Manuel C. Lemos - Dissemin

All papers authored by Manuel C. Lemos

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2022 Senthil Selvaraj, Dírcea Rodrigues, Navaneethakrishnan Krishnamoorthy

, Khalid A. Fakhro

, Luís R. Saraiva

, Manuel C. Lemos

Clinical, Genetic and Functional Characterization of a Novel AVPR2 Missense Mutation in a Woman with X-Linked Recessive Nephrogenic Diabetes Insipidus

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2021 Ivone Castro-Vale

, Cecília Durães, Elisabeth F. C. van Rossum, Sabine M. Staufenbiel, Milton Severo, Manuel C. Lemos

, Davide Carvalho

The Glucocorticoid Receptor Gene (NR3C1) 9β SNP Is Associated with Posttraumatic Stress Disorder

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2019 Catarina Inês Gonçalves, Filipa Marina Patriarca, José Maria Aragüés, Davide Carvalho

, Fernando Fonseca, Sofia Martins, Olinda Marques, Bernardo Dias Pereira, José Martinez-De-Oliveira, Manuel Carlos Lemos

High frequency of CHD7 mutations in congenital hypogonadotropic hypogonadism

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2017 M. Horta, C. Lino, M. C. Lemos

Hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome and GATA3

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This paper was not found in any repository, but could be made available legally by the author.

2016 Joana Raimundo, Maria I. Alvelos, Teresa Azevedo, Teresa Martins, Fernando J. Rodrigues, Manuel C. Lemos

Association of FOXE1 polyalanine repeat region with thyroid cancer is dependent on tumour size

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Joana B. Infante, Maria I. Alvelos, Margarida Bastos, Francisco Carrilho, Manuel C. Lemos

Complete androgen insensitivity syndrome caused by a novel splice donor site mutation and activation of a cryptic splice donor site in the androgen receptor gene

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2015 Blum Wf, Petra Dusatkova, Roland Pfäffle, Milton R. Brown, Brown Mr, Natallia Akulevich, Ivo Jp Arnhold, Arnhold Ij, Maria A. Kalina, Karolina Kot, Kalina Ma, Ciril Krzisnik, Manuel C. Lemos

, Jana Malikova, Lemos Mc and 12 other authors

Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations

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2014 Marina Santos, Teresa Azevedo, Teresa Martins, Fernando J. Rodrigues, Manuel C. Lemos

Association of RET Genetic Polymorphisms and Haplotypes with Papillary Thyroid Carcinoma in the Portuguese Population: A Case-Control Study

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2012 Gerard V. Walls, Manuel C. Lemos

, Mahsa Javid, Miriam Bazan-Peregrino, Jeshmi Jeyabalan, Anita A. C. Reed, Brian Harding, Damian J. Tyler, Daniel J. Stuckey, Sian Piret, Paul T. Christie, Olaf Ansorge, Kieran Clarke, Len Seymour, Rajesh V. Thakker

MEN1 Gene Replacement Therapy Reduces Proliferation Rates in a Mouse Model of Pituitary Adenomas

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M. Andrew Nesbit, M. Andrew Nesbit, Fadil M. Hannan, Chen Zhang, Treena Cranston, Alan J. Curley, Brian Harding, Carl Fratter, Nigel Rust, Paul T. Christie, Jeremy J. O. Turner, Manuel C. Lemos

, Michael R. Bowl, Roger Bouillon, Caroline Brain and 12 other authors

Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites

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2009 Brian Harding, Mc C. Lemos

, Aa A. C. Reed, Gv V. Walls, Jeshmi Jeyabalan, Mr R. Bowl, Hilda Tateossian, Nicky Sullivan, William D. Fraser, Tertius Hough, W. D. Fraser, Wd Fraser, Olaf Ansorge, Mt T. Cheeseman, Rv V. Thakker

and 1 other authors

Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia.

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Mc C. Lemos

, Brian Harding, Aa A. C. Reed, Jeshmi Jeyabalan, Gv V. Walls, Mr R. Bowl, James Sharpe, Sarah Wedden, Je E. Moss, Allyson Ross, Duncan Davidson, Rv V. Thakker

Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiers.

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M. C. Lemos

, E. Coutinho, L. Gomes, M. Bastos, A. Fagulha, L. Barros, F. Carrilho, E. Geraldes, F. J. Regateiro, M. Carvalheiro

TheCTLA4+49 A/G polymorphism is not associated with susceptibility to type 1 diabetes mellitus in the Portuguese population

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2008 M. C. Lemos

, E. Coutinho, L. Gomes, F. Carrilho, F. Rodrigues, F. J. Regateiro, M. Carvalheiro

Combined GSTM1 and GSTT1 null genotypes are associated with a lower risk of papillary thyroid cancer

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Mc Lemos

, Rv Thakker

Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene.

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Mc Lemos

, Ana Fagulha, Eduarda Coutinho, Leonor Gomes, Margarida Bastos, Luisa Barros, Francisco Carrilho, Elizabete Geraldes, Fj Regateiro, Manuela Carvalheiro

Lack of association of vitamin D receptor gene polymorphisms with susceptibility to type 1 diabetes mellitus in the Portuguese population

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2007 Mc Lemos

, Brian Harding, Sm Shalet, Rv Thakker

A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1.

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Mc Lemos

, Francisco Carrilho, Fernando Rodrigues, Eduarda Coutinho, Leonor Gomes, Manuela Carvalheiro, Fj Regateiro

Genetic polymorphism of CYP2D6 influences susceptibility to papillary thyroid cancer

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2006 Mc Lemos

, Leonor Gomes, Margarida Bastos, Valeriano Leite, Edward Limbert, Davide Carvalho

, Conceição Bacelar, Mariana Monteiro, Fernando Fonseca, Ana Agapito, João Jj Castro, Fj Regateiro, Manuela Carvalheiro

PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency

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2005 Leonor Gomes, Manuel C. Lemos

, Isabel Paiva, Cristina Ribeiro, Manuela Carvalheiro, Fernando J. Regateiro

CYP2D6 genetic polymorphisms are associated with susceptibility to pituitary tumors

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All papers authored by Manuel C. Lemos