UM ESTUDO COMPARATIVO DA EMPATIA ENTRE ESTUDANTES UNIVERSITÁRIOS
- 期刊名称POLÊM!CA
- 作者Carneiro, Rachel Shimba; Paulo Pires, Pedro; Parrine dos Reis, Tatiane; Pereira dos Santos, Araceli; De Andrade, Orlando Ferreira
- 卷第17卷
- 期第1期
- 电子ISSN1676-0727
- 文件大小318.80KB
- 发表时间2017-04-12
- DOI10.12957/polemica.2017.28299
Mutation Spectrum of NF1 and Clinical Characteristics in 78 Korean Patients With Neurofibromatosis Type 1Ko, Jung Min; Sohn, Young Bae; Jeong, Seon Yong; Kim, Hyon-Ju; Messiaen, Ludwine M. · Pediatric Neurology · 2013
Aberrant mutation spectrum and clinical characteristics of patients with mucopolysaccharidosis type I in an Iranian seriesAbdi, M.; Taghikhani, M.; Khatami, S.; Alaei, M.; Zamanfar, D.; Vakili, R.; Hakhamaneshi, M. · Clinica Chimica Acta · 2019
Clinical characteristics and spectrum of NF1 mutations in 12 unrelated Chinese families with neurofibromatosis type 1Mao, Bin; Chen, Siyu; Chen, Xin; Yu, Xiumei; Zhai, Xiaojia; Yang, Tao; Li, Lulu; Wang, Zheng; Zhao, Xiuli; Zhang, Xue · BMC Medical Genetics · 2018
Distal myopathy with rimmed vacuoles: clinical and muscle morphological characteristics and spectrum of GNE gene mutations in 53 Chinese patientsLu, Xianghui; Pu, Chuanqiang; Huang, Xusheng; Liu, Jiexiao; Mao, Yanling · Neurological Research · 2011
Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 PatientsPigg, M; Bygum, A; Gånemo, A; Virtanen, M; Brandrup, F; Zimmer, A; Hotz, A; Vahlquist, A; Fischer, J · Acta Dermato Venereologica · 2016
Clinical Characteristics, Mutation Spectrum, and Prevalence of Åland Eye Disease/Incomplete Congenital Stationary Night Blindness in DenmarkHove, Marianne N.; Kilic-Biyik, Kevser Z.; Trotter, Alana; Grønskov, Karen; Sander, Birgit; Larsen, Michael; Carroll, Joseph; Bech-Hansen, Torben; Rosenberg, Thomas · Investigative Opthalmology & Visual Science · 2016
O41 – 1941 Mutation spectrum and clinical characteristics in hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC)Hamilton, EM; Vanderver, A; Siriwardena, K; Pinelli, L; Schiffmann, R; Blaser, S; Naidu, S; van Berkel, CG; Polder, E; Abbink, TE; Wolf, NI; van der Knaap, MS · European Journal of Paediatric Neurology · 2013
Annual acknowledgement of reviewersSands, Timothy R · BMC Medical Genetics · 2014
Annual acknowledgement of reviewersSands, Tim · BMC Medical Genetics · 2015
Annual acknowledgement of reviewersSands, Timothy R. · BMC Medical Genetics · 2016
Cardiac manifestations of PRKAG2 mutationBanankhah, Pooya; Fishbein, Gregory A.; Dota, Anthony; Ardehali, Reza · BMC Medical Genetics · 2018
Mitochondrial mutations in maternally inherited hearing lossHideki Mutai,Takahisa Watabe,Kenjiro Kosaki,Kaoru Ogawa… · BMC Medical Genetics · 2017
A case report of Proteus syndrome (PS)Zeng, Xiaoyun; Wen, Xiaoming; Liang, Xinxin; Wang, Lina; Xu, Lingling · BMC Medical Genetics · 2020
Hair shaft structures inEDARinduced ectodermal dysplasiaStecksén-Blicks, C.; Falk Kieri, C.; Hägg, D.; Schmitt-Egenolf, M. · BMC Medical Genetics · 2015
Bilateral giant retinal tears in Osteogenesis ImperfectaScollo, Paolo; Snead, Martin Paul; Richards, Allan James; Pollitt, Rebecca; DeVile, Catherine · BMC Medical Genetics · 2018