HELPSCIENTIFIC DISCOVERY

Virtually every element of the world around us that has advanced in any meaningful way ...

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WHAT WE DORESEARCH INTERESTS

Our major research interests are (1) to uncover fundamental principles of clinical pediatric research and (2) to enable such studies ...

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RESEARCH INRARE PEDIATRIC GENETIC DISEASES

Welcome to Ped Mind Institute,

Human genom include 3.1 Milliards paired bases in a simple chromosom set. To date, there are known more than 6100 rare genetic diseases in human being, whereas 70 % of them are found exclusively in children. Nearly 15 % of all children treated in intensive care units have a rare genetic disease. The diagnosis of a rare genetic disease is difficult due to the variability of the diseases.

Ped Mind Institute focus on innovative research in rare genetic diseases in children.

Ped Mind Institute was established in 2010 to take care for children, who have born with a rare genetic disease or syndrome like Allan-Herndon Dudley syndrome, Hutchinson-Gilford syndrome, Kawasaki disease and others.

Since 2010, we spend enormous engagement in genetic rare diseases in pediatric patients and established scientific cooperations all over the world. We aim to find innovative genetic therapies and targets for treatment and follow innovative new aspects of research.

The best for our children.

Best wishes,

Prof. Stefan Bittmann M.A.
Professor for Pediatrics
Head of Department of Pediatrics and Ped Mind institute (PMI)
Visiting Professor, Faculty of Medicine, Shangluo Vocational and Technical College (SVTC), Shangluo, China

Last publications

    • Stefan Bittmann, Elisabeth Luchter, Elena Moschüring:
    • A New Heterozygous Duplication Variant c.953G>A p.(Arg318His) in MECP2 Gene in a 6 Years-Old Female Confirming Rett Syndrome
    • Novel Research in Sciences, 16 (4). NRS.000892 (2024)
    • Stefan Bittmann:
    • The Role of Synaptic Cargo Transporters in Regulating Neuronal Excitation/Inhibition Balance in Autism Spectrum Disorders: A Focus on Syntabulin syntaxin 1 A/B Axis
    • Asian Journal of Pediatric Research, Volume 14, Issue 12, Page 37-46, 2024; Article no.AJPR.126643
    • Stefan Bittmann:
    • The Role of Synaptic Dysfunction as a Key Driver in Autism Pathogenesis
    • Asian Journal of Pediatric Research, Volume 14, Issue 11, Page 55-67, 2024; Article no.AJPR.126641

Editorial engagement (last)

    • Editorial Board Member
    • Chinese Journal of Contemporary Pediatrics
    • (Oct.1, 2024 - Sep.30, 2027)
    • Organizing Committee Member
    • Advanced Pediatrics and Neonatology
    • October 21-22, 2024 | Rome, Italy
    • Reviewer
    • Springer Nature
    • Guest Editor for „Special Issue“, CHILDREN, MDPI
    • Kawasaki Disease in Children: Advance and Challenges

Advances in Pediatric Research

    • Bittmann S, Liuchter E:
    • An innovative new technique of pediatric vaccination: Take both hands and hold the needle to avoid damage of nociceptors and capillaries
    • Editorial as Editor-in Chief; Advances in Pediatric Research, Special Issue „Insights in Pediatric Research and Vaccine Pain Management in Children“, accepted 5/2019
    • Bittmann S
    • The origin of Alice in Wonderland Syndrome: Charles Dodgson and his attraction to small children
    • Editorial, Advances in Pediatric Research 5:24, 2019

Contact

Stefan Bittmann, M.D., M.A.
Hindenburgring 4
48599 Gronau, Germany

  +49 2565 97323
  +49 2565 97324
  info@ped-mind-institute.de