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Génétique de l’hypertension artérielle

Annales d'endocrinologie, 2016-09, Vol.77 (4), p.239-240

Jeunemaitre, X., Pr

2016

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Inflammation and Hypertension: The Interplay of Interleukin-6, Dietary Sodium, and the Renin-Angiotensin System in Humans

American journal of hypertension, 2011-10, Vol.24 (10), p.1143-1148

2011

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A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma

Hormone and metabolic research, 2012-05, Vol.44 (5), p.359

2012

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Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56

Journal of internal medicine, 2021-05, Vol.289 (5), p.709-725

2021

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Bilateral Idiopathic Adrenal Hyperplasia: Genetics and Beyond

Hormone and metabolic research, 2015-12, Vol.47 (13), p.947

2015

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Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndrome

American journal of medical genetics. Part A, 2023-11, Vol.191 (11), p.2728-2735

2023

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A novel mutation in KLHL3 gene causes familial hyperkalemic hypertension

QJM : An International Journal of Medicine, 2016-07, Vol.109 (7), p.487-488

2016

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The R22X Mutation of the SDHD Gene in Hereditary Paraganglioma Abolishes the Enzymatic Activity of Complex II in the Mitochondrial Respiratory Chain and Activates the Hypoxia Pathway

American journal of human genetics, 2001-12, Vol.69 (6), p.1186-1197

2001

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[OP.LB01.10] THE SKIPPING OF EXON 9 IN CULLIN-3 CAUSES A SEVERE FORM OF FAMILIAL HYPERKALEMIC HYPERTENSION IN MICE

Journal of hypertension, 2016-09, Vol.34 Suppl 2 - ESH 2016 Abstract Book (Supplement 2), p.e38-e39

2016

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Polymorphisms in the serum- and glucocorticoid-inducible kinase 1 gene are associated with blood pressure and renin response to dietary salt intake

Journal of human hypertension, 2013-03, Vol.27 (3), p.176-180

2013

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Phenotypic variability and diffuse arterial lesions in a family with Loeys–Dietz syndrome type 4

Clinical genetics, 2017-03, Vol.91 (3), p.458-462

2017

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Inheritance of arterial lesions in renal fibromuscular dysplasia

Journal of human hypertension, 2007-05, Vol.21 (5), p.393-400

2007

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Lysine-Specific Demethylase 1: An Epigenetic Regulator of Salt-Sensitive Hypertension

American journal of hypertension, 2012-07, Vol.25 (7), p.812-817

2012

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[OP.LB01.12] CACNA1H MUTATIONS ARE ASSOCIATED WITH YOUNG ONSET AND FAMILIAL FORMS OF PRIMARY ALDOSTERONISM

Journal of hypertension, 2016-09, Vol.34 Suppl 2 - ESH 2016 Abstract Book (Supplement 2), p.e39-e39

2016

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[OP.1C.04] STRUCTURAL AND FUNCTIONAL ARTERIAL ABNORMALITIES IN FIBROMUSCULAR DYSPLASIA ARE IN THE CONTINUUM OF HYPERTENSION: AN IMAGING AND BIOMECHANICAL STUDY

Journal of hypertension, 2016-09, Vol.34 Suppl 2 - ESH 2016 Abstract Book (Supplement 2), p.e8-e9

2016

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6C.02: EXOME SEQUENCING IN SEVEN FAMILIES AND GENE-BASED ASSOCIATION STUDIES SUPPORT GENETIC HETEROGENEITY AND SUGGEST POSSIBLE CANDIDATES FOR FIBROMUSCULAR DYSPLASIA

Journal of hypertension, 2015-06, Vol.33 Suppl 1 - ESH 2015 Abstract Book (Supplement 1), p.e79-e79

2015

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6D.03: FLOW-MEDIATED DILATATION (FMD) AND ENDOTHELIUM-INDEPENDENT DILATATION (EID) IN PATIENTS WITH MULTIFOCAL FIBROMUSCULAR DYSPLASIA: A CROSS-SECTIONAL STUDY

Journal of hypertension, 2015-06, Vol.33 Suppl 1 - ESH 2015 Abstract Book (Supplement 1), p.e82-e83

2015

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[OP.7C.04] GENETIC ASSOCIATION STUDY IDENTIFIES COMMON VARIATION IN PHACTR1 TO ASSOCIATE WITH FIBROMUSCULAR DYSPLASIA

Journal of hypertension, 2016-09, Vol.34 Suppl 2 - ESH 2016 Abstract Book (Supplement 2), p.e91-e91

2016

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1A.01: MUTATIONS AFFECTING THE CONSERVED ACIDIC MOTIF OF WNK1 CAUSE INHERITED NORMOTENSIVE HYPERKALEMIC ACIDOSIS

Journal of hypertension, 2015-06, Vol.33 Suppl 1 - ESH 2015 Abstract Book (Supplement 1), p.e1-e1

2015

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Prevalence of primary hyperaldosteronism in mild to moderate hypertension without hypokalaemia

Journal of human hypertension, 2006-02, Vol.20 (2), p.129-136

2006

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Gordon syndrome: The importance of measuring blood pressure in children

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2016-08, Vol.23 (8), p.827-831

2016

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6C.01: CULLIN-3 MUTATIONS LEADING TO SKIPPING OF EXON 9 ARE RESPONSIBLE FOR SEVERE CASES OF FAMILIAL HYPERKALAEMIC HYPERTENSION

Journal of hypertension, 2015-06, Vol.33 Suppl 1 - ESH 2015 Abstract Book (Supplement 1), p.e79-e79

2015

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Compliance and pulse wave velocity assessed by MRI detect early aortic impairment in young patients with mutation of the smooth muscle myosin heavy chain

Journal of magnetic resonance imaging, 2008-11, Vol.28 (5), p.1180-1187

2008

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Presymptomatic genetic testing in minors at risk of paraganglioma and pheochromocytoma: our experience of oncogenetic multidisciplinary consultation

Hormone and metabolic research, 2012-05, Vol.44 (5), p.354

2012

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Contribution of genetic polymorphism in the renin-angiotensin system to the development of renal complications in insulin-dependent diabetes: Genetique de la Nephropathie Diabetique (GENEDIAB) study group

The Journal of clinical investigation, 1997-04, Vol.99 (7), p.1585-1595

1997

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Génétique de l’hypertension artérielle

Inflammation and Hypertension: The Interplay of Interleukin-6, Dietary Sodium, and the Renin-Angiotensin System in Humans

A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma

Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56

Bilateral Idiopathic Adrenal Hyperplasia: Genetics and Beyond

Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndrome

A novel mutation in KLHL3 gene causes familial hyperkalemic hypertension

The R22X Mutation of the SDHD Gene in Hereditary Paraganglioma Abolishes the Enzymatic Activity of Complex II in the Mitochondrial Respiratory Chain and Activates the Hypoxia Pathway

[OP.LB01.10] THE SKIPPING OF EXON 9 IN CULLIN-3 CAUSES A SEVERE FORM OF FAMILIAL HYPERKALEMIC HYPERTENSION IN MICE

Polymorphisms in the serum- and glucocorticoid-inducible kinase 1 gene are associated with blood pressure and renin response to dietary salt intake

Phenotypic variability and diffuse arterial lesions in a family with Loeys–Dietz syndrome type 4

Inheritance of arterial lesions in renal fibromuscular dysplasia

Lysine-Specific Demethylase 1: An Epigenetic Regulator of Salt-Sensitive Hypertension

[OP.LB01.12] CACNA1H MUTATIONS ARE ASSOCIATED WITH YOUNG ONSET AND FAMILIAL FORMS OF PRIMARY ALDOSTERONISM

[OP.1C.04] STRUCTURAL AND FUNCTIONAL ARTERIAL ABNORMALITIES IN FIBROMUSCULAR DYSPLASIA ARE IN THE CONTINUUM OF HYPERTENSION: AN IMAGING AND BIOMECHANICAL STUDY

6C.02: EXOME SEQUENCING IN SEVEN FAMILIES AND GENE-BASED ASSOCIATION STUDIES SUPPORT GENETIC HETEROGENEITY AND SUGGEST POSSIBLE CANDIDATES FOR FIBROMUSCULAR DYSPLASIA

6D.03: FLOW-MEDIATED DILATATION (FMD) AND ENDOTHELIUM-INDEPENDENT DILATATION (EID) IN PATIENTS WITH MULTIFOCAL FIBROMUSCULAR DYSPLASIA: A CROSS-SECTIONAL STUDY

[OP.7C.04] GENETIC ASSOCIATION STUDY IDENTIFIES COMMON VARIATION IN PHACTR1 TO ASSOCIATE WITH FIBROMUSCULAR DYSPLASIA

1A.01: MUTATIONS AFFECTING THE CONSERVED ACIDIC MOTIF OF WNK1 CAUSE INHERITED NORMOTENSIVE HYPERKALEMIC ACIDOSIS

Prevalence of primary hyperaldosteronism in mild to moderate hypertension without hypokalaemia

Gordon syndrome: The importance of measuring blood pressure in children

6C.01: CULLIN-3 MUTATIONS LEADING TO SKIPPING OF EXON 9 ARE RESPONSIBLE FOR SEVERE CASES OF FAMILIAL HYPERKALAEMIC HYPERTENSION

Compliance and pulse wave velocity assessed by MRI detect early aortic impairment in young patients with mutation of the smooth muscle myosin heavy chain

Presymptomatic genetic testing in minors at risk of paraganglioma and pheochromocytoma: our experience of oncogenetic multidisciplinary consultation

Contribution of genetic polymorphism in the renin-angiotensin system to the development of renal complications in insulin-dependent diabetes: Genetique de la Nephropathie Diabetique (GENEDIAB) study group

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