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论文共 140 篇作者统计合作学者相似作者

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Congenital Oropouche in Humans: Clinical Characterization of a Possible New Teratogenic Syndrome
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
Virusesno. 3 (2025)
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THE SPECTRUM OF DISEASE EXPRESSION IN X-LINKED DISORDERS USING COFFIN LOWRY SYNDROME CASE
K. Barbour,M. del Campo
JOURNAL OF INVESTIGATIVE MEDICINEno. 1 (2024): 233-234
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VASCULAR EHLERS-DANLOS SYNDROME AND VON WILLEBRAND DISEASE: CASE REPORT AND REVIEW OF LITERATURE
A. Gomes,M. del Campo
JOURNAL OF INVESTIGATIVE MEDICINEno. 1 (2024): 235-236
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FAMILIAL PARTIAL DELETION WILLIAMS SYNDROME - A CASE REPORT
K. Parashar,L. M. Bird,M. del Campo
JOURNAL OF INVESTIGATIVE MEDICINEno. 1 (2024): 382-383
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作者统计

#Papers: 140

#Citation: 3663

H-Index: 30

G-Index: 60

Sociability: 7

Diversity: 3

Activity: 7

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