Dirk Prawitt
Mainz, RP 55121, Germany
Last Updated: 09/26/2026
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Found 32 publications
Expression, transport, and storage of fetuin-B in human granulosa cells.
Journal: Scientific reports
Published: January 28, 2025
Molecular mechanisms of human overgrowth and use of omics in its diagnostics: chances and challenges.
Journal: Frontiers in genetics
Published: February 05, 2024
Further understanding of paternal uniparental disomy in Beckwith-Wiedemann syndrome.
Journal: Expert review of endocrinology & metabolism
Published: November 15, 2022
Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives.
Journal: Endocrine connections
Published: August 30, 2022
Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation.
Journal: EXCLI journal
Published: November 02, 2021
Correction to: Molecular karyotyping and gene expression analysis in childhood cancer patients.
Journal: Journal of molecular medicine (Berlin, Germany)
Published: September 26, 2020
Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN).
Journal: Orphanet journal of rare diseases
Published: March 06, 2020
Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany: a retrospective cohort study.
Journal: British journal of cancer
Published: December 17, 2019
In renal cell carcinoma the PTEN splice variant PTEN-Δ shows similar function as the tumor suppressor PTEN itself.
Journal: Cell communication and signaling : CCS
Published: June 04, 2018
Beckwith-Wiedemann Syndrome (BWS) Current Status of Diagnosis and Clinical Management: Summary of the First International Consensus Statement
Journal: Klinische Padiatrie
Published: April 17, 2018
Last Updated: 09/26/2026