Manuel Carlos Loureiro de Lemos
AuthID: R-000-K5Y
1
TITLE: Regulation of ABC transporters by sex steroids may explain differences in drug resistance between sexes
AUTHORS: Mineiro, Rafael; Santos, Cecilia; Goncalves, Isabel; Lemos, Manuel; Cavaco, Jose Eduardo B.; Quintela, Telma;
PUBLISHED: 2023, SOURCE: JOURNAL OF PHYSIOLOGY AND BIOCHEMISTRY
AUTHORS: Mineiro, Rafael; Santos, Cecilia; Goncalves, Isabel; Lemos, Manuel; Cavaco, Jose Eduardo B.; Quintela, Telma;
PUBLISHED: 2023, SOURCE: JOURNAL OF PHYSIOLOGY AND BIOCHEMISTRY
INDEXED IN: 
Scopus 
WOS
Scopus WOS2
TITLE: The impact of biological clock and sex hormones on the risk of disease
AUTHORS: Furtado, A; Costa, D; Lemos, MC; Cavaco, JE; Santos, CRA; Quintela, T;
PUBLISHED: 2023, SOURCE: Advances in Protein Chemistry and Structural Biology
AUTHORS: Furtado, A; Costa, D; Lemos, MC; Cavaco, JE; Santos, CRA; Quintela, T;
PUBLISHED: 2023, SOURCE: Advances in Protein Chemistry and Structural Biology
INDEXED IN: Scopus
Scopus3
TITLE: Low frequency of AIP mutations in patients with young-onset sporadic pituitary macroadenomas
AUTHORS: Gaspar, L. M.; Goncalves, C. I.; Saraiva, C.; Cortez, L.; Amaral, C.; Nobre, E.; Lemos, M. C.;
PUBLISHED: 2023, SOURCE: JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
AUTHORS: Gaspar, L. M.; Goncalves, C. I.; Saraiva, C.; Cortez, L.; Amaral, C.; Nobre, E.; Lemos, M. C.;
PUBLISHED: 2023, SOURCE: JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
INDEXED IN: Scopus WOS
Scopus WOS4
TITLE: Hypoparathyroidism, deafness and renal dysplasia syndrome caused by a GATA3 splice site mutation leading to the activation of a cryptic splice site Full Text
AUTHORS: Goncalves, Catarina I. I.; Carrico, Josianne N. N.; Omar, Omneya M. M.; Abdalla, Ebtesam; Lemos, Manuel C. C.;
PUBLISHED: 2023, SOURCE: FRONTIERS IN ENDOCRINOLOGY, VOLUME: 14
AUTHORS: Goncalves, Catarina I. I.; Carrico, Josianne N. N.; Omar, Omneya M. M.; Abdalla, Ebtesam; Lemos, Manuel C. C.;
PUBLISHED: 2023, SOURCE: FRONTIERS IN ENDOCRINOLOGY, VOLUME: 14
INDEXED IN: WOS
WOS5
TITLE: Maternal Urinary Iodine Concentration during Pregnancy and Its Impact on Child Growth and Neurodevelopment: An 11-Year Follow-Up Study Full Text
AUTHORS: Lopes, Carla A.; Duarte, Marta; Prazeres, Susana; Carvalho, Ivone; Vilarinho, Laura; Martinez de Oliveira, Jose; Limbert, Edward; Lemos, Manuel C.;
PUBLISHED: 2023, SOURCE: NUTRIENTS, VOLUME: 15, ISSUE: 20
AUTHORS: Lopes, Carla A.; Duarte, Marta; Prazeres, Susana; Carvalho, Ivone; Vilarinho, Laura; Martinez de Oliveira, Jose; Limbert, Edward; Lemos, Manuel C.;
PUBLISHED: 2023, SOURCE: NUTRIENTS, VOLUME: 15, ISSUE: 20
INDEXED IN: Scopus WOS
Scopus WOS6
TITLE: Clinical, Genetic and Functional Characterization of a Novel AVPR2 Missense Mutation in a Woman with X-Linked Recessive Nephrogenic Diabetes Insipidus
AUTHORS: Selvaraj, S; Rodrigues, D; Krishnamoorthy, N; Fakhro, KA; Saraiva, LR; Lemos, MC;
PUBLISHED: 2022, SOURCE: JOURNAL OF PERSONALIZED MEDICINE, VOLUME: 12, ISSUE: 1
AUTHORS: Selvaraj, S; Rodrigues, D; Krishnamoorthy, N; Fakhro, KA; Saraiva, LR; Lemos, MC;
PUBLISHED: 2022, SOURCE: JOURNAL OF PERSONALIZED MEDICINE, VOLUME: 12, ISSUE: 1
INDEXED IN: Scopus WOS
Scopus WOS7
TITLE: Iodine Supplementation in Pregnancy in an Iodine-Deficient Region: A Cross-Sectional Survey Full Text
AUTHORS: Lopes, Carla A.; Prazeres, Susana; Martinez de Oliveira, Jose; Limbert, Edward; Lemos, Manuel C.;
PUBLISHED: 2022, SOURCE: NUTRIENTS, VOLUME: 14, ISSUE: 7
AUTHORS: Lopes, Carla A.; Prazeres, Susana; Martinez de Oliveira, Jose; Limbert, Edward; Lemos, Manuel C.;
PUBLISHED: 2022, SOURCE: NUTRIENTS, VOLUME: 14, ISSUE: 7
INDEXED IN: Scopus WOS
Scopus WOS8
TITLE: A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism Full Text
AUTHORS: Fadiga, Lucia; Lavrador, Mariana; Vicente, Nuno; Barros, Luisa; Goncalves, Catarina, I; Al Naama, Asma; Saraiva, Luis R.; Lemos, Manuel C.;
PUBLISHED: 2022, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 23, ISSUE: 8
AUTHORS: Fadiga, Lucia; Lavrador, Mariana; Vicente, Nuno; Barros, Luisa; Goncalves, Catarina, I; Al Naama, Asma; Saraiva, Luis R.; Lemos, Manuel C.;
PUBLISHED: 2022, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 23, ISSUE: 8
INDEXED IN: Scopus WOS
Scopus WOS9
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 Full Text
AUTHORS: Goncalves, Catarina, I; Carrico, Josianne; Bastos, Margarida; Lemos, Manuel C.;
PUBLISHED: 2022, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 23, ISSUE: 17
AUTHORS: Goncalves, Catarina, I; Carrico, Josianne; Bastos, Margarida; Lemos, Manuel C.;
PUBLISHED: 2022, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 23, ISSUE: 17
INDEXED IN: WOS
WOS10
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
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
