Microcephaly, an etiopathogenic vision by Luis Eduardo Becerra-Solano, Leovigildo Mateos-Sánchez, Eunice López-Muñoz

Subjects: “…acquired microcephaly…”
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Autosomal recessive primary microcephaly in sibs in time of Zika epidemic: a Case Report by Julia V. Almeida, Bianca Barbosa Abdala, Natana Chaves Rabelo, Maria Eduarda Gomes, Elenice Ferreira Bastos, Juan Clinton Llerena, Sayonara Gonzalez

Subjects: “…microcephaly…”
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Clinical, Radiological, and Molecular Findings in Cases with TRAPPopathies by Ayça Dilruba Aslanger, Esma Sengenç, Emrah Yücesan, Beyza Göncü, Akın İşcan, Gözde Yeşil Sayın

Subjects: “…microcephaly…”
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Clinical characteristics of children with congenital Zika syndrome: a case series by Thais MASSETTI, Dafne HERRERO, Julliana ALENCAR, Talita SILVA, Cristina MORIYAMA, Flavia GEHRKE, James TONKS, Fernando FONSECA, Suzanna WATSON, Carlos MONTEIRO, Mariana VOOS

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Zika virus: a new pandemic threat by Ahmed Ali Al-Qahtani, Nyla Nazir, Mashael R. Al-Anazi, Salvatore Rubino, Mohammed N. Al-Ahdal

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The role of microglia in Zika virus pathogenesis: Possible diagnostic and therapeutic strategies by Subhrajyoti Paul, Sudipta Patra, Ayan Mondal, Gungun Sharma Adhikari, Piu Ghosh, Manojit Bysack, Rajen Dey

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Detecting microcephaly and macrocephaly from ultrasound images using artificial intelligence by Abraham Keffale Mengistu, Bayou Tilahun Assaye, Addisu Baye Flatie, Zewdie Mossie

Subjects: “…Microcephaly…”
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A Novel Homozygote Pathogenic Variant in the DIAPH1 Gene Associated With Seizures, Cortical Blindness, and Microcephaly Syndrome (SCBMS): Report of a Family and Literature Review by Emran Esmaeilzadeh, Sajjad Biglari, Meysam Mosallaei, Hamid Reza Khorram Khorshid, Hassan Vahidnezhad, Mohammad Amin Tabatabaiefar

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Cornelia de Lange syndrome- Report of the Second Case from Ahvaz by Ali Ahmadzadeh, Azin Ahmadzadeh, Mohammadreza Fathi, Arash Ahmadzadeh

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Neonatal Microcephaly and Central Nervous System Abnormalities During the Zika Outbreak in Rio de Janeiro by Marlos Melo Martins, Roberto de Andrade Medronho, Carlos Eduardo Raymundo, Arnaldo Prata-Barbosa, Antonio José Ledo Alves da Cunha

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Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogenase deficiency by Mustafa Kılıç, Saliha Şenel, Kadri Karaer, Serdar Ceylaner

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Congenital Oropouche in Humans: Clinical Characterization of a Possible New Teratogenic Syndrome by Bethânia de Freitas Rodrigues Ribeiro, André Rodrigues Façanha Barreto, André Pessoa, Raimunda do Socorro da Silva Azevedo, Flávia de Freitas Rodrigues, Bruna da Cruz Beyruth Borges, Natália Pimentel Moreno Mantilla, Davi Dantas Muniz, Jannifer Oliveira Chiang, Lucas Rosa Fraga, Fernanda Sales Luiz Vianna, Maria Teresa Vieira Sanseverino, Lilith Schuler Faccini, Fernanda Eduarda das Neves Martins, Rafael da Silva Azevedo, Lívia Carício Martins, Livia Medeiros Neves Casseb, Consuelo Silva Oliveira, Pedro Fernando da Costa Vasconcelos, Juarez Antônio Simões Quaresma, Alberto Mantovani Abeche, Vania de Mesquita Gadelha Prazeres, Lucia Andreia Nunes de Oliveira, Simone de Menezes Karam, Giulia Radin, Miguel Del Campo, Camila V. Ventura, Lavinia Schuler-Faccini

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NIJMEGEN BREAKAGE SYNDROME by M. Y. Kagan, N. S. Shulakova, R. A. Gumirova, E. A. Zlodeeva, N. V. Resnick

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Epidemiology of Craniofacial Anomalies: A Retrospective Analysis at a Tertiary Care Teaching Hospital in Southern India by Archi Rai, Lahari U, Abhipsha Tikayat Ray, Sneha Deepak Mallya, Adarsh Kudva, Saniya Shetty, Leslie Edward S Lewis

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Interneuron migration impairment and brain region-specific DNA damage response following irradiation during early neurogenesis in mice by Lisa Berden, Nicholas Rajan, André Claude Mbouombouo Mfossa, Isabeau De Bie, Emre Etlioglu, Mohammed Abderrafi Benotmane, Mieke Verslegers, Najat Aourz, Ilse Smolders, Jean-Michel Rigo, Bert Brône, Roel Quintens

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Orofacial myofunctional and anthropometric characteristics of children with and without microcephaly: a case-control study by Andréa Monteiro Correia MEDEIROS, Gabriela Rodrigues Dourado NOBRE, Geyse do Espírito Santo REZENDE, Íkaro Daniel de Carvalho BARRETO, Jonan Emi Valencia CARDENAS, Sarah Catarina Santos NASCIMENTO, Anna Luiza dos Santos MATOS, Asenate Soares de Matos PEREIRA, Ricardo Queiroz GURGEL, Giédre BERRETIN-FELIX

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TUBGCP2 variants cause lissencephaly spectrum disorders: a case report and literature review by Tao Yu, Miao Yu, Xueyan Liu, Hua Wang

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Diagnostic Algorithm for Microcephaly by J Gordon Millichap

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Foxr1 deletion causes microcephaly and leads to cortical and hippocampal hypoplasia by Hannah Waxman, Marcus Kankkunen, Arya Gupta, Margo Dowgiewicz, Uwe Beffert, Angela Ho

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Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation associated with KIF11 pathogenic variant: case report and genotype-phenotype correlation analysis by Jiajia Peng, Yan Xie, Hui Wang, Lijuan Huang, Yangfan Yang, Ningdong Li

Subjects: “…Microcephaly…”
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