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Identification of a novel deletion in SURF1 gene: Heterogeneity in Leigh syndrome with COX deficiency. [electronic resource] by
- Ribeiro, Carolina
- do Carmo Macário, Maria
- Viegas, Ana Teresa
- Pratas, João
- Santos, Maria João
- Simões, Marta
- Mendes, Cândida
- Bacalhau, Mafalda
- Garcia, Paula
- Diogo, Luísa
- Grazina, Manuela
Producer: 20170509
In:
Mitochondrion vol. 31
Availability: No items available.
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Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant. [electronic resource] by
- Bacalhau, Mafalda
- Simões, Marta
- Rocha, Mariana C
- Hardy, Steven A
- Vincent, Amy E
- Durães, João
- Macário, Maria C
- Santos, Maria João
- Rebelo, Olinda
- Lopes, Carla
- Pratas, João
- Mendes, Cândida
- Zuzarte, Mónica
- Rego, A Cristina
- Girão, Henrique
- Wong, Lee-Jun C
- Taylor, Robert W
- Grazina, Manuela
Producer: 20191017
In:
Neuromuscular disorders : NMD vol. 28
Availability: No items available.
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Validation of control of allergic rhinitis and asthma test for children (CARATKids)--a prospective multicenter study. [electronic resource] by
- Linhares, Daniela V B R
- da Fonseca, João Almeida L
- Borrego, Luís Miguel
- Matos, Agueda
- Pereira, Ana Margarida
- Sá-Sousa, Ana
- Gaspar, Angela
- Mendes, Cândida
- Moreira, Carla
- Gomes, Eva
- Rebelo, Filomena F
- Cidrais Rodrigues, José Carlos
- Onofre, José Manuel
- Azevedo, Luís Filipe
- Alfaro, Maria
- Calix, Maria José
- Amaral, Rita
- Rodrigues-Alves, Rodrigo
- Correia de Sousa, Jaime
- Morais-Almeida, Mário
Producer: 20150219
In:
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology vol. 25
Availability: No items available.
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