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Consensus of the Spanish society of laboratory medicine and the Spanish society of medical oncology on the methodology and criteria for evaluation of circulating tumour markers in breast cancer

Clinical & translational oncology, 2021-07, Vol.23 (7), p.1272-1280

2021

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Pro-gastrin-releasing Peptide (ProGRP) in Patients with Benign and Malignant Diseases: Comparison with CEA, SCC, CYFRA 21-1 and NSE in Patients with Lung Cancer

Anticancer research, 2005-05, Vol.25 (3A), p.1773-1778

2005

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Serum Protein S-100 Predicts Clinical Outcome in Patients with Melanoma Treated with Adjuvant Interferon – Comparison with Tyrosinase RT-PCR

Oncology, 2005-01, Vol.68 (4-6), p.341-349

2005

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Melanoma Inhibiting Activity Protein (MIA), Beta-2 Microglobulin and Lactate Dehydrogenase (LDH) in Metastatic Melanoma

Anticancer research, 2007-01, Vol.27 (1B), p.595-599

2007

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Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing Holoprosencephaly

Human molecular genetics, 1999-09, Vol.8 (9), p.1683-1689

1999

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Tumor markers (CEA, CA 125, CYFRA 21-1, SCC and NSE) in patients with non-small cell lung cancer as an aid in histological diagnosis and prognosis: Comparison with the main clinical and pathological prognostic factors

Tumor biology, 2003-08, Vol.24 (4), p.209-218

2003

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Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain

American journal of human genetics, 2000-05, Vol.66 (5), p.1496-1503

2000

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Variability of assay methods for total and free PSA after WHO standardization

Tumor biology, 2014-03, Vol.35 (3), p.1867-1873

2014

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Pro-Gastrin-Releasing Peptide in Patients with Benign and Malignant Diseases

Tumor biology, 2004-01, Vol.25 (1-2), p.56-61

2004

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PAX8, TITF1, and FOXE1 Gene Expression Patterns during Human Development: New Insights into Human Thyroid Development and Thyroid Dysgenesis-Associated Malformations

The journal of clinical endocrinology and metabolism, 2005-01, Vol.90 (1), p.455-462

2005

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PAX2 mutations in renal-coloboma syndrome: mutational hotspot and germline mosaicism

European journal of human genetics : EJHG, 2000-11, Vol.8 (11), p.820-826

2000

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Reticular drusen over time with SD-OCT

Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft, 2014-08, Vol.111 (8), p.765-771

2014

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Significance of Angiographic Coronary Dissection After Cutting Balloon Angioplasty

The American journal of cardiology, 1998-06, Vol.81 (11), p.1349-1352

1998

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Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome

Journal of medical genetics, 2004-05, Vol.41 (5), p.381-386

2004

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Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental Retardation

Science (American Association for the Advancement of Science), 2002-11, Vol.298 (5599), p.1779-1781

2002

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Interstitial duplication of the short arm of chromosome 2: report of a new case and review

Journal of medical genetics, 1997-09, Vol.34 (9), p.783-786

1997

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Spectrum of Alcohol-Induced Myocardial Damage Detected by Indium-111–Labeled Monoclonal Antimyosin Antibodies

Journal of the American College of Cardiology, 1997-01, Vol.29 (1), p.160-167

1997

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Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome

American journal of human genetics, 2005-03, Vol.76 (3), p.493-504

2005

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Impact of Ultrasensitive Cardiac Troponin I Dynamic Changes in the New Universal Definition of Myocardial Infarction

American journal of clinical pathology, 2008-12, Vol.130 (6), p.964-968

2008

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Coronary stenting for symptomatic myocardial bridging

Heart (British Cardiac Society), 1998-07, Vol.80 (1), p.102-103

1998

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Efficacy of augmented immunosuppressive therapy for early vasculopathy in heart transplantation

Journal of the American College of Cardiology, 1998-08, Vol.32 (2), p.413-419

1998

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Cutting balloon versus conventional balloon angioplasty for the treatment of in-stent restenosis: Results of the Restenosis Cutting Balloon Evaluation Trial (RESCUT)

Journal of the American College of Cardiology, 2004-03, Vol.43 (6), p.943-949

2004

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Influence of residual stenosis in determining restenosis after cutting balloon angioplasty

Catheterization and cardiovascular interventions, 2000-04, Vol.49 (4), p.410-414

2000

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Long-chain fatty acid oxidation during early human development

Pediatric research, 2005-06, Vol.57 (6), p.753-754

2005

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Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse)

Human molecular genetics, 2003-12, Vol.12 (23), p.3173-3180

2003

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Consensus of the Spanish society of laboratory medicine and the Spanish society of medical oncology on the methodology and criteria for evaluation of circulating tumour markers in breast cancer

Pro-gastrin-releasing Peptide (ProGRP) in Patients with Benign and Malignant Diseases: Comparison with CEA, SCC, CYFRA 21-1 and NSE in Patients with Lung Cancer

Serum Protein S-100 Predicts Clinical Outcome in Patients with Melanoma Treated with Adjuvant Interferon – Comparison with Tyrosinase RT-PCR

Melanoma Inhibiting Activity Protein (MIA), Beta-2 Microglobulin and Lactate Dehydrogenase (LDH) in Metastatic Melanoma

Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing Holoprosencephaly

Tumor markers (CEA, CA 125, CYFRA 21-1, SCC and NSE) in patients with non-small cell lung cancer as an aid in histological diagnosis and prognosis: Comparison with the main clinical and pathological prognostic factors

Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain

Variability of assay methods for total and free PSA after WHO standardization

Pro-Gastrin-Releasing Peptide in Patients with Benign and Malignant Diseases

PAX8, TITF1, and FOXE1 Gene Expression Patterns during Human Development: New Insights into Human Thyroid Development and Thyroid Dysgenesis-Associated Malformations

PAX2 mutations in renal-coloboma syndrome: mutational hotspot and germline mosaicism

Reticular drusen over time with SD-OCT

Significance of Angiographic Coronary Dissection After Cutting Balloon Angioplasty

Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome

Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental Retardation

Interstitial duplication of the short arm of chromosome 2: report of a new case and review

Spectrum of Alcohol-Induced Myocardial Damage Detected by Indium-111–Labeled Monoclonal Antimyosin Antibodies

Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome

Impact of Ultrasensitive Cardiac Troponin I Dynamic Changes in the New Universal Definition of Myocardial Infarction

Coronary stenting for symptomatic myocardial bridging

Efficacy of augmented immunosuppressive therapy for early vasculopathy in heart transplantation

Cutting balloon versus conventional balloon angioplasty for the treatment of in-stent restenosis: Results of the Restenosis Cutting Balloon Evaluation Trial (RESCUT)

Influence of residual stenosis in determining restenosis after cutting balloon angioplasty

Long-chain fatty acid oxidation during early human development

Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse)

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