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Seventy years of pheochromocytomas and paragangliomas in Argentina. The FRENAR database

Hipertensión y riesgo vascular, 2024-07, Vol.41 (3), p.170-178

2024

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Carcinoma medular de tiroides: estudio multicéntrico. Presentación y evolución en 219 pacientes

Revista argentina de endocrinología y metabolismo, 2013-07, Vol.50 (2), p.63-70

2013

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Prehepatic portal hypertension in rats modifies norepinephrine metabolism in hypothalamus medulla oblongata and portal vein

Digestive diseases and sciences, 1993-07, Vol.38 (7), p.1259-1262

1993

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Prenatal screening for congenital heart disease with four‐chamber and outflow‐tract views: a multicenter study

Ultrasound in obstetrics & gynecology, 2006-11, Vol.28 (6), p.779-784

2006

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Allele-Specific Amplification (AS-PCR) for Point Mutation Screening of G Protein α-Subunit (Gsα) in McCune-Albright Syndrome (MAS)

Pediatric research, 1999-03, Vol.45 (3), p.441-441

1999

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Calcium-dependent diuretic system in preascitic liver cirrhosis

Journal of hepatology, 2010-11, Vol.53 (5), p.856-862

2010

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Familial isolated pheochromocytoma presenting a new mutation in the von Hippel-Lindau gene

American journal of hypertension, 2004-12, Vol.17 (12), p.1107-1111

2004

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Stability of ursodeoxycholic acid 7-oleyl ester to enzymatic hydrolysis

Bollettino chimico farmaceutico, 1985-03, Vol.124 (3), p.150

1985

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Early diagnosis of multiple endocrine neoplasia type 2 (MEN 2) by detection of mutated RET proto-oncogene carriers

Medicina (Buenos Aires), 1998, Vol.58 (2), p.179

1998

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Very early detection of RET proto-oncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children presence of c-cell malignant disease in asymptomatic carriers

Cancer, 2002-01, Vol.94 (2), p.323-330

2002

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The C105fs114X is the prevalent thyrotropin beta-subunit gene mutation in Argentinean patients with congenital central hypothyroidism

Hormone research, 2004-01, Vol.61 (1), p.41-46

2004

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Accuracy of routine ultrasonography in screening heart disease prenatally

Prenatal diagnosis, 1997-10, Vol.17 (10), p.901-906

1997

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Early Diagnosis of Multiple Endocrine Neoplasia Type 2 by Detection of Mutated Ret Proto-Oncogen Carriers

Pediatric research, 1999-03, Vol.45 (3), p.439-439

1999

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Hormonal profiles in Italian late-onset adrenal hyperplasia correlate with HLA class III polymorphisms

Gynecological endocrinology, 1992, Vol.6 (2), p.91-98

1992

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Diagnosis of G-Protein Gene Mutations in Mc Cune-Albright Syndrome. 15

Pediatric research, 1998-02, Vol.43 (2), p.297-297

1998

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3D structures of individual mammalian genomes studied by single-cell Hi-C

Nature (London), 2017-04, Vol.544 (7648), p.59-64

2017

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Thyroid performance in an iodine-rich environment (Salsomaggiore spa)

The Journal of nuclear medicine and allied sciences, 1977-01, Vol.21 (1-2), p.30

1977

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Open access to regional geoid models: the International Service for the Geoid

Earth system science data, 2021-04, Vol.13 (4), p.1653-1666

2021

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Promoter bivalency favors an open chromatin architecture in embryonic stem cells

Nature genetics, 2018-10, Vol.50 (10), p.1452-1462

2018

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Chromatographic identification of cysteine, also in the presence of cystine and other amino acids

Bollettino chimico farmaceutico, 1970-04, Vol.109 (4), p.266

1970

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Behavior of the serum immunoglobulins in cases of malignant neoplasms

Rivista di anatomia patologica e di oncologia, 1967-03, Vol.31 (3), p.331

1967

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Evaluation of tsunami flooding using geomorphologic evidence

Marine geology, 2009-05, Vol.260 (1), p.6-18

2009

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Geodetic Boundary Value Problems in View of the One Centimeter Geoid

2005

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Geodetic Boundary Value Problem: the Equivalence between Molodensky’s and Helmert’s Solutions

2016

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Seventy years of pheochromocytomas and paragangliomas in Argentina. The FRENAR database

Carcinoma medular de tiroides: estudio multicéntrico. Presentación y evolución en 219 pacientes

A HIF1α Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas

Prehepatic portal hypertension in rats modifies norepinephrine metabolism in hypothalamus medulla oblongata and portal vein

Prenatal screening for congenital heart disease with four‐chamber and outflow‐tract views: a multicenter study

Allele-Specific Amplification (AS-PCR) for Point Mutation Screening of G Protein α-Subunit (Gsα) in McCune-Albright Syndrome (MAS)

Calcium-dependent diuretic system in preascitic liver cirrhosis

Familial isolated pheochromocytoma presenting a new mutation in the von Hippel-Lindau gene

Stability of ursodeoxycholic acid 7-oleyl ester to enzymatic hydrolysis

Early diagnosis of multiple endocrine neoplasia type 2 (MEN 2) by detection of mutated RET proto-oncogene carriers

Very early detection of RET proto-oncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children presence of c-cell malignant disease in asymptomatic carriers

The C105fs114X is the prevalent thyrotropin beta-subunit gene mutation in Argentinean patients with congenital central hypothyroidism

Accuracy of routine ultrasonography in screening heart disease prenatally

Early Diagnosis of Multiple Endocrine Neoplasia Type 2 by Detection of Mutated Ret Proto-Oncogen Carriers

Hormonal profiles in Italian late-onset adrenal hyperplasia correlate with HLA class III polymorphisms

Diagnosis of G-Protein Gene Mutations in Mc Cune-Albright Syndrome. 15

3D structures of individual mammalian genomes studied by single-cell Hi-C

Thyroid performance in an iodine-rich environment (Salsomaggiore spa)

Open access to regional geoid models: the International Service for the Geoid

Promoter bivalency favors an open chromatin architecture in embryonic stem cells

Chromatographic identification of cysteine, also in the presence of cystine and other amino acids

Behavior of the serum immunoglobulins in cases of malignant neoplasms

Evaluation of tsunami flooding using geomorphologic evidence

Geodetic Boundary Value Problems in View of the One Centimeter Geoid

Geodetic Boundary Value Problem: the Equivalence between Molodensky’s and Helmert’s Solutions

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