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Novel FGFR1 mutations in Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: evidence for the involvement of an alternatively spliced isoform.
Gonçalves C, Bastos M, Pignatelli D, Borges T, Aragüés JM, Fonseca F, Pereira BD, Socorro S, Lemos MC. Gonçalves C, et al. Among authors: lemos mc. Fertil Steril. 2015 Nov;104(5):1261-7.e1. doi: 10.1016/j.fertnstert.2015.07.1142. Epub 2015 Aug 12. Fertil Steril. 2015. PMID: 26277103 Free article.
High frequency of CHD7 mutations in congenital hypogonadotropic hypogonadism.
Gonçalves CI, Patriarca FM, Aragüés JM, Carvalho D, Fonseca F, Martins S, Marques O, Pereira BD, Martinez-de-Oliveira J, Lemos MC. Gonçalves CI, et al. Among authors: lemos mc. Sci Rep. 2019 Feb 7;9(1):1597. doi: 10.1038/s41598-018-38178-y. Sci Rep. 2019. PMID: 30733481 Free PMC article.
Association of Vitamin D Pathway Genetic Variation and Thyroid Cancer.
Carvalho IS, Gonçalves CI, Almeida JT, Azevedo T, Martins T, Rodrigues FJ, Lemos MC. Carvalho IS, et al. Among authors: lemos mc. Genes (Basel). 2019 Jul 28;10(8):572. doi: 10.3390/genes10080572. Genes (Basel). 2019. PMID: 31357732 Free PMC article.
Maturity-Onset Diabetes of the Young (MODY) in Portugal: Novel GCK, HNFA1 and HNFA4 Mutations.
Alvelos MI, Gonçalves 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. Alvelos MI, et al. Among authors: lemos mc. J Clin Med. 2020 Jan 20;9(1):288. doi: 10.3390/jcm9010288. J Clin Med. 2020. PMID: 31968686 Free PMC article.
100 results