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EP26.24: The etiology of fetal renal dysplasias investigated by means of a prenatal CAKUT targeted NGS gene panel

Ultrasound in obstetrics & gynecology, 2022-09, Vol.60 (S1), p.204-205

2022

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Perfil de expresión génica en el cáncer de próstata: identificación de marcadores candidatos para el diagnóstico no invasivo

Actas urologicas españolas, 2014-04, Vol.38 (3), p.143-149

2014

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Hábitos alimentares: aconselhamento breve

Revista portuguesa de medicina geral e familiar, 2023-05, Vol.39 (2), p.172-174

2023

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Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility

Journal of medical genetics, 2014-05, Vol.51 (5), p.340-344

2014

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Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients

Journal of medical genetics, 2003-06, Vol.40 (6), p.e82-82

2003

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Early Macrophage Infiltration and Sustained Inflammation in Kidneys From Deceased Donors Are Associated With Long‐Term Renal Function

American journal of transplantation, 2017-03, Vol.17 (3), p.733-743

2017

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Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1

Human molecular genetics, 2000-01, Vol.9 (2), p.237-247

2000

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Monocyte implication in renal allograft dysfunction

Clinical and experimental immunology, 2014-02, Vol.175 (2), p.323-331

2014

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Y-chromosome microdeletions are not associated with SHOX haploinsufficiency

Human reproduction (Oxford), 2013-11, Vol.28 (11), p.3155-3160

2013

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Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia

Andrology (Oxford), 2015-03, Vol.3 (2), p.203-212

2015

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Seguimento da SAOS numa Unidade de Saúde Familiar: avaliação e melhoria contínua da qualidade

Revista portuguesa de medicina geral e familiar, 2023-12, Vol.39 (6), p.609-610

2023

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Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency

Human reproduction (Oxford), 2014-05, Vol.29 (5), p.1114-1115

2014

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Aprendizagem relacional: oportunidades e desafios na formação em medicina geral e familiar

Revista portuguesa de medicina geral e familiar, 2022-11, Vol.38 (5), p.436-448

2022

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Hiperpigmentação da mucosa oral como apresentação da síndroma de Laugier-Hunziker: um relato de caso

Revista portuguesa de medicina geral e familiar, 2022-04, Vol.38 (2), p.198-202

2022

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Collagen type IV (α3–α4) nephropathy: from isolated haematuria to renal failure

Nephrology, dialysis, transplantation, 2004-10, Vol.19 (10), p.2429-2432

2004

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Gene expression profiles in prostate cancer: identification of candidate non-invasive diagnostic markers

Actas urologicas españolas, 2014-04, Vol.38 (3), p.143-149

2014

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Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutations

Human genetics, 2001-05, Vol.108 (5), p.416-429

2001

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Molecular Staging of Bladder Cancer with RT-PCR Assay for CK20 in Peripheral Blood, Bone Marrow and Lymph Nodes: Comparison with Standard Histological Staging

Anticancer research, 2006-01, Vol.26 (1A), p.411-419

2006

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Isolamento social e solidão dos idosos em tempo de COVID-19

Revista portuguesa de medicina geral e familiar, 2022-11, Vol.38 (5), p.539-544

Ribeiro, Andreia Soares Teles

2022

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A importância do rastreio do aneurisma da aorta abdominal: a propósito de um caso clínico

Revista portuguesa de medicina geral e familiar, 2022-04, Vol.38 (2), p.193-197

2022

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WT1 mutations may be a cause of severe renal failure due to nephroblastomatosis in Wilms' tumor patients

Clinical nephrology, 2011-09, Vol.76 (3), p.244

2011

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Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1

American journal of kidney diseases, 2018-09, Vol.72 (3), p.411-418

2018

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Molecular diagnosis of autosomal dominant polycystic kidney disease

Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, 2011, Vol.31 (1), p.35

2011

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Preservation of renal function in a patient with Fabry nephropathy on enzyme replacement therapy

Clinical nephrology, 2008-06, Vol.69 (6), p.445

2008

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Further insights into the role of T222P variant of RXFP2 in non-syndromic cryptorchidism in two Mediterranean populations

International journal of andrology, 2011-08, Vol.34 (4pt1), p.333-338

2011

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EP26.24: The etiology of fetal renal dysplasias investigated by means of a prenatal CAKUT targeted NGS gene panel

Perfil de expresión génica en el cáncer de próstata: identificación de marcadores candidatos para el diagnóstico no invasivo

Hábitos alimentares: aconselhamento breve

Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility

Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients

Early Macrophage Infiltration and Sustained Inflammation in Kidneys From Deceased Donors Are Associated With Long‐Term Renal Function

Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1

Monocyte implication in renal allograft dysfunction

Y-chromosome microdeletions are not associated with SHOX haploinsufficiency

Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia

Seguimento da SAOS numa Unidade de Saúde Familiar: avaliação e melhoria contínua da qualidade

Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency

Aprendizagem relacional: oportunidades e desafios na formação em medicina geral e familiar

Hiperpigmentação da mucosa oral como apresentação da síndroma de Laugier-Hunziker: um relato de caso

Collagen type IV (α3–α4) nephropathy: from isolated haematuria to renal failure

Gene expression profiles in prostate cancer: identification of candidate non-invasive diagnostic markers

Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutations

Molecular Staging of Bladder Cancer with RT-PCR Assay for CK20 in Peripheral Blood, Bone Marrow and Lymph Nodes: Comparison with Standard Histological Staging

Isolamento social e solidão dos idosos em tempo de COVID-19

A importância do rastreio do aneurisma da aorta abdominal: a propósito de um caso clínico

WT1 mutations may be a cause of severe renal failure due to nephroblastomatosis in Wilms' tumor patients

Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1

Molecular diagnosis of autosomal dominant polycystic kidney disease

Preservation of renal function in a patient with Fabry nephropathy on enzyme replacement therapy

Further insights into the role of T222P variant of RXFP2 in non-syndromic cryptorchidism in two Mediterranean populations

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