Vascular mechanisms of testosterone: The non-genomic point of view von Lorigo, Margarida, Mariana, Melissa, Lemos, Manuel C., Cairrao, Elisa

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Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene von Lemos, Manuel C, Thakker, Rajesh V

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Disorder of Sex Development Due to 17-Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Report and Review of 70 Different HSD17B3 Mutations Reported in 239 Patients von Gonçalves, Catarina I, Carriço, Josianne, Bastos, Margarida, Lemos, Manuel C

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Hypoparathyroidism, deafness and renal dysplasia syndrome caused by a GATA3 splice site mutation leading to the activation of a cryptic splice site von Gonçalves, Catarina I., Carriço, Josianne N., Omar, Omneya M., Abdalla, Ebtesam, Lemos, Manuel C.

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Iodine Supplementation in Pregnancy in an Iodine-Deficient Region: A Cross-Sectional Survey von Lopes, Carla A, Prazeres, Susana, Martinez-de-Oliveira, José, Limbert, Edward, Lemos, Manuel C

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A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism von Fadiga, Lúcia, Lavrador, Mariana, Vicente, Nuno, Barros, Luísa, Gonçalves, Catarina I, Al-Naama, Asma, Saraiva, Luis R, Lemos, Manuel C

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Age, Sex Hormones, and Circadian Rhythm Regulate the Expression of Amyloid-Beta Scavengers at the Choroid Plexus von Duarte, Ana C., Furtado, Andre, Hrynchak, Mariya, Costa, Ana R., Talhada, Daniela, Goncalves, Isabel, Lemos, Manuel C., Quintela, Telma, Santos, Cecilia R. A.

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Parathyroid identification by autofluorescence - preliminary report on five cases of surgery for primary hyperparathyroidism von Serra, Carlos, Silveira, Luís, Canudo, António, Lemos, Manuel C

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UV-B Filter Octylmethoxycinnamate Induces Vasorelaxation by Ca2+ Channel Inhibition and Guanylyl Cyclase Activation in Human Umbilical Arteries von Lorigo, Margarida, Quintaneiro, Carla, Lemos, Manuel, Martinez-de-Oliveira, José, Breitenfeld, Luiza, Cairrao, Elisa

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Maternal Urinary Iodine Concentration during Pregnancy and Its Impact on Child Growth and Neurodevelopment: An 11-Year Follow-Up Study von Lopes, Carla A., Duarte, Marta, Prazeres, Susana, Carvalho, Ivone, Vilarinho, Laura, Martinez-de-Oliveira, José, Limbert, Edward, Lemos, Manuel C.

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A Common Variant in the CDK8 Gene Is Associated with Sporadic Pituitary Adenomas in the Portuguese Population: A Case-Control Study von Gaspar, Leonor M., Gonçalves, Catarina I., Fonseca, Fernando, Carvalho, Davide, Cortez, Luísa, Palha, Ana, Barros, Inês F., Nobre, Ema, Duarte, João S., Amaral, Cláudia, Bugalho, Maria J., Marques, Olinda, Pereira, Bernardo D., Lemos, Manuel C.

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Association of RET genetic polymorphisms and haplotypes with papillary thyroid carcinoma in the Portuguese population: a case-control study von Santos, Marina, Azevedo, Teresa, Martins, Teresa, Rodrigues, Fernando J, Lemos, Manuel C

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GNAS Mutations in Pseudohypoparathyroidism Type 1a and Related Disorders von Lemos, Manuel C., Thakker, Rajesh V.

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Novel FGFR1 mutations in Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: evidence for the involvement of an alternatively spliced isoform von Gonçalves, Catarina, M.Sc, Bastos, Margarida, M.D, Pignatelli, Duarte, M.D., Ph.D, Borges, Teresa, M.D, Aragüés, José M., M.D, Fonseca, Fernando, M.D, Pereira, Bernardo D., M.D, Socorro, Sílvia, Ph.D, Lemos, Manuel C., M.D., Ph.D

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Hypoparathyroidism, deafness, and renal dysplasia syndrome: 20 Years after the identification of the first GATA3 mutations von Lemos, Manuel C., Thakker, Rajesh V.

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The Glucocorticoid Receptor Gene (NR3C1) 9 beta SNP Is Associated with Posttraumatic Stress Disorder von Castro-Vale, Ivone, Duraes, Cecilia, van Rossum, Elisabeth F. C., Staufenbiel, Sabine M., Severo, Milton, Lemos, Manuel C., Carvalho, Davide

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Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia von Harding, Brian, Lemos, Manuel C, Reed, Anita A C, Walls, Gerard V, Jeyabalan, Jeshmi, Bowl, Michael R, Tateossian, Hilda, Sullivan, Nicky, Hough, Tertius, Fraser, William D, Ansorge, Olaf, Cheeseman, Michael T, Thakker, Rajesh V

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Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis von Rocha, Sandra M., Sousa, Ines, Gomes, Ines M., Arinto, Patricia, Costa-Pinheiro, Pedro, Coutinho, Eduarda, Santos, Cecilia R., Jeronimo, Carmen, Lemos, Manuel C., Passarinha, Luis A., Socorro, Silvia, Maia, Claudio J.

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MEN1 Gene Replacement Therapy Reduces Proliferation Rates in a Mouse Model of Pituitary Adenomas von WALLS, Gerard V, LEMOS, Manuel C, CHRISTIE, Paul T, ANSORGE, Olaf, CLARKE, Kieran, SEYMOUR, Len, THAKKER, Rajesh V, JAVID, Mahsa, BAZAN-PEREGRINO, Miriam, JEYABALAN, Jeshmi, REED, Anita A. C, HARDING, Brian, TYLER, Damian J, STUCKEY, Daniel J, PIRET, Sian

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Vascular Pathways of Testosterone: Clinical Implications von Lorigo, Margarida, Mariana, Melissa, Oliveira, Nelson, Lemos, Manuel C., Cairrao, Elisa

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