Concepedia

Author

Milka Pringsheim

Schön Klinik Vogtareuth

Also Known As

Milka Pringsheim, Pringsheim, Milka

36

Publications

566

Citations

11

H-Index

8

Concepts

All Affiliations

Schön Klinik VogtareuthDeutsches Herzzentrum MünchenGoethe University FrankfurtUniversity of FreiburgParacelsus Medical University
MP

About

Milka Pringsheim is an author at Schön Klinik Vogtareuth specializing in molecular genetics, monogenic disorders, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

1

1

108

2

Public Health

1

1

108

3

Molecular Genetics

1

1

108

4

Pathology

1

1

108

5

Clinical Genetics

1

1

108

Milka Pringsheim

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9

Publications

433

Citations

9

H-Index

YearCitations

FOXG1 syndrome: genotype–phenotype association in 83 patients with FOXG1 variants

Diana Mitter, Milka Pringsheim, Marc Kaulisch,

Genetics in Medicine

2017

108

Fenfluramine HCl (Fintepla<sup>®</sup>) provides long‐term clinically meaningful reduction in seizure frequency: Analysis of an ongoing open‐label extension study

Joseph Sullivan, Ingrid E. Scheffer, Lieven Lagae,

Epilepsia

2020

64

Cardiovascular safety of fenfluramine in the treatment of Dravet syndrome: Analysis of an ongoing long‐term open‐label safety extension study

Wyman W. Lai, Bradley S. Galer, Pierre C. Wong,

Epilepsia

2020

45

Real‐world data on cannabidiol treatment of various epilepsy subtypes: A retrospective, multicenter study

Fabienne Kühne, Lena‐Luise Becker, Thomas Bast,

Epilepsia Open

2023

45

Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: Compassionate use program in Germany

Adam Strzelczyk, Milka Pringsheim, Tilman Polster,

Epilepsia

2021

39

An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a <scp>real‐world</scp> practice setting: A report from the Fenfluramine European Early Access Program

Renzo Guerrini, Nicola Specchio, Ángel Aledo‐Serrano,

Epilepsia Open

2022

39

Perampanel as precision therapy in rare genetic epilepsies

Andreea Nissenkorn, Gerhard Kluger, Susanne Schubert‐Bast,

Epilepsia

2023

38

Structural brain anomalies in patients with <scp>FOXG</scp>1 syndrome and in Foxg1+/− mice

Milka Pringsheim, Diana Mitter, Simone Schröder,

Annals of Clinical and Translational Neurology

2019

34

Motor training of sixty minutes once per week improves motor ability in children with congenital heart disease and retarded motor development: a pilot study

Jan Müller, Milka Pringsheim, Juliana Meixner,

Cardiology in the Young

2012

21

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