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Sara Morais

Showing results (31-40 of 49) with videos related to

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Parkinsonism & Related Disorders|December 10, 2025
Atypical parkinsonism with dystonia and bulbar dysfunction with a ATP1A3 gene disease-causing variantRita Nunes Rato, André Fernandes, Daniela Ferro, et al.
Pediatric Reports|April 3, 2021
Aggressive Neuroblastoma in a Pediatric Patient with Severe Hemophilia ALidia Costa, Maria Eduarda Couto, Juliana Moutinho, et al.
GE Portuguese Journal of Gastroenterology|April 1, 2021
Long-Term Follow-Up of a Portuguese Single-Centre Cohort of Persons with Haemophilia and Hepatitis C Virus InfectionTiago Pereira Guedes, Mónica Garrido, Ricardo Kuttner Magalhães, et al.
Clinical Genetics|March 8, 2021
Congenital ataxia due to novel variant in ATP8A2Joana Damásio, Diana Santos, Sara Morais, et al.
Platelets|February 27, 2004
Mutations in the beta3 gene giving rise to type I Glanzmann thrombasthenia in two families in PortugalLoida Corbillon Garcia, Christelle Breillat, Margarida Lima, et al.
International Journal of Molecular Sciences|November 27, 2021
CalDAG-GEFI Deficiency in a Family with Symptomatic Heterozygous and Homozygous Carriers of a Likely Pathogenic Variant in <i>RASGRP2</i>Sara Morais, Mónica Pereira, Catarina Lau, et al.
Environmental Science & Technology|January 9, 2019
Bulk pH and Carbon Source Are Key Factors for Calcium Phosphate GranulationJorge Ricardo Cunha, Sara Morais, Joana C Silva, et al.
European Journal of Human Genetics : EJHG|August 24, 2017
Massive sequencing of 70 genes reveals a myriad of missing genes or mechanisms to be uncovered in hereditary spastic paraplegiasSara Morais, Laure Raymond, Mathilde Mairey, et al.
Haematologica|June 14, 2006
The spectrum of mutations and molecular pathogenesis of hemophilia A in 181 Portuguese patientsDezsö David, Célia Ventura, Isabel Moreira, et al.
Ergonomics|December 21, 2021
Can increased load carriage affect lower limbs kinematics during military gait?Manoela Vieira Sousa, Ricardo Sebastião, Pedro Fonseca, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Parkinsonism & Related Disorders|December 10, 2025
Atypical parkinsonism with dystonia and bulbar dysfunction with a ATP1A3 gene disease-causing variantRita Nunes Rato, André Fernandes, Daniela Ferro, et al.
Pediatric Reports|April 3, 2021
Aggressive Neuroblastoma in a Pediatric Patient with Severe Hemophilia ALidia Costa, Maria Eduarda Couto, Juliana Moutinho, et al.
GE Portuguese Journal of Gastroenterology|April 1, 2021
Long-Term Follow-Up of a Portuguese Single-Centre Cohort of Persons with Haemophilia and Hepatitis C Virus InfectionTiago Pereira Guedes, Mónica Garrido, Ricardo Kuttner Magalhães, et al.
Clinical Genetics|March 8, 2021
Congenital ataxia due to novel variant in ATP8A2Joana Damásio, Diana Santos, Sara Morais, et al.
Platelets|February 27, 2004
Mutations in the beta3 gene giving rise to type I Glanzmann thrombasthenia in two families in PortugalLoida Corbillon Garcia, Christelle Breillat, Margarida Lima, et al.
International Journal of Molecular Sciences|November 27, 2021
CalDAG-GEFI Deficiency in a Family with Symptomatic Heterozygous and Homozygous Carriers of a Likely Pathogenic Variant in <i>RASGRP2</i>Sara Morais, Mónica Pereira, Catarina Lau, et al.
Environmental Science & Technology|January 9, 2019
Bulk pH and Carbon Source Are Key Factors for Calcium Phosphate GranulationJorge Ricardo Cunha, Sara Morais, Joana C Silva, et al.
European Journal of Human Genetics : EJHG|August 24, 2017
Massive sequencing of 70 genes reveals a myriad of missing genes or mechanisms to be uncovered in hereditary spastic paraplegiasSara Morais, Laure Raymond, Mathilde Mairey, et al.
Haematologica|June 14, 2006
The spectrum of mutations and molecular pathogenesis of hemophilia A in 181 Portuguese patientsDezsö David, Célia Ventura, Isabel Moreira, et al.
Ergonomics|December 21, 2021
Can increased load carriage affect lower limbs kinematics during military gait?Manoela Vieira Sousa, Ricardo Sebastião, Pedro Fonseca, et al.
Pageof 5