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Multidisciplinary consensus on the criteria for fertility preservation in cancer patients

Clinical & translational oncology, 2022-02, Vol.24 (2), p.227-243

2022

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Hidden mosaicism in patients with Klinefelter's syndrome: implications for genetic reproductive counselling

Human reproduction (Oxford), 2011-12, Vol.26 (12), p.3486-3493

2011

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Altered gene expression signature of early stages of the germ line supports the pre‐meiotic origin of human spermatogenic failure

Andrology (Oxford), 2014-07, Vol.2 (4), p.596-606

2014

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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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Chromosome 16 Abnormalities in Embryos and in Sperm from a Male with a Fragile Site at 16q22.1

Cytogenetic and genome research, 2014-01, Vol.142 (2), p.134-139

2014

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Protocolo de evaluación y tratamiento de la disfunción sexual en el varón con diabetes

Medicine - programa de formación médica continuada acreditado, 2016-09, Vol.12 (17), p.995-999

Bassas Arnau, L

2016

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P-055 Influence of a dynamic exposome on the genetic component of male infertility

Human reproduction (Oxford), 2024-07, Vol.39 (Supplement_1)

2024

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Complete selective absence of protamine P2 in humans

The Journal of biological chemistry, 1993-05, Vol.268 (14), p.10553-10557

1993

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O3 Preimplantation genetic diagnosis as a strategy to prevent a fetomaternal incompatibility for a highly immunogenic platelet antigen causing severe Fetal/Neonatal Alloimmune Thrombocytopenia (FNAIT)

Reproductive biomedicine online, 2010, Vol.20, p.S15-S16

2010

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P16 Preimplantation Genetic Diagnosis (PGD) cycles for translocations carriers. Results in a public hospital

Reproductive biomedicine online, 2010, Vol.20, p.S28-S28

2010

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P18 PGD for a woman carrier of a balanced reciprocal translocation (11;22) and a man with high expression of 16q22 fragile site

Reproductive biomedicine online, 2010, Vol.20, p.S28-S29

2010

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Quality of Life and Sexual Function Benefits of Long-Term Testosterone Treatment: Longitudinal Results From the Registry of Hypogonadism in Men (RHYME)

Journal of sexual medicine, 2017-09, Vol.14 (9), p.1104-1115

2017

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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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Testicular CFTR Splice Variants in Patients with Congenital Absence of the Vas Deferens

Human molecular genetics, 1998-10, Vol.7 (11), p.1739-1744

1998

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Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility

Communications biology, 2022-11, Vol.5 (1), p.1220-1220, Article 1220

2022

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Genome-wide compound heterozygote analysis highlights DPY19L2 alleles in a non-consanguineous Spanish family with a complete form of globozoospermia

European urology open science (Online), 2021-10, Vol.32, p.S183

2021

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P02 - Genome-wide compound heterozygote analysis highlights DPY19L2 alleles in a non-consanguineous Spanish family with a complete form of globozoospermia

European urology open science (Online), 2021-10, Vol.32, p.S183-S183

2021

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Adenosine Triphosphate-Binding Cassette Superfamily Transporter Gene Expression in Severe Male Infertility

Biology of reproduction, 2001-08, Vol.65 (2), p.394-400

2001

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Testosterone treatment is not associated with increased risk of adverse cardiovascular events: results from the Registry of Hypogonadism in Men (RHYME)

International journal of clinical practice (Esher), 2016-10, Vol.70 (10), p.843-852

2016

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Developmental regulation of insulin and type I insulin-like growth factor receptors and absence of type II receptors in chicken embryo tissues

Diabetes (New York, N.Y.), 1988-05, Vol.37 (5), p.637-644

1988

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Cyclamate intake and cyclohexylamine excretion are not related to male fertility in humans

Food additives and contaminants, 2003-12, Vol.20 (12), p.1097-1104

2003

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Molecular evaluation of CFTR sequence variants in male infertility of testicular origin

International journal of andrology, 2005-10, Vol.28 (5), p.284-290

2005

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Extensive analysis of 40 infertile patients with congenital absence of the vas deferens : in 50 % of cases only one CFTR allele could be detected

Human genetics, 1995-02, Vol.95 (2), p.205-211

1995

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Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens

The New England journal of medicine, 1995-06, Vol.332 (22), p.1475-1480

1995

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Multidisciplinary consensus on the criteria for fertility preservation in cancer patients

Hidden mosaicism in patients with Klinefelter's syndrome: implications for genetic reproductive counselling

Altered gene expression signature of early stages of the germ line supports the pre‐meiotic origin of human spermatogenic failure

Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia

Chromosome 16 Abnormalities in Embryos and in Sperm from a Male with a Fragile Site at 16q22.1

Protocolo de evaluación y tratamiento de la disfunción sexual en el varón con diabetes

P-055 Influence of a dynamic exposome on the genetic component of male infertility

Complete selective absence of protamine P2 in humans

O3 Preimplantation genetic diagnosis as a strategy to prevent a fetomaternal incompatibility for a highly immunogenic platelet antigen causing severe Fetal/Neonatal Alloimmune Thrombocytopenia (FNAIT)

P16 Preimplantation Genetic Diagnosis (PGD) cycles for translocations carriers. Results in a public hospital

P18 PGD for a woman carrier of a balanced reciprocal translocation (11;22) and a man with high expression of 16q22 fragile site

Quality of Life and Sexual Function Benefits of Long-Term Testosterone Treatment: Longitudinal Results From the Registry of Hypogonadism in Men (RHYME)

Testosterone treatment is not associated with increased risk of prostate cancer or worsening of lower urinary tract symptoms: prostate health outcomes in the Registry of Hypogonadism in Men

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

Testicular CFTR Splice Variants in Patients with Congenital Absence of the Vas Deferens

Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility

Genome-wide compound heterozygote analysis highlights DPY19L2 alleles in a non-consanguineous Spanish family with a complete form of globozoospermia

P02 - Genome-wide compound heterozygote analysis highlights DPY19L2 alleles in a non-consanguineous Spanish family with a complete form of globozoospermia

Adenosine Triphosphate-Binding Cassette Superfamily Transporter Gene Expression in Severe Male Infertility

Testosterone treatment is not associated with increased risk of adverse cardiovascular events: results from the Registry of Hypogonadism in Men (RHYME)

Developmental regulation of insulin and type I insulin-like growth factor receptors and absence of type II receptors in chicken embryo tissues

Cyclamate intake and cyclohexylamine excretion are not related to male fertility in humans

Molecular evaluation of CFTR sequence variants in male infertility of testicular origin

Extensive analysis of 40 infertile patients with congenital absence of the vas deferens : in 50 % of cases only one CFTR allele could be detected

Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens

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