或参与国家自然科学基金、省厅局级科研项目8项，发表论文10余篇，SCI收录3篇。参与专著编写1部。

1. Jiang L, Mao S, Xu J, Gao F*. Reversible splenial lesion syndrome in children with benign convulsions associated with mild gastroenteritis: A retrospective study of five cases[J]. Brain Dev, 2018

2. Jiang T, Shen Y, Chen H, Yuan Z, Mao S, Gao F*. Clinical and molecular analysis of epilepsy-related genes in patients with Dravet syndrome[J]. Medicine, 2018,97(50):e13565.

3. Jiang J, Jiang T, Xu J, Shen J, Gao F*. Novel Mutation of the Dystrophin Gene in a Child with Duchenne Muscular Dystrophy[J]. Fetal and pediatric pathology, 2018,37(1):1-6.

4. Lihua J, Feng G, Shanshan M, Jialu X, Kewen J. Somatic KRAS mutation in an infant with linear nevus sebaceous syndrome associated with lymphatic malformations: A case report and literature review[J]. Medicine, 2017,96(47):e8016.

5. Jiang P, Shen J, Yu Y, Jiang L, Xu J, Xu L, Yu H, Gao F*. Dravet syndrome with favourable cognitive and behavioral development due to a novel SCN1A frameshift mutation[J]. Clinical neurology and neurosurgery, 2016,146:144-146.

6. Gao J, Gao F, Hong F, Yu H, Jiang P. Hyperammonemic encephalopathy in a child with ornithine transcarbamylase deficiency due to a novel combined heterozygous mutations[J]. The American journal of emergency medicine, 2015,33(3):474 e471-473.