Juan Politei - Concepedia

Author

Juan Politei

Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia ORCID

Also Known As

Francisca Masllorens, J. M. Politei, J. Politei, J.M. Politei, Juan M Politei, Juan M. POLITEI, Juan M. Politei, Juan Manuel Politei, Juan Politei

171

Publications

Citations

H-Index

Concepts

All Affiliations

Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia Hospital Fernández Hospital Universitario Fundación Jiménez Díaz Universidad Autónoma de Madrid Hospital Británico de Buenos Aires

About

Juan Politei is an author at Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia specializing in medicine, pathology, and renal pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	155
2	Public Health	2	2	29
3	Engineering	1	1	19
4	Health Sciences	1	1	22
5	Anatomy	1	1	22

Juan Politei

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Stroke in Fabry Disease Frequently Occurs Before Diagnosis and in the Absence of Other Clinical Events Katherine B. Sims, Juan Politei, Maryam Banikazemi, Stroke	2009	331
Screening, diagnosis, and management of patients with Fabry disease: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference Raphael Schiffmann, Derralynn Hughes, Gabor E. Linthorst, Kidney International	2016	175
Time to treatment benefit for adult patients with Fabry disease receiving agalsidase β: data from the Fabry Registry Alberto Ortíz, Ademola K. Abiose, Daniel G. Bichet, Journal of Medical Genetics	2016	144
Pain in Fabry Disease: Practical Recommendations for Diagnosis and Treatment Juan Politei, Didier Bouhassira, Dominique P. Germain, CNS Neuroscience & Therapeutics	2016	112
Foot Process Effacement Is an Early Marker of Nephropathy in Young Classic Fabry Patients without Albuminuria Camilla Tøndel, Takahiro Kanai, Kristin Kampevold Larsen, The Nephron journals/Nephron journals	2014	97
Use of a rare disease registry for establishing phenotypic classification of previously unassigned <i>GLA</i> variants: a consensus classification system by a multispecialty Fabry disease genotype–phenotype workgroup Dominique P. Germain, João Paulo Oliveira, Daniel G. Bichet, Journal of Medical Genetics	2020	63
Familial gain-of-function Na<sub>v</sub>1.9 mutation in a painful channelopathy Chongyang Han, Yang Yang, René H te Morsche, Journal of Neurology Neurosurgery & Psychiatry	2016	60
Determinants of white matter hyperintensity burden in patients with Fabry disease Natalia S. Rost, Lisa Cloonan, Allison Kanakis, Neurology	2016	57
Podocyturia is significantly elevated in untreated vs treated Fabry adult patients Hernán Trimarchi, Romina Canzonieri, Amalia Schiel, Journal of Nephrology	2016	50
Increased urinary CD80 excretion and podocyturia in Fabry disease Hernán Trimarchi, Romina Canzonieri, Amalia Schiel, Journal of Translational Medicine	2016	38

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