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TITLE: 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
AUTHORS: Gonçalves, CI; Carriço, J; Bastos, M; Lemos, MC;
PUBLISHED: 2022, SOURCE: International journal of molecular sciences, VOLUME: 23, ISSUE: 17
INDEXED IN: Scopus CrossRef: 8
IN MY: ORCID
12
TITLE: A Common Variant in the CDK8 Gene Is Associated with Sporadic Pituitary Adenomas in the Portuguese Population: A Case-Control Study  Full Text
AUTHORS: Gaspar, Leonor M.; Goncalves, Catarina, I; Fonseca, Fernando; Carvalho, Davide ; Cortez, Luisa; Palha, Ana; Barros, Ines F.; Nobre, Ema; Duarte, Joao S.; Amaral, Claudia; Bugalho, Maria J.; Marques, Olinda; Pereira, Bernardo D.; Lemos, Manuel C.;
PUBLISHED: 2022, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 23, ISSUE: 19
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID
13
TITLE: The Choroid Plexus Is an Alternative Source of Prolactin to the Rat Brain  Full Text
AUTHORS: Costa Brito, AR; Quintela, T; Goncalves, I; Duarte, AC; Costa, AR; Arosa, FA; Cavaco, JE; Lemos, MC; Santos, CRA;
PUBLISHED: 2021, SOURCE: MOLECULAR NEUROBIOLOGY
INDEXED IN: Scopus WOS
14
TITLE: The Glucocorticoid Receptor Gene (NR3C1) 9 beta SNP Is Associated with Posttraumatic Stress Disorder  Full Text
AUTHORS: Castro Vale, I ; Duraes, C; van Rossum, EFC; Staufenbiel, SM; Severo, M ; Lemos, MC; Carvalho, D ;
PUBLISHED: 2021, SOURCE: HEALTHCARE, VOLUME: 9, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 9
IN MY: ORCID
15
TITLE: Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis  Full Text
AUTHORS: Rocha, SM; Sousa, I; Gomes, IM; Arinto, P; Costa Pinheiro, P; Coutinho, E; Santos, CR; Carmen Jerónimo ; Lemos, MC; Passarinha, LA; Socorro, S; Maia, CJ;
PUBLISHED: 2021, SOURCE: LIFE-BASEL, VOLUME: 11, ISSUE: 11
INDEXED IN: Scopus WOS CrossRef: 4
IN MY: ORCID
16
TITLE: Maturity-Onset Diabetes of the Young (MODY) in Portugal: Novel GCK, HNFA1 and HNFA4 Mutations
AUTHORS: Alvelos, MI; Goncalves, CI; Coutinho, E; Almeida, JT; Bastos, M; Sampaio, ML; Melo, M; Martins, S; Dinis, I; Mirante, A; Gomes, L; Saraiva, J; Pereira, BD; Gama de Sousa, S; Moreno, C; Guelho, D; Martins, D; Baptista, C; Barros, L; Ventura, M; Gomes, MM; Lemos, MC; ...More
PUBLISHED: 2020, SOURCE: JOURNAL OF CLINICAL MEDICINE, VOLUME: 9, ISSUE: 1
INDEXED IN: WOS CrossRef: 8
IN MY: ORCID
18
TITLE: Hypoparathyroidism, deafness, and renal dysplasia syndrome: 20 Years after the identification of the firstGATA3mutations
AUTHORS: Lemos, MC; Thakker, RV;
PUBLISHED: 2020, SOURCE: HUMAN MUTATION, VOLUME: 41, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 23
IN MY: ORCID
19
TITLE: Vitamin D Pathway Genetic Variation and Type 1 Diabetes: A Case-Control Association Study
AUTHORS: Almeida, JT; Rodrigues, D; Guimaraes, J; Lemos, MC;
PUBLISHED: 2020, SOURCE: GENES, VOLUME: 11, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 11
IN MY: ORCID
20
TITLE: Neonatal presentation of growth hormone deficiency in CHARGE syndrome: the benefit of early treatment on long-term growth
AUTHORS: Costa, C ; Coutinho, E; Santos Silva, R ; Castro Correia, C ; Lemos, MC; Fontoura, M;
PUBLISHED: 2020, SOURCE: ARCHIVES OF ENDOCRINOLOGY METABOLISM, VOLUME: 64, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
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