Advanced in Chromosome 4q Deletion

Philippe Loget

Rennes, FR 
Advanced in Chromosome 4q Deletion
Rennes, FR 
OverviewLocationsClinical Research

Overview

Philippe Loget practices in Rennes, France. Mr. Loget is rated as an Advanced expert by MediFind in the treatment of Chromosome 4q Deletion. His top areas of expertise are Pallister-Hall Syndrome, Lissencephaly 2, Potter Syndrome, and Bilateral Renal Agenesis Dominant Type.

His clinical research consists of co-authoring 45 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Chromosome 4q Deletion.

Gender
Male

Locations

Rennes, France
Other Locations
Nantes, France
Besancon, France

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

1 Clinical Trials

Congenital Malformations and Intrauterine Pollutants Exposure (Alcohol, Solvents and Pesticides) in Brittany. Population Based Case-control Study Short Title : Malformations and Environment Acronym : PENEW for Pregnancy Environment and Newborn Malformations
Congenital Malformations and Intrauterine Pollutants Exposure (Alcohol, Solvents and Pesticides) in Brittany. Population Based Case-control Study Short Title : Malformations and Environment Acronym : PENEW for Pregnancy Environment and Newborn Malformations
Enrollment Status: Completed
Publish Date: May 24, 2023
Intervention Type: Other
Study Phase: Not Applicable

45 Total Publications

Characterization of autopsy findings including multivisceral glomeruloid vascular bodies in hereditary thrombotic thrombocytopenic purpura with two new variants in ADAMTS13 gene.
Characterization of autopsy findings including multivisceral glomeruloid vascular bodies in hereditary thrombotic thrombocytopenic purpura with two new variants in ADAMTS13 gene.
Journal: Virchows Archiv : an international journal of pathology
Published: May 26, 2025

Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

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