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Influence of the exon 3 deletion of GH receptor and IGF-I level at diagnosis on the efficacy and safety of treatment with somatotropin in adults with GH deficiency

Pituitary, 2015-02, Vol.18 (1), p.101-107

2015

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Use of chemometric analyses to assess biological wastewater treatment plants by protozoa and metazoa monitoring

Environmental monitoring and assessment, 2018-09, Vol.190 (9), p.497-15, Article 497

2018

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Genetic basis of short stature

Journal of endocrinological investigation, 2005, Vol.28 (5 Suppl), p.30-37

2005

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LightCycler PCR assay for genotyping codon 634 mutations in the RET protooncogene

Clinical chemistry (Baltimore, Md.), 2001-06, Vol.47 (6), p.1131-1132

2001

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Novel mutation involving the translation initiation codon of the growth hormone receptor gene (GHR) in a patient with Laron syndrome

Journal of pediatric endocrinology & metabolism : JPEM, 2002-07, Vol.15 (7), p.1041

2002

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P.2.b.043 - Dysthymia and double depression in a mental health unit

European neuropsychopharmacology, 2017-10, Vol.27, p.S809-S809

2017

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Dysthymia and double depression in a mental health unit

European neuropsychopharmacology, 2017-10, Vol.27, p.S809

2017

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Numerical analysis of alternative mining sequences to minimise potential for fault slip rockbursting

Mining Technology (Transactions of the Institution of Mining and Metallurgy, Section A), 2012-01, Vol.121 (4), p.226-235

2012

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Therapeutic optimization of growth hormone deficiency in children and adolescents

Journal of pediatric endocrinology & metabolism : JPEM, 2004-03, Vol.17 Suppl 3, p.401

2004

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Gene by Environment Interaction: The −159C/T Polymorphism in the Promoter Region of the CD14 Gene Modifies the Effect of Alcohol Consumption on Serum IgE Levels

Alcoholism, clinical and experimental research, 2006-01, Vol.30 (1), p.7-14

2006

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The −159C/T Polymorphism in the Promoter Region of the CD14 Gene Is Associated With Advanced Liver Disease and Higher Serum Levels of Acute-Phase Proteins in Heavy Drinkers

Alcoholism, clinical and experimental research, 2005-07, Vol.29 (7), p.1206-1213

2005

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High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect

Clinical endocrinology (Oxford), 2006-03, Vol.64 (3), p.330-336

2006

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LIF, a Novel STAT5-Regulated Gene, Is Aberrantly Expressed in Myeloproliferative Neoplasms

Genes & cancer, 2011-05, Vol.2 (5), p.593-596

2011

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Interferences of bilirubin, ascorbic acid, dipyrone, and D-penicillamine in two assays of 5'-nucleotidase

Clinical chemistry (Baltimore, Md.), 1993-05, Vol.39 (5), p.906

1993

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Screening of JAK2 V617F Mutation in 84 Patients with Thrombocythemia and Erythrocytosis. Is Necesary for Diagnosis of a Chronic Myeloproliferative Disorders?

Blood, 2006-11, Vol.108 (11), p.4891-4891

2006

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Relation of tumor necrosis factor (TNF) gene polymorphisms with serum concentrations and in vitro production of TNF-alpha and interleukin-8 in heavy drinkers

Alcohol (Fayetteville, N.Y.), 2004-10, Vol.34 (2), p.273-277

2004

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Kallmann's syndrome with a novel missense mutation in the KAL1 gene that modifies the major cell adhesion site of the anosmin-1 protein

Journal of pediatric endocrinology & metabolism : JPEM, 2005-06, Vol.18 (6), p.545

2005

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Determination of oligosaccharides in Brazilian honeys of different botanical origin

Food chemistry, 2000-07, Vol.70 (1), p.93-98

2000

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Nell’acromegalia la delezione dell’esone 3 del recettore del GH si associa a una migliore risposta alla terapia con pegvisomant

L'Endocrinologo, 2010-10, Vol.11 (5), p.231-232

2010

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Nell’acromegalia la delezione dell’esone 3 del recettore del GH si associa a una migliore risposta alla terapia con pegvisomant

L'Endocrinologo, 2010-08, Vol.11 (4), p.182-183

2010

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High serum IgA concentrations in patients with diabetes mellitus: agewise distribution and relation to chronic complications

Clinical chemistry (Baltimore, Md.), 1996-07, Vol.42 (7), p.1064-1067

1996

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The C494F variant in the CYP11B1 gene is a sequence polymorphism in the Spanish population

The journal of clinical endocrinology and metabolism, 1999-12, Vol.84 (12), p.4749-4749

1999

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Effect of 5-caffeoylquinic acid on soybean oil oxidative stability

International journal of food science & technology, 1997-02, Vol.32 (1), p.15-19

1997

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Determination of non-volatile compounds of different botanical origin Brazilian honeys

Food chemistry, 1999-05, Vol.65 (3), p.347-352

1999

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Morris syndrome

Anales de pediatría (Barcelona, Spain : 2003), 2003-10, Vol.59 (4), p.403

2003

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Influence of the exon 3 deletion of GH receptor and IGF-I level at diagnosis on the efficacy and safety of treatment with somatotropin in adults with GH deficiency

Use of chemometric analyses to assess biological wastewater treatment plants by protozoa and metazoa monitoring

Genetic basis of short stature

LightCycler PCR assay for genotyping codon 634 mutations in the RET protooncogene

Novel mutation involving the translation initiation codon of the growth hormone receptor gene (GHR) in a patient with Laron syndrome

P.2.b.043 - Dysthymia and double depression in a mental health unit

Dysthymia and double depression in a mental health unit

Numerical analysis of alternative mining sequences to minimise potential for fault slip rockbursting

Therapeutic optimization of growth hormone deficiency in children and adolescents

Gene by Environment Interaction: The −159C/T Polymorphism in the Promoter Region of the CD14 Gene Modifies the Effect of Alcohol Consumption on Serum IgE Levels

The −159C/T Polymorphism in the Promoter Region of the CD14 Gene Is Associated With Advanced Liver Disease and Higher Serum Levels of Acute-Phase Proteins in Heavy Drinkers

High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect

LIF, a Novel STAT5-Regulated Gene, Is Aberrantly Expressed in Myeloproliferative Neoplasms

Interferences of bilirubin, ascorbic acid, dipyrone, and D-penicillamine in two assays of 5'-nucleotidase

Screening of JAK2 V617F Mutation in 84 Patients with Thrombocythemia and Erythrocytosis. Is Necesary for Diagnosis of a Chronic Myeloproliferative Disorders?

Relation of tumor necrosis factor (TNF) gene polymorphisms with serum concentrations and in vitro production of TNF-alpha and interleukin-8 in heavy drinkers

Kallmann's syndrome with a novel missense mutation in the KAL1 gene that modifies the major cell adhesion site of the anosmin-1 protein

Determination of oligosaccharides in Brazilian honeys of different botanical origin

Nell’acromegalia la delezione dell’esone 3 del recettore del GH si associa a una migliore risposta alla terapia con pegvisomant

Nell’acromegalia la delezione dell’esone 3 del recettore del GH si associa a una migliore risposta alla terapia con pegvisomant

High serum IgA concentrations in patients with diabetes mellitus: agewise distribution and relation to chronic complications

The C494F variant in the CYP11B1 gene is a sequence polymorphism in the Spanish population

Effect of 5-caffeoylquinic acid on soybean oil oxidative stability

Determination of non-volatile compounds of different botanical origin Brazilian honeys

Morris syndrome

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