Béatrice Fiquet‐Kempf

Author

Also Known As

B Fiquet-Kempf, B. Fiquet-Kempf, B??atrice Fiquet-Kempf, Beatrice Fiquet-Kempf, Béatrice Fiquet-Kempf, Béatrice Fiquet‐Kempf

Publications

491

Citations

H-Index

Concepts

All Affiliations

Hôpital Européen Inserm Hôpital Européen Georges-Pompidou Collège de France Assistance Publique – Hôpitaux de Paris

About

Béatrice Fiquet‐Kempf is an author at Hôpital Européen specializing in hypertension, medicine, and cardiovascular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	147
2	Health Sciences	1	1	98
3	Public Health	1	1	36
4	Biostatistics	1	1	36
5	Endocrinology	1	1	98

Béatrice Fiquet‐Kempf

Publications

473

Citations

H-Index

Page 1

	Year	Citations
Possible familial origin of multifocal renal artery fibromuscular dysplasia I Pannier-Moreau, Philippe Grimbert, Béatrice Fiquet‐Kempf, Journal of Hypertension	1997	136
Apparent Mineralocorticoid Excess Gilles Morineau, V. Sulmont, Rémi Salomon, Journal of the American Society of Nephrology HypertensionElectrolyte DisorderApparent Mineralocorticoid ExcessOsteoporosisMetabolic Syndrome	2006	98
Phenotypic And Genetic Heterogeneity Of Familial Hyperkalaemic Hypertension (Gordon Syndrome) Jean‐Michel Achard, Sandra Disse-Nicodème, Béatrice Fiquet‐Kempf, Clinical and Experimental Pharmacology and Physiology	2001	86
Evidence for carotid and radial artery wall subclinical lesions in renal fibromuscular dysplasia Pierre Boutouyrie, Anne‐Paule Gimenez‐Roqueplo, Erika Fine, Journal of Hypertension	2003	53
Genetic heterogeneity of familial hyperkalaemic hypertension Sandra Disse-Nicodème, Isabelle Desitter, Béatrice Fiquet‐Kempf, Journal of Hypertension HypertensionGeneticsGenetic EpidemiologyHuman PolymorphismGenetic Linkage	2001	36
α1-antitrypsin gene polymorphisms are not associated with renal arterial fibromuscular dysplasia Jérôme Perdu, Anne‐Paule Gimenez‐Roqueplo, Pierre Boutouyrie, Journal of Hypertension	2006	35
Is Primary Aldosteronism Underdiagnosed In Clinical Practice? Béatrice Fiquet‐Kempf, P Launay-Mignot, Guillaume Bobrie, Clinical and Experimental Pharmacology and Physiology	2001	16
Familial hyperkalemic hypertension (Gordon syndrome): evidence for phenotypic variability in a study of 7 families. Sandra Disse-Nicodème, Achard Jm, Julie F. N. Potier, PubMed HypertensionGordon SyndromeGenetic DisorderGeneticsGenetic Epidemiology	2001	13

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