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Rui César

Observed names: César, Rui, César,Rui, R Cesar, R. Cesar, Rui Cesar
OpenAlex ID: A5073747010
A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?
2018 · Bernardo Dias Pereira, Tiago Nunes da Silva, et al. · International Journal of Endocrinology · 13
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Aporte do iodo nas Regiões Autónomas da Madeira e dos Açores
2012 · Edward Limbert, Susana Prazeres, et al. · Revista Portuguesa de Endocrinologia Diabetes e Metabolismo · 11
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[A rare case of malabsorption of thyroid hormones].
2004 · E Lacerda Nobre, Zulmira Jorge, et al. · PubMed · 9
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Successful long-term use of pioglitazone in Berardinelli–Seip lipodystrophy-associated diabetes
2021 · Carolina Chaves, Mariana Chaves, et al. · Endocrinology Diabetes and Metabolism Case Reports · 8
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Transient neonatal diabetes due to a missense mutation (E227K) in the gene encoding the ATP ‐sensitive potassium channel ( KCNJ 11)
2015 · Luísa Martins, Rita Lourenço, et al. · Clinical Case Reports · 7
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Resistance to Thyroid Hormone: Report of 2 Kindreds with 35 Patients
1998 · João Anselmo, Rui César · Endocrine Practice · 6
Yes, there is (quality of) life after liver transplantation
1996 · S H Uchman, R Cesar · Hepatology · 5
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Efficacy of a Salt Iodization Program on Iodine Status and Intakes in Schoolchildren of São Miguel Island, Azores, Portugal
2020 · Catarina Senra Moniz, Rita Carvalho, et al. · European Thyroid Journal · 3
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Anthropometric evaluation of pre-school and school age children from Azores archipelago, Portugal
2019 · Cíntia Ferreira-Pêgo, Sara Gaipo, et al. · Biomedical and Biopharmaceutical Research · 3
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Hipotiroidismo congénito
2014 · Ana Luísa Rodrigues, Ana Carvalho, et al. · Revista Portuguesa de Endocrinologia Diabetes e Metabolismo · 3
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Iodine deficiency in pregnant women on São Miguel Island, Azores. Assessing the Impact of Corrective Measures
2021 · Isabel Sousa, André Sampaio, et al. · Revista Portuguesa de Endocrinologia Diabetes e Metabolismo · 2
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Frutos gordos e neurodegenerescência
2016 · Raquel Bradford, Teresa F Amaral, et al. · Acta Portuguesa de Nutrição · 1
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Contribution for Validation of a Questionnaire about Carbohydrate Count and Insulin Dosage in Youth with Type 1 Diabetes Intensive Insulin Therapy
2020 · Inês Mendes, Rita Carvalho, et al. · Revista Portuguesa de Endocrinologia Diabetes e Metabolismo
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Partial hydatidiform mole with spontaneous ovarian hyperstimulation syndrome.
2020 · Isabel Sousa, André Luiz Lopes Sampaio, et al. · Gynecology and Reproductive Endocrinology
Lymphocytic hypophysitis - A case report
2020 · Isabel Sousa, André Luiz Lopes Sampaio, et al. · Gynecology and Reproductive Endocrinology
SUN-447 Screening of Genetic Alterations in Patients with Giant Prolactinomas
2019 · Carolina Chaves, Mariana Chaves, et al. · Journal of the Endocrine Society
OR15-3 Extreme Phenotypic Variability of a Novel Mutation of MEN1 Gene in a Family with 14 Carriers across 3 Generations
2019 · Carolina Chaves, Mariana Chaves, et al. · Journal of the Endocrine Society
A dramatic improvement in metabolic parameters and cutaneous manifestations of insulin-resistance in a type 2 diabetic patient with Congenital Generalized Lipodystrophy (Berardinelli-Seip Syndrome) treated with pioglitazone
2017 · Carolina Chaves, Catarina Moniz, et al. · Endocrine Abstracts
Is there a threshold of Vitamin D sufficiency that can prevent secondary hyperparathyroidism?
2017 · Andre Amaral, Tatiana Nunes, et al. · Endocrine Abstracts
Characterization of the Young Azorean Portuguese Population with Diabetes Type 1: Study of Nutritional and Environmental Risk Factors
2017 · Dias, Tiago, Teixeira, Vitor Hugo, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Caracterização da População Jovem Açoriana com Diabetes Tipo 1: Estudo de Fatores de Risco Nutricionais e Ambientais
2017 · Tiago Dias, Vitor Hugo Teixeira, et al. · Revista Portuguesa de Endocrinologia Diabetes e Metabolismo
Avaliação do risco de desnutrição (através do Strongkids) e da desnutrição em crianças hospitalizadas
2016 · Bela Franchini, Joana Lopes, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Familial Hypercholesterolemia in an Azorean Family: A Novel Mutation in the Low-Density Lipoprotein Receptor Gene
2014 · Rita Lourenço, Luísa Martins, et al. · Advances in Bioscience and Biotechnology
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Hipercolesterolémia Familiar: Em Cada Amostra Sanguínea Uma Oportunidade Diagnóstica
2012 · Luísa M. D. R. S. Martins, Rita Lourenco, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
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Development of primary hyperparathyroidism is closely associated with the onset of dyslipidemia and insulin resistance in a large family harboring a MEN1 gene mutation
2012 · João Anselmo, C. Moniz, et al. · 15th International & 14th European Congress of Endocrinology
Works count: 31
Citation count: 71
H-index: 6
I10-index: 2
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